{ "disease_id": "DOID:0050737", "recommended_name": { "id": "DOID:0050737", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0050737", "name": "autosomal recessive disease", "description": "An autosomal genetic disease that is characterized by the presence of two mutated copies of the gene, both of which must be present in order for the disease or trait to develop." }, "synonyms": [], "children": [ { "id": "DOID:0050335", "label": "bradyopsia", "link_status": true, "children": [ { "id": "DOID:0070363", "label": "bradyopsia 1", "link_status": true, "children": [] }, { "id": "DOID:0070364", "label": "bradyopsia 2", "link_status": true, "children": [] } ] }, { "id": "DOID:0050427", "label": "xeroderma pigmentosum", "link_status": true, "children": [ { "id": "DOID:0110843", "label": "xeroderma pigmentosum group A", "link_status": true, "children": [] }, { "id": "DOID:0110844", "label": "xeroderma pigmentosum group C", "link_status": true, "children": [] }, { "id": "DOID:0110845", "label": "xeroderma pigmentosum group D", "link_status": true, "children": [] }, { "id": "DOID:0110846", "label": "xeroderma pigmentosum group E", "link_status": true, "children": [] }, { "id": "DOID:0110847", "label": "xeroderma pigmentosum variant type", "link_status": true, "children": [] }, { "id": "DOID:0110848", "label": "xeroderma pigmentosum group F", "link_status": true, "children": [] }, { "id": "DOID:0110849", "label": "xeroderma pigmentosum group G", "link_status": true, "children": [] }, { "id": "DOID:0110850", "label": "xeroderma pigmentosum group B", "link_status": true, "children": [] }, { "id": "DOID:0112158", "label": "De Sanctis-Cacchione syndrome", "link_status": true, "children": [] } ] }, { "id": "DOID:0050436", "label": "mulibrey nanism", "link_status": true, "children": [] }, { "id": "DOID:0050439", "label": "Usher syndrome", "link_status": true, "children": [ { "id": "DOID:0110826", "label": "Usher syndrome type 1", "link_status": true, "children": [ { "id": "DOID:0110830", "label": "Usher syndrome type 1C", "link_status": true, "children": [] }, { "id": "DOID:0110831", "label": "Usher syndrome type 1D", "link_status": true, "children": [] }, { "id": "DOID:0110832", "label": "Usher syndrome type 1F", "link_status": true, "children": [] }, { "id": "DOID:0110834", "label": "Usher syndrome type 1G", "link_status": true, "children": [] } ] }, { "id": "DOID:0110827", "label": "Usher syndrome type 2", "link_status": true, "children": [ { "id": "DOID:0110838", "label": "Usher syndrome type 2A", "link_status": true, "children": [] }, { "id": "DOID:0110839", "label": "Usher syndrome type 2C", "link_status": true, "children": [] }, { "id": "DOID:0110840", "label": "Usher syndrome type 2D", "link_status": true, "children": [] } ] }, { "id": "DOID:0110828", "label": "Usher syndrome type 3", "link_status": true, "children": [ { "id": "DOID:0110841", "label": "Usher syndrome type 3A", "link_status": true, "children": [] }, { "id": "DOID:0110842", "label": "Usher syndrome type 3B", "link_status": true, "children": [] } ] } ] }, { "id": "DOID:0050441", "label": "mucosulfatidosis", "link_status": true, "children": [] }, { "id": "DOID:0050450", "label": "Gitelman syndrome", "link_status": true, "children": [] }, { "id": "DOID:0050462", "label": "Antley-Bixler syndrome with disordered steroidogenesis", "link_status": true, "children": [] }, { "id": "DOID:0050470", "label": "Donohue syndrome", "link_status": true, "children": [] }, { "id": "DOID:0050473", "label": "Alstrom syndrome", "link_status": true, "children": [] }, { "id": "DOID:0050474", "label": "Netherton syndrome", "link_status": true, "children": [] }, { "id": "DOID:0050528", "label": "nonphotosensitive trichothiodystrophy 4", "link_status": true, "children": [] }, { "id": "DOID:0050529", "label": "adult spinal muscular atrophy", "link_status": true, "children": [] }, { "id": "DOID:0050530", "label": "intermediate spinal muscular atrophy", "link_status": true, "children": [] }, { "id": "DOID:0050540", "label": "Charcot-Marie-Tooth disease type 3", "link_status": true, "children": [] }, { "id": "DOID:0050546", "label": "congenital adrenal insufficiency", "link_status": true, "children": [] }, { "id": "DOID:0050553", "label": "proteasome-associated autoinflammatory syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0050558", "label": "Ullrich congenital muscular dystrophy", "link_status": true, "children": [ { "id": "DOID:0060942", "label": "Ullrich congenital muscular dystrophy 1B", "link_status": true, "children": [] }, { "id": "DOID:0060943", "label": "Ullrich congenital muscular dystrophy 1C", "link_status": true, "children": [] }, { "id": "DOID:0060946", "label": "Ullrich congenital muscular dystrophy 1A", "link_status": true, "children": [] }, { "id": "DOID:0060948", "label": "Ullrich congenital muscular dystrophy 2", "link_status": true, "children": [] } ] }, { "id": "DOID:0050560", "label": "Walker-Warburg syndrome", "link_status": true, "children": [] }, { "id": "DOID:0050565", "label": "autosomal recessive nonsyndromic deafness", "link_status": true, "children": [ { "id": "DOID:0061124", "label": "autosomal recessive nonsyndromic deafness 125", "link_status": true, "children": [] }, { "id": "DOID:0080261", "label": "autosomal recessive nonsyndromic deafness 106", "link_status": true, "children": [] }, { "id": "DOID:0080262", "label": "autosomal recessive nonsyndromic deafness 107", "link_status": true, "children": [] }, { "id": "DOID:0080263", "label": "autosomal recessive nonsyndromic deafness 108", "link_status": true, "children": [] }, { "id": "DOID:0110462", "label": "autosomal recessive nonsyndromic deafness 101", "link_status": true, "children": [] }, { "id": "DOID:0110463", "label": "autosomal recessive nonsyndromic deafness 102", "link_status": true, "children": [] }, { "id": "DOID:0110464", "label": "autosomal recessive nonsyndromic deafness 103", "link_status": true, "children": [] }, { "id": "DOID:0110465", "label": "autosomal recessive nonsyndromic deafness 104", "link_status": true, "children": [] }, { "id": "DOID:0110467", "label": "autosomal recessive nonsyndromic deafness 12", "link_status": true, "children": [] }, { "id": "DOID:0110470", "label": "autosomal recessive nonsyndromic deafness 15", "link_status": true, "children": [] }, { "id": "DOID:0110471", "label": "autosomal recessive nonsyndromic deafness 16", "link_status": true, "children": [] }, { "id": "DOID:0110473", "label": "autosomal recessive nonsyndromic deafness 18A", "link_status": true, "children": [] }, { "id": "DOID:0110474", "label": "autosomal recessive nonsyndromic deafness 18B", "link_status": true, "children": [] }, { "id": "DOID:0110475", "label": "autosomal recessive nonsyndromic deafness 1A", "link_status": true, "children": [] }, { "id": "DOID:0110476", "label": "autosomal recessive nonsyndromic deafness 1B", "link_status": true, "children": [] }, { "id": "DOID:0110477", "label": "autosomal recessive nonsyndromic deafness 2", "link_status": true, "children": [] }, { "id": "DOID:0110479", "label": "autosomal recessive nonsyndromic deafness 21", "link_status": true, "children": [] }, { "id": "DOID:0110480", "label": "autosomal recessive nonsyndromic deafness 22", "link_status": true, "children": [] }, { "id": "DOID:0110481", "label": "autosomal recessive nonsyndromic deafness 23", "link_status": true, "children": [] }, { "id": "DOID:0110482", "label": "autosomal recessive nonsyndromic deafness 24", "link_status": true, "children": [] }, { "id": "DOID:0110483", "label": "autosomal recessive nonsyndromic deafness 25", "link_status": true, "children": [] }, { "id": "DOID:0110484", "label": "autosomal recessive nonsyndromic deafness 26", "link_status": true, "children": [] }, { "id": "DOID:0110486", "label": "autosomal recessive nonsyndromic deafness 28", "link_status": true, "children": [] }, { "id": "DOID:0110487", "label": "autosomal recessive nonsyndromic deafness 29", "link_status": true, "children": [] }, { "id": "DOID:0110488", "label": "autosomal recessive nonsyndromic deafness 3", "link_status": true, "children": [] }, { "id": "DOID:0110489", "label": "autosomal recessive nonsyndromic deafness 30", "link_status": true, "children": [] }, { "id": "DOID:0110490", "label": "autosomal recessive nonsyndromic deafness 31", "link_status": true, "children": [] }, { "id": "DOID:0110491", "label": "autosomal recessive nonsyndromic deafness 32", "link_status": true, "children": [] }, { "id": "DOID:0110493", "label": "autosomal recessive nonsyndromic deafness 35", "link_status": true, "children": [] }, { "id": "DOID:0110494", "label": "autosomal recessive nonsyndromic deafness 36", "link_status": true, "children": [] }, { "id": "DOID:0110495", "label": "autosomal recessive nonsyndromic deafness 37", "link_status": true, "children": [] }, { "id": "DOID:0110497", "label": "autosomal recessive nonsyndromic deafness 39", "link_status": true, "children": [] }, { "id": "DOID:0110498", "label": "autosomal recessive nonsyndromic deafness 4", "link_status": true, "children": [] }, { "id": "DOID:0110500", "label": "autosomal recessive nonsyndromic deafness 42", "link_status": true, "children": [] }, { "id": "DOID:0110501", "label": "autosomal recessive nonsyndromic deafness 44", "link_status": true, "children": [] }, { "id": "DOID:0110505", "label": "autosomal recessive nonsyndromic deafness 48", "link_status": true, "children": [] }, { "id": "DOID:0110506", "label": "autosomal recessive nonsyndromic deafness 49", "link_status": true, "children": [] }, { "id": "DOID:0110509", "label": "autosomal recessive nonsyndromic deafness 53", "link_status": true, "children": [] }, { "id": "DOID:0110511", "label": "autosomal recessive nonsyndromic deafness 59", "link_status": true, "children": [] }, { "id": "DOID:0110512", "label": "autosomal recessive nonsyndromic deafness 6", "link_status": true, "children": [] }, { "id": "DOID:0110513", "label": "autosomal recessive nonsyndromic deafness 61", "link_status": true, "children": [] }, { "id": "DOID:0110515", "label": "autosomal recessive nonsyndromic deafness 63", "link_status": true, "children": [] }, { "id": "DOID:0110517", "label": "autosomal recessive nonsyndromic deafness 66", "link_status": true, "children": [] }, { "id": "DOID:0110518", "label": "autosomal recessive nonsyndromic deafness 67", "link_status": true, "children": [] }, { "id": "DOID:0110519", "label": "autosomal recessive nonsyndromic deafness 68", "link_status": true, "children": [] }, { "id": "DOID:0110520", "label": "autosomal recessive nonsyndromic deafness 7", "link_status": true, "children": [] }, { "id": "DOID:0110521", "label": "autosomal recessive nonsyndromic deafness 70", "link_status": true, "children": [] }, { "id": "DOID:0110523", "label": "autosomal recessive nonsyndromic deafness 74", "link_status": true, "children": [] }, { "id": "DOID:0110524", "label": "autosomal recessive nonsyndromic deafness 76", "link_status": true, "children": [] }, { "id": "DOID:0110525", "label": "autosomal recessive nonsyndromic deafness 77", "link_status": true, "children": [] }, { "id": "DOID:0110526", "label": "autosomal recessive nonsyndromic deafness 79", "link_status": true, "children": [] }, { "id": "DOID:0110527", "label": "autosomal recessive nonsyndromic deafness 8", "link_status": true, "children": [] }, { "id": "DOID:0110529", "label": "autosomal recessive nonsyndromic deafness 84A", "link_status": true, "children": [] }, { "id": "DOID:0110530", "label": "autosomal recessive nonsyndromic deafness 84B", "link_status": true, "children": [] }, { "id": "DOID:0110532", "label": "autosomal recessive nonsyndromic deafness 86", "link_status": true, "children": [] }, { "id": "DOID:0110533", "label": "autosomal recessive nonsyndromic deafness 88", "link_status": true, "children": [] }, { "id": "DOID:0110534", "label": "autosomal recessive nonsyndromic deafness 89", "link_status": true, "children": [] }, { "id": "DOID:0110535", "label": "autosomal recessive nonsyndromic deafness 9", "link_status": true, "children": [] }, { "id": "DOID:0110536", "label": "autosomal recessive nonsyndromic deafness 91", "link_status": true, "children": [] }, { "id": "DOID:0110537", "label": "autosomal recessive nonsyndromic deafness 93", "link_status": true, "children": [] }, { "id": "DOID:0110539", "label": "autosomal recessive nonsyndromic deafness 97", "link_status": true, "children": [] }, { "id": "DOID:0110540", "label": "autosomal recessive nonsyndromic deafness 98", "link_status": true, "children": [] }, { "id": "DOID:0111634", "label": "autosomal recessive nonsyndromic deafness 99", "link_status": true, "children": [] }, { "id": "DOID:0111635", "label": "autosomal recessive nonsyndromic deafness 57", "link_status": true, "children": [] }, { "id": "DOID:0111636", "label": "autosomal recessive nonsyndromic deafness 113", "link_status": true, "children": [] }, { "id": "DOID:0111637", "label": "autosomal recessive nonsyndromic deafness 112", "link_status": true, "children": [] }, { "id": "DOID:0111638", "label": "autosomal recessive nonsyndromic deafness 100", "link_status": true, "children": [] }, { "id": "DOID:0111639", "label": "autosomal recessive nonsyndromic deafness 109", "link_status": true, "children": [] }, { "id": "DOID:0111640", "label": "autosomal recessive nonsyndromic deafness 111", "link_status": true, "children": [] }, { "id": "DOID:0111641", "label": "autosomal recessive nonsyndromic deafness 94", "link_status": true, "children": [] }, { "id": "DOID:0111642", "label": "autosomal recessive nonsyndromic deafness 114", "link_status": true, "children": [] }, { "id": "DOID:0111643", "label": "autosomal recessive nonsyndromic deafness 115", "link_status": true, "children": [] }, { "id": "DOID:0111644", "label": "autosomal recessive nonsyndromic deafness 110", "link_status": true, "children": [] }, { "id": "DOID:0112162", "label": "autosomal recessive nonsyndromic deafness 116", "link_status": true, "children": [] } ] }, { "id": "DOID:0050569", "label": "Seckel syndrome", "link_status": true, "children": [ { "id": "DOID:0070005", "label": "Seckel syndrome 9", "link_status": true, "children": [] }, { "id": "DOID:0070006", "label": "Seckel syndrome 6", "link_status": true, "children": [] }, { "id": "DOID:0070007", "label": "Seckel syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0070008", "label": "Seckel syndrome 10", "link_status": true, "children": [] }, { "id": "DOID:0070009", "label": "Seckel syndrome 8", "link_status": true, "children": [] }, { "id": "DOID:0070010", "label": "Seckel syndrome 4", "link_status": true, "children": [] }, { "id": "DOID:0070011", "label": "Seckel syndrome 7", "link_status": true, "children": [] }, { "id": "DOID:0070012", "label": "Seckel syndrome 5", "link_status": true, "children": [] }, { "id": "DOID:0070013", "label": "Seckel syndrome 2", "link_status": true, "children": [] } ] }, { "id": "DOID:0050576", "label": "Senior-Loken syndrome", "link_status": true, "children": [] }, { "id": "DOID:0050577", "label": "cranioectodermal dysplasia", "link_status": true, "children": [ { "id": "DOID:0080803", "label": "cranioectodermal dysplasia 1", "link_status": true, "children": [] }, { "id": "DOID:0080804", "label": "cranioectodermal dysplasia 2", "link_status": true, "children": [] }, { "id": "DOID:0080805", "label": "cranioectodermal dysplasia 3", "link_status": true, "children": [] }, { "id": "DOID:0080806", "label": "cranioectodermal dysplasia 4", "link_status": true, "children": [] } ] }, { "id": "DOID:0050579", "label": "glycogen storage disease XV", "link_status": true, "children": [] }, { "id": "DOID:0050585", "label": "congenital generalized lipodystrophy", "link_status": true, "children": [ { "id": "DOID:0111135", "label": "congenital generalized lipodystrophy type 1", "link_status": true, "children": [] }, { "id": "DOID:0111136", "label": "congenital generalized lipodystrophy type 2", "link_status": true, "children": [] }, { "id": "DOID:0111137", "label": "congenital generalized lipodystrophy type 3", "link_status": true, "children": [] }, { "id": "DOID:0111138", "label": "congenital generalized lipodystrophy type 4", "link_status": true, "children": [] } ] }, { "id": "DOID:0050588", "label": "muscular dystrophy-dystroglycanopathy type B1", "link_status": true, "children": [] }, { "id": "DOID:0050600", "label": "ABCD syndrome", "link_status": true, "children": [] }, { "id": "DOID:0050602", "label": "triple-A syndrome", "link_status": true, "children": [] }, { "id": "DOID:0050603", "label": "acheiropody", "link_status": true, "children": [] }, { "id": "DOID:0050604", "label": "acrocapitofemoral dysplasia", "link_status": true, "children": [] }, { "id": "DOID:0050632", "label": "oculocutaneous albinism", "link_status": true, "children": [ { "id": "DOID:0070094", "label": "oculocutaneous albinism type IA", "link_status": true, "children": [] }, { "id": "DOID:0070095", "label": "oculocutaneous albinism type IB", "link_status": true, "children": [] }, { "id": "DOID:0070096", "label": "oculocutaneous albinism type II", "link_status": true, "children": [] }, { "id": "DOID:0070097", "label": "oculocutaneous albinism type III", "link_status": true, "children": [] }, { "id": "DOID:0070098", "label": "oculocutaneous albinism type IV", "link_status": true, "children": [] }, { "id": "DOID:0070100", "label": "oculocutaneous albinism type VII", "link_status": true, "children": [] }, { "id": "DOID:0080614", "label": "oculocutaneous albinism type VI", "link_status": true, "children": [] } ] }, { "id": "DOID:0050634", "label": "alopecia universalis", "link_status": true, "children": [] }, { "id": "DOID:0050649", "label": "atransferrinemia", "link_status": true, "children": [] }, { "id": "DOID:0050656", "label": "pseudo-TORCH syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0050677", "label": "Bjornstad syndrome", "link_status": true, "children": [] }, { "id": "DOID:0050682", "label": "Athabaskan brainstem dysgenesis syndrome", "link_status": true, "children": [] }, { "id": "DOID:0050684", "label": "Bowen-Conradi syndrome", "link_status": true, "children": [] }, { "id": "DOID:0050710", "label": "3-methylcrotonyl-CoA carboxylase deficiency", "link_status": true, "children": [ { "id": "DOID:0080579", "label": "3-methylcrotonyl-CoA carboxylase 1 deficiency", "link_status": true, "children": [] }, { "id": "DOID:0080580", "label": "3-methylcrotonyl-CoA carboxylase 2 deficiency", "link_status": true, "children": [] } ] }, { "id": "DOID:0050711", "label": "aceruloplasminemia", "link_status": true, "children": [] }, { "id": "DOID:0050712", "label": "AGAT deficiency", "link_status": true, "children": [] }, { "id": "DOID:0050719", "label": "cerebral folate receptor alpha deficiency", "link_status": true, "children": [] }, { "id": "DOID:0050763", "label": "ARC syndrome", "link_status": true, "children": [ { "id": "DOID:0111353", "label": "arthrogryposis, renal dysfunction, and cholestasis 1", "link_status": true, "children": [] }, { "id": "DOID:0111354", "label": "arthrogryposis, renal dysfunction, and cholestasis 2", "link_status": true, "children": [] } ] }, { "id": "DOID:0050766", "label": "choreaacanthocytosis", "link_status": true, "children": [] }, { "id": "DOID:0050774", "label": "rapadilino syndrome", "link_status": true, "children": [] }, { "id": "DOID:0050779", "label": "hydrolethalus syndrome", "link_status": true, "children": [ { "id": "DOID:0111355", "label": "hydrolethalus syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0111356", "label": "hydrolethalus syndrome 2", "link_status": true, "children": [] } ] }, { "id": "DOID:0050790", "label": "fibular hypoplasia and complex brachydactyly", "link_status": true, "children": [] }, { "id": "DOID:0050797", "label": "peroxisomal acyl-CoA oxidase deficiency", "link_status": true, "children": [] }, { "id": "DOID:0050802", "label": "Ehlers-Danlos syndrome spondylodysplastic type 2", "link_status": true, "children": [] }, { "id": "DOID:0050807", "label": "Kahrizi syndrome", "link_status": true, "children": [] }, { "id": "DOID:0050812", "label": "spondyloepimetaphyseal dysplasia, Pakistani type", "link_status": true, "children": [] }, { "id": "DOID:0050814", "label": "temtamy preaxial brachydactyly syndrome", "link_status": true, "children": [] }, { "id": "DOID:0050816", "label": "urofacial syndrome", "link_status": true, "children": [] }, { "id": "DOID:0050857", "label": "Perrault syndrome", "link_status": true, "children": [ { "id": "DOID:0061073", "label": "Perrault syndrome 7", "link_status": true, "children": [] }, { "id": "DOID:0061117", "label": "Perrault syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0080256", "label": "Perrault syndrome 6", "link_status": true, "children": [] } ] }, { "id": "DOID:0050883", "label": "infantile cerebellar-retinal degeneration", "link_status": true, "children": [] }, { "id": "DOID:0050886", "label": "Troyer syndrome", "link_status": true, "children": [] }, { "id": "DOID:0050941", "label": "spastic ataxia 2", "link_status": true, "children": [] }, { "id": "DOID:0050942", "label": "spastic ataxia 3", "link_status": true, "children": [] }, { "id": "DOID:0050943", "label": "spastic ataxia 4", "link_status": true, "children": [] }, { "id": "DOID:0050944", "label": "spastic ataxia 5", "link_status": true, "children": [] }, { "id": "DOID:0050949", "label": "autosomal recessive hypophosphatemic rickets", "link_status": true, "children": [] }, { "id": "DOID:0050950", "label": "autosomal recessive cerebellar ataxia", "link_status": true, "children": [ { "id": "DOID:0050754", "label": "early-onset ataxia with oculomotor apraxia and hypoalbuminemia", "link_status": true, "children": [] }, { "id": "DOID:0050755", "label": "spinocerebellar ataxia with axonal neuropathy 2", "link_status": true, "children": [] }, { "id": "DOID:0050946", "label": "Charlevoix-Saguenay spastic ataxia", "link_status": true, "children": [] }, { "id": "DOID:0050999", "label": "autosomal recessive spinocerebellar ataxia 10", "link_status": true, "children": [] }, { "id": "DOID:0060557", "label": "ataxia-oculomotor apraxia 3", "link_status": true, "children": [] }, { "id": "DOID:0060694", "label": "Cayman type cerebellar ataxia", "link_status": true, "children": [] }, { "id": "DOID:0070409", "label": "autosomal recessive spinocerebellar ataxia 28", "link_status": true, "children": [] }, { "id": "DOID:0070410", "label": "autosomal recessive spinocerebellar ataxia 29", "link_status": true, "children": [] }, { "id": "DOID:0070411", "label": "autosomal recessive spinocerebellar ataxia 30", "link_status": true, "children": [] }, { "id": "DOID:0070412", "label": "autosomal recessive spinocerebellar ataxia 31", "link_status": true, "children": [] }, { "id": "DOID:0070413", "label": "autosomal recessive spinocerebellar ataxia 32", "link_status": true, "children": [] }, { "id": "DOID:0070465", "label": "autosomal recessive spinocerebellar ataxia with axonal neuropathy 3", "link_status": true, "children": [] }, { "id": "DOID:0070558", "label": "autosomal recessive spinocerebellar ataxia 34", "link_status": true, "children": [] }, { "id": "DOID:0080029", "label": "autosomal recessive spinocerebellar ataxia 16", "link_status": true, "children": [] }, { "id": "DOID:0080042", "label": "autosomal recessive spinocerebellar ataxia 18", "link_status": true, "children": [] }, { "id": "DOID:0080057", "label": "autosomal recessive spinocerebellar ataxia 15", "link_status": true, "children": [] }, { "id": "DOID:0080058", "label": "autosomal recessive spinocerebellar ataxia 14", "link_status": true, "children": [] }, { "id": "DOID:0080059", "label": "autosomal recessive spinocerebellar ataxia 7", "link_status": true, "children": [] }, { "id": "DOID:0080060", "label": "autosomal recessive spinocerebellar ataxia 12", "link_status": true, "children": [] }, { "id": "DOID:0080061", "label": "autosomal recessive spinocerebellar ataxia 2", "link_status": true, "children": [] }, { "id": "DOID:0080062", "label": "autosomal recessive spinocerebellar ataxia 13", "link_status": true, "children": [] }, { "id": "DOID:0080063", "label": "autosomal recessive spinocerebellar ataxia 11", "link_status": true, "children": [] }, { "id": "DOID:0080064", "label": "autosomal recessive spinocerebellar ataxia 17", "link_status": true, "children": [] }, { "id": "DOID:0080065", "label": "autosomal recessive spinocerebellar ataxia 19", "link_status": true, "children": [] }, { "id": "DOID:0080066", "label": "autosomal recessive spinocerebellar ataxia 20", "link_status": true, "children": [] }, { "id": "DOID:0080259", "label": "autosomal recessive spinocerebellar ataxia 25", "link_status": true, "children": [] }, { "id": "DOID:0080260", "label": "autosomal recessive spinocerebellar ataxia 26", "link_status": true, "children": [] }, { "id": "DOID:0081383", "label": "ataxia-oculomotor apraxia 4", "link_status": true, "children": [] }, { "id": "DOID:0081384", "label": "ataxia-telangiectasia-like disorder 1", "link_status": true, "children": [] }, { "id": "DOID:0081385", "label": "ataxia-telangiectasia-like disorder 2", "link_status": true, "children": [] }, { "id": "DOID:0090115", "label": "spinocerebellar ataxia with axonal neuropathy 1", "link_status": true, "children": [] }, { "id": "DOID:0111155", "label": "autosomal recessive spinocerebellar ataxia 21", "link_status": true, "children": [] }, { "id": "DOID:0111611", "label": "autosomal recessive spinocerebellar ataxia 4", "link_status": true, "children": [] }, { "id": "DOID:0111613", "label": "autosomal recessive spinocerebellar ataxia 23", "link_status": true, "children": [] }, { "id": "DOID:0111614", "label": "autosomal recessive spinocerebellar ataxia 22", "link_status": true, "children": [] }, { "id": "DOID:0111615", "label": "autosomal recessive spinocerebellar ataxia 24", "link_status": true, "children": [] }, { "id": "DOID:0111616", "label": "autosomal recessive spinocerebellar ataxia 27", "link_status": true, "children": [] }, { "id": "DOID:0111618", "label": "autosomal recessive spinocerebellar ataxia 8", "link_status": true, "children": [] }, { "id": "DOID:12704", "label": "ataxia telangiectasia", "link_status": true, "children": [] }, { "id": "DOID:12705", "label": "Friedreich ataxia", "link_status": true, "children": [ { "id": "DOID:0111218", "label": "Friedreich ataxia 1", "link_status": true, "children": [] } ] } ] }, { "id": "DOID:0050997", "label": "cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome", "link_status": true, "children": [ { "id": "DOID:0070556", "label": "cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0070557", "label": "cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0070559", "label": "cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 4", "link_status": true, "children": [] } ] }, { "id": "DOID:0051001", "label": "congenital dyserythropoietic anemia type IIIb", "link_status": true, "children": [] }, { "id": "DOID:0051004", "label": "congenital nonspherocytic hemolytic anemia 3", "link_status": true, "children": [] }, { "id": "DOID:0051005", "label": "congenital nonspherocytic hemolytic anemia 4", "link_status": true, "children": [] }, { "id": "DOID:0051006", "label": "congenital nonspherocytic hemolytic anemia 5", "link_status": true, "children": [] }, { "id": "DOID:0051007", "label": "congenital nonspherocytic hemolytic anemia 8", "link_status": true, "children": [] }, { "id": "DOID:0051020", "label": "visceral heterotaxy 6", "link_status": true, "children": [] }, { "id": "DOID:0051021", "label": "visceral heterotaxy 7", "link_status": true, "children": [] }, { "id": "DOID:0051022", "label": "visceral heterotaxy 8", "link_status": true, "children": [] }, { "id": "DOID:0051023", "label": "visceral heterotaxy 9", "link_status": true, "children": [] }, { "id": "DOID:0051024", "label": "visceral heterotaxy 10", "link_status": true, "children": [] }, { "id": "DOID:0051025", "label": "visceral heterotaxy 11", "link_status": true, "children": [] }, { "id": "DOID:0051026", "label": "visceral heterotaxy 12", "link_status": true, "children": [] }, { "id": "DOID:0051027", "label": "visceral heterotaxy 13", "link_status": true, "children": [] }, { "id": "DOID:0051028", "label": "autosomal recessive axonal Charcot-Marie-Tooth disease with vocal cord paresis", "link_status": true, "children": [] }, { "id": "DOID:0051044", "label": "infantile-onset myofibrillar myopathy 12 with cardiomyopathy", "link_status": true, "children": [] }, { "id": "DOID:0051047", "label": "congenital disorder of glycosylation type IIbb", "link_status": true, "children": [] }, { "id": "DOID:0051049", "label": "congenital disorder of glycosylation type IIt", "link_status": true, "children": [] }, { "id": "DOID:0051050", "label": "congenital disorder of glycosylation type IIv", "link_status": true, "children": [] }, { "id": "DOID:0051052", "label": "congenital disorder of glycosylation type IIy", "link_status": true, "children": [] }, { "id": "DOID:0051053", "label": "congenital disorder of glycosylation type IIz", "link_status": true, "children": [] }, { "id": "DOID:0060020", "label": "reticular dysgenesis", "link_status": true, "children": [] }, { "id": "DOID:0060021", "label": "DNA ligase IV deficiency", "link_status": true, "children": [] }, { "id": "DOID:0060023", "label": "immunodeficiency with hyper IgM type 3", "link_status": true, "children": [] }, { "id": "DOID:0060025", "label": "immunoglobulin alpha deficiency", "link_status": true, "children": [] }, { "id": "DOID:0060027", "label": "agammaglobulinemia 4", "link_status": true, "children": [] }, { "id": "DOID:0060065", "label": "autosomal recessive pyridoxine-refractory sideroblastic anemia 2", "link_status": true, "children": [] }, { "id": "DOID:0060193", "label": "amyotrophic lateral sclerosis type 1", "link_status": true, "children": [] }, { "id": "DOID:0060225", "label": "3MC syndrome", "link_status": true, "children": [ { "id": "DOID:0060575", "label": "3MC syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0060576", "label": "3MC syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0060577", "label": "3MC syndrome 3", "link_status": true, "children": [] } ] }, { "id": "DOID:0060236", "label": "xanthinuria", "link_status": true, "children": [ { "id": "DOID:0070452", "label": "xanthinuria type I", "link_status": true, "children": [] }, { "id": "DOID:0070453", "label": "xanthinuria type II", "link_status": true, "children": [] } ] }, { "id": "DOID:0060237", "label": "Warburg micro syndrome", "link_status": true, "children": [ { "id": "DOID:0110716", "label": "Warburg micro syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0110717", "label": "Warburg micro syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0110718", "label": "Warburg micro syndrome 3", "link_status": true, "children": [] }, { "id": "DOID:0110719", "label": "Warburg micro syndrome 4", "link_status": true, "children": [] } ] }, { "id": "DOID:0060238", "label": "Van Maldergem syndrome", "link_status": true, "children": [ { "id": "DOID:0080585", "label": "Van Maldergem syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0080586", "label": "Van Maldergem syndrome 2", "link_status": true, "children": [] } ] }, { "id": "DOID:0060240", "label": "UV-sensitive syndrome", "link_status": true, "children": [] }, { "id": "DOID:0060241", "label": "3-M syndrome", "link_status": true, "children": [] }, { "id": "DOID:0060265", "label": "pontocerebellar hypoplasia type 1A", "link_status": true, "children": [] }, { "id": "DOID:0060266", "label": "pontocerebellar hypoplasia type 1B", "link_status": true, "children": [] }, { "id": "DOID:0060267", "label": "pontocerebellar hypoplasia type 2A", "link_status": true, "children": [] }, { "id": "DOID:0060268", "label": "pontocerebellar hypoplasia type 2B", "link_status": true, "children": [] }, { "id": "DOID:0060269", "label": "pontocerebellar hypoplasia type 2C", "link_status": true, "children": [] }, { "id": "DOID:0060270", "label": "pontocerebellar hypoplasia type 2D", "link_status": true, "children": [] }, { "id": "DOID:0060271", "label": "pontocerebellar hypoplasia type 2E", "link_status": true, "children": [] }, { "id": "DOID:0060283", "label": "peeling skin syndrome", "link_status": true, "children": [ { "id": "DOID:0070520", "label": "peeling skin syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0070521", "label": "peeling skin syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0070523", "label": "peeling skin syndrome 4", "link_status": true, "children": [] }, { "id": "DOID:0070524", "label": "peeling skin syndrome 5", "link_status": true, "children": [] }, { "id": "DOID:0070525", "label": "peeling skin syndrome 6", "link_status": true, "children": [] } ] }, { "id": "DOID:0060294", "label": "cold-induced sweating syndrome", "link_status": true, "children": [ { "id": "DOID:0080329", "label": "cold-induced sweating syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0080330", "label": "cold-induced sweating syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0080331", "label": "cold-induced sweating syndrome 3", "link_status": true, "children": [] } ] }, { "id": "DOID:0060296", "label": "congenital secretory chloride diarrhea 1", "link_status": true, "children": [] }, { "id": "DOID:0060308", "label": "autosomal recessive intellectual developmental disorder", "link_status": true, "children": [ { "id": "DOID:0051030", "label": "neurodevelopmental disorder with microcephaly, absent speech, and hypotonia", "link_status": true, "children": [] }, { "id": "DOID:0060934", "label": "neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy", "link_status": true, "children": [] }, { "id": "DOID:0060935", "label": "infantile hypotonia with psychomotor retardation and characteristic facies-3", "link_status": true, "children": [] }, { "id": "DOID:0060947", "label": "autosomal recessive intellectual developmental disorder 82", "link_status": true, "children": [] }, { "id": "DOID:0061114", "label": "autosomal recessive intellectual developmental disorder 83", "link_status": true, "children": [] }, { "id": "DOID:0061126", "label": "Brunet-Wagner neurodevelopmental syndrome", "link_status": true, "children": [] }, { "id": "DOID:0070421", "label": "neurodevelopmental disorder with spasticity and poor growth", "link_status": true, "children": [] }, { "id": "DOID:0070423", "label": "early onset progressive encephalopathy with brain atrophy and thin corpus callosum", "link_status": true, "children": [] }, { "id": "DOID:0070431", "label": "hyperphosphatasia with impaired intellectual development syndrome", "link_status": true, "children": [ { "id": "DOID:0070432", "label": "hyperphosphatasia with impaired intellectual development syndrome 5", "link_status": true, "children": [] }, { "id": "DOID:0070433", "label": "hyperphosphatasia with impaired intellectual development syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0070434", "label": "hyperphosphatasia with impaired intellectual development syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0070435", "label": "hyperphosphatasia with impaired intellectual development syndrome 3", "link_status": true, "children": [] }, { "id": "DOID:0070436", "label": "hyperphosphatasia with impaired intellectual development syndrome 4", "link_status": true, "children": [] }, { "id": "DOID:0070437", "label": "hyperphosphatasia with impaired intellectual development syndrome 6", "link_status": true, "children": [] } ] }, { "id": "DOID:0070443", "label": "neurodevelopmental disorder with cerebellar atrophy and motor dysfunction", "link_status": true, "children": [] }, { "id": "DOID:0070444", "label": "neurodevelopmental disorder with language delay and seizures", "link_status": true, "children": [] }, { "id": "DOID:0070537", "label": "spastic tetraplegia, thin corpus callosum, and progressive microcephaly", "link_status": true, "children": [] }, { "id": "DOID:0070542", "label": "neurodevelopmental disorder with spastic paraplegia and microcephaly", "link_status": true, "children": [] }, { "id": "DOID:0080239", "label": "autosomal recessive intellectual developmental disorder 61", "link_status": true, "children": [] }, { "id": "DOID:0080765", "label": "autosomal recessive intellectual developmental disorder 72", "link_status": true, "children": [] }, { "id": "DOID:0081097", "label": "Rafiq syndrome", "link_status": true, "children": [] }, { "id": "DOID:0081098", "label": "autosomal recessive intellectual developmental disorder 13", "link_status": true, "children": [] }, { "id": "DOID:0081099", "label": "neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies", "link_status": true, "children": [] }, { "id": "DOID:0081177", "label": "autosomal recessive intellectual developmental disorder 1", "link_status": true, "children": [] }, { "id": "DOID:0081178", "label": "autosomal recessive intellectual developmental disorder 2", "link_status": true, "children": [] }, { "id": "DOID:0081179", "label": "autosomal recessive intellectual developmental disorder 3", "link_status": true, "children": [] }, { "id": "DOID:0081180", "label": "autosomal recessive intellectual developmental disorder 12", "link_status": true, "children": [] }, { "id": "DOID:0081181", "label": "autosomal recessive intellectual developmental disorder 5", "link_status": true, "children": [] }, { "id": "DOID:0081182", "label": "autosomal recessive intellectual developmental disorder 6", "link_status": true, "children": [] }, { "id": "DOID:0081183", "label": "autosomal recessive intellectual developmental disorder 7", "link_status": true, "children": [] }, { "id": "DOID:0081188", "label": "autosomal recessive intellectual developmental disorder 14", "link_status": true, "children": [] }, { "id": "DOID:0081190", "label": "autosomal recessive intellectual developmental disorder 18", "link_status": true, "children": [] }, { "id": "DOID:0081193", "label": "autosomal recessive intellectual developmental disorder 27", "link_status": true, "children": [] }, { "id": "DOID:0081200", "label": "autosomal recessive intellectual developmental disorder 34", "link_status": true, "children": [] }, { "id": "DOID:0081202", "label": "autosomal recessive intellectual developmental disorder 37", "link_status": true, "children": [] }, { "id": "DOID:0081203", "label": "autosomal recessive intellectual developmental disorder 38", "link_status": true, "children": [] }, { "id": "DOID:0081204", "label": "autosomal recessive intellectual developmental disorder 39", "link_status": true, "children": [] }, { "id": "DOID:0081205", "label": "autosomal recessive intellectual developmental disorder 40", "link_status": true, "children": [] }, { "id": "DOID:0081206", "label": "autosomal recessive intellectual developmental disorder 41", "link_status": true, "children": [] }, { "id": "DOID:0081207", "label": "autosomal recessive intellectual developmental disorder 43", "link_status": true, "children": [] }, { "id": "DOID:0081208", "label": "autosomal recessive intellectual developmental disorder 44", "link_status": true, "children": [] }, { "id": "DOID:0081209", "label": "autosomal recessive intellectual developmental disorder 45", "link_status": true, "children": [] }, { "id": "DOID:0081210", "label": "autosomal recessive intellectual developmental disorder 46", "link_status": true, "children": [] }, { "id": "DOID:0081211", "label": "autosomal recessive intellectual developmental disorder 47", "link_status": true, "children": [] }, { "id": "DOID:0081212", "label": "autosomal recessive intellectual developmental disorder 48", "link_status": true, "children": [] }, { "id": "DOID:0081213", "label": "autosomal recessive intellectual developmental disorder 50", "link_status": true, "children": [] }, { "id": "DOID:0081214", "label": "autosomal recessive intellectual developmental disorder 51", "link_status": true, "children": [] }, { "id": "DOID:0081215", "label": "autosomal recessive intellectual developmental disorder 52", "link_status": true, "children": [] }, { "id": "DOID:0081216", "label": "autosomal recessive intellectual developmental disorder 54", "link_status": true, "children": [] }, { "id": "DOID:0081217", "label": "autosomal recessive intellectual developmental disorder 56", "link_status": true, "children": [] }, { "id": "DOID:0081218", "label": "autosomal recessive intellectual developmental disorder 74", "link_status": true, "children": [] }, { "id": "DOID:0081219", "label": "autosomal recessive intellectual developmental disorder 57", "link_status": true, "children": [] }, { "id": "DOID:0081220", "label": "autosomal recessive intellectual developmental disorder 58", "link_status": true, "children": [] }, { "id": "DOID:0081221", "label": "autosomal recessive intellectual developmental disorder 59", "link_status": true, "children": [] }, { "id": "DOID:0081222", "label": "autosomal recessive intellectual developmental disorder 60", "link_status": true, "children": [] }, { "id": "DOID:0081223", "label": "glycosylphosphatidylinositol biosynthesis defect 16", "link_status": true, "children": [] }, { "id": "DOID:0081224", "label": "autosomal recessive intellectual developmental disorder 63", "link_status": true, "children": [] }, { "id": "DOID:0081225", "label": "autosomal recessive intellectual developmental disorder 64", "link_status": true, "children": [] }, { "id": "DOID:0081226", "label": "autosomal recessive intellectual developmental disorder 65", "link_status": true, "children": [] }, { "id": "DOID:0081227", "label": "autosomal recessive intellectual developmental disorder 66", "link_status": true, "children": [] }, { "id": "DOID:0081228", "label": "autosomal recessive intellectual developmental disorder 67", "link_status": true, "children": [] }, { "id": "DOID:0081229", "label": "autosomal recessive intellectual developmental disorder 68", "link_status": true, "children": [] }, { "id": "DOID:0081230", "label": "autosomal recessive intellectual developmental disorder 69", "link_status": true, "children": [] }, { "id": "DOID:0081231", "label": "autosomal recessive intellectual developmental disorder 70", "link_status": true, "children": [] }, { "id": "DOID:0081232", "label": "autosomal recessive intellectual developmental disorder 71", "link_status": true, "children": [] }, { "id": "DOID:0081233", "label": "autosomal recessive intellectual developmental disorder 73", "link_status": true, "children": [] }, { "id": "DOID:0081234", "label": "autosomal recessive intellectual developmental disorder 75", "link_status": true, "children": [] }, { "id": "DOID:0081235", "label": "autosomal recessive intellectual developmental disorder 76", "link_status": true, "children": [] }, { "id": "DOID:0081236", "label": "autosomal recessive intellectual developmental disorder 77", "link_status": true, "children": [] }, { "id": "DOID:0081263", "label": "neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities", "link_status": true, "children": [] }, { "id": "DOID:0081265", "label": "intellectual developmental disorder with abnormal behavior, microcephaly, and short stature", "link_status": true, "children": [] }, { "id": "DOID:0081324", "label": "neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss", "link_status": true, "children": [] }, { "id": "DOID:0081387", "label": "neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities", "link_status": true, "children": [] }, { "id": "DOID:0081444", "label": "neurodevelopmental disorder with poor growth and behavioral abnormalities", "link_status": true, "children": [] } ] }, { "id": "DOID:0060337", "label": "CEDNIK syndrome", "link_status": true, "children": [] }, { "id": "DOID:0060346", "label": "congenital myopathy 13", "link_status": true, "children": [] }, { "id": "DOID:0060348", "label": "hypoparathyroidism-retardation-dysmorphism syndrome", "link_status": true, "children": [] }, { "id": "DOID:0060350", "label": "adenine phosphoribosyltransferase deficiency", "link_status": true, "children": [] }, { "id": "DOID:0060356", "label": "Vici syndrome", "link_status": true, "children": [] }, { "id": "DOID:0060364", "label": "Galloway-Mowat syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0060368", "label": "Parkinson's disease 2", "link_status": true, "children": [] }, { "id": "DOID:0060369", "label": "Parkinson's disease 6", "link_status": true, "children": [] }, { "id": "DOID:0060370", "label": "Parkinson's disease 7", "link_status": true, "children": [] }, { "id": "DOID:0060372", "label": "Parkinson's disease 15", "link_status": true, "children": [] }, { "id": "DOID:0060374", "label": "orofaciodigital syndrome IV", "link_status": true, "children": [] }, { "id": "DOID:0060375", "label": "orofaciodigital syndrome V", "link_status": true, "children": [] }, { "id": "DOID:0060382", "label": "orofaciodigital syndrome IX", "link_status": true, "children": [] }, { "id": "DOID:0060449", "label": "gelatinous drop-like corneal dystrophy", "link_status": true, "children": [] }, { "id": "DOID:0060470", "label": "salt and pepper syndrome", "link_status": true, "children": [] }, { "id": "DOID:0060474", "label": "familial erythrocytosis 2", "link_status": true, "children": [] }, { "id": "DOID:0060481", "label": "Goldberg-Shprintzen syndrome", "link_status": true, "children": [] }, { "id": "DOID:0060484", "label": "EAST syndrome", "link_status": true, "children": [] }, { "id": "DOID:0060490", "label": "Schimke immuno-osseous dysplasia", "link_status": true, "children": [] }, { "id": "DOID:0060491", "label": "SPOAN syndrome", "link_status": true, "children": [] }, { "id": "DOID:0060535", "label": "Warsaw breakage syndrome", "link_status": true, "children": [] }, { "id": "DOID:0060551", "label": "poikiloderma with neutropenia", "link_status": true, "children": [] }, { "id": "DOID:0060556", "label": "Kufor-Rakeb syndrome", "link_status": true, "children": [] }, { "id": "DOID:0060558", "label": "lethal congenital contracture syndrome", "link_status": true, "children": [ { "id": "DOID:0060559", "label": "lethal congenital contracture syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0060560", "label": "lethal congenital contracture syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0060653", "label": "lethal congenital contracture syndrome 3", "link_status": true, "children": [] }, { "id": "DOID:0060654", "label": "lethal congenital contracture syndrome 4", "link_status": true, "children": [] } ] }, { "id": "DOID:0060571", "label": "Ritscher-Schinzel syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0060580", "label": "Noonan syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0060589", "label": "Yunis-Varon syndrome", "link_status": true, "children": [] }, { "id": "DOID:0060590", "label": "XFE progeroid syndrome", "link_status": true, "children": [] }, { "id": "DOID:0060601", "label": "alpha-2-plasmin inhibitor deficiency", "link_status": true, "children": [] }, { "id": "DOID:0060609", "label": "microcephalic osteodysplastic primordial dwarfism type II", "link_status": true, "children": [] }, { "id": "DOID:0060638", "label": "neonatal diabetes mellitus with congenital hypothyroidism", "link_status": true, "children": [] }, { "id": "DOID:0060639", "label": "permanent neonatal diabetes mellitus", "link_status": true, "children": [] }, { "id": "DOID:0060641", "label": "endocrine-cerebro-osteodysplasia syndrome", "link_status": true, "children": [] }, { "id": "DOID:0060642", "label": "recessive dystrophic epidermolysis bullosa", "link_status": true, "children": [] }, { "id": "DOID:0060647", "label": "fetal encasement syndrome", "link_status": true, "children": [] }, { "id": "DOID:0060649", "label": "congenital hereditary endothelial dystrophy of cornea", "link_status": true, "children": [] }, { "id": "DOID:0060650", "label": "dicarboxylic aminoaciduria", "link_status": true, "children": [] }, { "id": "DOID:0060655", "label": "autosomal recessive congenital ichthyosis", "link_status": true, "children": [ { "id": "DOID:0060656", "label": "autosomal recessive congenital ichthyosis 1", "link_status": true, "children": [] }, { "id": "DOID:0060710", "label": "autosomal recessive congenital ichthyosis 2", "link_status": true, "children": [] }, { "id": "DOID:0060711", "label": "autosomal recessive congenital ichthyosis 3", "link_status": true, "children": [] }, { "id": "DOID:0060712", "label": "autosomal recessive congenital ichthyosis 4A", "link_status": true, "children": [] }, { "id": "DOID:0060713", "label": "autosomal recessive congenital ichthyosis 4B", "link_status": true, "children": [] }, { "id": "DOID:0060714", "label": "autosomal recessive congenital ichthyosis 5", "link_status": true, "children": [] }, { "id": "DOID:0060715", "label": "autosomal recessive congenital ichthyosis 6", "link_status": true, "children": [] }, { "id": "DOID:0060717", "label": "autosomal recessive congenital ichthyosis 8", "link_status": true, "children": [] }, { "id": "DOID:0060718", "label": "autosomal recessive congenital ichthyosis 9", "link_status": true, "children": [] }, { "id": "DOID:0060719", "label": "autosomal recessive congenital ichthyosis 10", "link_status": true, "children": [] }, { "id": "DOID:0060720", "label": "autosomal recessive congenital ichthyosis 11", "link_status": true, "children": [] }, { "id": "DOID:0080257", "label": "autosomal recessive congenital ichthyosis 13", "link_status": true, "children": [] }, { "id": "DOID:0080258", "label": "autosomal recessive congenital ichthyosis 14", "link_status": true, "children": [] } ] }, { "id": "DOID:0060672", "label": "frontotemporal dementia 2", "link_status": true, "children": [] }, { "id": "DOID:0060689", "label": "atrichia with papular lesions", "link_status": true, "children": [] }, { "id": "DOID:0060692", "label": "platelet-type bleeding disorder 8", "link_status": true, "children": [] }, { "id": "DOID:0060696", "label": "hyperekplexia 1", "link_status": true, "children": [] }, { "id": "DOID:0060697", "label": "hyperekplexia 2", "link_status": true, "children": [] }, { "id": "DOID:0060698", "label": "hyperekplexia 3", "link_status": true, "children": [] }, { "id": "DOID:0060707", "label": "lymphoproliferative syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0060708", "label": "lymphoproliferative syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0060728", "label": "congenital disorder of deglycosylation 1", "link_status": true, "children": [] }, { "id": "DOID:0060733", "label": "junctional epidermolysis bullosa with pyloric atresia", "link_status": true, "children": [] }, { "id": "DOID:0060737", "label": "junctional epidermolysis bullosa Herlitz type", "link_status": true, "children": [] }, { "id": "DOID:0060738", "label": "junctional epidermolysis bullosa non-Herlitz type", "link_status": true, "children": [] }, { "id": "DOID:0060744", "label": "Pendred Syndrome", "link_status": true, "children": [] }, { "id": "DOID:0060752", "label": "familial temporal lobe epilepsy 5", "link_status": true, "children": [] }, { "id": "DOID:0060756", "label": "sclerosteosis 1", "link_status": true, "children": [] }, { "id": "DOID:0060757", "label": "sclerosteosis 2", "link_status": true, "children": [] }, { "id": "DOID:0060758", "label": "immunodeficiency with hyper-IgM type 2", "link_status": true, "children": [] }, { "id": "DOID:0060759", "label": "immunodeficiency with hyper IgM type 5", "link_status": true, "children": [] }, { "id": "DOID:0060764", "label": "autosomal recessive Robinow syndrome", "link_status": true, "children": [] }, { "id": "DOID:0060769", "label": "T-cell immunodeficiency, congenital alopecia, and nail dystrophy", "link_status": true, "children": [] }, { "id": "DOID:0060773", "label": "cleft lip-palate-ectodermal dysplasia syndrome", "link_status": true, "children": [] }, { "id": "DOID:0060775", "label": "microvillus inclusion disease", "link_status": true, "children": [] }, { "id": "DOID:0060776", "label": "congenital diarrhea 5 with tufting enteropathy", "link_status": true, "children": [] }, { "id": "DOID:0060777", "label": "congenital secretory sodium diarrhea 8", "link_status": true, "children": [] }, { "id": "DOID:0060778", "label": "congenital diarrhea 7 with exudative enteropathy", "link_status": true, "children": [] }, { "id": "DOID:0060779", "label": "congenital malabsorptive diarrhea 4", "link_status": true, "children": [] }, { "id": "DOID:0060781", "label": "congenital secretory sodium diarrhea 3", "link_status": true, "children": [] }, { "id": "DOID:0060787", "label": "hypomyelinating leukodystrophy 2", "link_status": true, "children": [] }, { "id": "DOID:0060788", "label": "hypomyelinating leukodystrophy 10", "link_status": true, "children": [] }, { "id": "DOID:0060789", "label": "hypomyelinating leukodystrophy 4", "link_status": true, "children": [] }, { "id": "DOID:0060790", "label": "hypomyelinating leukodystrophy 3", "link_status": true, "children": [] }, { "id": "DOID:0060791", "label": "hypomyelinating leukodystrophy 9", "link_status": true, "children": [] }, { "id": "DOID:0060792", "label": "hypomyelinating leukodystrophy 11", "link_status": true, "children": [] }, { "id": "DOID:0060793", "label": "hypomyelinating leukodystrophy 5", "link_status": true, "children": [] }, { "id": "DOID:0060794", "label": "hypomyelinating leukodystrophy 7", "link_status": true, "children": [] }, { "id": "DOID:0060795", "label": "hypomyelinating leukodystrophy 13", "link_status": true, "children": [] }, { "id": "DOID:0060796", "label": "hypomyelinating leukodystrophy 12", "link_status": true, "children": [] }, { "id": "DOID:0060797", "label": "hypomyelinating leukodystrophy 8", "link_status": true, "children": [] }, { "id": "DOID:0060831", "label": "Griscelli syndrome", "link_status": true, "children": [ { "id": "DOID:0060832", "label": "Griscelli syndrome type 1", "link_status": true, "children": [] }, { "id": "DOID:0060833", "label": "Griscelli syndrome type 2", "link_status": true, "children": [] }, { "id": "DOID:0060834", "label": "Griscelli syndrome type 3", "link_status": true, "children": [] } ] }, { "id": "DOID:0060835", "label": "isolated microphthalmia 6", "link_status": true, "children": [] }, { "id": "DOID:0060837", "label": "isolated microphthalmia 5", "link_status": true, "children": [] }, { "id": "DOID:0060839", "label": "isolated microphthalmia 2", "link_status": true, "children": [] }, { "id": "DOID:0060841", "label": "isolated microphthalmia 8", "link_status": true, "children": [] }, { "id": "DOID:0060842", "label": "isolated microphthalmia 3", "link_status": true, "children": [] }, { "id": "DOID:0060849", "label": "osteoporosis-pseudoglioma syndrome", "link_status": true, "children": [] }, { "id": "DOID:0060852", "label": "Pierson syndrome", "link_status": true, "children": [] }, { "id": "DOID:0060854", "label": "autosomal recessive pseudohypoaldosteronism type 1", "link_status": true, "children": [] }, { "id": "DOID:0060856", "label": "right atrial isomerism", "link_status": true, "children": [] }, { "id": "DOID:0060861", "label": "microphthalmia with limb anomalies", "link_status": true, "children": [] }, { "id": "DOID:0060862", "label": "mal de Meleda", "link_status": true, "children": [] }, { "id": "DOID:0060868", "label": "leukoencephalopathy with vanishing white matter", "link_status": true, "children": [ { "id": "DOID:0070367", "label": "leukoencephalopathy with vanishing white matter 5", "link_status": true, "children": [] }, { "id": "DOID:0070371", "label": "leukoencephalopathy with vanishing white matter 4", "link_status": true, "children": [] }, { "id": "DOID:0070372", "label": "leukoencephalopathy with vanishing white matter 3", "link_status": true, "children": [] }, { "id": "DOID:0070373", "label": "leukoencephalopathy with vanishing white matter 2", "link_status": true, "children": [] }, { "id": "DOID:0070374", "label": "leukoencephalopathy with vanishing white matter 1", "link_status": true, "children": [] } ] }, { "id": "DOID:0060889", "label": "prune belly syndrome", "link_status": true, "children": [] }, { "id": "DOID:0060891", "label": "Parkinson's disease 19A", "link_status": true, "children": [] }, { "id": "DOID:0060896", "label": "Parkinson's disease 23", "link_status": true, "children": [] }, { "id": "DOID:0060898", "label": "Parkinson's disease 20", "link_status": true, "children": [] }, { "id": "DOID:0060900", "label": "Parkinson's disease 14", "link_status": true, "children": [] }, { "id": "DOID:0060902", "label": "Norman-Roberts syndrome", "link_status": true, "children": [] }, { "id": "DOID:0060911", "label": "karyomegalic interstitial nephritis", "link_status": true, "children": [] }, { "id": "DOID:0060915", "label": "proteosome-associated autoinflammatory syndrome 4", "link_status": true, "children": [] }, { "id": "DOID:0060916", "label": "proteasome-associated autoinflammatory syndrome 3", "link_status": true, "children": [] }, { "id": "DOID:0060919", "label": "proteosome-associated autoinflammatory syndrome 5", "link_status": true, "children": [] }, { "id": "DOID:0060938", "label": "dystonia 31", "link_status": true, "children": [] }, { "id": "DOID:0060939", "label": "dystonia 32", "link_status": true, "children": [] }, { "id": "DOID:0060940", "label": "dystonia 33", "link_status": true, "children": [] }, { "id": "DOID:0060941", "label": "interstitial lung disease 1", "link_status": true, "children": [] }, { "id": "DOID:0060949", "label": "3-hydroxyisobutryl-CoA hydrolase deficiency", "link_status": true, "children": [] }, { "id": "DOID:0060950", "label": "hypervalinemia and hyperleucine-isoleucinemia", "link_status": true, "children": [] }, { "id": "DOID:0060955", "label": "dystonia 35, childhood-onset", "link_status": true, "children": [] }, { "id": "DOID:0060956", "label": "dystonia 37, early-onset with striatal lesions", "link_status": true, "children": [] }, { "id": "DOID:0060958", "label": "orofaciodigital syndrome XIV", "link_status": true, "children": [] }, { "id": "DOID:0060959", "label": "orofaciodigital syndrome II", "link_status": true, "children": [] }, { "id": "DOID:0060960", "label": "orofaciodigital syndrome XIX", "link_status": true, "children": [] }, { "id": "DOID:0060961", "label": "orofaciodigital syndrome XVIII", "link_status": true, "children": [] }, { "id": "DOID:0060962", "label": "orofaciodigital syndrome XX", "link_status": true, "children": [] }, { "id": "DOID:0060966", "label": "dystonia 22, juvenile-onset", "link_status": true, "children": [] }, { "id": "DOID:0060967", "label": "dystonia 22, adult-onset", "link_status": true, "children": [] }, { "id": "DOID:0060968", "label": "hypotrichosis 15", "link_status": true, "children": [] }, { "id": "DOID:0060973", "label": "WHIM syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0060974", "label": "autosomal recessive Robinow syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0060978", "label": "Fanconi anemia complementation group W", "link_status": true, "children": [] }, { "id": "DOID:0060979", "label": "Fanconi anemia complementation group S", "link_status": true, "children": [] }, { "id": "DOID:0060981", "label": "mosaic variegated aneuploidy syndrome 4", "link_status": true, "children": [] }, { "id": "DOID:0060987", "label": "preaxial polydactyly I", "link_status": true, "children": [] }, { "id": "DOID:0060988", "label": "pancreatic agenesis 2", "link_status": true, "children": [] }, { "id": "DOID:0060990", "label": "congenital disorder of deglycosylation 2", "link_status": true, "children": [] }, { "id": "DOID:0060993", "label": "bent bone dysplasia syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0060994", "label": "encephalopathy due to defective mitochondrial and peroxisomal fission 2", "link_status": true, "children": [] }, { "id": "DOID:0061003", "label": "pancreatic agenesis 1", "link_status": true, "children": [] }, { "id": "DOID:0061007", "label": "sideroblastic anemia 5", "link_status": true, "children": [] }, { "id": "DOID:0061013", "label": "ovarian dysgenesis 9", "link_status": true, "children": [] }, { "id": "DOID:0061014", "label": "ovarian dysgenesis 10", "link_status": true, "children": [] }, { "id": "DOID:0061016", "label": "combined or isolated pituitary growth hormone deficiency 7", "link_status": true, "children": [] }, { "id": "DOID:0061019", "label": "combined or isolated pituitary hormone deficiency 1", "link_status": true, "children": [] }, { "id": "DOID:0061020", "label": "combined pituitary hormone deficiency 2", "link_status": true, "children": [] }, { "id": "DOID:0061021", "label": "combined pituitary hormone deficiency 3", "link_status": true, "children": [] }, { "id": "DOID:0061023", "label": "nonphotosensitive trichothiodystrophy 8", "link_status": true, "children": [] }, { "id": "DOID:0061024", "label": "nonphotosensitive trichothiodystrophy 9", "link_status": true, "children": [] }, { "id": "DOID:0061025", "label": "familial restrictive cardiomyopathy 6", "link_status": true, "children": [] }, { "id": "DOID:0061026", "label": "hereditary pyropoikilocytosis", "link_status": true, "children": [] }, { "id": "DOID:0061051", "label": "immunodeficiency 80", "link_status": true, "children": [] }, { "id": "DOID:0061052", "label": "immunodeficiency 81", "link_status": true, "children": [] }, { "id": "DOID:0061056", "label": "immunodeficiency 86", "link_status": true, "children": [] }, { "id": "DOID:0061057", "label": "immunodeficiency 87", "link_status": true, "children": [] }, { "id": "DOID:0061058", "label": "immunodeficiency 88", "link_status": true, "children": [] }, { "id": "DOID:0061059", "label": "immunodeficiency 89", "link_status": true, "children": [] }, { "id": "DOID:0061060", "label": "immunodeficiency 90", "link_status": true, "children": [] }, { "id": "DOID:0061061", "label": "immunodeficiency 91", "link_status": true, "children": [] }, { "id": "DOID:0061062", "label": "immunodeficiency 92", "link_status": true, "children": [] }, { "id": "DOID:0061063", "label": "immunodeficiency 93", "link_status": true, "children": [] }, { "id": "DOID:0061065", "label": "immunodeficiency 95", "link_status": true, "children": [] }, { "id": "DOID:0061066", "label": "immunodeficiency 96", "link_status": true, "children": [] }, { "id": "DOID:0061067", "label": "immunodeficiency 97", "link_status": true, "children": [] }, { "id": "DOID:0061069", "label": "immunodeficiency 99", "link_status": true, "children": [] }, { "id": "DOID:0061074", "label": "severe combined immunodeficiency 105", "link_status": true, "children": [] }, { "id": "DOID:0061075", "label": "immunodeficiency 106", "link_status": true, "children": [] }, { "id": "DOID:0061077", "label": "immunodeficiency 108", "link_status": true, "children": [] }, { "id": "DOID:0061078", "label": "immunodeficiency 109", "link_status": true, "children": [] }, { "id": "DOID:0061079", "label": "immunodeficiency 112", "link_status": true, "children": [] }, { "id": "DOID:0061080", "label": "immunodeficiency 114", "link_status": true, "children": [] }, { "id": "DOID:0061081", "label": "immunodeficiency 115", "link_status": true, "children": [] }, { "id": "DOID:0061082", "label": "immunodeficiency 116", "link_status": true, "children": [] }, { "id": "DOID:0061083", "label": "immunodeficiency 117", "link_status": true, "children": [] }, { "id": "DOID:0061085", "label": "immunodeficiency 119", "link_status": true, "children": [] }, { "id": "DOID:0061086", "label": "immunodeficiency 120", "link_status": true, "children": [] }, { "id": "DOID:0061088", "label": "immunodeficiency 122", "link_status": true, "children": [] }, { "id": "DOID:0061089", "label": "immunodeficiency 123", "link_status": true, "children": [] }, { "id": "DOID:0061090", "label": "severe combined immunodeficiency 124", "link_status": true, "children": [] }, { "id": "DOID:0061091", "label": "immunodeficiency 125", "link_status": true, "children": [] }, { "id": "DOID:0061092", "label": "immunodeficiency 127", "link_status": true, "children": [] }, { "id": "DOID:0061093", "label": "immunodeficiency 128", "link_status": true, "children": [] }, { "id": "DOID:0061094", "label": "immunodeficiency 129", "link_status": true, "children": [] }, { "id": "DOID:0061098", "label": "Carpenter syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0061099", "label": "Carpenter syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0061102", "label": "hypertrophic cardiomyopathy 27", "link_status": true, "children": [] }, { "id": "DOID:0061103", "label": "retinitis pigmentosa 76", "link_status": true, "children": [] }, { "id": "DOID:0061105", "label": "retinitis pigmentosa 93", "link_status": true, "children": [] }, { "id": "DOID:0061107", "label": "retinitis pigmentosa 92", "link_status": true, "children": [] }, { "id": "DOID:0061109", "label": "retinitis pigmentosa 98", "link_status": true, "children": [] }, { "id": "DOID:0061111", "label": "retinitis pigmentosa 80", "link_status": true, "children": [] }, { "id": "DOID:0061112", "label": "retinitis pigmentosa 95", "link_status": true, "children": [] }, { "id": "DOID:0061113", "label": "retinitis pigmentosa 78", "link_status": true, "children": [] }, { "id": "DOID:0061115", "label": "Carey-Fineman-Ziter syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0061116", "label": "Carey-Fineman-Ziter syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0061123", "label": "visceral heterotaxy 14", "link_status": true, "children": [] }, { "id": "DOID:0070000", "label": "3-methylglutaconic aciduria type 8", "link_status": true, "children": [] }, { "id": "DOID:0070002", "label": "3-methylglutaconic aciduria type 9", "link_status": true, "children": [] }, { "id": "DOID:0070015", "label": "autosomal recessive dyskeratosis congenita 1", "link_status": true, "children": [] }, { "id": "DOID:0070017", "label": "autosomal recessive dyskeratosis congenita 2", "link_status": true, "children": [] }, { "id": "DOID:0070019", "label": "autosomal recessive dyskeratosis congenita 3", "link_status": true, "children": [] }, { "id": "DOID:0070022", "label": "autosomal recessive dyskeratosis congenita 5", "link_status": true, "children": [] }, { "id": "DOID:0070024", "label": "autosomal recessive dyskeratosis congenita 6", "link_status": true, "children": [] }, { "id": "DOID:0070123", "label": "congenital nongoitrous hypothyroidism 4", "link_status": true, "children": [] }, { "id": "DOID:0070126", "label": "congenital nongoitrous hypothyroidism 1", "link_status": true, "children": [] }, { "id": "DOID:0070137", "label": "autosomal recessive cutis laxa type IIB", "link_status": true, "children": [] }, { "id": "DOID:0070141", "label": "autosomal recessive cutis laxa type II classic type", "link_status": false, "children": [ { "id": "DOID:0070129", "label": "autosomal recessive cutis laxa type IID", "link_status": true, "children": [] }, { "id": "DOID:0070134", "label": "autosomal recessive cutis laxa type IIA", "link_status": true, "children": [] }, { "id": "DOID:0070140", "label": "autosomal recessive cutis laxa type IIC", "link_status": true, "children": [] } ] }, { "id": "DOID:0070143", "label": "autosomal recessive cutis laxa type III", "link_status": true, "children": [ { "id": "DOID:0070132", "label": "autosomal recessive cutis laxa type IIIA", "link_status": true, "children": [] }, { "id": "DOID:0070138", "label": "autosomal recessive cutis laxa type IIIB", "link_status": true, "children": [] } ] }, { "id": "DOID:0070144", "label": "autosomal recessive cutis laxa type I", "link_status": false, "children": [ { "id": "DOID:0070133", "label": "autosomal recessive cutis laxa type IB", "link_status": true, "children": [] }, { "id": "DOID:0070135", "label": "autosomal recessive cutis laxa type IA", "link_status": true, "children": [] }, { "id": "DOID:0070139", "label": "autosomal recessive cutis laxa type IC", "link_status": true, "children": [] } ] }, { "id": "DOID:0070145", "label": "hereditary sensory and autonomic neuropathy type 5", "link_status": true, "children": [] }, { "id": "DOID:0070146", "label": "hereditary sensory neuropathy type 4", "link_status": true, "children": [] }, { "id": "DOID:0070147", "label": "hereditary sensory neuropathy type 2C", "link_status": true, "children": [] }, { "id": "DOID:0070150", "label": "hereditary sensory and autonomic neuropathy type 2B", "link_status": true, "children": [] }, { "id": "DOID:0070151", "label": "hereditary sensory and autonomic neuropathy type 6", "link_status": true, "children": [] }, { "id": "DOID:0070153", "label": "hereditary sensory and autonomic neuropathy type 8", "link_status": true, "children": [] }, { "id": "DOID:0070155", "label": "hereditary sensory and autonomic neuropathy type 2A", "link_status": true, "children": [] }, { "id": "DOID:0070163", "label": "spermatogenic failure 21", "link_status": true, "children": [] }, { "id": "DOID:0070165", "label": "spermatogenic failure 18", "link_status": true, "children": [] }, { "id": "DOID:0070166", "label": "spermatogenic failure 20", "link_status": true, "children": [] }, { "id": "DOID:0070167", "label": "spermatogenic failure 6", "link_status": true, "children": [] }, { "id": "DOID:0070170", "label": "spermatogenic failure 19", "link_status": true, "children": [] }, { "id": "DOID:0070172", "label": "spermatogenic failure 15", "link_status": true, "children": [] }, { "id": "DOID:0070173", "label": "spermatogenic failure 7", "link_status": true, "children": [] }, { "id": "DOID:0070174", "label": "spermatogenic failure 17", "link_status": true, "children": [] }, { "id": "DOID:0070177", "label": "spermatogenic failure 22", "link_status": true, "children": [] }, { "id": "DOID:0070179", "label": "spermatogenic failure 14", "link_status": true, "children": [] }, { "id": "DOID:0070181", "label": "spermatogenic failure 23", "link_status": true, "children": [] }, { "id": "DOID:0070182", "label": "spermatogenic failure 13", "link_status": true, "children": [] }, { "id": "DOID:0070183", "label": "spermatogenic failure 5", "link_status": true, "children": [] }, { "id": "DOID:0070184", "label": "spermatogenic failure 16", "link_status": true, "children": [] }, { "id": "DOID:0070191", "label": "autosomal recessive chronic granulomatous disease 2", "link_status": true, "children": [] }, { "id": "DOID:0070192", "label": "autosomal recessive chronic granulomatous disease 1", "link_status": true, "children": [] }, { "id": "DOID:0070193", "label": "autosomal recessive chronic granulomatous disease 4", "link_status": true, "children": [] }, { "id": "DOID:0070194", "label": "autosomal recessive chronic granulomatous disease 3", "link_status": true, "children": [] }, { "id": "DOID:0070199", "label": "Miyoshi muscular dystrophy 1", "link_status": true, "children": [] }, { "id": "DOID:0070201", "label": "Miyoshi muscular dystrophy 3", "link_status": true, "children": [] }, { "id": "DOID:0070203", "label": "familial partial lipodystrophy type 5", "link_status": true, "children": [] }, { "id": "DOID:0070206", "label": "familial partial lipodystrophy type 6", "link_status": true, "children": [] }, { "id": "DOID:0070215", "label": "familial hyperinsulinemic hypoglycemia 4", "link_status": true, "children": [] }, { "id": "DOID:0070218", "label": "familial hyperinsulinemic hypoglycemia 2", "link_status": true, "children": [] }, { "id": "DOID:0070219", "label": "familial hyperinsulinemic hypoglycemia 1", "link_status": true, "children": [] }, { "id": "DOID:0070222", "label": "progressive familial intrahepatic cholestasis 2", "link_status": true, "children": [] }, { "id": "DOID:0070223", "label": "progressive familial intrahepatic cholestasis 3", "link_status": true, "children": [] }, { "id": "DOID:0070224", "label": "progressive familial intrahepatic cholestasis 4", "link_status": true, "children": [] }, { "id": "DOID:0070225", "label": "progressive familial intrahepatic cholestasis 5", "link_status": true, "children": [] }, { "id": "DOID:0070226", "label": "progressive familial intrahepatic cholestasis 1", "link_status": true, "children": [] }, { "id": "DOID:0070231", "label": "benign recurrent intrahepatic cholestasis 1", "link_status": true, "children": [] }, { "id": "DOID:0070232", "label": "benign recurrent intrahepatic cholestasis 2", "link_status": true, "children": [] }, { "id": "DOID:0070248", "label": "autosomal recessive Emery-Dreifuss muscular dystrophy 3", "link_status": true, "children": [] }, { "id": "DOID:0070253", "label": "congenital disorder of glycosylation type IIa", "link_status": true, "children": [] }, { "id": "DOID:0070254", "label": "congenital disorder of glycosylation type IIb", "link_status": true, "children": [] }, { "id": "DOID:0070255", "label": "congenital disorder of glycosylation type IIc", "link_status": true, "children": [] }, { "id": "DOID:0070256", "label": "congenital disorder of glycosylation type IId", "link_status": true, "children": [] }, { "id": "DOID:0070257", "label": "congenital disorder of glycosylation type IIe", "link_status": true, "children": [] }, { "id": "DOID:0070258", "label": "congenital disorder of glycosylation type IIf", "link_status": true, "children": [] }, { "id": "DOID:0070259", "label": "congenital disorder of glycosylation type IIg", "link_status": true, "children": [] }, { "id": "DOID:0070260", "label": "congenital disorder of glycosylation type IIh", "link_status": true, "children": [] }, { "id": "DOID:0070261", "label": "congenital disorder of glycosylation type IIi", "link_status": true, "children": [] }, { "id": "DOID:0070262", "label": "congenital disorder of glycosylation type IIj", "link_status": true, "children": [] }, { "id": "DOID:0070263", "label": "congenital disorder of glycosylation type IIk", "link_status": true, "children": [] }, { "id": "DOID:0070264", "label": "congenital disorder of glycosylation type IIl", "link_status": true, "children": [] }, { "id": "DOID:0070266", "label": "congenital disorder of glycosylation type IIn", "link_status": true, "children": [] }, { "id": "DOID:0070267", "label": "congenital disorder of glycosylation type IIo", "link_status": true, "children": [] }, { "id": "DOID:0070268", "label": "congenital disorder of glycosylation type IIp", "link_status": true, "children": [] }, { "id": "DOID:0070269", "label": "congenital disorder of glycosylation type IIq", "link_status": true, "children": [] }, { "id": "DOID:0070296", "label": "autosomal recessive primary microcephaly", "link_status": true, "children": [ { "id": "DOID:0051031", "label": "primary autosomal recessive microcephaly 20", "link_status": true, "children": [] }, { "id": "DOID:0051032", "label": "primary autosomal recessive microcephaly 21", "link_status": true, "children": [] }, { "id": "DOID:0051033", "label": "primary autosomal recessive microcephaly 22", "link_status": true, "children": [] }, { "id": "DOID:0051034", "label": "primary autosomal recessive microcephaly 23", "link_status": true, "children": [] }, { "id": "DOID:0051035", "label": "primary autosomal recessive microcephaly 24", "link_status": true, "children": [] }, { "id": "DOID:0051036", "label": "primary autosomal recessive microcephaly 25", "link_status": true, "children": [] }, { "id": "DOID:0051039", "label": "primary autosomal recessive microcephaly 28", "link_status": true, "children": [] }, { "id": "DOID:0051040", "label": "primary autosomal recessive microcephaly 29", "link_status": true, "children": [] }, { "id": "DOID:0051041", "label": "primary autosomal recessive microcephaly 30", "link_status": true, "children": [] }, { "id": "DOID:0070277", "label": "primary autosomal recessive microcephaly 15", "link_status": true, "children": [] }, { "id": "DOID:0070278", "label": "primary autosomal recessive microcephaly 7", "link_status": true, "children": [] }, { "id": "DOID:0070279", "label": "primary autosomal recessive microcephaly 14", "link_status": true, "children": [] }, { "id": "DOID:0070280", "label": "primary autosomal recessive microcephaly 5", "link_status": true, "children": [] }, { "id": "DOID:0070281", "label": "primary autosomal recessive microcephaly 19", "link_status": true, "children": [] }, { "id": "DOID:0070282", "label": "primary autosomal recessive microcephaly 8", "link_status": true, "children": [] }, { "id": "DOID:0070283", "label": "primary autosomal recessive microcephaly 13", "link_status": true, "children": [] }, { "id": "DOID:0070284", "label": "primary autosomal recessive microcephaly 12", "link_status": true, "children": [] }, { "id": "DOID:0070285", "label": "primary autosomal recessive microcephaly 1", "link_status": true, "children": [] }, { "id": "DOID:0070286", "label": "primary autosomal recessive microcephaly 3", "link_status": true, "children": [] }, { "id": "DOID:0070287", "label": "primary autosomal recessive microcephaly 11", "link_status": true, "children": [] }, { "id": "DOID:0070288", "label": "primary autosomal recessive microcephaly 17", "link_status": true, "children": [] }, { "id": "DOID:0070289", "label": "primary autosomal recessive microcephaly 16", "link_status": true, "children": [] }, { "id": "DOID:0070290", "label": "primary autosomal recessive microcephaly 6", "link_status": true, "children": [] }, { "id": "DOID:0070291", "label": "primary autosomal recessive microcephaly 4", "link_status": true, "children": [] }, { "id": "DOID:0070292", "label": "primary autosomal recessive microcephaly 9", "link_status": true, "children": [] }, { "id": "DOID:0070293", "label": "primary autosomal recessive microcephaly 2 with or without cortical malformations", "link_status": true, "children": [] }, { "id": "DOID:0070294", "label": "primary autosomal recessive microcephaly 10", "link_status": true, "children": [] } ] }, { "id": "DOID:0070300", "label": "multiple epiphyseal dysplasia 4", "link_status": true, "children": [] }, { "id": "DOID:0070302", "label": "multiple epiphyseal dysplasia 7", "link_status": true, "children": [] }, { "id": "DOID:0070307", "label": "craniolenticulosutural dysplasia", "link_status": true, "children": [] }, { "id": "DOID:0070331", "label": "mitochondrial DNA depletion syndrome 8b", "link_status": true, "children": [] }, { "id": "DOID:0070332", "label": "multiple mitochondrial dysfunctions syndrome 6", "link_status": true, "children": [] }, { "id": "DOID:0070341", "label": "neonatal-onset type II citrullinemia", "link_status": true, "children": [] }, { "id": "DOID:0070352", "label": "stress-induced childhood-onset neurodegeneration with variable ataxia and seizures", "link_status": true, "children": [] }, { "id": "DOID:0070354", "label": "cataract 48", "link_status": true, "children": [] }, { "id": "DOID:0070356", "label": "visual impairment and progressive phthisis bulbi", "link_status": true, "children": [] }, { "id": "DOID:0070368", "label": "autosomal recessive chronic granulomatous disease 5", "link_status": true, "children": [] }, { "id": "DOID:0070369", "label": "restrictive dermopathy 1", "link_status": true, "children": [] }, { "id": "DOID:0070376", "label": "developmental and epileptic encephalopathy 31B", "link_status": true, "children": [] }, { "id": "DOID:0070382", "label": "developmental and epileptic encephalopathy 95", "link_status": true, "children": [] }, { "id": "DOID:0070387", "label": "developmental and epileptic encephalopathy 101", "link_status": true, "children": [] }, { "id": "DOID:0070388", "label": "developmental and epileptic encephalopathy 102", "link_status": true, "children": [] }, { "id": "DOID:0070391", "label": "developmental and epileptic encephalopathy 105", "link_status": true, "children": [] }, { "id": "DOID:0070392", "label": "developmental and epileptic encephalopathy 106", "link_status": true, "children": [] }, { "id": "DOID:0070393", "label": "developmental and epileptic encephalopathy 107", "link_status": true, "children": [] }, { "id": "DOID:0070395", "label": "developmental and epileptic encephalopathy 110", "link_status": true, "children": [] }, { "id": "DOID:0070396", "label": "progressive leukoencephalopathy with ovarian failure", "link_status": true, "children": [] }, { "id": "DOID:0070397", "label": "hypomyelinating leukodystrophy 23", "link_status": true, "children": [] }, { "id": "DOID:0070398", "label": "hypomyelinating leukodystrophy 15", "link_status": true, "children": [] }, { "id": "DOID:0070399", "label": "hypomyelinating leukodystrophy 18", "link_status": true, "children": [] }, { "id": "DOID:0070403", "label": "hypomyelinating leukodystrophy 26", "link_status": true, "children": [] }, { "id": "DOID:0070404", "label": "hypomyelinating leukodystrophy 17", "link_status": true, "children": [] }, { "id": "DOID:0070407", "label": "hypomyelinating leukodystrophy 21", "link_status": true, "children": [] }, { "id": "DOID:0070408", "label": "Hengel-Maroofian-Schols syndrome", "link_status": true, "children": [] }, { "id": "DOID:0070424", "label": "combined oxidative phosphorylation deficiency 44", "link_status": true, "children": [] }, { "id": "DOID:0070425", "label": "combined oxidative phosphorylation deficiency 52", "link_status": true, "children": [] }, { "id": "DOID:0070426", "label": "combined oxidative phosphorylation deficiency 53", "link_status": true, "children": [] }, { "id": "DOID:0070427", "label": "combined oxidative phosphorylation deficiency 54", "link_status": true, "children": [] }, { "id": "DOID:0070429", "label": "combined oxidative phosphorylation deficiency 56", "link_status": true, "children": [] }, { "id": "DOID:0070430", "label": "combined oxidative phosphorylation deficiency 57", "link_status": true, "children": [] }, { "id": "DOID:0070446", "label": "mitochondrial DNA depletion syndrome 16", "link_status": true, "children": [] }, { "id": "DOID:0070447", "label": "mitochondrial DNA depletion syndrome 16B", "link_status": true, "children": [] }, { "id": "DOID:0070448", "label": "mitochondrial DNA depletion syndrome 17", "link_status": true, "children": [] }, { "id": "DOID:0070449", "label": "mitochondrial DNA depletion syndrome 18", "link_status": true, "children": [] }, { "id": "DOID:0070450", "label": "mitochondrial DNA depletion syndrome 19", "link_status": true, "children": [] }, { "id": "DOID:0070451", "label": "mitochondrial DNA depletion syndrome 20", "link_status": true, "children": [] }, { "id": "DOID:0070454", "label": "hereditary spastic paraplegia 70", "link_status": true, "children": [] }, { "id": "DOID:0070456", "label": "hereditary spastic paraplegia 87", "link_status": true, "children": [] }, { "id": "DOID:0070458", "label": "hereditary spastic paraplegia 89", "link_status": true, "children": [] }, { "id": "DOID:0070462", "label": "mitochondrial complex V (ATP synthase) deficiency nuclear type 4B", "link_status": true, "children": [] }, { "id": "DOID:0070463", "label": "mitochondrial complex V (ATP synthase) deficiency nuclear type 5", "link_status": true, "children": [] }, { "id": "DOID:0070464", "label": "mitochondrial complex V (ATP synthase) deficiency nuclear type 7", "link_status": true, "children": [] }, { "id": "DOID:0070468", "label": "Yoon-Bellen neurodevelopmental syndrome", "link_status": true, "children": [] }, { "id": "DOID:0070473", "label": "Zaki syndrome", "link_status": true, "children": [] }, { "id": "DOID:0070476", "label": "diphthamide deficiency syndrome", "link_status": true, "children": [ { "id": "DOID:0070477", "label": "diphthamide deficiency syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0070478", "label": "diphthamide deficiency syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0070479", "label": "neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties", "link_status": true, "children": [] } ] }, { "id": "DOID:0070485", "label": "mitochondrial complex IV deficiency nuclear type 23", "link_status": true, "children": [] }, { "id": "DOID:0070486", "label": "Parkinson's disease 25", "link_status": true, "children": [] }, { "id": "DOID:0070489", "label": "classic dopamine transporter deficiency syndrome", "link_status": true, "children": [] }, { "id": "DOID:0070490", "label": "infantile parkinsonism-dystonia 2", "link_status": true, "children": [] }, { "id": "DOID:0070491", "label": "mitochondrial complex IV deficiency nuclear type 1", "link_status": true, "children": [] }, { "id": "DOID:0070492", "label": "mitochondrial complex IV deficiency nuclear type 3", "link_status": true, "children": [] }, { "id": "DOID:0070493", "label": "mitochondrial complex IV deficiency nuclear type 4", "link_status": true, "children": [] }, { "id": "DOID:0070494", "label": "mitochondrial complex IV deficiency nuclear type 7", "link_status": true, "children": [] }, { "id": "DOID:0070495", "label": "mitochondrial complex IV deficiency nuclear type 8", "link_status": true, "children": [] }, { "id": "DOID:0070496", "label": "mitochondrial complex IV deficiency nuclear type 10", "link_status": true, "children": [] }, { "id": "DOID:0070497", "label": "mitochondrial complex IV deficiency nuclear type 11", "link_status": true, "children": [] }, { "id": "DOID:0070498", "label": "mitochondrial complex IV deficiency nuclear type 12", "link_status": true, "children": [] }, { "id": "DOID:0070499", "label": "mitochondrial complex IV deficiency nuclear type 14", "link_status": true, "children": [] }, { "id": "DOID:0070500", "label": "mitochondrial complex IV deficiency nuclear type 15", "link_status": true, "children": [] }, { "id": "DOID:0070501", "label": "mitochondrial complex IV deficiency nuclear type 16", "link_status": true, "children": [] }, { "id": "DOID:0070502", "label": "mitochondrial complex IV deficiency nuclear type 17", "link_status": true, "children": [] }, { "id": "DOID:0070503", "label": "mitochondrial complex IV deficiency nuclear type 18", "link_status": true, "children": [] }, { "id": "DOID:0070504", "label": "mitochondrial complex IV deficiency nuclear type 19", "link_status": true, "children": [] }, { "id": "DOID:0070505", "label": "mitochondrial complex IV deficiency nuclear type 20", "link_status": true, "children": [] }, { "id": "DOID:0070506", "label": "mitochondrial complex IV deficiency nuclear type 21", "link_status": true, "children": [] }, { "id": "DOID:0070507", "label": "mitochondrial complex IV deficiency nuclear type 22", "link_status": true, "children": [] }, { "id": "DOID:0070510", "label": "inflammatory poikiloderma with hair abnormalities and acral keratoses", "link_status": true, "children": [] }, { "id": "DOID:0070511", "label": "polyhydramnios, megalencephaly, and symptomatic epilepsy", "link_status": true, "children": [] }, { "id": "DOID:0070526", "label": "PLACK syndrome", "link_status": true, "children": [] }, { "id": "DOID:0070531", "label": "foveal hypoplasia 2", "link_status": true, "children": [] }, { "id": "DOID:0070539", "label": "Halperin-Birk syndrome", "link_status": true, "children": [] }, { "id": "DOID:0070540", "label": "mitochondrial short-chain enoyl-CoA hydratase 1 deficiency", "link_status": true, "children": [] }, { "id": "DOID:0070541", "label": "3-hydroxy-3-methylglutaryl-CoA lyase deficiency", "link_status": true, "children": [] }, { "id": "DOID:0070543", "label": "neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities", "link_status": true, "children": [] }, { "id": "DOID:0070544", "label": "congenital glutamine deficiency", "link_status": true, "children": [] }, { "id": "DOID:0070554", "label": "palmoplantar keratoderma and woolly hair", "link_status": true, "children": [] }, { "id": "DOID:0070555", "label": "Nagashima-type palmoplantar keratosis", "link_status": true, "children": [] }, { "id": "DOID:0070562", "label": "Fanconi-Bickel syndrome", "link_status": true, "children": [] }, { "id": "DOID:0070563", "label": "glucose-galactose malabsorption", "link_status": true, "children": [] }, { "id": "DOID:0070565", "label": "spermatogenic failure 66", "link_status": true, "children": [] }, { "id": "DOID:0070566", "label": "spermatogenic failure 67", "link_status": true, "children": [] }, { "id": "DOID:0070567", "label": "spermatogenic failure 68", "link_status": true, "children": [] }, { "id": "DOID:0070568", "label": "spermatogenic failure 69", "link_status": true, "children": [] }, { "id": "DOID:0070569", "label": "spermatogenic failure 70", "link_status": true, "children": [] }, { "id": "DOID:0070570", "label": "spermatogenic failure 71", "link_status": true, "children": [] }, { "id": "DOID:0070571", "label": "spermatogenic failure 72", "link_status": true, "children": [] }, { "id": "DOID:0070572", "label": "spermatogenic failure 73", "link_status": true, "children": [] }, { "id": "DOID:0070573", "label": "spermatogenic failure 74", "link_status": true, "children": [] }, { "id": "DOID:0070574", "label": "spermatogenic failure 75", "link_status": true, "children": [] }, { "id": "DOID:0070575", "label": "spermatogenic failure 76", "link_status": true, "children": [] }, { "id": "DOID:0070576", "label": "spermatogenic failure 77", "link_status": true, "children": [] }, { "id": "DOID:0070577", "label": "spermatogenic failure 78", "link_status": true, "children": [] }, { "id": "DOID:0070578", "label": "spermatogenic failure 79", "link_status": true, "children": [] }, { "id": "DOID:0070579", "label": "spermatogenic failure 80", "link_status": true, "children": [] }, { "id": "DOID:0070580", "label": "spermatogenic failure 81", "link_status": true, "children": [] }, { "id": "DOID:0070581", "label": "spermatogenic failure 82", "link_status": true, "children": [] }, { "id": "DOID:0070582", "label": "spermatogenic failure 83", "link_status": true, "children": [] }, { "id": "DOID:0070583", "label": "spermatogenic failure 84", "link_status": true, "children": [] }, { "id": "DOID:0070584", "label": "spermatogenic failure 85", "link_status": true, "children": [] }, { "id": "DOID:0070585", "label": "spermatogenic failure 86", "link_status": true, "children": [] }, { "id": "DOID:0070586", "label": "spermatogenic failure 87", "link_status": true, "children": [] }, { "id": "DOID:0070587", "label": "spermatogenic failure 88", "link_status": true, "children": [] }, { "id": "DOID:0070588", "label": "spermatogenic failure 89", "link_status": true, "children": [] }, { "id": "DOID:0070589", "label": "spermatogenic failure 90", "link_status": true, "children": [] }, { "id": "DOID:0070590", "label": "spermatogenic failure 91", "link_status": true, "children": [] }, { "id": "DOID:0070591", "label": "spermatogenic failure 92", "link_status": true, "children": [] }, { "id": "DOID:0070592", "label": "spermatogenic failure 93", "link_status": true, "children": [] }, { "id": "DOID:0070593", "label": "spermatogenic failure 94", "link_status": true, "children": [] }, { "id": "DOID:0070594", "label": "spermatogenic failure 95", "link_status": true, "children": [] }, { "id": "DOID:0070613", "label": "familial renal glucosuria", "link_status": true, "children": [] }, { "id": "DOID:0080026", "label": "otospondylomegaepiphyseal dysplasia, autosomal recessive", "link_status": true, "children": [] }, { "id": "DOID:0080036", "label": "SOST-related sclerosing bone dysplasia", "link_status": true, "children": [] }, { "id": "DOID:0080038", "label": "pycnodysostosis", "link_status": true, "children": [] }, { "id": "DOID:0080050", "label": "acromesomelic dysplasia, Maroteaux type", "link_status": true, "children": [] }, { "id": "DOID:0080051", "label": "acromesomelic dysplasia, Hunter-Thompson type", "link_status": true, "children": [] }, { "id": "DOID:0080052", "label": "acromesomelic dysplasia, Grebe type", "link_status": true, "children": [] }, { "id": "DOID:0080054", "label": "achondrogenesis type IA", "link_status": true, "children": [] }, { "id": "DOID:0080055", "label": "achondrogenesis type IB", "link_status": true, "children": [] }, { "id": "DOID:0080071", "label": "mucolipidosis III alpha/beta", "link_status": true, "children": [] }, { "id": "DOID:0080081", "label": "nonsyndromic congenital nail disorder 3", "link_status": true, "children": [] }, { "id": "DOID:0080082", "label": "nonsyndromic congenital nail disorder 4", "link_status": true, "children": [] }, { "id": "DOID:0080092", "label": "myofibrillar myopathy 1", "link_status": true, "children": [] }, { "id": "DOID:0080098", "label": "myofibrillar myopathy 7", "link_status": true, "children": [] }, { "id": "DOID:0080101", "label": "Compton-North congenital myopathy", "link_status": true, "children": [] }, { "id": "DOID:0080105", "label": "microcephaly and chorioretinopathy 1", "link_status": true, "children": [] }, { "id": "DOID:0080106", "label": "microcephaly and chorioretinopathy 2", "link_status": true, "children": [] }, { "id": "DOID:0080107", "label": "microcephaly and chorioretinopathy 3", "link_status": true, "children": [] }, { "id": "DOID:0080119", "label": "mitochondrial DNA depletion syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0080120", "label": "mitochondrial DNA depletion syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0080121", "label": "mitochondrial DNA depletion syndrome 3", "link_status": true, "children": [] }, { "id": "DOID:0080122", "label": "Alpers-Huttenlocher syndrome", "link_status": true, "children": [] }, { "id": "DOID:0080123", "label": "mitochondrial DNA depletion syndrome 4b", "link_status": true, "children": [] }, { "id": "DOID:0080124", "label": "mitochondrial DNA depletion syndrome 5", "link_status": true, "children": [] }, { "id": "DOID:0080125", "label": "mitochondrial DNA depletion syndrome 6", "link_status": true, "children": [] }, { "id": "DOID:0080126", "label": "mitochondrial DNA depletion syndrome 7", "link_status": true, "children": [] }, { "id": "DOID:0080127", "label": "mitochondrial DNA depletion syndrome 8a", "link_status": true, "children": [] }, { "id": "DOID:0080128", "label": "mitochondrial DNA depletion syndrome 9", "link_status": true, "children": [] }, { "id": "DOID:0080129", "label": "mitochondrial DNA depletion syndrome 11", "link_status": true, "children": [] }, { "id": "DOID:0080131", "label": "mitochondrial DNA depletion syndrome 13", "link_status": true, "children": [] }, { "id": "DOID:0080132", "label": "Sengers syndrome", "link_status": true, "children": [] }, { "id": "DOID:0080133", "label": "multiple mitochondrial dysfunctions syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0080134", "label": "multiple mitochondrial dysfunctions syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0080135", "label": "multiple mitochondrial dysfunctions syndrome 3", "link_status": true, "children": [] }, { "id": "DOID:0080136", "label": "multiple mitochondrial dysfunctions syndrome 4", "link_status": true, "children": [] }, { "id": "DOID:0080138", "label": "multiple congenital anomalies-hypotonia-seizures syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0080140", "label": "multiple congenital anomalies-hypotonia-seizures syndrome 3", "link_status": true, "children": [] }, { "id": "DOID:0080141", "label": "mosaic variegated aneuploidy syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0080142", "label": "mosaic variegated aneuploidy syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0080163", "label": "autosomal recessive autoinflammation, panniculitis, and dermatosis syndrome", "link_status": true, "children": [] }, { "id": "DOID:0080172", "label": "poor metabolism of thiopurines", "link_status": true, "children": [ { "id": "DOID:0060996", "label": "poor metabolism of thiopurines 2", "link_status": true, "children": [] }, { "id": "DOID:0061004", "label": "poor metabolism of thiopurines 1", "link_status": true, "children": [] } ] }, { "id": "DOID:0080181", "label": "PHARC syndrome", "link_status": true, "children": [] }, { "id": "DOID:0080195", "label": "Marinesco-Sjogren syndrome", "link_status": true, "children": [] }, { "id": "DOID:0080197", "label": "congenital muscular dystrophy with cataracts and intellectual disability", "link_status": true, "children": [] }, { "id": "DOID:0080209", "label": "sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay", "link_status": true, "children": [] }, { "id": "DOID:0080217", "label": "lysosomal acid lipase deficiency", "link_status": true, "children": [ { "id": "DOID:14497", "label": "Wolman disease", "link_status": true, "children": [] }, { "id": "DOID:14502", "label": "cholesterol ester storage disease", "link_status": true, "children": [] } ] }, { "id": "DOID:0080245", "label": "Galloway-Mowat syndrome 3", "link_status": true, "children": [] }, { "id": "DOID:0080246", "label": "Galloway-Mowat syndrome 4", "link_status": true, "children": [] }, { "id": "DOID:0080250", "label": "erythrokeratodermia variabilis et progressiva 4", "link_status": true, "children": [] }, { "id": "DOID:0080251", "label": "erythrokeratodermia variabilis et progressiva 5", "link_status": true, "children": [] }, { "id": "DOID:0080252", "label": "spastic ataxia 8", "link_status": true, "children": [] }, { "id": "DOID:0080253", "label": "Meckel syndrome 13", "link_status": true, "children": [] }, { "id": "DOID:0080254", "label": "orofaciodigital syndrome XVI", "link_status": true, "children": [] }, { "id": "DOID:0080255", "label": "Meier-Gorlin syndrome 8", "link_status": true, "children": [] }, { "id": "DOID:0080265", "label": "RENI syndrome", "link_status": true, "children": [] }, { "id": "DOID:0080271", "label": "nephrotic syndrome type 15", "link_status": true, "children": [] }, { "id": "DOID:0080272", "label": "nephrotic syndrome type 16", "link_status": true, "children": [] }, { "id": "DOID:0080274", "label": "multiple mitochondrial dysfunctions syndrome 5", "link_status": true, "children": [] }, { "id": "DOID:0080283", "label": "developmental and epileptic encephalopathy 55", "link_status": true, "children": [] }, { "id": "DOID:0080289", "label": "orofaciodigital syndrome XVII", "link_status": true, "children": [] }, { "id": "DOID:0080292", "label": "retinitis pigmentosa 81", "link_status": true, "children": [] }, { "id": "DOID:0080293", "label": "short-rib thoracic dysplasia 18 with polydactyly", "link_status": true, "children": [] }, { "id": "DOID:0080295", "label": "short-rib thoracic dysplasia 19 with or without polydactyly", "link_status": true, "children": [] }, { "id": "DOID:0080296", "label": "hypomyelinating leukodystrophy 14", "link_status": true, "children": [] }, { "id": "DOID:0080308", "label": "myofibrillar myopathy 8", "link_status": true, "children": [] }, { "id": "DOID:0080309", "label": "infantile-onset myofibrillar myopathy-2B", "link_status": true, "children": [] }, { "id": "DOID:0080312", "label": "neurodevelopmental disorder with midbrain and hindbrain malformations", "link_status": true, "children": [] }, { "id": "DOID:0080316", "label": "megalencephalic leukoencephalopathy with subcortical cysts 1", "link_status": true, "children": [] }, { "id": "DOID:0080318", "label": "megalencephalic leukoencephalopathy with subcortical cysts 2A", "link_status": true, "children": [] }, { "id": "DOID:0080327", "label": "multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly", "link_status": true, "children": [] }, { "id": "DOID:0080335", "label": "mitochondrial DNA depletion syndrome 12b", "link_status": true, "children": [] }, { "id": "DOID:0080337", "label": "mitochondrial DNA depletion syndrome 15", "link_status": true, "children": [] }, { "id": "DOID:0080343", "label": "autosomal recessive pyridoxine-refractory sideroblastic anemia 3", "link_status": true, "children": [] }, { "id": "DOID:0080349", "label": "developmental and epileptic encephalopathy 39", "link_status": true, "children": [] }, { "id": "DOID:0080350", "label": "retinitis pigmentosa 77", "link_status": true, "children": [] }, { "id": "DOID:0080357", "label": "mitochondrial complex IV deficiency nuclear type 2", "link_status": true, "children": [] }, { "id": "DOID:0080358", "label": "mitochondrial complex IV deficiency nuclear type 6", "link_status": true, "children": [] }, { "id": "DOID:0080359", "label": "mitochondrial complex IV deficiency nuclear type 9", "link_status": true, "children": [] }, { "id": "DOID:0080360", "label": "mitochondrial complex IV deficiency nuclear type 13", "link_status": true, "children": [] }, { "id": "DOID:0080361", "label": "trimethylaminuria", "link_status": true, "children": [] }, { "id": "DOID:0080363", "label": "mitochondrial pyruvate carrier deficiency", "link_status": true, "children": [] }, { "id": "DOID:0080379", "label": "nephrotic syndrome type 2", "link_status": true, "children": [] }, { "id": "DOID:0080380", "label": "nephrotic syndrome type 5", "link_status": true, "children": [] }, { "id": "DOID:0080381", "label": "nephrotic syndrome type 13", "link_status": true, "children": [] }, { "id": "DOID:0080382", "label": "nephrotic syndrome type 3", "link_status": true, "children": [] }, { "id": "DOID:0080384", "label": "nephrotic syndrome type 6", "link_status": true, "children": [] }, { "id": "DOID:0080385", "label": "nephrotic syndrome type 11", "link_status": true, "children": [] }, { "id": "DOID:0080386", "label": "nephrotic syndrome type 10", "link_status": true, "children": [] }, { "id": "DOID:0080387", "label": "nephrotic syndrome type 12", "link_status": true, "children": [] }, { "id": "DOID:0080388", "label": "nephrotic syndrome type 7", "link_status": true, "children": [] }, { "id": "DOID:0080389", "label": "nephrotic syndrome type 8", "link_status": true, "children": [] }, { "id": "DOID:0080390", "label": "nephrotic syndrome type 1", "link_status": true, "children": [] }, { "id": "DOID:0080391", "label": "nephrotic syndrome type 9", "link_status": true, "children": [] }, { "id": "DOID:0080392", "label": "nephrotic syndrome type 17", "link_status": true, "children": [] }, { "id": "DOID:0080393", "label": "nephrotic syndrome type 18", "link_status": true, "children": [] }, { "id": "DOID:0080394", "label": "nephrotic syndrome type 19", "link_status": true, "children": [] }, { "id": "DOID:0080410", "label": "familial adenomatous polyposis 2", "link_status": true, "children": [] }, { "id": "DOID:0080411", "label": "familial adenomatous polyposis 3", "link_status": true, "children": [] }, { "id": "DOID:0080412", "label": "familial adenomatous polyposis 4", "link_status": true, "children": [] }, { "id": "DOID:0080413", "label": "developmental and epileptic encephalopathy 18", "link_status": true, "children": [] }, { "id": "DOID:0080414", "label": "developmental and epileptic encephalopathy 15", "link_status": true, "children": [] }, { "id": "DOID:0080415", "label": "developmental and epileptic encephalopathy 23", "link_status": true, "children": [] }, { "id": "DOID:0080417", "label": "developmental and epileptic encephalopathy 38", "link_status": true, "children": [] }, { "id": "DOID:0080419", "label": "developmental and epileptic encephalopathy 50", "link_status": true, "children": [] }, { "id": "DOID:0080424", "label": "developmental and epileptic encephalopathy 44", "link_status": true, "children": [] }, { "id": "DOID:0080426", "label": "developmental and epileptic encephalopathy 63", "link_status": true, "children": [] }, { "id": "DOID:0080427", "label": "developmental and epileptic encephalopathy 40", "link_status": true, "children": [] }, { "id": "DOID:0080432", "label": "developmental and epileptic encephalopathy 60", "link_status": true, "children": [] }, { "id": "DOID:0080433", "label": "developmental and epileptic encephalopathy 51", "link_status": true, "children": [] }, { "id": "DOID:0080434", "label": "developmental and epileptic encephalopathy 61", "link_status": true, "children": [] }, { "id": "DOID:0080435", "label": "developmental and epileptic encephalopathy 37", "link_status": true, "children": [] }, { "id": "DOID:0080440", "label": "developmental and epileptic encephalopathy 3", "link_status": true, "children": [] }, { "id": "DOID:0080441", "label": "developmental and epileptic encephalopathy 49", "link_status": true, "children": [] }, { "id": "DOID:0080443", "label": "developmental and epileptic encephalopathy 21", "link_status": true, "children": [] }, { "id": "DOID:0080448", "label": "developmental and epileptic encephalopathy 48", "link_status": true, "children": [] }, { "id": "DOID:0080449", "label": "developmental and epileptic encephalopathy 16", "link_status": true, "children": [] }, { "id": "DOID:0080451", "label": "developmental and epileptic encephalopathy 29", "link_status": true, "children": [] }, { "id": "DOID:0080452", "label": "developmental and epileptic encephalopathy 28", "link_status": true, "children": [] }, { "id": "DOID:0080453", "label": "developmental and epileptic encephalopathy 25", "link_status": true, "children": [] }, { "id": "DOID:0080455", "label": "developmental and epileptic encephalopathy 52", "link_status": true, "children": [] }, { "id": "DOID:0080457", "label": "microcephaly, seizures, and developmental delay", "link_status": true, "children": [] }, { "id": "DOID:0080458", "label": "developmental and epileptic encephalopathy 35", "link_status": true, "children": [] }, { "id": "DOID:0080459", "label": "developmental and epileptic encephalopathy 12", "link_status": true, "children": [] }, { "id": "DOID:0080460", "label": "developmental and epileptic encephalopathy 34", "link_status": true, "children": [] }, { "id": "DOID:0080464", "label": "developmental and epileptic encephalopathy 53", "link_status": true, "children": [] }, { "id": "DOID:0080493", "label": "ovarian dysgenesis 1", "link_status": true, "children": [] }, { "id": "DOID:0080495", "label": "ovarian dysgenesis 3", "link_status": true, "children": [] }, { "id": "DOID:0080496", "label": "ovarian dysgenesis 4", "link_status": true, "children": [] }, { "id": "DOID:0080497", "label": "ovarian dysgenesis 5", "link_status": true, "children": [] }, { "id": "DOID:0080498", "label": "ovarian dysgenesis 6", "link_status": true, "children": [] }, { "id": "DOID:0080499", "label": "ovarian dysgenesis 7", "link_status": true, "children": [] }, { "id": "DOID:0080512", "label": "Meier-Gorlin syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0080513", "label": "Meier-Gorlin syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0080514", "label": "Meier-Gorlin syndrome 3", "link_status": true, "children": [] }, { "id": "DOID:0080515", "label": "Meier-Gorlin syndrome 4", "link_status": true, "children": [] }, { "id": "DOID:0080516", "label": "Meier-Gorlin syndrome 5", "link_status": true, "children": [] }, { "id": "DOID:0080518", "label": "Meier-Gorlin syndrome 7", "link_status": true, "children": [] }, { "id": "DOID:0080542", "label": "hyperprolinemia type 1", "link_status": true, "children": [] }, { "id": "DOID:0080543", "label": "hyperprolinemia type 2", "link_status": true, "children": [] }, { "id": "DOID:0080552", "label": "congenital disorder of glycosylation Ia", "link_status": true, "children": [] }, { "id": "DOID:0080553", "label": "congenital disorder of glycosylation Iaa", "link_status": true, "children": [] }, { "id": "DOID:0080554", "label": "congenital disorder of glycosylation Ib", "link_status": true, "children": [] }, { "id": "DOID:0080555", "label": "congenital disorder of glycosylation Ic", "link_status": true, "children": [] }, { "id": "DOID:0080556", "label": "congenital disorder of glycosylation Id", "link_status": true, "children": [] }, { "id": "DOID:0080557", "label": "congenital disorder of glycosylation Ie", "link_status": true, "children": [] }, { "id": "DOID:0080558", "label": "congenital disorder of glycosylation If", "link_status": true, "children": [] }, { "id": "DOID:0080559", "label": "congenital disorder of glycosylation Ig", "link_status": true, "children": [] }, { "id": "DOID:0080560", "label": "congenital disorder of glycosylation Ih", "link_status": true, "children": [] }, { "id": "DOID:0080561", "label": "congenital disorder of glycosylation Ii", "link_status": true, "children": [] }, { "id": "DOID:0080562", "label": "congenital disorder of glycosylation Ij", "link_status": true, "children": [] }, { "id": "DOID:0080563", "label": "congenital disorder of glycosylation Ik", "link_status": true, "children": [] }, { "id": "DOID:0080564", "label": "congenital disorder of glycosylation Il", "link_status": true, "children": [] }, { "id": "DOID:0080565", "label": "congenital disorder of glycosylation Im", "link_status": true, "children": [] }, { "id": "DOID:0080566", "label": "congenital disorder of glycosylation In", "link_status": true, "children": [] }, { "id": "DOID:0080567", "label": "congenital disorder of glycosylation Ip", "link_status": true, "children": [] }, { "id": "DOID:0080568", "label": "congenital disorder of glycosylation Iq", "link_status": true, "children": [] }, { "id": "DOID:0080569", "label": "congenital disorder of glycosylation Ir", "link_status": true, "children": [] }, { "id": "DOID:0080570", "label": "congenital disorder of glycosylation It", "link_status": true, "children": [] }, { "id": "DOID:0080571", "label": "congenital disorder of glycosylation Iu", "link_status": true, "children": [] }, { "id": "DOID:0080572", "label": "congenital disorder of glycosylation Iw", "link_status": true, "children": [] }, { "id": "DOID:0080573", "label": "congenital disorder of glycosylation Ix", "link_status": true, "children": [] }, { "id": "DOID:0080575", "label": "Larsen-like syndrome B3GAT3 type", "link_status": true, "children": [] }, { "id": "DOID:0080576", "label": "spondyloepimetaphyseal dysplasia, Genevieve-type", "link_status": true, "children": [] }, { "id": "DOID:0080581", "label": "hyperekplexia 4", "link_status": true, "children": [] }, { "id": "DOID:0080587", "label": "congenital myasthenic syndrome 22", "link_status": true, "children": [] }, { "id": "DOID:0080590", "label": "Klippel-Feil syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0080592", "label": "Klippel-Feil syndrome 4", "link_status": true, "children": [] }, { "id": "DOID:0080594", "label": "hyper IgE recurrent infection syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0080595", "label": "autosomal recessive hyper-IgE syndrome 3 with recurrent infections", "link_status": true, "children": [] }, { "id": "DOID:0080596", "label": "hyper IgE recurrent infection syndrome 4", "link_status": true, "children": [] }, { "id": "DOID:0080607", "label": "anterior segment dysgenesis 2", "link_status": true, "children": [] }, { "id": "DOID:0080612", "label": "anterior segment dysgenesis 7", "link_status": true, "children": [] }, { "id": "DOID:0080613", "label": "anterior segment dysgenesis 8", "link_status": true, "children": [] }, { "id": "DOID:0080621", "label": "glucocorticoid deficiency 1", "link_status": true, "children": [] }, { "id": "DOID:0080622", "label": "peroxisome biogenesis disorder 2B", "link_status": true, "children": [] }, { "id": "DOID:0080623", "label": "Heimler syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0080624", "label": "Heimler syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0080626", "label": "corticosterone methyloxidase deficiency 1", "link_status": true, "children": [] }, { "id": "DOID:0080628", "label": "alopecia-mental retardation syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0080632", "label": "Fazio-Londe disease", "link_status": true, "children": [] }, { "id": "DOID:0080635", "label": "optic disc anomalies with retinal and/or macular dystrophy", "link_status": true, "children": [] }, { "id": "DOID:0080663", "label": "atrial standstill 2", "link_status": true, "children": [] }, { "id": "DOID:0080672", "label": "fibrochondrogenesis 1", "link_status": true, "children": [] }, { "id": "DOID:0080673", "label": "fibrochondrogenesis 2", "link_status": true, "children": [] }, { "id": "DOID:0080678", "label": "mucolipidosis III gamma", "link_status": true, "children": [] }, { "id": "DOID:0080689", "label": "mosaic variegated aneuploidy syndrome 3", "link_status": true, "children": [] }, { "id": "DOID:0080715", "label": "developmental and epileptic encephalopathy 82", "link_status": true, "children": [] }, { "id": "DOID:0080717", "label": "infantile liver failure syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0080718", "label": "GNE myopathy", "link_status": true, "children": [] }, { "id": "DOID:0080719", "label": "congenital myopathy 6", "link_status": true, "children": [] }, { "id": "DOID:0080722", "label": "Kenny-Caffey syndrome type 1", "link_status": true, "children": [] }, { "id": "DOID:0080729", "label": "brittle cornea syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0080730", "label": "Ehlers-Danlos syndrome cardiac valvular type", "link_status": true, "children": [] }, { "id": "DOID:0080731", "label": "Ehlers-Danlos syndrome classic-like 1", "link_status": true, "children": [] }, { "id": "DOID:0080732", "label": "Ehlers-Danlos syndrome classic-like 2", "link_status": true, "children": [] }, { "id": "DOID:0080733", "label": "Ehlers-Danlos syndrome dermatosparaxis type", "link_status": true, "children": [] }, { "id": "DOID:0080734", "label": "Ehlers-Danlos syndrome kyphoscoliotic type 1", "link_status": true, "children": [] }, { "id": "DOID:0080735", "label": "Ehlers-Danlos syndrome kyphoscoliotic type 2", "link_status": true, "children": [] }, { "id": "DOID:0080736", "label": "Ehlers-Danlos syndrome musculocontractural type 1", "link_status": true, "children": [] }, { "id": "DOID:0080737", "label": "Ehlers-Danlos syndrome musculocontractural type 2", "link_status": true, "children": [] }, { "id": "DOID:0080738", "label": "Ehlers-Danlos syndrome spondylodysplastic type 1", "link_status": true, "children": [] }, { "id": "DOID:0080751", "label": "keratosis pilaris atrophicans", "link_status": true, "children": [ { "id": "DOID:0080753", "label": "keratosis follicularis spinulosa decalvans", "link_status": true, "children": [ { "id": "DOID:0080754", "label": "X-linked keratosis follicularis spinulosa decalvans", "link_status": true, "children": [] } ] } ] }, { "id": "DOID:0080758", "label": "Fanconi renotubular syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0080761", "label": "Fanconi renotubular syndrome 5", "link_status": true, "children": [] }, { "id": "DOID:0080768", "label": "pyridoxine-dependent epilepsy", "link_status": true, "children": [ { "id": "DOID:0070519", "label": "early-onset vitamin B6-dependent epilepsy 4", "link_status": true, "children": [] }, { "id": "DOID:0080769", "label": "early-onset vitamin B6-dependent epilepsy 1", "link_status": true, "children": [] } ] }, { "id": "DOID:0080778", "label": "transient infantile liver failure", "link_status": true, "children": [] }, { "id": "DOID:0080785", "label": "Brown-Vialetto-Van Laere syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0080786", "label": "Brown-Vialetto-Van Laere syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0080790", "label": "Treacher Collins syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0080791", "label": "Treacher Collins syndrome 3", "link_status": true, "children": [] }, { "id": "DOID:0080802", "label": "autosomal recessive craniometaphyseal dysplasia", "link_status": true, "children": [] }, { "id": "DOID:0080836", "label": "growth hormone insensitivity syndrome with immune dysregulation 1", "link_status": true, "children": [] }, { "id": "DOID:0080844", "label": "omodysplasia 1", "link_status": true, "children": [] }, { "id": "DOID:0080865", "label": "primary ovarian insufficiency 8", "link_status": true, "children": [] }, { "id": "DOID:0080866", "label": "primary ovarian insufficiency 9", "link_status": true, "children": [] }, { "id": "DOID:0080867", "label": "primary ovarian insufficiency 10", "link_status": true, "children": [] }, { "id": "DOID:0080869", "label": "primary ovarian insufficiency 12", "link_status": true, "children": [] }, { "id": "DOID:0080870", "label": "primary ovarian insufficiency 13", "link_status": true, "children": [] }, { "id": "DOID:0080871", "label": "primary ovarian insufficiency 14", "link_status": true, "children": [] }, { "id": "DOID:0080872", "label": "primary ovarian insufficiency 15", "link_status": true, "children": [] }, { "id": "DOID:0080884", "label": "vitamin D-dependent rickets type 2A", "link_status": true, "children": [] }, { "id": "DOID:0080886", "label": "vitamin D-dependent rickets type 1A", "link_status": true, "children": [] }, { "id": "DOID:0080887", "label": "vitamin D-dependent rickets type 1B", "link_status": true, "children": [] }, { "id": "DOID:0080898", "label": "cerebellofaciodental syndrome", "link_status": true, "children": [] }, { "id": "DOID:0080922", "label": "bilateral frontoparietal polymicrogyria", "link_status": true, "children": [] }, { "id": "DOID:0080923", "label": "bilateral parasagittal parieto-occipital polymicrogyria", "link_status": true, "children": [] }, { "id": "DOID:0080925", "label": "cytochrome P450 oxidoreductase deficiency", "link_status": true, "children": [] }, { "id": "DOID:0080939", "label": "hereditary angioedema type I", "link_status": true, "children": [] }, { "id": "DOID:0080946", "label": "retinal dystrophy with leukodystrophy", "link_status": true, "children": [] }, { "id": "DOID:0080950", "label": "alopecia-mental retardation syndrome 4", "link_status": true, "children": [] }, { "id": "DOID:0080952", "label": "AMED syndrome", "link_status": true, "children": [] }, { "id": "DOID:0080953", "label": "amelogenesis imperfecta type 1J", "link_status": true, "children": [] }, { "id": "DOID:0080954", "label": "arthrogryposis multiplex congenita", "link_status": true, "children": [ { "id": "DOID:0070336", "label": "arthrogryposis multiplex congenita-6", "link_status": true, "children": [] }, { "id": "DOID:0080978", "label": "arthrogryposis multiplex congenita-1", "link_status": true, "children": [] }, { "id": "DOID:0080979", "label": "arthrogryposis multiplex congenita-3", "link_status": true, "children": [] }, { "id": "DOID:0080980", "label": "arthrogryposis multiplex congenita-4", "link_status": true, "children": [] }, { "id": "DOID:0080981", "label": "arthrogryposis multiplex congenita-5", "link_status": true, "children": [] }, { "id": "DOID:0090124", "label": "neurogenic-type arthrogryposis multiplex congenita-2", "link_status": true, "children": [] } ] }, { "id": "DOID:0080960", "label": "amelogenesis imperfecta type 2A6", "link_status": true, "children": [] }, { "id": "DOID:0080962", "label": "anauxetic dysplasia 2", "link_status": true, "children": [] }, { "id": "DOID:0080963", "label": "anauxetic dysplasia 3", "link_status": true, "children": [] }, { "id": "DOID:0081007", "label": "RNASET2-deficient cystic leukoencephalopathy", "link_status": true, "children": [] }, { "id": "DOID:0081008", "label": "Lodder-Merla syndrome type 1 with impaired intellectual development and cardiac arrhythmia", "link_status": true, "children": [] }, { "id": "DOID:0081016", "label": "congenital fibrosis of the extraocular muscles 2", "link_status": true, "children": [] }, { "id": "DOID:0081020", "label": "congenital fibrosis of the extraocular muscles 5", "link_status": true, "children": [] }, { "id": "DOID:0081022", "label": "retinal cone dystrophy 3B", "link_status": true, "children": [] }, { "id": "DOID:0081034", "label": "glutatione synthetase deficiency with 5-oxoprolinuria", "link_status": true, "children": [] }, { "id": "DOID:0081045", "label": "frontonasal dysplasia 1", "link_status": true, "children": [] }, { "id": "DOID:0081046", "label": "frontonasal dysplasia 2", "link_status": true, "children": [] }, { "id": "DOID:0081047", "label": "frontonasal dysplasia 3", "link_status": true, "children": [] }, { "id": "DOID:0081061", "label": "nephrogenic diabetes insipidus type 2", "link_status": true, "children": [] }, { "id": "DOID:0081111", "label": "osteosclerotic metaphyseal dysplasia", "link_status": true, "children": [] }, { "id": "DOID:0081124", "label": "craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0081129", "label": "mandibuloacral dysplasia type B lipodystrophy", "link_status": true, "children": [] }, { "id": "DOID:0081130", "label": "BH4-deficient hyperphenylalaninemia C", "link_status": true, "children": [] }, { "id": "DOID:0081131", "label": "BH4-deficient hyperphenylalaninemia D", "link_status": true, "children": [] }, { "id": "DOID:0081135", "label": "agammaglobulinemia 2", "link_status": true, "children": [] }, { "id": "DOID:0081136", "label": "agammaglobulinemia 1", "link_status": true, "children": [] }, { "id": "DOID:0081137", "label": "agammaglobulinemia 3", "link_status": true, "children": [] }, { "id": "DOID:0081138", "label": "agammaglobulinemia 6", "link_status": true, "children": [] }, { "id": "DOID:0081139", "label": "agammaglobulinemia 7", "link_status": true, "children": [] }, { "id": "DOID:0081141", "label": "agammaglobulinemia 9", "link_status": true, "children": [] }, { "id": "DOID:0081143", "label": "agammaglobulinemia 8B", "link_status": true, "children": [] }, { "id": "DOID:0081159", "label": "dilated cardiomyopathy 2C", "link_status": true, "children": [] }, { "id": "DOID:0081160", "label": "dilated cardiomyopathy 2D", "link_status": true, "children": [] }, { "id": "DOID:0081161", "label": "dilated cardiomyopathy 2E", "link_status": true, "children": [] }, { "id": "DOID:0081162", "label": "dilated cardiomyopathy 2F", "link_status": true, "children": [] }, { "id": "DOID:0081163", "label": "dilated cardiomyopathy 2G", "link_status": true, "children": [] }, { "id": "DOID:0081168", "label": "HMG-CoA synthase 2 deficiency", "link_status": true, "children": [] }, { "id": "DOID:0081175", "label": "short stature, hearing loss, retinitis pigmentosa, and distinctive facies", "link_status": true, "children": [] }, { "id": "DOID:0081237", "label": "acromesomelic dysplasia 3", "link_status": true, "children": [] }, { "id": "DOID:0081238", "label": "acromesomelic dysplasia 4", "link_status": true, "children": [] }, { "id": "DOID:0081240", "label": "peroxisome biogenesis disorder 1B", "link_status": true, "children": [] }, { "id": "DOID:0081241", "label": "peroxisome biogenesis disorder 3B", "link_status": true, "children": [] }, { "id": "DOID:0081269", "label": "pulmonary venoocclusive disease 2", "link_status": true, "children": [] }, { "id": "DOID:0081272", "label": "Sandestig-Stefanova syndrome", "link_status": true, "children": [] }, { "id": "DOID:0081274", "label": "peroxisome biogenesis disorder 14B", "link_status": true, "children": [] }, { "id": "DOID:0081276", "label": "cerebellar atrophy, visual impairment, and psychomotor retardation", "link_status": true, "children": [] }, { "id": "DOID:0081322", "label": "contractures, pterygia, and spondylocarpotarsal fusion syndrome 1B", "link_status": true, "children": [] }, { "id": "DOID:0081326", "label": "oxoglutarate dehydrogenase deficiency", "link_status": true, "children": [] }, { "id": "DOID:0081328", "label": "familial hyperinsulinemic hypoglycemia 8", "link_status": true, "children": [] }, { "id": "DOID:0081330", "label": "glycogen storage disease Ib", "link_status": true, "children": [] }, { "id": "DOID:0081331", "label": "glycogen storage disease Ic", "link_status": true, "children": [] }, { "id": "DOID:0081333", "label": "Wiedemann-Rautenstrauch syndrome", "link_status": true, "children": [] }, { "id": "DOID:0081334", "label": "Nestor-Guillermo progeria syndrome", "link_status": true, "children": [] }, { "id": "DOID:0081335", "label": "Becker disease", "link_status": true, "children": [] }, { "id": "DOID:0081339", "label": "congenital myopathy 2B", "link_status": true, "children": [] }, { "id": "DOID:0081341", "label": "congenital myopathy 5", "link_status": true, "children": [] }, { "id": "DOID:0081343", "label": "congenital myopathy 9A", "link_status": true, "children": [] }, { "id": "DOID:0081344", "label": "congenital myopathy 9B", "link_status": true, "children": [] }, { "id": "DOID:0081345", "label": "congenital myopathy 10B", "link_status": true, "children": [] }, { "id": "DOID:0081346", "label": "congenital myopathy 14", "link_status": true, "children": [] }, { "id": "DOID:0081349", "label": "congenital myopathy 17", "link_status": true, "children": [] }, { "id": "DOID:0081350", "label": "congenital myopathy 18", "link_status": true, "children": [] }, { "id": "DOID:0081351", "label": "congenital myopathy 19", "link_status": true, "children": [] }, { "id": "DOID:0081352", "label": "congenital myopathy 20", "link_status": true, "children": [] }, { "id": "DOID:0081353", "label": "congenital myopathy 21", "link_status": true, "children": [] }, { "id": "DOID:0081354", "label": "congenital myopathy 22A", "link_status": true, "children": [] }, { "id": "DOID:0081355", "label": "congenital myopathy 22B", "link_status": true, "children": [] }, { "id": "DOID:0081361", "label": "spastic quadriplegic cerebral palsy 3", "link_status": true, "children": [] }, { "id": "DOID:0081368", "label": "Paget's disease of bone 5", "link_status": true, "children": [] }, { "id": "DOID:0081374", "label": "nemaline myopathy 5B", "link_status": true, "children": [] }, { "id": "DOID:0081386", "label": "TANGO2-related metabolic encephalopathy and arrythmias", "link_status": true, "children": [] }, { "id": "DOID:0081394", "label": "Caroli syndrome", "link_status": true, "children": [] }, { "id": "DOID:0081395", "label": "Harel-Yoon syndrome", "link_status": true, "children": [] }, { "id": "DOID:0081396", "label": "neonatal lethal pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome", "link_status": true, "children": [] }, { "id": "DOID:0081419", "label": "childhood-onset dystonia with optic atrophy and basal ganglia abnormalities", "link_status": true, "children": [] }, { "id": "DOID:0081431", "label": "microcephaly, short stature, and limb abnormalities", "link_status": true, "children": [] }, { "id": "DOID:0081433", "label": "Peroxisome biogenesis disorder 4B", "link_status": true, "children": [] }, { "id": "DOID:0081434", "label": "Peroxisome biogenesis disorder 5B", "link_status": true, "children": [] }, { "id": "DOID:0081435", "label": "Peroxisome biogenesis disorder 6B", "link_status": true, "children": [] }, { "id": "DOID:0081436", "label": "Peroxisome biogenesis disorder 7B", "link_status": true, "children": [] }, { "id": "DOID:0081437", "label": "Peroxisome biogenesis disorder 8B", "link_status": true, "children": [] }, { "id": "DOID:0081438", "label": "Peroxisome biogenesis disorder 9B", "link_status": true, "children": [] }, { "id": "DOID:0081439", "label": "Peroxisome biogenesis disorder 11B", "link_status": true, "children": [] }, { "id": "DOID:0081440", "label": "Peroxisome biogenesis disorder 10B", "link_status": true, "children": [] }, { "id": "DOID:0081446", "label": "dimethylglycine dehydrogenase deficiency", "link_status": true, "children": [] }, { "id": "DOID:0081447", "label": "cone-rod dystrophy 21", "link_status": true, "children": [] }, { "id": "DOID:0081448", "label": "cone-rod dystrophy 22", "link_status": true, "children": [] }, { "id": "DOID:0090001", "label": "Fraser syndrome", "link_status": true, "children": [ { "id": "DOID:0111405", "label": "Fraser syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0111406", "label": "Fraser syndrome 3", "link_status": true, "children": [] }, { "id": "DOID:0111407", "label": "Fraser syndrome 2", "link_status": true, "children": [] } ] }, { "id": "DOID:0090003", "label": "agenesis of the corpus callosum with peripheral neuropathy", "link_status": true, "children": [] }, { "id": "DOID:0090004", "label": "progressive pseudorheumatoid arthropathy of childhood", "link_status": true, "children": [] }, { "id": "DOID:0090005", "label": "Schwartz-Jampel syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0090007", "label": "immunodeficiency-centromeric instability-facial anomalies syndrome", "link_status": true, "children": [ { "id": "DOID:0090008", "label": "immunodeficiency-centromeric instability-facial anomalies syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0090009", "label": "immunodeficiency-centromeric instability-facial anomalies syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0090010", "label": "immunodeficiency-centromeric instability-facial anomalies syndrome 3", "link_status": true, "children": [] }, { "id": "DOID:0090011", "label": "immunodeficiency-centromeric instability-facial anomalies syndrome 4", "link_status": true, "children": [] } ] }, { "id": "DOID:0090012", "label": "severe combined immunodeficiency with sensitivity to ionizing radiation", "link_status": true, "children": [] }, { "id": "DOID:0090013", "label": "severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive", "link_status": true, "children": [] }, { "id": "DOID:0090014", "label": "severe combined immunodeficiency 104", "link_status": true, "children": [] }, { "id": "DOID:0090017", "label": "epidermolysis bullosa simplex with muscular dystrophy", "link_status": true, "children": [] }, { "id": "DOID:0090019", "label": "sitosterolemia", "link_status": true, "children": [ { "id": "DOID:0060983", "label": "sitosterolemia 2", "link_status": true, "children": [] }, { "id": "DOID:0070634", "label": "sitosterolemia 1", "link_status": true, "children": [] } ] }, { "id": "DOID:0090024", "label": "split hand-foot malformation 1 with sensorineural hearing loss", "link_status": true, "children": [] }, { "id": "DOID:0090026", "label": "split hand-foot malformation 6", "link_status": true, "children": [] }, { "id": "DOID:0090032", "label": "Silverman-Handmaker type dyssegmental dysplasia", "link_status": true, "children": [] }, { "id": "DOID:0090038", "label": "torsion dystonia 2", "link_status": true, "children": [] }, { "id": "DOID:0090043", "label": "dopa-responsive dystonia", "link_status": true, "children": [] }, { "id": "DOID:0090048", "label": "dystonia 16", "link_status": true, "children": [] }, { "id": "DOID:0090050", "label": "dystonia 27", "link_status": true, "children": [] }, { "id": "DOID:0090059", "label": "enhanced S-cone syndrome", "link_status": true, "children": [] }, { "id": "DOID:0090060", "label": "Wolcott-Rallison syndrome", "link_status": true, "children": [] }, { "id": "DOID:0090067", "label": "Fuhrmann syndrome", "link_status": true, "children": [] }, { "id": "DOID:0090068", "label": "giant axonal neuropathy 1", "link_status": true, "children": [] }, { "id": "DOID:0090071", "label": "hypogonadotropic hypogonadism 11 with or without anosmia", "link_status": true, "children": [] }, { "id": "DOID:0090072", "label": "hypogonadotropic hypogonadism 12 with or without anosmia", "link_status": true, "children": [] }, { "id": "DOID:0090073", "label": "hypogonadotropic hypogonadism 13 with or without anosmia", "link_status": true, "children": [] }, { "id": "DOID:0090074", "label": "hypogonadotropic hypogonadism 8 with or without anosmia", "link_status": true, "children": [] }, { "id": "DOID:0090076", "label": "hypogonadotropic hypogonadism 18 with or without anosmia", "link_status": true, "children": [] }, { "id": "DOID:0090078", "label": "hypogonadotropic hypogonadism 7 with or without anosmia", "link_status": true, "children": [] }, { "id": "DOID:0090081", "label": "hypogonadotropic hypogonadism 22 with or without anosmia", "link_status": true, "children": [] }, { "id": "DOID:0090088", "label": "hypogonadotropic hypogonadism 24 without anosmia", "link_status": true, "children": [] }, { "id": "DOID:0090089", "label": "hypogonadotropic hypogonadism 10 with or without anosmia", "link_status": true, "children": [] }, { "id": "DOID:0090091", "label": "hypogonadotropic hypogonadism 23 with or without anosmia", "link_status": true, "children": [] }, { "id": "DOID:0090106", "label": "BH4-deficient hyperphenylalaninemia A", "link_status": true, "children": [] }, { "id": "DOID:0090112", "label": "Nasu-Hakola disease", "link_status": true, "children": [] }, { "id": "DOID:0090113", "label": "RIDDLE syndrome", "link_status": true, "children": [] }, { "id": "DOID:0090116", "label": "spondylocarpotarsal synostosis syndrome", "link_status": true, "children": [] }, { "id": "DOID:0090117", "label": "thiamine-responsive megaloblastic anemia syndrome", "link_status": true, "children": [] }, { "id": "DOID:0090118", "label": "congenital amegakaryocytic thrombocytopenia", "link_status": true, "children": [ { "id": "DOID:0061002", "label": "congenital amegakaryocytic thrombocytopenia 2", "link_status": true, "children": [] }, { "id": "DOID:0061005", "label": "congenital amegakaryocytic thrombocytopenia 1", "link_status": true, "children": [] } ] }, { "id": "DOID:0090126", "label": "branched-chain keto acid dehydrogenase kinase deficiency", "link_status": true, "children": [] }, { "id": "DOID:0090127", "label": "camptodactyly-arthropathy-coxa vara-pericarditis syndrome", "link_status": true, "children": [] }, { "id": "DOID:0090130", "label": "cortical dysplasia-focal epilepsy syndrome", "link_status": true, "children": [] }, { "id": "DOID:0090141", "label": "cortisone reductase deficiency 1", "link_status": true, "children": [] }, { "id": "DOID:0090142", "label": "cystathioninuria", "link_status": true, "children": [] }, { "id": "DOID:0090143", "label": "brachyolmia-amelogenesis imperfecta syndrome", "link_status": true, "children": [] }, { "id": "DOID:0090144", "label": "Donnai-Barrow syndrome", "link_status": true, "children": [] }, { "id": "DOID:0110000", "label": "3-methylglutaconic aciduria type 5", "link_status": true, "children": [] }, { "id": "DOID:0110001", "label": "3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome", "link_status": true, "children": [] }, { "id": "DOID:0110002", "label": "3-methylglutaconic aciduria type 1", "link_status": true, "children": [] }, { "id": "DOID:0110003", "label": "3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia", "link_status": false, "children": [ { "id": "DOID:0081133", "label": "3-methylglutaconic aciduria type 7a", "link_status": true, "children": [] }, { "id": "DOID:0081134", "label": "3-methylglutaconic aciduria type 7b", "link_status": true, "children": [] } ] }, { "id": "DOID:0110004", "label": "3-methylglutaconic aciduria type 3", "link_status": true, "children": [] }, { "id": "DOID:0110005", "label": "Leber congenital amaurosis 9", "link_status": true, "children": [] }, { "id": "DOID:0110007", "label": "achromatopsia 2", "link_status": true, "children": [] }, { "id": "DOID:0110008", "label": "achromatopsia 3", "link_status": true, "children": [] }, { "id": "DOID:0110009", "label": "achromatopsia 7", "link_status": true, "children": [] }, { "id": "DOID:0110016", "label": "Leber congenital amaurosis 2", "link_status": true, "children": [] }, { "id": "DOID:0110033", "label": "autosomal recessive Alport syndrome", "link_status": true, "children": [] }, { "id": "DOID:0110056", "label": "amelogenesis imperfecta type 1C", "link_status": true, "children": [] }, { "id": "DOID:0110057", "label": "amelogenesis imperfecta type 2A1", "link_status": true, "children": [] }, { "id": "DOID:0110060", "label": "amelogenesis imperfecta hypomaturation type 2A2", "link_status": true, "children": [] }, { "id": "DOID:0110061", "label": "amelogenesis imperfecta hypomaturation type 2A3", "link_status": true, "children": [] }, { "id": "DOID:0110062", "label": "amelogenesis imperfecta hypomaturation type 2A4", "link_status": true, "children": [] }, { "id": "DOID:0110063", "label": "amelogenesis imperfecta hypomaturation type 2A5", "link_status": true, "children": [] }, { "id": "DOID:0110064", "label": "amelogenesis imperfecta type 1H", "link_status": true, "children": [] }, { "id": "DOID:0110065", "label": "amelogenesis imperfecta type 1F", "link_status": true, "children": [] }, { "id": "DOID:0110066", "label": "amelogenesis imperfecta type 1G", "link_status": true, "children": [] }, { "id": "DOID:0110078", "label": "Leber congenital amaurosis 1", "link_status": true, "children": [] }, { "id": "DOID:0110079", "label": "Leber congenital amaurosis 8", "link_status": true, "children": [] }, { "id": "DOID:0110080", "label": "Leber congenital amaurosis 12", "link_status": true, "children": [] }, { "id": "DOID:0110085", "label": "asphyxiating thoracic dystrophy 1", "link_status": true, "children": [] }, { "id": "DOID:0110086", "label": "asphyxiating thoracic dystrophy 2", "link_status": true, "children": [] }, { "id": "DOID:0110087", "label": "asphyxiating thoracic dystrophy 3", "link_status": true, "children": [] }, { "id": "DOID:0110088", "label": "asphyxiating thoracic dystrophy 4", "link_status": true, "children": [] }, { "id": "DOID:0110089", "label": "asphyxiating thoracic dystrophy 5", "link_status": true, "children": [] }, { "id": "DOID:0110090", "label": "short-rib thoracic dysplasia 7 with or without polydactyly", "link_status": true, "children": [] }, { "id": "DOID:0110091", "label": "short-rib thoracic dysplasia 10 with or without polydactyly", "link_status": true, "children": [] }, { "id": "DOID:0110092", "label": "short-rib thoracic dysplasia 6 with or without polydactyly", "link_status": true, "children": [] }, { "id": "DOID:0110093", "label": "short-rib thoracic dysplasia 13 with or without polydactyly", "link_status": true, "children": [] }, { "id": "DOID:0110094", "label": "short-rib thoracic dysplasia 8 with or without polydactyly", "link_status": true, "children": [] }, { "id": "DOID:0110095", "label": "short-rib thoracic dysplasia 11 with or without polydactyly", "link_status": true, "children": [] }, { "id": "DOID:0110096", "label": "short-rib thoracic dysplasia 14 with polydactyly", "link_status": true, "children": [] }, { "id": "DOID:0110097", "label": "short-rib thoracic dysplasia 9 with or without polydactyly", "link_status": true, "children": [] }, { "id": "DOID:0110116", "label": "autoimmune lymphoproliferative syndrome type 2B", "link_status": true, "children": [] }, { "id": "DOID:0110118", "label": "Leber congenital amaurosis 16", "link_status": true, "children": [] }, { "id": "DOID:0110119", "label": "autoimmune lymphoproliferative syndrome type 3", "link_status": true, "children": [] }, { "id": "DOID:0110149", "label": "Charcot-Marie-Tooth disease type 1F", "link_status": true, "children": [] }, { "id": "DOID:0110156", "label": "Charcot-Marie-Tooth disease type 2B1", "link_status": true, "children": [] }, { "id": "DOID:0110160", "label": "Charcot-Marie-Tooth disease axonal type 2T", "link_status": true, "children": [] }, { "id": "DOID:0110161", "label": "Charcot-Marie-Tooth disease type 2R", "link_status": true, "children": [] }, { "id": "DOID:0110167", "label": "Charcot-Marie-Tooth disease axonal type 2K", "link_status": true, "children": [] }, { "id": "DOID:0110169", "label": "Charcot-Marie-Tooth disease axonal type 2P", "link_status": true, "children": [] }, { "id": "DOID:0110171", "label": "Charcot-Marie-Tooth disease axonal type 2S", "link_status": true, "children": [] }, { "id": "DOID:0110176", "label": "Charcot-Marie-Tooth disease axonal type 2X", "link_status": true, "children": [] }, { "id": "DOID:0110179", "label": "Charcot-Marie-Tooth disease type 2B2", "link_status": true, "children": [] }, { "id": "DOID:0110183", "label": "Charcot-Marie-Tooth disease type 4C", "link_status": true, "children": [] }, { "id": "DOID:0110184", "label": "Charcot-Marie-Tooth disease type 4J", "link_status": true, "children": [] }, { "id": "DOID:0110185", "label": "Charcot-Marie-Tooth disease type 4A", "link_status": true, "children": [] }, { "id": "DOID:0110186", "label": "Charcot-Marie-Tooth disease type 4D", "link_status": true, "children": [] }, { "id": "DOID:0110187", "label": "Charcot-Marie-Tooth disease type 4K", "link_status": true, "children": [] }, { "id": "DOID:0110188", "label": "Leber congenital amaurosis 14", "link_status": true, "children": [] }, { "id": "DOID:0110189", "label": "Leber congenital amaurosis 15", "link_status": true, "children": [] }, { "id": "DOID:0110190", "label": "Charcot-Marie-Tooth disease type 4B2", "link_status": true, "children": [] }, { "id": "DOID:0110191", "label": "Charcot-Marie-Tooth disease type 4B1", "link_status": true, "children": [] }, { "id": "DOID:0110192", "label": "Charcot-Marie-Tooth disease type 4H", "link_status": true, "children": [] }, { "id": "DOID:0110193", "label": "Charcot-Marie-Tooth disease type 4F", "link_status": true, "children": [] }, { "id": "DOID:0110194", "label": "Charcot-Marie-Tooth disease type 4B3", "link_status": true, "children": [] }, { "id": "DOID:0110195", "label": "Charcot-Marie-Tooth disease type 4E", "link_status": true, "children": [] }, { "id": "DOID:0110196", "label": "Charcot-Marie-Tooth disease type 4G", "link_status": true, "children": [] }, { "id": "DOID:0110198", "label": "Charcot-Marie-Tooth disease recessive intermediate C", "link_status": true, "children": [] }, { "id": "DOID:0110201", "label": "Charcot-Marie-Tooth disease recessive intermediate A", "link_status": true, "children": [] }, { "id": "DOID:0110203", "label": "Charcot-Marie-Tooth disease recessive intermediate D", "link_status": true, "children": [] }, { "id": "DOID:0110204", "label": "Charcot-Marie-Tooth disease recessive intermediate B", "link_status": true, "children": [] }, { "id": "DOID:0110215", "label": "Leber congenital amaurosis 5", "link_status": true, "children": [] }, { "id": "DOID:0110217", "label": "Leber congenital amaurosis 17", "link_status": true, "children": [] }, { "id": "DOID:0110238", "label": "cataract 18", "link_status": true, "children": [] }, { "id": "DOID:0110242", "label": "cataract 13 with adult i phenotype", "link_status": true, "children": [] }, { "id": "DOID:0110243", "label": "cataract 46 juvenile-onset", "link_status": true, "children": [] }, { "id": "DOID:0110245", "label": "cataract 38", "link_status": true, "children": [] }, { "id": "DOID:0110247", "label": "cataract 36", "link_status": true, "children": [] }, { "id": "DOID:0110249", "label": "cataract 11 multiple types", "link_status": true, "children": [] }, { "id": "DOID:0110250", "label": "cataract 16 multiple types", "link_status": true, "children": [] }, { "id": "DOID:0110262", "label": "cataract 45", "link_status": true, "children": [] }, { "id": "DOID:0110263", "label": "cataract 19 multiple types", "link_status": true, "children": [] }, { "id": "DOID:0110264", "label": "cataract 33", "link_status": true, "children": [] }, { "id": "DOID:0110266", "label": "cataract 9 multiple types", "link_status": true, "children": [] }, { "id": "DOID:0110267", "label": "cataract 44", "link_status": true, "children": [] }, { "id": "DOID:0110268", "label": "cataract 22 multiple types", "link_status": true, "children": [] }, { "id": "DOID:0110270", "label": "cataract 17 multiple types", "link_status": true, "children": [] }, { "id": "DOID:0110274", "label": "autosomal recessive limb-girdle muscular dystrophy", "link_status": true, "children": [ { "id": "DOID:0061130", "label": "autosomal recessive limb-girdle muscular dystrophy type 28", "link_status": true, "children": [] }, { "id": "DOID:0061131", "label": "autosomal recessive limb-girdle muscular dystrophy type 26", "link_status": true, "children": [] }, { "id": "DOID:0061132", "label": "autosomal recessive limb-girdle muscular dystrophy type 23", "link_status": true, "children": [] }, { "id": "DOID:0061133", "label": "autosomal recessive limb-girdle muscular dystrophy type 27", "link_status": true, "children": [] }, { "id": "DOID:0061134", "label": "autosomal recessive limb-girdle muscular dystrophy type 29", "link_status": true, "children": [] }, { "id": "DOID:0080762", "label": "autosomal recessive limb-girdle muscular dystrophy type 2Z", "link_status": true, "children": [] }, { "id": "DOID:0110275", "label": "autosomal recessive limb-girdle muscular dystrophy type 2A", "link_status": true, "children": [] }, { "id": "DOID:0110276", "label": "autosomal recessive limb-girdle muscular dystrophy type 2B", "link_status": true, "children": [] }, { "id": "DOID:0110277", "label": "autosomal recessive limb-girdle muscular dystrophy type 2C", "link_status": true, "children": [] }, { "id": "DOID:0110278", "label": "autosomal recessive limb-girdle muscular dystrophy type 2D", "link_status": true, "children": [] }, { "id": "DOID:0110279", "label": "autosomal recessive limb-girdle muscular dystrophy type 2E", "link_status": true, "children": [] }, { "id": "DOID:0110280", "label": "autosomal recessive limb-girdle muscular dystrophy type 2F", "link_status": true, "children": [] }, { "id": "DOID:0110281", "label": "autosomal recessive limb-girdle muscular dystrophy type 2G", "link_status": true, "children": [] }, { "id": "DOID:0110282", "label": "autosomal recessive limb-girdle muscular dystrophy type 2H", "link_status": true, "children": [] }, { "id": "DOID:0110283", "label": "autosomal recessive limb-girdle muscular dystrophy type 2J", "link_status": true, "children": [] }, { "id": "DOID:0110284", "label": "autosomal recessive limb-girdle muscular dystrophy type 2L", "link_status": true, "children": [] }, { "id": "DOID:0110285", "label": "autosomal recessive limb-girdle muscular dystrophy type 2Q", "link_status": true, "children": [] }, { "id": "DOID:0110287", "label": "autosomal recessive limb-girdle muscular dystrophy type 2S", "link_status": true, "children": [] }, { "id": "DOID:0110288", "label": "autosomal recessive limb-girdle muscular dystrophy type 2W", "link_status": true, "children": [] }, { "id": "DOID:0110289", "label": "autosomal recessive limb-girdle muscular dystrophy type 2Y", "link_status": true, "children": [] }, { "id": "DOID:0110290", "label": "autosomal recessive limb-girdle muscular dystrophy type 2X", "link_status": true, "children": [] }, { "id": "DOID:0110292", "label": "autosomal recessive limb-girdle muscular dystrophy type 2O", "link_status": true, "children": [] }, { "id": "DOID:0110293", "label": "autosomal recessive limb-girdle muscular dystrophy type 2P", "link_status": true, "children": [] }, { "id": "DOID:0110294", "label": "autosomal recessive limb-girdle muscular dystrophy type 2T", "link_status": true, "children": [] }, { "id": "DOID:0110295", "label": "autosomal recessive limb-girdle muscular dystrophy type 2U", "link_status": true, "children": [] }, { "id": "DOID:0110296", "label": "autosomal recessive limb-girdle muscular dystrophy type 2M", "link_status": true, "children": [] }, { "id": "DOID:0110297", "label": "autosomal recessive limb-girdle muscular dystrophy type 2K", "link_status": true, "children": [] }, { "id": "DOID:0110298", "label": "autosomal recessive limb-girdle muscular dystrophy type 2N", "link_status": true, "children": [] }, { "id": "DOID:0110299", "label": "autosomal recessive limb-girdle muscular dystrophy type 2I", "link_status": true, "children": [] } ] }, { "id": "DOID:0110329", "label": "Leber congenital amaurosis 6", "link_status": true, "children": [] }, { "id": "DOID:0110330", "label": "Leber congenital amaurosis 13", "link_status": true, "children": [] }, { "id": "DOID:0110332", "label": "Leber congenital amaurosis 4", "link_status": true, "children": [] }, { "id": "DOID:0110336", "label": "osteogenesis imperfecta type 8", "link_status": true, "children": [] }, { "id": "DOID:0110337", "label": "osteogenesis imperfecta type 7", "link_status": true, "children": [] }, { "id": "DOID:0110338", "label": "osteogenesis imperfecta type 17", "link_status": true, "children": [] }, { "id": "DOID:0110342", "label": "osteogenesis imperfecta type 13", "link_status": true, "children": [] }, { "id": "DOID:0110346", "label": "osteogenesis imperfecta type 10", "link_status": true, "children": [] }, { "id": "DOID:0110347", "label": "osteogenesis imperfecta type 15", "link_status": true, "children": [] }, { "id": "DOID:0110348", "label": "osteogenesis imperfecta type 12", "link_status": true, "children": [] }, { "id": "DOID:0110349", "label": "osteogenesis imperfecta type 9", "link_status": true, "children": [] }, { "id": "DOID:0110351", "label": "osteogenesis imperfecta type 11", "link_status": true, "children": [] }, { "id": "DOID:0110352", "label": "retinitis pigmentosa 59", "link_status": true, "children": [] }, { "id": "DOID:0110353", "label": "retinitis pigmentosa 20", "link_status": true, "children": [] }, { "id": "DOID:0110354", "label": "retinitis pigmentosa 19", "link_status": true, "children": [] }, { "id": "DOID:0110357", "label": "retinitis pigmentosa 35", "link_status": true, "children": [] }, { "id": "DOID:0110358", "label": "retinitis pigmentosa 12", "link_status": true, "children": [] }, { "id": "DOID:0110361", "label": "retinitis pigmentosa 75", "link_status": true, "children": [] }, { "id": "DOID:0110363", "label": "retinitis pigmentosa 71", "link_status": true, "children": [] }, { "id": "DOID:0110365", "label": "retinitis pigmentosa 28", "link_status": true, "children": [] }, { "id": "DOID:0110367", "label": "retinitis pigmentosa 38", "link_status": true, "children": [] }, { "id": "DOID:0110368", "label": "retinitis pigmentosa 26", "link_status": true, "children": [] }, { "id": "DOID:0110371", "label": "retinitis pigmentosa 56", "link_status": true, "children": [] }, { "id": "DOID:0110372", "label": "retinitis pigmentosa 4", "link_status": true, "children": [] }, { "id": "DOID:0110374", "label": "retinitis pigmentosa 68", "link_status": true, "children": [] }, { "id": "DOID:0110375", "label": "retinitis pigmentosa 40", "link_status": true, "children": [] }, { "id": "DOID:0110376", "label": "retinitis pigmentosa 41", "link_status": true, "children": [] }, { "id": "DOID:0110380", "label": "retinitis pigmentosa 62", "link_status": true, "children": [] }, { "id": "DOID:0110381", "label": "retinitis pigmentosa 14", "link_status": true, "children": [] }, { "id": "DOID:0110383", "label": "retinitis pigmentosa 7", "link_status": true, "children": [] }, { "id": "DOID:0110384", "label": "retinitis pigmentosa 25", "link_status": true, "children": [] }, { "id": "DOID:0110389", "label": "retinitis pigmentosa 73", "link_status": true, "children": [] }, { "id": "DOID:0110390", "label": "retinitis pigmentosa 1", "link_status": true, "children": [] }, { "id": "DOID:0110395", "label": "retinitis pigmentosa 72", "link_status": true, "children": [] }, { "id": "DOID:0110396", "label": "retinitis pigmentosa 50", "link_status": true, "children": [] }, { "id": "DOID:0110399", "label": "retinitis pigmentosa 37", "link_status": true, "children": [] }, { "id": "DOID:0110401", "label": "retinitis pigmentosa 74", "link_status": true, "children": [] }, { "id": "DOID:0110402", "label": "retinitis pigmentosa 45", "link_status": true, "children": [] }, { "id": "DOID:0110407", "label": "retinitis pigmentosa 57", "link_status": true, "children": [] }, { "id": "DOID:0110410", "label": "retinitis pigmentosa 69", "link_status": true, "children": [] }, { "id": "DOID:0110419", "label": "retinitis pigmentosa with or without situs inversus", "link_status": true, "children": [] }, { "id": "DOID:0110441", "label": "dilated cardiomyopathy 2B", "link_status": true, "children": [] }, { "id": "DOID:0110444", "label": "dilated cardiomyopathy 1X", "link_status": true, "children": [] }, { "id": "DOID:0110460", "label": "dilated cardiomyopathy 2A", "link_status": true, "children": [] }, { "id": "DOID:0110629", "label": "Wolfram syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0110630", "label": "Wolfram syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0110632", "label": "megaconial type congenital muscular dystrophy", "link_status": true, "children": [] }, { "id": "DOID:0110633", "label": "rigid spine muscular dystrophy 1", "link_status": true, "children": [] }, { "id": "DOID:0110635", "label": "muscular dystrophy-dystroglycanopathy type B5", "link_status": true, "children": [] }, { "id": "DOID:0110636", "label": "congenital merosin-deficient muscular dystrophy 1A", "link_status": true, "children": [] }, { "id": "DOID:0110637", "label": "muscular dystrophy-dystroglycanopathy type B6", "link_status": true, "children": [] }, { "id": "DOID:0110639", "label": "congenital muscular dystrophy due to integrin alpha-7 deficiency", "link_status": true, "children": [] }, { "id": "DOID:0110657", "label": "congenital myasthenic syndrome 8", "link_status": true, "children": [] }, { "id": "DOID:0110658", "label": "congenital myasthenic syndrome 15", "link_status": true, "children": [] }, { "id": "DOID:0110660", "label": "congenital myasthenic syndrome 12", "link_status": true, "children": [] }, { "id": "DOID:0110661", "label": "congenital myasthenic syndrome 20", "link_status": true, "children": [] }, { "id": "DOID:0110662", "label": "congenital myasthenic syndrome 1B", "link_status": true, "children": [] }, { "id": "DOID:0110664", "label": "congenital myasthenic syndrome 3C", "link_status": true, "children": [] }, { "id": "DOID:0110665", "label": "congenital myasthenic syndrome 3B", "link_status": true, "children": [] }, { "id": "DOID:0110667", "label": "congenital myasthenic syndrome 5", "link_status": true, "children": [] }, { "id": "DOID:0110668", "label": "congenital myasthenic syndrome 10", "link_status": true, "children": [] }, { "id": "DOID:0110669", "label": "congenital myasthenic syndrome 14", "link_status": true, "children": [] }, { "id": "DOID:0110670", "label": "congenital myasthenic syndrome 9", "link_status": true, "children": [] }, { "id": "DOID:0110671", "label": "congenital myasthenic syndrome 6", "link_status": true, "children": [] }, { "id": "DOID:0110672", "label": "congenital myasthenic syndrome 21", "link_status": true, "children": [] }, { "id": "DOID:0110673", "label": "congenital myasthenic syndrome 19", "link_status": true, "children": [] }, { "id": "DOID:0110674", "label": "congenital myasthenic syndrome 17", "link_status": true, "children": [] }, { "id": "DOID:0110675", "label": "congenital myasthenic syndrome 11", "link_status": true, "children": [] }, { "id": "DOID:0110676", "label": "congenital myasthenic syndrome 13", "link_status": true, "children": [] }, { "id": "DOID:0110677", "label": "congenital myasthenic syndrome 4B", "link_status": true, "children": [] }, { "id": "DOID:0110678", "label": "congenital myasthenic syndrome 4A", "link_status": true, "children": [] }, { "id": "DOID:0110679", "label": "congenital myasthenic syndrome 4C", "link_status": true, "children": [] }, { "id": "DOID:0110680", "label": "congenital myasthenic syndrome 2C", "link_status": true, "children": [] }, { "id": "DOID:0110682", "label": "congenital myasthenic syndrome 16", "link_status": true, "children": [] }, { "id": "DOID:0110703", "label": "hypotrichosis 6", "link_status": true, "children": [] }, { "id": "DOID:0110704", "label": "hypotrichosis 7", "link_status": true, "children": [] }, { "id": "DOID:0110705", "label": "hypotrichosis 8", "link_status": true, "children": [] }, { "id": "DOID:0110711", "label": "congenital hypotrichosis with juvenile macular dystrophy", "link_status": true, "children": [] }, { "id": "DOID:0110712", "label": "Oguchi disease-1", "link_status": true, "children": [] }, { "id": "DOID:0110713", "label": "Oguchi disease-2", "link_status": true, "children": [] }, { "id": "DOID:0110714", "label": "congenital stationary night blindness 1G", "link_status": true, "children": [] }, { "id": "DOID:0110721", "label": "neuronal ceroid lipofuscinosis 1", "link_status": true, "children": [] }, { "id": "DOID:0110722", "label": "neuronal ceroid lipofuscinosis 7", "link_status": true, "children": [] }, { "id": "DOID:0110723", "label": "neuronal ceroid lipofuscinosis 8", "link_status": true, "children": [] }, { "id": "DOID:0110724", "label": "neuronal ceroid lipofuscinosis 8 northern epilepsy variant", "link_status": true, "children": [] }, { "id": "DOID:0110725", "label": "neuronal ceroid lipofuscinosis 10", "link_status": true, "children": [] }, { "id": "DOID:0110726", "label": "neuronal ceroid lipofuscinosis 2", "link_status": true, "children": [] }, { "id": "DOID:0110727", "label": "neuronal ceroid lipofuscinosis 13", "link_status": true, "children": [] }, { "id": "DOID:0110728", "label": "neuronal ceroid lipofuscinosis 5", "link_status": true, "children": [] }, { "id": "DOID:0110729", "label": "neuronal ceroid lipofuscinosis 6A", "link_status": true, "children": [] }, { "id": "DOID:0110730", "label": "neuronal ceroid lipofuscinosis 6B", "link_status": true, "children": [] }, { "id": "DOID:0110731", "label": "neuronal ceroid lipofuscinosis 3", "link_status": true, "children": [] }, { "id": "DOID:0110732", "label": "neuronal ceroid lipofuscinosis 11", "link_status": true, "children": [] }, { "id": "DOID:0110735", "label": "neurodegeneration with brain iron accumulation 2a", "link_status": true, "children": [] }, { "id": "DOID:0110736", "label": "neurodegeneration with brain iron accumulation 2b", "link_status": true, "children": [] }, { "id": "DOID:0110738", "label": "neurodegeneration with brain iron accumulation 4", "link_status": true, "children": [] }, { "id": "DOID:0110740", "label": "neurodegeneration with brain iron accumulation 6", "link_status": true, "children": [] }, { "id": "DOID:0110764", "label": "hereditary spastic paraplegia 11", "link_status": true, "children": [] }, { "id": "DOID:0110768", "label": "hereditary spastic paraplegia 15", "link_status": true, "children": [] }, { "id": "DOID:0110774", "label": "hereditary spastic paraplegia 23", "link_status": true, "children": [] }, { "id": "DOID:0110777", "label": "hereditary spastic paraplegia 26", "link_status": true, "children": [] }, { "id": "DOID:0110779", "label": "hereditary spastic paraplegia 28", "link_status": true, "children": [] }, { "id": "DOID:0110786", "label": "hereditary spastic paraplegia 35", "link_status": true, "children": [] }, { "id": "DOID:0110790", "label": "hereditary spastic paraplegia 39", "link_status": true, "children": [] }, { "id": "DOID:0110795", "label": "hereditary spastic paraplegia 43", "link_status": true, "children": [] }, { "id": "DOID:0110796", "label": "hereditary spastic paraplegia 44", "link_status": true, "children": [] }, { "id": "DOID:0110797", "label": "hereditary spastic paraplegia 45", "link_status": true, "children": [] }, { "id": "DOID:0110798", "label": "hereditary spastic paraplegia 46", "link_status": true, "children": [] }, { "id": "DOID:0110799", "label": "hereditary spastic paraplegia 47", "link_status": true, "children": [] }, { "id": "DOID:0110800", "label": "hereditary spastic paraplegia 48", "link_status": true, "children": [] }, { "id": "DOID:0110801", "label": "hereditary spastic paraplegia 49", "link_status": true, "children": [] }, { "id": "DOID:0110802", "label": "hereditary spastic paraplegia 50", "link_status": true, "children": [] }, { "id": "DOID:0110803", "label": "hereditary spastic paraplegia 51", "link_status": true, "children": [] }, { "id": "DOID:0110804", "label": "hereditary spastic paraplegia 52", "link_status": true, "children": [] }, { "id": "DOID:0110805", "label": "hereditary spastic paraplegia 53", "link_status": true, "children": [] }, { "id": "DOID:0110806", "label": "hereditary spastic paraplegia 54", "link_status": true, "children": [] }, { "id": "DOID:0110807", "label": "hereditary spastic paraplegia 55", "link_status": true, "children": [] }, { "id": "DOID:0110808", "label": "hereditary spastic paraplegia 56", "link_status": true, "children": [] }, { "id": "DOID:0110809", "label": "hereditary spastic paraplegia 57", "link_status": true, "children": [] }, { "id": "DOID:0110810", "label": "hereditary spastic paraplegia 5A", "link_status": true, "children": [] }, { "id": "DOID:0110812", "label": "hereditary spastic paraplegia 61", "link_status": true, "children": [] }, { "id": "DOID:0110813", "label": "hereditary spastic paraplegia 62", "link_status": true, "children": [] }, { "id": "DOID:0110814", "label": "hereditary spastic paraplegia 63", "link_status": true, "children": [] }, { "id": "DOID:0110815", "label": "hereditary spastic paraplegia 64", "link_status": true, "children": [] }, { "id": "DOID:0110816", "label": "hereditary spastic paraplegia 7", "link_status": true, "children": [] }, { "id": "DOID:0110819", "label": "hereditary spastic paraplegia 74", "link_status": true, "children": [] }, { "id": "DOID:0110820", "label": "hereditary spastic paraplegia 75", "link_status": true, "children": [] }, { "id": "DOID:0110821", "label": "hereditary spastic paraplegia 76", "link_status": true, "children": [] }, { "id": "DOID:0110822", "label": "hereditary spastic paraplegia 77", "link_status": true, "children": [] }, { "id": "DOID:0110825", "label": "hereditary spastic paraplegia 9B", "link_status": true, "children": [] }, { "id": "DOID:0110861", "label": "autosomal recessive polycystic kidney disease", "link_status": true, "children": [ { "id": "DOID:0080212", "label": "polycystic kidney disease 4", "link_status": true, "children": [] }, { "id": "DOID:0080273", "label": "polycystic kidney disease 5", "link_status": true, "children": [] } ] }, { "id": "DOID:0110864", "label": "congenital stationary night blindness 1F", "link_status": true, "children": [] }, { "id": "DOID:0110865", "label": "congenital stationary night blindness 1B", "link_status": true, "children": [] }, { "id": "DOID:0110866", "label": "congenital stationary night blindness 1H", "link_status": true, "children": [] }, { "id": "DOID:0110867", "label": "congenital stationary night blindness 1C", "link_status": true, "children": [] }, { "id": "DOID:0110868", "label": "congenital stationary night blindness 1D", "link_status": true, "children": [] }, { "id": "DOID:0110869", "label": "congenital stationary night blindness 1E", "link_status": true, "children": [] }, { "id": "DOID:0110899", "label": "inflammatory bowel disease 28", "link_status": true, "children": [] }, { "id": "DOID:0110909", "label": "inflammatory bowel disease 25", "link_status": true, "children": [] }, { "id": "DOID:0110916", "label": "hereditary spherocytosis type 1", "link_status": true, "children": [] }, { "id": "DOID:0110918", "label": "hereditary spherocytosis type 3", "link_status": true, "children": [] }, { "id": "DOID:0110920", "label": "hereditary spherocytosis type 5", "link_status": true, "children": [] }, { "id": "DOID:0110922", "label": "familial hemophagocytic lymphohistiocytosis 2", "link_status": true, "children": [] }, { "id": "DOID:0110923", "label": "familial hemophagocytic lymphohistiocytosis 3", "link_status": true, "children": [] }, { "id": "DOID:0110924", "label": "familial hemophagocytic lymphohistiocytosis 4", "link_status": true, "children": [] }, { "id": "DOID:0110926", "label": "congenital myopathy 4B", "link_status": true, "children": [] }, { "id": "DOID:0110927", "label": "nemaline myopathy 3", "link_status": true, "children": [] }, { "id": "DOID:0110928", "label": "nemaline myopathy 2", "link_status": true, "children": [] }, { "id": "DOID:0110929", "label": "nemaline myopathy 9", "link_status": true, "children": [] }, { "id": "DOID:0110930", "label": "nemaline myopathy 8", "link_status": true, "children": [] }, { "id": "DOID:0110931", "label": "nemaline myopathy 10", "link_status": true, "children": [] }, { "id": "DOID:0110933", "label": "nemaline myopathy 11", "link_status": true, "children": [] }, { "id": "DOID:0110934", "label": "nemaline myopathy 7", "link_status": true, "children": [] }, { "id": "DOID:0110936", "label": "nemaline myopathy 5A", "link_status": true, "children": [] }, { "id": "DOID:0110939", "label": "autosomal recessive osteopetrosis 5", "link_status": true, "children": [] }, { "id": "DOID:0110940", "label": "autosomal recessive osteopetrosis 8", "link_status": true, "children": [] }, { "id": "DOID:0110941", "label": "autosomal recessive osteopetrosis 3", "link_status": true, "children": [] }, { "id": "DOID:0110942", "label": "autosomal recessive osteopetrosis 1", "link_status": true, "children": [] }, { "id": "DOID:0110943", "label": "autosomal recessive osteopetrosis 2", "link_status": true, "children": [] }, { "id": "DOID:0110944", "label": "autosomal recessive osteopetrosis 4", "link_status": true, "children": [] }, { "id": "DOID:0110945", "label": "autosomal recessive osteopetrosis 6", "link_status": true, "children": [] }, { "id": "DOID:0110946", "label": "autosomal recessive osteopetrosis 7", "link_status": true, "children": [] }, { "id": "DOID:0110959", "label": "Gaucher's disease type III", "link_status": true, "children": [ { "id": "DOID:0112250", "label": "Gaucher's disease type IIIC", "link_status": true, "children": [] } ] }, { "id": "DOID:0111043", "label": "glycogen storage disease IXc", "link_status": true, "children": [] }, { "id": "DOID:0111044", "label": "gray platelet syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111046", "label": "platelet-type bleeding disorder 10", "link_status": true, "children": [] }, { "id": "DOID:0111048", "label": "platelet-type bleeding disorder 19", "link_status": true, "children": [] }, { "id": "DOID:0111051", "label": "platelet-type bleeding disorder 18", "link_status": true, "children": [] }, { "id": "DOID:0111057", "label": "platelet-type bleeding disorder 11", "link_status": true, "children": [] }, { "id": "DOID:0111063", "label": "hyperphosphatemic familial tumoral calcinosis", "link_status": true, "children": [] }, { "id": "DOID:0111077", "label": "congenital nonspherocytic hemolytic anemia 2", "link_status": true, "children": [] }, { "id": "DOID:0111080", "label": "Fanconi anemia complementation group V", "link_status": true, "children": [] }, { "id": "DOID:0111081", "label": "Fanconi anemia complementation group T", "link_status": true, "children": [] }, { "id": "DOID:0111082", "label": "Fanconi anemia complementation group L", "link_status": true, "children": [] }, { "id": "DOID:0111083", "label": "Fanconi anemia complementation group D2", "link_status": true, "children": [] }, { "id": "DOID:0111084", "label": "Fanconi anemia complementation group E", "link_status": true, "children": [] }, { "id": "DOID:0111085", "label": "Fanconi anemia complementation group U", "link_status": true, "children": [] }, { "id": "DOID:0111087", "label": "Fanconi anemia complementation group C", "link_status": true, "children": [] }, { "id": "DOID:0111089", "label": "Fanconi anemia complementation group D1", "link_status": true, "children": [] }, { "id": "DOID:0111091", "label": "Fanconi anemia complementation group I", "link_status": true, "children": [] }, { "id": "DOID:0111092", "label": "Fanconi anemia complementation group P", "link_status": true, "children": [] }, { "id": "DOID:0111093", "label": "Fanconi anemia complementation group Q", "link_status": true, "children": [] }, { "id": "DOID:0111095", "label": "Fanconi anemia complementation group A", "link_status": true, "children": [] }, { "id": "DOID:0111096", "label": "Fanconi anemia complementation group O", "link_status": true, "children": [] }, { "id": "DOID:0111131", "label": "focal segmental glomerulosclerosis 6", "link_status": true, "children": [] }, { "id": "DOID:0111134", "label": "focal segmental glomerulosclerosis 9", "link_status": true, "children": [] }, { "id": "DOID:0111149", "label": "autosomal recessive isolated ectopia lentis 2", "link_status": true, "children": [] }, { "id": "DOID:0111156", "label": "spermatogenic failure 9", "link_status": true, "children": [] }, { "id": "DOID:0111167", "label": "Dyggve-Melchior-Clausen disease", "link_status": true, "children": [ { "id": "DOID:0060247", "label": "Smith-McCort dysplasia", "link_status": true, "children": [ { "id": "DOID:0081270", "label": "Smith-McCort dysplasia 1", "link_status": true, "children": [] }, { "id": "DOID:0081271", "label": "Smith-McCort dysplasia 2", "link_status": true, "children": [] } ] } ] }, { "id": "DOID:0111168", "label": "sepiapterin reductase deficiency", "link_status": true, "children": [] }, { "id": "DOID:0111187", "label": "distal myopathy with anterior tibial onset", "link_status": true, "children": [] }, { "id": "DOID:0111195", "label": "erythrokeratodermia variabilis et progressiva 1", "link_status": true, "children": [] }, { "id": "DOID:0111197", "label": "autosomal recessive distal hereditary motor neuronopathy", "link_status": true, "children": [ { "id": "DOID:0081425", "label": "autosomal recessive distal hereditary motor neuronopathy 6", "link_status": true, "children": [] }, { "id": "DOID:0081426", "label": "autosomal recessive distal hereditary motor neuronopathy 7", "link_status": true, "children": [] }, { "id": "DOID:0081427", "label": "autosomal recessive distal hereditary motor neuronopathy 8", "link_status": true, "children": [] }, { "id": "DOID:0081428", "label": "autosomal recessive distal hereditary motor neuronopathy 9", "link_status": true, "children": [] }, { "id": "DOID:0081429", "label": "autosomal recessive distal hereditary motor neuronopathy 10", "link_status": true, "children": [] }, { "id": "DOID:0111064", "label": "autosomal recessive distal hereditary motor neuronopathy 1", "link_status": true, "children": [] }, { "id": "DOID:0111065", "label": "autosomal recessive distal hereditary motor neuronopathy 2", "link_status": true, "children": [] }, { "id": "DOID:0111213", "label": "autosomal recessive distal hereditary motor neuronopathy 4", "link_status": true, "children": [] }, { "id": "DOID:0111214", "label": "autosomal recessive distal hereditary motor neuronopathy 5", "link_status": true, "children": [] } ] }, { "id": "DOID:0111216", "label": "autosomal recessive centronuclear myopathy", "link_status": true, "children": [ { "id": "DOID:0111220", "label": "centronuclear myopathy 2", "link_status": true, "children": [] }, { "id": "DOID:0111221", "label": "centronuclear myopathy 6 with fiber-type disproportion", "link_status": true, "children": [] }, { "id": "DOID:0111222", "label": "centronuclear myopathy 5", "link_status": true, "children": [] } ] }, { "id": "DOID:0111229", "label": "congenital muscular dystrophy-dystroglycanopathy type A", "link_status": true, "children": [ { "id": "DOID:0050559", "label": "Fukuyama congenital muscular dystrophy", "link_status": true, "children": [] }, { "id": "DOID:0111230", "label": "congenital muscular dystrophy-dystroglycanopathy type A11", "link_status": true, "children": [] }, { "id": "DOID:0111231", "label": "congenital muscular dystrophy-dystroglycanopathy type A8", "link_status": true, "children": [] }, { "id": "DOID:0111232", "label": "congenital muscular dystrophy-dystroglycanopathy type A9", "link_status": true, "children": [] }, { "id": "DOID:0111233", "label": "congenital muscular dystrophy-dystroglycanopathy type A14", "link_status": true, "children": [] }, { "id": "DOID:0111234", "label": "congenital muscular dystrophy-dystroglycanopathy type A7", "link_status": true, "children": [] }, { "id": "DOID:0111235", "label": "congenital muscular dystrophy-dystroglycanopathy type A12", "link_status": true, "children": [] }, { "id": "DOID:0111236", "label": "congenital muscular dystrophy-dystroglycanopathy type A3", "link_status": true, "children": [] }, { "id": "DOID:0111237", "label": "congenital muscular dystrophy-dystroglycanopathy type A1", "link_status": true, "children": [] }, { "id": "DOID:0111238", "label": "congenital muscular dystrophy-dystroglycanopathy type A13", "link_status": true, "children": [] }, { "id": "DOID:0111239", "label": "congenital muscular dystrophy-dystroglycanopathy type A10", "link_status": true, "children": [] }, { "id": "DOID:0111240", "label": "congenital muscular dystrophy-dystroglycanopathy type A2", "link_status": true, "children": [] }, { "id": "DOID:0111241", "label": "congenital muscular dystrophy-dystroglycanopathy type A5", "link_status": true, "children": [] }, { "id": "DOID:0111242", "label": "congenital muscular dystrophy-dystroglycanopathy type A6", "link_status": true, "children": [] } ] }, { "id": "DOID:0111254", "label": "glutaric acidemia I", "link_status": true, "children": [] }, { "id": "DOID:0111255", "label": "McKusick-Kaufman syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111257", "label": "gamma-glutamyl transpeptidase deficiency", "link_status": true, "children": [] }, { "id": "DOID:0111258", "label": "pentosuria", "link_status": true, "children": [] }, { "id": "DOID:0111259", "label": "postaxial acrofacial dysostosis", "link_status": true, "children": [] }, { "id": "DOID:0111261", "label": "fumarase deficiency", "link_status": true, "children": [] }, { "id": "DOID:0111262", "label": "infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly", "link_status": true, "children": [] }, { "id": "DOID:0111263", "label": "combined malonic and methylmalonic acidemia", "link_status": true, "children": [] }, { "id": "DOID:0111264", "label": "Ruijs-Aalfs syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111265", "label": "Boucher-Neuhauser syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111266", "label": "geroderma osteodysplasticum", "link_status": true, "children": [] }, { "id": "DOID:0111268", "label": "autosomal recessive hyaline body myopathy", "link_status": true, "children": [] }, { "id": "DOID:0111270", "label": "isolated sulfite oxidase deficiency", "link_status": true, "children": [] }, { "id": "DOID:0111271", "label": "Oliver-McFarlane syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111274", "label": "CODAS syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111276", "label": "sensory ataxic neuropathy, dysarthria, and ophthalmoparesis", "link_status": true, "children": [] }, { "id": "DOID:0111277", "label": "mitochondrial trifunctional protein deficiency", "link_status": true, "children": [ { "id": "DOID:0060999", "label": "mitochondrial trifunctional protein deficiency 2", "link_status": true, "children": [] }, { "id": "DOID:0070619", "label": "mitochondrial trifunctional protein deficiency 1", "link_status": true, "children": [] } ] }, { "id": "DOID:0111278", "label": "histiocytosis-lymphadenopathy plus syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111332", "label": "Pitt-Hopkins-like syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0111333", "label": "early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111334", "label": "congenital leptin deficiency", "link_status": true, "children": [] }, { "id": "DOID:0111335", "label": "myopathy with extrapyramidal signs", "link_status": true, "children": [] }, { "id": "DOID:0111337", "label": "Jackson-Weiss syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111345", "label": "transient bullous dermolysis of the newborn", "link_status": true, "children": [] }, { "id": "DOID:0111351", "label": "D-2-hydroxyglutaric aciduria 1", "link_status": true, "children": [] }, { "id": "DOID:0111361", "label": "hypotrichosis-lymphedema-telangiectasia syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111366", "label": "familial hepatic adenoma", "link_status": true, "children": [] }, { "id": "DOID:0111371", "label": "isolated hyperchlorhidrosis", "link_status": true, "children": [] }, { "id": "DOID:0111376", "label": "fetal akinesia deformation sequence syndrome 3", "link_status": true, "children": [] }, { "id": "DOID:0111377", "label": "fetal akinesia deformation sequence syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0111378", "label": "fetal akinesia deformation sequence syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0111379", "label": "fetal akinesia deformation sequence syndrome 4", "link_status": true, "children": [] }, { "id": "DOID:0111389", "label": "mucopolysaccharidosis Ih/s", "link_status": true, "children": [] }, { "id": "DOID:0111390", "label": "mucopolysaccharidosis Ih", "link_status": true, "children": [] }, { "id": "DOID:0111391", "label": "mucopolysaccharidosis IVA", "link_status": true, "children": [] }, { "id": "DOID:0111392", "label": "mucopolysaccharidosis type IVB", "link_status": true, "children": [] }, { "id": "DOID:0111393", "label": "mucopolysaccharidosis type IIIC", "link_status": true, "children": [] }, { "id": "DOID:0111394", "label": "mucopolysaccharidosis type IIIB", "link_status": true, "children": [] }, { "id": "DOID:0111395", "label": "mucopolysaccharidosis type IIIA", "link_status": true, "children": [] }, { "id": "DOID:0111397", "label": "congenital dyserythropoietic anemia type Ib", "link_status": true, "children": [] }, { "id": "DOID:0111398", "label": "congenital dyserythropoietic anemia type Ia", "link_status": true, "children": [] }, { "id": "DOID:0111401", "label": "congenital dyserythropoietic anemia type II", "link_status": true, "children": [] }, { "id": "DOID:0111402", "label": "mucopolysaccharidosis type IIID", "link_status": true, "children": [] }, { "id": "DOID:0111404", "label": "Jalili syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111414", "label": "trichohepatoenteric syndrome", "link_status": true, "children": [ { "id": "DOID:0111415", "label": "trichohepatoenteric syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0111416", "label": "trichohepatoenteric syndrome 2", "link_status": true, "children": [] } ] }, { "id": "DOID:0111418", "label": "familial apolipoprotein C-II deficiency", "link_status": true, "children": [] }, { "id": "DOID:0111420", "label": "familial GPIHBP1 deficiency", "link_status": true, "children": [] }, { "id": "DOID:0111422", "label": "familial lipase maturation factor 1 deficiency", "link_status": true, "children": [] }, { "id": "DOID:0111436", "label": "optic atrophy 11", "link_status": true, "children": [] }, { "id": "DOID:0111437", "label": "optic atrophy 7", "link_status": true, "children": [] }, { "id": "DOID:0111442", "label": "optic atrophy 9", "link_status": true, "children": [] }, { "id": "DOID:0111444", "label": "progressive myoclonus epilepsy 4", "link_status": true, "children": [] }, { "id": "DOID:0111445", "label": "progressive myoclonus epilepsy 10", "link_status": true, "children": [] }, { "id": "DOID:0111446", "label": "progressive myoclonus epilepsy 3", "link_status": true, "children": [] }, { "id": "DOID:0111448", "label": "progressive myoclonus epilepsy 1B", "link_status": true, "children": [] }, { "id": "DOID:0111449", "label": "progressive myoclonus epilepsy 6", "link_status": true, "children": [] }, { "id": "DOID:0111450", "label": "progressive myoclonus epilepsy 9", "link_status": true, "children": [] }, { "id": "DOID:0111451", "label": "progressive myoclonus epilepsy 8", "link_status": true, "children": [] }, { "id": "DOID:0111452", "label": "progressive myoclonus epilepsy 1A", "link_status": true, "children": [] }, { "id": "DOID:0111453", "label": "2-aminoadipic 2-oxoadipic aciduria", "link_status": true, "children": [] }, { "id": "DOID:0111455", "label": "GRACILE syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111456", "label": "Kaufman oculocerebrofacial syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111458", "label": "galactose epimerase deficiency", "link_status": true, "children": [] }, { "id": "DOID:0111459", "label": "classic galactosemia", "link_status": true, "children": [] }, { "id": "DOID:0111464", "label": "combined oxidative phosphorylation deficiency 35", "link_status": true, "children": [] }, { "id": "DOID:0111465", "label": "combined oxidative phosphorylation deficiency 21", "link_status": true, "children": [] }, { "id": "DOID:0111466", "label": "combined oxidative phosphorylation deficiency 38", "link_status": true, "children": [] }, { "id": "DOID:0111467", "label": "combined oxidative phosphorylation deficiency 13", "link_status": true, "children": [] }, { "id": "DOID:0111468", "label": "combined oxidative phosphorylation deficiency 25", "link_status": true, "children": [] }, { "id": "DOID:0111469", "label": "combined oxidative phosphorylation deficiency 16", "link_status": true, "children": [] }, { "id": "DOID:0111470", "label": "combined oxidative phosphorylation deficiency 28", "link_status": true, "children": [] }, { "id": "DOID:0111471", "label": "combined oxidative phosphorylation deficiency 30", "link_status": true, "children": [] }, { "id": "DOID:0111472", "label": "combined oxidative phosphorylation deficiency 9", "link_status": true, "children": [] }, { "id": "DOID:0111473", "label": "combined oxidative phosphorylation deficiency 5", "link_status": true, "children": [] }, { "id": "DOID:0111474", "label": "combined oxidative phosphorylation deficiency 1", "link_status": true, "children": [] }, { "id": "DOID:0111475", "label": "combined oxidative phosphorylation deficiency 39", "link_status": true, "children": [] }, { "id": "DOID:0111476", "label": "combined oxidative phosphorylation deficiency 19", "link_status": true, "children": [] }, { "id": "DOID:0111477", "label": "combined oxidative phosphorylation deficiency 14", "link_status": true, "children": [] }, { "id": "DOID:0111478", "label": "combined oxidative phosphorylation deficiency 20", "link_status": true, "children": [] }, { "id": "DOID:0111479", "label": "combined oxidative phosphorylation deficiency 8", "link_status": true, "children": [] }, { "id": "DOID:0111480", "label": "combined oxidative phosphorylation deficiency 10", "link_status": true, "children": [] }, { "id": "DOID:0111481", "label": "combined oxidative phosphorylation deficiency 11", "link_status": true, "children": [] }, { "id": "DOID:0111482", "label": "combined oxidative phosphorylation deficiency 36", "link_status": true, "children": [] }, { "id": "DOID:0111483", "label": "combined oxidative phosphorylation deficiency 2", "link_status": true, "children": [] }, { "id": "DOID:0111484", "label": "combined oxidative phosphorylation deficiency 18", "link_status": true, "children": [] }, { "id": "DOID:0111485", "label": "combined oxidative phosphorylation deficiency 24", "link_status": true, "children": [] }, { "id": "DOID:0111486", "label": "combined oxidative phosphorylation deficiency 3", "link_status": true, "children": [] }, { "id": "DOID:0111487", "label": "combined oxidative phosphorylation deficiency 7", "link_status": true, "children": [] }, { "id": "DOID:0111488", "label": "combined oxidative phosphorylation deficiency 31", "link_status": true, "children": [] }, { "id": "DOID:0111489", "label": "combined oxidative phosphorylation deficiency 27", "link_status": true, "children": [] }, { "id": "DOID:0111490", "label": "combined oxidative phosphorylation deficiency 26", "link_status": true, "children": [] }, { "id": "DOID:0111491", "label": "combined oxidative phosphorylation deficiency 15", "link_status": true, "children": [] }, { "id": "DOID:0111492", "label": "combined oxidative phosphorylation deficiency 32", "link_status": true, "children": [] }, { "id": "DOID:0111493", "label": "combined oxidative phosphorylation deficiency 12", "link_status": true, "children": [] }, { "id": "DOID:0111494", "label": "combined oxidative phosphorylation deficiency 4", "link_status": true, "children": [] }, { "id": "DOID:0111495", "label": "combined oxidative phosphorylation deficiency 33", "link_status": true, "children": [] }, { "id": "DOID:0111496", "label": "combined oxidative phosphorylation deficiency 17", "link_status": true, "children": [] }, { "id": "DOID:0111497", "label": "combined oxidative phosphorylation deficiency 34", "link_status": true, "children": [] }, { "id": "DOID:0111498", "label": "combined oxidative phosphorylation deficiency 22", "link_status": true, "children": [] }, { "id": "DOID:0111499", "label": "combined oxidative phosphorylation deficiency 37", "link_status": true, "children": [] }, { "id": "DOID:0111500", "label": "combined oxidative phosphorylation deficiency 23", "link_status": true, "children": [] }, { "id": "DOID:0111501", "label": "combined oxidative phosphorylation deficiency 29", "link_status": true, "children": [] }, { "id": "DOID:0111515", "label": "autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 2", "link_status": true, "children": [] }, { "id": "DOID:0111516", "label": "autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 4", "link_status": true, "children": [] }, { "id": "DOID:0111522", "label": "autosomal recessive progressive external ophthalmoplegia 1", "link_status": true, "children": [] }, { "id": "DOID:0111523", "label": "autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 3", "link_status": true, "children": [] }, { "id": "DOID:0111524", "label": "autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5", "link_status": true, "children": [] }, { "id": "DOID:0111527", "label": "spinal muscular atrophy with progressive myoclonic epilepsy", "link_status": true, "children": [] }, { "id": "DOID:0111540", "label": "prolidase deficiency", "link_status": true, "children": [] }, { "id": "DOID:0111555", "label": "Alkuraya-Kucinskas syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111557", "label": "Charcot-Marie-Tooth disease type 2A2B", "link_status": true, "children": [] }, { "id": "DOID:0111559", "label": "Charcot-Marie-Tooth disease type 2EE", "link_status": true, "children": [] }, { "id": "DOID:0111566", "label": "familial isolated trichomegaly", "link_status": true, "children": [] }, { "id": "DOID:0111574", "label": "autosomal recessive woolly hair 3", "link_status": true, "children": [] }, { "id": "DOID:0111580", "label": "Behr syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111582", "label": "hereditary arterial and articular multiple calcification syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111583", "label": "carboxypeptidase N deficiency", "link_status": true, "children": [] }, { "id": "DOID:0111585", "label": "carnitine-acylcarnitine translocase deficiency", "link_status": true, "children": [] }, { "id": "DOID:0111586", "label": "Martsolf syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111587", "label": "Gordon Holmes syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111588", "label": "Greenberg dysplasia", "link_status": true, "children": [] }, { "id": "DOID:0111589", "label": "COACH syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111590", "label": "Cohen syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111591", "label": "congenital heart defects, hamartomas of tongue, and polysyndactyly", "link_status": true, "children": [] }, { "id": "DOID:0111592", "label": "plasminogen deficiency type I", "link_status": true, "children": [] }, { "id": "DOID:0111594", "label": "distal arthrogryposis type 5D", "link_status": true, "children": [] }, { "id": "DOID:0111619", "label": "combined D-2- and L-2-hydroxyglutaric aciduria", "link_status": true, "children": [] }, { "id": "DOID:0111620", "label": "corneal dystrophy-perceptive deafness syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111621", "label": "Temtamy syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111625", "label": "ventriculomegaly - cystic kidney disease", "link_status": true, "children": [] }, { "id": "DOID:0111626", "label": "D-glyceric aciduria", "link_status": true, "children": [] }, { "id": "DOID:0111627", "label": "DOORS syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111628", "label": "high myopia-sensorineural deafness syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111629", "label": "dihydropyrimidinase deficiency", "link_status": true, "children": [] }, { "id": "DOID:0111633", "label": "congenital sucrase-isomaltase deficiency", "link_status": true, "children": [] }, { "id": "DOID:0111645", "label": "Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111646", "label": "congenital lactase deficiency", "link_status": true, "children": [] }, { "id": "DOID:0111648", "label": "ectopia lentis with ectopia of pupil", "link_status": true, "children": [] }, { "id": "DOID:0111649", "label": "ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111650", "label": "ectodermal dysplasia 13", "link_status": true, "children": [] }, { "id": "DOID:0111651", "label": "ectodermal dysplasia 15", "link_status": true, "children": [] }, { "id": "DOID:0111654", "label": "ectodermal dysplasia 11B", "link_status": true, "children": [] }, { "id": "DOID:0111656", "label": "ectodermal dysplasia 9", "link_status": true, "children": [] }, { "id": "DOID:0111658", "label": "ectodermal dysplasia 4", "link_status": true, "children": [] }, { "id": "DOID:0111660", "label": "ectodermal dysplasia 7", "link_status": true, "children": [] }, { "id": "DOID:0111662", "label": "ectodermal dysplasia 14", "link_status": true, "children": [] }, { "id": "DOID:0111665", "label": "ectodermal dysplasia 10B", "link_status": true, "children": [] }, { "id": "DOID:0111666", "label": "proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111667", "label": "enterokinase deficiency", "link_status": true, "children": [] }, { "id": "DOID:0111668", "label": "Kohlschutter-Tonz syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111669", "label": "hyaline fibromatosis syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111674", "label": "intellectual developmental disorder with short stature and behavioral abnormalities", "link_status": true, "children": [] }, { "id": "DOID:0111676", "label": "high molecular weight kininogen deficiency", "link_status": true, "children": [] }, { "id": "DOID:0111677", "label": "familial benign fleck retina", "link_status": true, "children": [] }, { "id": "DOID:0111678", "label": "hereditary folate malabsorption", "link_status": true, "children": [] }, { "id": "DOID:0111679", "label": "glutamate formiminotransferase deficiency", "link_status": true, "children": [] }, { "id": "DOID:0111680", "label": "essential fructosuria", "link_status": true, "children": [] }, { "id": "DOID:0111681", "label": "congenital nonspherocytic hemolytic anemia 7", "link_status": true, "children": [] }, { "id": "DOID:0111691", "label": "familial adult myoclonic epilepsy 5", "link_status": true, "children": [] }, { "id": "DOID:0111698", "label": "proprotein convertase 1/3 deficiency", "link_status": true, "children": [] }, { "id": "DOID:0111699", "label": "Van den Ende-Gupta syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111703", "label": "familial hypertryptophanemia", "link_status": true, "children": [] }, { "id": "DOID:0111722", "label": "amelogenesis imperfecta type 3C", "link_status": true, "children": [] }, { "id": "DOID:0111725", "label": "geleophysic dysplasia 1", "link_status": true, "children": [] }, { "id": "DOID:0111732", "label": "Eiken syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111773", "label": "46,XY sex reversal 8", "link_status": true, "children": [] }, { "id": "DOID:0111774", "label": "46,XY sex reversal 7", "link_status": true, "children": [] }, { "id": "DOID:0111776", "label": "46,XY sex reversal 5", "link_status": true, "children": [] }, { "id": "DOID:0111789", "label": "Frank-Ter Haar syndrome", "link_status": true, "children": [] }, { "id": "DOID:0111797", "label": "autosomal recessive congenital nystagmus", "link_status": true, "children": [] }, { "id": "DOID:0111807", "label": "syndromic microphthalmia 9", "link_status": true, "children": [] }, { "id": "DOID:0111836", "label": "congenital nongoitrous hypothyroidism 7", "link_status": true, "children": [] }, { "id": "DOID:0111848", "label": "osteogenesis imperfecta type 18", "link_status": true, "children": [] }, { "id": "DOID:0111849", "label": "osteogenesis imperfecta type 20", "link_status": true, "children": [] }, { "id": "DOID:0111851", "label": "primary ciliary dyskinesia 44", "link_status": true, "children": [] }, { "id": "DOID:0111852", "label": "primary ciliary dyskinesia 38", "link_status": true, "children": [] }, { "id": "DOID:0111853", "label": "primary ciliary dyskinesia 40", "link_status": true, "children": [] }, { "id": "DOID:0111854", "label": "primary ciliary dyskinesia 39", "link_status": true, "children": [] }, { "id": "DOID:0111855", "label": "primary ciliary dyskinesia 42", "link_status": true, "children": [] }, { "id": "DOID:0111857", "label": "primary ciliary dyskinesia 45", "link_status": true, "children": [] }, { "id": "DOID:0111858", "label": "primary ciliary dyskinesia 41", "link_status": true, "children": [] }, { "id": "DOID:0111864", "label": "autosomal recessive congenital bilateral absence of vas deferens", "link_status": true, "children": [] }, { "id": "DOID:0111869", "label": "photosensitive trichothiodystrophy 2", "link_status": true, "children": [] }, { "id": "DOID:0111870", "label": "nonphotosensitive trichothiodystrophy 7", "link_status": true, "children": [] }, { "id": "DOID:0111871", "label": "photosensitive trichothiodystrophy 3", "link_status": true, "children": [] }, { "id": "DOID:0111872", "label": "nonphotosensitive trichothiodystrophy 6", "link_status": true, "children": [] }, { "id": "DOID:0111873", "label": "photosensitive trichothiodystrophy 1", "link_status": true, "children": [] }, { "id": "DOID:0111904", "label": "autosomal recessive thrombophilia due to protein C deficiency", "link_status": true, "children": [] }, { "id": "DOID:0111905", "label": "autosomal recessive thrombophilia due to protein S deficiency", "link_status": true, "children": [] }, { "id": "DOID:0111911", "label": "spermatogenic failure 34", "link_status": true, "children": [] }, { "id": "DOID:0111912", "label": "spermatogenic failure 41", "link_status": true, "children": [] }, { "id": "DOID:0111913", "label": "spermatogenic failure 30", "link_status": true, "children": [] }, { "id": "DOID:0111914", "label": "spermatogenic failure 35", "link_status": true, "children": [] }, { "id": "DOID:0111915", "label": "spermatogenic failure 33", "link_status": true, "children": [] }, { "id": "DOID:0111916", "label": "spermatogenic failure 28", "link_status": true, "children": [] }, { "id": "DOID:0111917", "label": "spermatogenic failure 43", "link_status": true, "children": [] }, { "id": "DOID:0111918", "label": "spermatogenic failure 40", "link_status": true, "children": [] }, { "id": "DOID:0111919", "label": "spermatogenic failure 38", "link_status": true, "children": [] }, { "id": "DOID:0111920", "label": "spermatogenic failure 25", "link_status": true, "children": [] }, { "id": "DOID:0111922", "label": "spermatogenic failure 31", "link_status": true, "children": [] }, { "id": "DOID:0111923", "label": "spermatogenic failure 42", "link_status": true, "children": [] }, { "id": "DOID:0111924", "label": "spermatogenic failure 26", "link_status": true, "children": [] }, { "id": "DOID:0111926", "label": "spermatogenic failure 39", "link_status": true, "children": [] }, { "id": "DOID:0111927", "label": "spermatogenic failure 37", "link_status": true, "children": [] }, { "id": "DOID:0111928", "label": "spermatogenic failure 27", "link_status": true, "children": [] }, { "id": "DOID:0111929", "label": "spermatogenic failure 24", "link_status": true, "children": [] }, { "id": "DOID:0111930", "label": "spermatogenic failure 29", "link_status": true, "children": [] }, { "id": "DOID:0111934", "label": "immunodeficiency 38", "link_status": true, "children": [] }, { "id": "DOID:0111935", "label": "immunodeficiency 16", "link_status": true, "children": [] }, { "id": "DOID:0111937", "label": "immunodeficiency 22", "link_status": true, "children": [] }, { "id": "DOID:0111938", "label": "immunodeficiency 24", "link_status": true, "children": [] }, { "id": "DOID:0111939", "label": "immunodeficiency 37", "link_status": true, "children": [] }, { "id": "DOID:0111940", "label": "immunodeficiency 42", "link_status": true, "children": [] }, { "id": "DOID:0111941", "label": "immunodeficiency 20", "link_status": true, "children": [] }, { "id": "DOID:0111942", "label": "immunodeficiency 25", "link_status": true, "children": [] }, { "id": "DOID:0111943", "label": "immunodeficiency 48", "link_status": true, "children": [] }, { "id": "DOID:0111944", "label": "immunodeficiency 31B", "link_status": true, "children": [] }, { "id": "DOID:0111948", "label": "immunodeficiency 46", "link_status": true, "children": [] }, { "id": "DOID:0111950", "label": "immunodeficiency 29", "link_status": true, "children": [] }, { "id": "DOID:0111951", "label": "immunodeficiency 40", "link_status": true, "children": [] }, { "id": "DOID:0111952", "label": "immunodeficiency 57", "link_status": true, "children": [] }, { "id": "DOID:0111953", "label": "immunodeficiency 23", "link_status": true, "children": [] }, { "id": "DOID:0111955", "label": "immunodeficiency 27A", "link_status": true, "children": [] }, { "id": "DOID:0111957", "label": "immunodeficiency 11A", "link_status": true, "children": [] }, { "id": "DOID:0111959", "label": "immunodeficiency 15B", "link_status": true, "children": [] }, { "id": "DOID:0111961", "label": "immunodeficiency 26", "link_status": true, "children": [] }, { "id": "DOID:0111967", "label": "immunodeficiency 54", "link_status": true, "children": [] }, { "id": "DOID:0111968", "label": "immunodeficiency 41", "link_status": true, "children": [] }, { "id": "DOID:0111970", "label": "immunodeficiency 10", "link_status": true, "children": [] }, { "id": "DOID:0111971", "label": "immunodeficiency 18", "link_status": true, "children": [] }, { "id": "DOID:0111972", "label": "immunodeficiency 19", "link_status": true, "children": [] }, { "id": "DOID:0111973", "label": "immunodeficiency 17", "link_status": true, "children": [] }, { "id": "DOID:0111974", "label": "immunodeficiency 59", "link_status": true, "children": [] }, { "id": "DOID:0111975", "label": "immunodeficiency 44", "link_status": true, "children": [] }, { "id": "DOID:0111976", "label": "immunodeficiency 9", "link_status": true, "children": [] }, { "id": "DOID:0111977", "label": "immunodeficiency 7", "link_status": true, "children": [] }, { "id": "DOID:0111978", "label": "immunodeficiency 65", "link_status": true, "children": [] }, { "id": "DOID:0111980", "label": "immunodeficiency 64", "link_status": true, "children": [] }, { "id": "DOID:0111981", "label": "immunodeficiency 43", "link_status": true, "children": [] }, { "id": "DOID:0111982", "label": "immunodeficiency 56", "link_status": true, "children": [] }, { "id": "DOID:0111983", "label": "immunodeficiency 52", "link_status": true, "children": [] }, { "id": "DOID:0111984", "label": "immunodeficiency 58", "link_status": true, "children": [] }, { "id": "DOID:0111985", "label": "immunodeficiency 32B", "link_status": true, "children": [] }, { "id": "DOID:0111988", "label": "immunodeficiency 12", "link_status": true, "children": [] }, { "id": "DOID:0111989", "label": "immunodeficiency 35", "link_status": true, "children": [] }, { "id": "DOID:0111990", "label": "immunodeficiency 30", "link_status": true, "children": [] }, { "id": "DOID:0111991", "label": "immunodeficiency 62", "link_status": true, "children": [] }, { "id": "DOID:0111992", "label": "immunodeficiency 53", "link_status": true, "children": [] }, { "id": "DOID:0111993", "label": "immunodeficiency 55", "link_status": true, "children": [] }, { "id": "DOID:0111994", "label": "immunodeficiency 45", "link_status": true, "children": [] }, { "id": "DOID:0111995", "label": "immunodeficiency 28", "link_status": true, "children": [] }, { "id": "DOID:0111996", "label": "immunodeficiency 51", "link_status": true, "children": [] }, { "id": "DOID:0111997", "label": "immunodeficiency 63", "link_status": true, "children": [] }, { "id": "DOID:0111998", "label": "immunodeficiency 66", "link_status": true, "children": [] }, { "id": "DOID:0111999", "label": "immunodeficiency 61", "link_status": true, "children": [] }, { "id": "DOID:0112004", "label": "immunodeficiency 71", "link_status": true, "children": [] }, { "id": "DOID:0112006", "label": "immunodeficiency 69", "link_status": true, "children": [] }, { "id": "DOID:0112015", "label": "immunodeficiency 72", "link_status": true, "children": [] }, { "id": "DOID:0112062", "label": "immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia", "link_status": true, "children": [] }, { "id": "DOID:0112066", "label": "nuclear type mitochondrial complex I deficiency 6", "link_status": true, "children": [] }, { "id": "DOID:0112067", "label": "nuclear type mitochondrial complex I deficiency 25", "link_status": true, "children": [] }, { "id": "DOID:0112068", "label": "nuclear type mitochondrial complex I deficiency 5", "link_status": true, "children": [] }, { "id": "DOID:0112069", "label": "nuclear type mitochondrial complex I deficiency 22", "link_status": true, "children": [] }, { "id": "DOID:0112070", "label": "nuclear type mitochondrial complex I deficiency 18", "link_status": true, "children": [] }, { "id": "DOID:0112071", "label": "nuclear type mitochondrial complex I deficiency 31", "link_status": true, "children": [] }, { "id": "DOID:0112072", "label": "nuclear type mitochondrial complex I deficiency 20", "link_status": true, "children": [] }, { "id": "DOID:0112073", "label": "nuclear type mitochondrial complex I deficiency 9", "link_status": true, "children": [] }, { "id": "DOID:0112074", "label": "nuclear type mitochondrial complex I deficiency 1", "link_status": true, "children": [] }, { "id": "DOID:0112075", "label": "nuclear type mitochondrial complex I deficiency 10", "link_status": true, "children": [] }, { "id": "DOID:0112076", "label": "nuclear type mitochondrial complex I deficiency 13", "link_status": true, "children": [] }, { "id": "DOID:0112077", "label": "nuclear type mitochondrial complex I deficiency 15", "link_status": true, "children": [] }, { "id": "DOID:0112078", "label": "nuclear type mitochondrial complex I deficiency 17", "link_status": true, "children": [] }, { "id": "DOID:0112079", "label": "nuclear type mitochondrial complex I deficiency 24", "link_status": true, "children": [] }, { "id": "DOID:0112080", "label": "nuclear type mitochondrial complex I deficiency 32", "link_status": true, "children": [] }, { "id": "DOID:0112081", "label": "nuclear type mitochondrial complex I deficiency 8", "link_status": true, "children": [] }, { "id": "DOID:0112082", "label": "nuclear type mitochondrial complex I deficiency 4", "link_status": true, "children": [] }, { "id": "DOID:0112083", "label": "nuclear type mitochondrial complex I deficiency 2", "link_status": true, "children": [] }, { "id": "DOID:0112084", "label": "nuclear type mitochondrial complex I deficiency 29", "link_status": true, "children": [] }, { "id": "DOID:0112085", "label": "nuclear type mitochondrial complex I deficiency 19", "link_status": true, "children": [] }, { "id": "DOID:0112086", "label": "nuclear type mitochondrial complex I deficiency 26", "link_status": true, "children": [] }, { "id": "DOID:0112087", "label": "nuclear type mitochondrial complex I deficiency 23", "link_status": true, "children": [] }, { "id": "DOID:0112088", "label": "nuclear type mitochondrial complex I deficiency 21", "link_status": true, "children": [] }, { "id": "DOID:0112089", "label": "nuclear type mitochondrial complex I deficiency 11", "link_status": true, "children": [] }, { "id": "DOID:0112090", "label": "nuclear type mitochondrial complex I deficiency 27", "link_status": true, "children": [] }, { "id": "DOID:0112091", "label": "nuclear type mitochondrial complex I deficiency 34", "link_status": true, "children": [] }, { "id": "DOID:0112092", "label": "nuclear type mitochondrial complex I deficiency 7", "link_status": true, "children": [] }, { "id": "DOID:0112093", "label": "nuclear type mitochondrial complex I deficiency 3", "link_status": true, "children": [] }, { "id": "DOID:0112094", "label": "nuclear type mitochondrial complex I deficiency 14", "link_status": true, "children": [] }, { "id": "DOID:0112095", "label": "nuclear type mitochondrial complex I deficiency 28", "link_status": true, "children": [] }, { "id": "DOID:0112096", "label": "nuclear type mitochondrial complex I deficiency 16", "link_status": true, "children": [] }, { "id": "DOID:0112097", "label": "nuclear type mitochondrial complex I deficiency 33", "link_status": true, "children": [] }, { "id": "DOID:0112104", "label": "Sotos syndrome 3", "link_status": true, "children": [] }, { "id": "DOID:0112108", "label": "myofibrillar myopathy 10", "link_status": true, "children": [] }, { "id": "DOID:0112109", "label": "spermatogenic failure 44", "link_status": true, "children": [] }, { "id": "DOID:0112110", "label": "combined oxidative phosphorylation deficiency 49", "link_status": true, "children": [] }, { "id": "DOID:0112111", "label": "combined oxidative phosphorylation deficiency 50", "link_status": true, "children": [] }, { "id": "DOID:0112112", "label": "combined oxidative phosphorylation deficiency 48", "link_status": true, "children": [] }, { "id": "DOID:0112113", "label": "combined oxidative phosphorylation deficiency 45", "link_status": true, "children": [] }, { "id": "DOID:0112114", "label": "combined oxidative phosphorylation deficiency 47", "link_status": true, "children": [] }, { "id": "DOID:0112115", "label": "combined oxidative phosphorylation deficiency 46", "link_status": true, "children": [] }, { "id": "DOID:0112116", "label": "combined oxidative phosphorylation deficiency 43", "link_status": true, "children": [] }, { "id": "DOID:0112117", "label": "combined oxidative phosphorylation deficiency 40", "link_status": true, "children": [] }, { "id": "DOID:0112118", "label": "combined oxidative phosphorylation deficiency 42", "link_status": true, "children": [] }, { "id": "DOID:0112119", "label": "combined oxidative phosphorylation deficiency 41", "link_status": true, "children": [] }, { "id": "DOID:0112129", "label": "severe congenital neutropenia 7", "link_status": true, "children": [] }, { "id": "DOID:0112132", "label": "severe congenital neutropenia 5", "link_status": true, "children": [] }, { "id": "DOID:0112133", "label": "severe congenital neutropenia 3", "link_status": true, "children": [] }, { "id": "DOID:0112134", "label": "severe congenital neutropenia 6", "link_status": true, "children": [] }, { "id": "DOID:0112136", "label": "severe congenital neutropenia 4", "link_status": true, "children": [] }, { "id": "DOID:0112137", "label": "combined oxidative phosphorylation deficiency 51", "link_status": true, "children": [] }, { "id": "DOID:0112138", "label": "primary coenzyme Q10 deficiency 9", "link_status": true, "children": [] }, { "id": "DOID:0112139", "label": "nuclear type mitochondrial complex I deficiency 35", "link_status": true, "children": [] }, { "id": "DOID:0112141", "label": "retinitis pigmentosa 84", "link_status": true, "children": [] }, { "id": "DOID:0112142", "label": "retinitis pigmentosa 85", "link_status": true, "children": [] }, { "id": "DOID:0112145", "label": "retinitis pigmentosa 88", "link_status": true, "children": [] }, { "id": "DOID:0112147", "label": "retinitis pigmentosa 90", "link_status": true, "children": [] }, { "id": "DOID:0112152", "label": "CHIME syndrome", "link_status": true, "children": [] }, { "id": "DOID:0112153", "label": "hypomyelinating leukodystrophy 20", "link_status": true, "children": [] }, { "id": "DOID:0112163", "label": "spermatogenic failure 45", "link_status": true, "children": [] }, { "id": "DOID:0112164", "label": "spermatogenic failure 46", "link_status": true, "children": [] }, { "id": "DOID:0112171", "label": "wrinkly skin syndrome", "link_status": true, "children": [] }, { "id": "DOID:0112173", "label": "combined deficiency of vitamin K-dependent clotting factors 1", "link_status": true, "children": [] }, { "id": "DOID:0112174", "label": "combined deficiency of vitamin K-dependent clotting factors 2", "link_status": true, "children": [] }, { "id": "DOID:0112175", "label": "spermatogenic failure 47", "link_status": true, "children": [] }, { "id": "DOID:0112176", "label": "spermatogenic failure 48", "link_status": true, "children": [] }, { "id": "DOID:0112180", "label": "urocanase deficiency", "link_status": true, "children": [] }, { "id": "DOID:0112181", "label": "Schinzel type phocomelia", "link_status": true, "children": [] }, { "id": "DOID:0112182", "label": "mismatch repair cancer syndrome", "link_status": true, "children": [] }, { "id": "DOID:0112184", "label": "thyroid dyshormonogenesis 5", "link_status": true, "children": [] }, { "id": "DOID:0112185", "label": "thyroid dyshormonogenesis 1", "link_status": true, "children": [] }, { "id": "DOID:0112186", "label": "thyroid dyshormonogenesis 2A", "link_status": true, "children": [] }, { "id": "DOID:0112187", "label": "thyroid dyshormonogenesis 3", "link_status": true, "children": [] }, { "id": "DOID:0112188", "label": "thyroid dyshormonogenesis 4", "link_status": true, "children": [] }, { "id": "DOID:0112189", "label": "thyroid dyshormonogenesis 6", "link_status": true, "children": [] }, { "id": "DOID:0112192", "label": "tetraamelia syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0112193", "label": "tetraamelia syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0112194", "label": "Filippi syndrome", "link_status": true, "children": [] }, { "id": "DOID:0112196", "label": "spondylometaepiphyseal dysplasia, short limb-hand type", "link_status": true, "children": [] }, { "id": "DOID:0112198", "label": "spondyloepimetaphyseal dysplasia with joint laxity type 1", "link_status": true, "children": [] }, { "id": "DOID:0112200", "label": "spondyloepimetaphyseal dysplasia with joint laxity type 3", "link_status": true, "children": [] }, { "id": "DOID:0112201", "label": "osteogenesis imperfecta type 21", "link_status": true, "children": [] }, { "id": "DOID:0112204", "label": "developmental and epileptic encephalopathy 68", "link_status": true, "children": [] }, { "id": "DOID:0112207", "label": "developmental and epileptic encephalopathy 71", "link_status": true, "children": [] }, { "id": "DOID:0112211", "label": "developmental and epileptic encephalopathy 75", "link_status": true, "children": [] }, { "id": "DOID:0112212", "label": "developmental and epileptic encephalopathy 76", "link_status": true, "children": [] }, { "id": "DOID:0112213", "label": "multiple congenital anomalies-hypotonia-seizures syndrome 4", "link_status": true, "children": [] }, { "id": "DOID:0112216", "label": "developmental and epileptic encephalopathy 80", "link_status": true, "children": [] }, { "id": "DOID:0112217", "label": "developmental and epileptic encephalopathy 81", "link_status": true, "children": [] }, { "id": "DOID:0112218", "label": "developmental and epileptic encephalopathy 83", "link_status": true, "children": [] }, { "id": "DOID:0112219", "label": "developmental and epileptic encephalopathy 84", "link_status": true, "children": [] }, { "id": "DOID:0112220", "label": "developmental and epileptic encephalopathy 86", "link_status": true, "children": [] }, { "id": "DOID:0112222", "label": "developmental and epileptic encephalopathy 88", "link_status": true, "children": [] }, { "id": "DOID:0112223", "label": "developmental and epileptic encephalopathy 89", "link_status": true, "children": [] }, { "id": "DOID:0112224", "label": "chondrodysplasia with joint dislocations gPAPP type", "link_status": true, "children": [] }, { "id": "DOID:0112225", "label": "BH4-deficient hyperphenylalaninemia B", "link_status": true, "children": [] }, { "id": "DOID:0112230", "label": "lissencephaly 5", "link_status": true, "children": [] }, { "id": "DOID:0112231", "label": "lissencephaly 7 with cerebellar hypoplasia", "link_status": true, "children": [] }, { "id": "DOID:0112233", "label": "lissencephaly 8", "link_status": true, "children": [] }, { "id": "DOID:0112235", "label": "lissencephaly 4", "link_status": true, "children": [] }, { "id": "DOID:0112236", "label": "lissencephaly 6", "link_status": true, "children": [] }, { "id": "DOID:0112244", "label": "alopecia, neurologic defects, and endocrinopathy syndrome", "link_status": true, "children": [] }, { "id": "DOID:0112246", "label": "glutaric acidemia type 3", "link_status": true, "children": [] }, { "id": "DOID:0112248", "label": "17-beta hydroxysteroid dehydrogenase 3 deficiency", "link_status": true, "children": [] }, { "id": "DOID:0112249", "label": "GAPO syndrome", "link_status": true, "children": [] }, { "id": "DOID:0112251", "label": "Ghosal hematodiaphyseal syndrome", "link_status": true, "children": [] }, { "id": "DOID:0112252", "label": "congenital nonspherocytic hemolytic anemia 6", "link_status": true, "children": [] }, { "id": "DOID:0112253", "label": "combined cellular and humoral immune defects with granulomas", "link_status": true, "children": [] }, { "id": "DOID:0112254", "label": "hepatic venoocclusive disease with immunodeficiency", "link_status": true, "children": [] }, { "id": "DOID:0112255", "label": "homocystinuria-megaloblastic anemia cblE type", "link_status": true, "children": [] }, { "id": "DOID:0112256", "label": "homocystinuria-megaloblastic anemia cblG type", "link_status": true, "children": [] }, { "id": "DOID:0112257", "label": "hydroxykynureninuria", "link_status": true, "children": [] }, { "id": "DOID:0112258", "label": "N-acetylglutamate synthase deficiency", "link_status": true, "children": [] }, { "id": "DOID:0112259", "label": "Leydig cell hypoplasia", "link_status": true, "children": [ { "id": "DOID:0112260", "label": "Leydig cell hypoplasia type I", "link_status": true, "children": [] } ] }, { "id": "DOID:0112264", "label": "Woodhouse-Sakati syndrome", "link_status": true, "children": [] }, { "id": "DOID:0112266", "label": "nephrotic syndrome type 23", "link_status": true, "children": [] }, { "id": "DOID:0112267", "label": "nephrotic syndrome type 21", "link_status": true, "children": [] }, { "id": "DOID:0112268", "label": "nephrotic syndrome type 22", "link_status": true, "children": [] }, { "id": "DOID:0112269", "label": "primary ovarian insufficiency 18", "link_status": true, "children": [] }, { "id": "DOID:0112270", "label": "spermatogenic failure 52", "link_status": true, "children": [] }, { "id": "DOID:0112271", "label": "spermatogenic failure 49", "link_status": true, "children": [] }, { "id": "DOID:0112272", "label": "spermatogenic failure 50", "link_status": true, "children": [] }, { "id": "DOID:0112273", "label": "spermatogenic failure 51", "link_status": true, "children": [] }, { "id": "DOID:0112277", "label": "immunodeficiency 79", "link_status": true, "children": [] }, { "id": "DOID:0112278", "label": "primary ovarian insufficiency 19", "link_status": true, "children": [] }, { "id": "DOID:0112279", "label": "spermatogenic failure 53", "link_status": true, "children": [] }, { "id": "DOID:0112283", "label": "spondyloepiphyseal dysplasia Kondo-Fu type", "link_status": true, "children": [] }, { "id": "DOID:0112290", "label": "spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis", "link_status": true, "children": [] }, { "id": "DOID:0112298", "label": "spondylometaphyseal dysplasia Sedaghatian type", "link_status": true, "children": [] }, { "id": "DOID:0112299", "label": "axial spondylometaphyseal dysplasia", "link_status": true, "children": [] }, { "id": "DOID:0112300", "label": "spondylometaphyseal dysplasia with cone-rod dystrophy", "link_status": true, "children": [] }, { "id": "DOID:0112303", "label": "spondylometaphyseal dysplasia with corneal dystrophy", "link_status": true, "children": [] }, { "id": "DOID:0112304", "label": "spondylometaphyseal dysplasia Megarbane-Dagher-Melike type", "link_status": true, "children": [] }, { "id": "DOID:0112306", "label": "Mahvash Disease", "link_status": true, "children": [] }, { "id": "DOID:0112307", "label": "sarcosinemia", "link_status": true, "children": [] }, { "id": "DOID:0112315", "label": "brain small vessel disease 3", "link_status": true, "children": [] }, { "id": "DOID:0112316", "label": "methemoglobinemia and ambiguous genitalia", "link_status": true, "children": [] }, { "id": "DOID:0112317", "label": "Schindler disease", "link_status": false, "children": [ { "id": "DOID:0112318", "label": "Schindler disease type 1", "link_status": true, "children": [] }, { "id": "DOID:0112319", "label": "Kanzaki disease", "link_status": true, "children": [] } ] }, { "id": "DOID:0112321", "label": "alacrima, achalasia, and impaired intellectual development syndrome", "link_status": true, "children": [] }, { "id": "DOID:0112323", "label": "pontocerebellar hypoplasia type 1D", "link_status": true, "children": [] }, { "id": "DOID:0112324", "label": "pontocerebellar hypoplasia type 11", "link_status": true, "children": [] }, { "id": "DOID:0112325", "label": "pontocerebellar hypoplasia type 14", "link_status": true, "children": [] }, { "id": "DOID:0112326", "label": "pontocerebellar hypoplasia type 15", "link_status": true, "children": [] }, { "id": "DOID:0112327", "label": "pontocerebellar hypoplasia type 12", "link_status": true, "children": [] }, { "id": "DOID:0112329", "label": "pontocerebellar hypoplasia type 2F", "link_status": true, "children": [] }, { "id": "DOID:0112330", "label": "pontocerebellar hypoplasia type 1E", "link_status": true, "children": [] }, { "id": "DOID:0112331", "label": "pontocerebellar hypoplasia type 1F", "link_status": true, "children": [] }, { "id": "DOID:0112332", "label": "pontocerebellar hypoplasia type 13", "link_status": true, "children": [] }, { "id": "DOID:0112333", "label": "pontocerebellar hypoplasia type 16", "link_status": true, "children": [] }, { "id": "DOID:0112334", "label": "pontocerebellar hypoplasia type 1C", "link_status": true, "children": [] }, { "id": "DOID:0112335", "label": "spermatogenic failure 54", "link_status": true, "children": [] }, { "id": "DOID:0112336", "label": "spermatogenic failure 56", "link_status": true, "children": [] }, { "id": "DOID:0112337", "label": "spermatogenic failure 55", "link_status": true, "children": [] }, { "id": "DOID:0112338", "label": "spermatogenic failure 57", "link_status": true, "children": [] }, { "id": "DOID:0112340", "label": "craniotubular dysplasia Ikegawa type", "link_status": true, "children": [] }, { "id": "DOID:0112342", "label": "hereditary spastic paraplegia 86", "link_status": true, "children": [] }, { "id": "DOID:0112343", "label": "hereditary spastic paraplegia 82", "link_status": true, "children": [] }, { "id": "DOID:0112344", "label": "hereditary spastic paraplegia 79B", "link_status": true, "children": [] }, { "id": "DOID:0112345", "label": "hereditary spastic paraplegia 85", "link_status": true, "children": [] }, { "id": "DOID:0112346", "label": "hereditary spastic paraplegia 83", "link_status": true, "children": [] }, { "id": "DOID:0112347", "label": "hereditary spastic paraplegia 84", "link_status": true, "children": [] }, { "id": "DOID:0112348", "label": "hereditary spastic paraplegia 78", "link_status": true, "children": [] }, { "id": "DOID:0112349", "label": "hereditary spastic paraplegia 81", "link_status": true, "children": [] }, { "id": "DOID:0112350", "label": "spermatogenic failure 61", "link_status": true, "children": [] }, { "id": "DOID:0112351", "label": "spermatogenic failure 62", "link_status": true, "children": [] }, { "id": "DOID:0112352", "label": "spermatogenic failure 58", "link_status": true, "children": [] }, { "id": "DOID:0112353", "label": "spermatogenic failure 64", "link_status": true, "children": [] }, { "id": "DOID:0112354", "label": "spermatogenic failure 65", "link_status": true, "children": [] }, { "id": "DOID:0112355", "label": "spermatogenic failure 60", "link_status": true, "children": [] }, { "id": "DOID:0112356", "label": "spermatogenic failure 63", "link_status": true, "children": [] }, { "id": "DOID:0112357", "label": "spermatogenic failure 59", "link_status": true, "children": [] }, { "id": "DOID:0112358", "label": "short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2", "link_status": true, "children": [] }, { "id": "DOID:0112360", "label": "spondylocostal dysostosis 6", "link_status": true, "children": [] }, { "id": "DOID:0112361", "label": "spondylocostal dysostosis 3", "link_status": true, "children": [] }, { "id": "DOID:0112362", "label": "spondylocostal dysostosis 2", "link_status": true, "children": [] }, { "id": "DOID:0112364", "label": "spondylocostal dysostosis 4", "link_status": true, "children": [] }, { "id": "DOID:0112365", "label": "spondylocostal dysostosis 1", "link_status": true, "children": [] }, { "id": "DOID:0112376", "label": "muscular dystrophy-dystroglycanopathy type B15", "link_status": true, "children": [] }, { "id": "DOID:0112377", "label": "muscular dystrophy-dystroglycanopathy type B14", "link_status": true, "children": [] }, { "id": "DOID:0112378", "label": "muscular dystrophy-dystroglycanopathy type B3", "link_status": true, "children": [] }, { "id": "DOID:0112379", "label": "muscular dystrophy-dystroglycanopathy type B4", "link_status": true, "children": [] }, { "id": "DOID:0112380", "label": "muscular dystrophy-dystroglycanopathy type B2", "link_status": true, "children": [] }, { "id": "DOID:0112381", "label": "muscular dystrophy-dystroglycanopathy type C12", "link_status": true, "children": [] }, { "id": "DOID:0112382", "label": "muscular dystrophy-dystroglycanopathy type C8", "link_status": true, "children": [] }, { "id": "DOID:10241", "label": "thalassemia", "link_status": true, "children": [ { "id": "DOID:1099", "label": "alpha thalassemia", "link_status": true, "children": [ { "id": "DOID:0110030", "label": "alpha thalassemia-X-linked intellectual disability syndrome", "link_status": true, "children": [] }, { "id": "DOID:0110031", "label": "hemoglobin H disease", "link_status": true, "children": [] } ] }, { "id": "DOID:12241", "label": "beta thalassemia", "link_status": true, "children": [ { "id": "DOID:0080770", "label": "autosomal dominant beta thalassemia", "link_status": true, "children": [] }, { "id": "DOID:0080771", "label": "beta-thalassemia major", "link_status": true, "children": [] }, { "id": "DOID:0080773", "label": "delta beta-thalassemia", "link_status": true, "children": [] } ] } ] }, { "id": "DOID:1064", "label": "cystinosis", "link_status": true, "children": [] }, { "id": "DOID:10923", "label": "sickle cell anemia", "link_status": true, "children": [] }, { "id": "DOID:11721", "label": "glycogen storage disease VII", "link_status": true, "children": [] }, { "id": "DOID:12177", "label": "common variable immunodeficiency", "link_status": true, "children": [ { "id": "DOID:0081144", "label": "common variable immunodeficiency 1", "link_status": true, "children": [] }, { "id": "DOID:0081145", "label": "common variable immunodeficiency 2", "link_status": true, "children": [] }, { "id": "DOID:0081146", "label": "common variable immunodeficiency 3", "link_status": true, "children": [] }, { "id": "DOID:0081147", "label": "common variable immunodeficiency 4", "link_status": true, "children": [] }, { "id": "DOID:0081148", "label": "common variable immunodeficiency 5", "link_status": true, "children": [] }, { "id": "DOID:0081149", "label": "common variable immunodeficiency 6", "link_status": true, "children": [] }, { "id": "DOID:0081150", "label": "common variable immunodeficiency 7", "link_status": true, "children": [] }, { "id": "DOID:0081151", "label": "common variable immunodeficiency 8", "link_status": true, "children": [] }, { "id": "DOID:0081152", "label": "common variable immunodeficiency 10", "link_status": true, "children": [] }, { "id": "DOID:0081153", "label": "common variable immunodeficiency 11", "link_status": true, "children": [] }, { "id": "DOID:0081154", "label": "common variable immunodeficiency 12", "link_status": true, "children": [] }, { "id": "DOID:0081155", "label": "common variable immunodeficiency 13", "link_status": true, "children": [] }, { "id": "DOID:0081156", "label": "common variable immunodeficiency 14", "link_status": true, "children": [] } ] }, { "id": "DOID:12712", "label": "nephronophthisis", "link_status": true, "children": [ { "id": "DOID:0111112", "label": "nephronophthisis 1", "link_status": true, "children": [] }, { "id": "DOID:0111113", "label": "nephronophthisis 2", "link_status": true, "children": [] }, { "id": "DOID:0111114", "label": "nephronophthisis 3", "link_status": true, "children": [] }, { "id": "DOID:0111115", "label": "nephronophthisis 4", "link_status": true, "children": [] }, { "id": "DOID:0111116", "label": "nephronophthisis 7", "link_status": true, "children": [] }, { "id": "DOID:0111117", "label": "nephronophthisis-like nephropathy 1", "link_status": true, "children": [] }, { "id": "DOID:0111118", "label": "nephronophthisis 11", "link_status": true, "children": [] }, { "id": "DOID:0111119", "label": "nephronophthisis 12", "link_status": true, "children": [] }, { "id": "DOID:0111120", "label": "nephronophthisis 9", "link_status": true, "children": [] }, { "id": "DOID:0111121", "label": "nephronophthisis 13", "link_status": true, "children": [] }, { "id": "DOID:0111122", "label": "nephronophthisis 14", "link_status": true, "children": [] }, { "id": "DOID:0111123", "label": "nephronophthisis 15", "link_status": true, "children": [] }, { "id": "DOID:0111124", "label": "nephronophthisis 16", "link_status": true, "children": [] }, { "id": "DOID:0111125", "label": "nephronophthisis 18", "link_status": true, "children": [] }, { "id": "DOID:0111126", "label": "nephronophthisis 19", "link_status": true, "children": [] }, { "id": "DOID:0111127", "label": "nephronophthisis 20", "link_status": true, "children": [] } ] }, { "id": "DOID:12714", "label": "Ellis-Van Creveld syndrome", "link_status": true, "children": [] }, { "id": "DOID:13777", "label": "epidermodysplasia verruciformis", "link_status": true, "children": [] }, { "id": "DOID:1386", "label": "abetalipoproteinemia", "link_status": true, "children": [] }, { "id": "DOID:14118", "label": "familial lipoprotein lipase deficiency", "link_status": true, "children": [] }, { "id": "DOID:14501", "label": "Sjogren-Larsson syndrome", "link_status": true, "children": [] }, { "id": "DOID:14671", "label": "multiple intestinal atresia", "link_status": true, "children": [] }, { "id": "DOID:14687", "label": "diastrophic dysplasia", "link_status": true, "children": [] }, { "id": "DOID:14694", "label": "Johanson-Blizzard syndrome", "link_status": true, "children": [] }, { "id": "DOID:14699", "label": "thrombocytopenia-absent radius syndrome", "link_status": true, "children": [] }, { "id": "DOID:14723", "label": "beta-ketothiolase deficiency", "link_status": true, "children": [] }, { "id": "DOID:14775", "label": "brittle cornea syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:1485", "label": "cystic fibrosis", "link_status": true, "children": [] }, { "id": "DOID:1930", "label": "Laurence-Moon syndrome", "link_status": true, "children": [] }, { "id": "DOID:1935", "label": "Bardet-Biedl syndrome", "link_status": true, "children": [ { "id": "DOID:0081009", "label": "Bardet-Biedl syndrome 20", "link_status": true, "children": [] }, { "id": "DOID:0081010", "label": "Bardet-Biedl syndrome 21", "link_status": true, "children": [] }, { "id": "DOID:0081011", "label": "Bardet-Biedl syndrome 22", "link_status": true, "children": [] }, { "id": "DOID:0110123", "label": "Bardet-Biedl syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0110124", "label": "Bardet-Biedl syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0110125", "label": "Bardet-Biedl syndrome 3", "link_status": true, "children": [] }, { "id": "DOID:0110126", "label": "Bardet-Biedl syndrome 4", "link_status": true, "children": [] }, { "id": "DOID:0110127", "label": "Bardet-Biedl syndrome 5", "link_status": true, "children": [] }, { "id": "DOID:0110128", "label": "Bardet-Biedl syndrome 6", "link_status": true, "children": [] }, { "id": "DOID:0110129", "label": "Bardet-Biedl syndrome 7", "link_status": true, "children": [] }, { "id": "DOID:0110130", "label": "Bardet-Biedl syndrome 8", "link_status": true, "children": [] }, { "id": "DOID:0110131", "label": "Bardet-Biedl syndrome 9", "link_status": true, "children": [] }, { "id": "DOID:0110132", "label": "Bardet-Biedl syndrome 10", "link_status": true, "children": [] }, { "id": "DOID:0110133", "label": "Bardet-Biedl syndrome 11", "link_status": true, "children": [] }, { "id": "DOID:0110134", "label": "Bardet-Biedl syndrome 12", "link_status": true, "children": [] }, { "id": "DOID:0110135", "label": "Bardet-Biedl syndrome 13", "link_status": true, "children": [] }, { "id": "DOID:0110136", "label": "Bardet-Biedl syndrome 14", "link_status": true, "children": [] }, { "id": "DOID:0110137", "label": "Bardet-Biedl syndrome 15", "link_status": true, "children": [] }, { "id": "DOID:0110138", "label": "Bardet-Biedl syndrome 16", "link_status": true, "children": [] }, { "id": "DOID:0110139", "label": "Bardet-Biedl syndrome 17", "link_status": true, "children": [] }, { "id": "DOID:0110140", "label": "Bardet-Biedl syndrome 18", "link_status": true, "children": [] }, { "id": "DOID:0110141", "label": "Bardet-Biedl syndrome 19", "link_status": true, "children": [] } ] }, { "id": "DOID:2012", "label": "Nezelof syndrome", "link_status": true, "children": [] }, { "id": "DOID:2211", "label": "factor XIII deficiency", "link_status": true, "children": [] }, { "id": "DOID:2215", "label": "factor VII deficiency", "link_status": true, "children": [] }, { "id": "DOID:2216", "label": "factor V deficiency", "link_status": true, "children": [] }, { "id": "DOID:2217", "label": "Bernard-Soulier syndrome", "link_status": true, "children": [ { "id": "DOID:0111059", "label": "Bernard-Soulier syndrome type A2", "link_status": true, "children": [] } ] }, { "id": "DOID:2222", "label": "factor X deficiency", "link_status": true, "children": [] }, { "id": "DOID:2231", "label": "factor XII deficiency", "link_status": true, "children": [] }, { "id": "DOID:2235", "label": "prothrombin deficiency", "link_status": true, "children": [] }, { "id": "DOID:2236", "label": "congenital afibrinogenemia", "link_status": true, "children": [] }, { "id": "DOID:2368", "label": "gangliosidosis", "link_status": false, "children": [ { "id": "DOID:3321", "label": "GM2 gangliosidosis", "link_status": true, "children": [ { "id": "DOID:3320", "label": "Tay-Sachs disease", "link_status": true, "children": [] }, { "id": "DOID:3323", "label": "Sandhoff disease", "link_status": true, "children": [] }, { "id": "DOID:4795", "label": "GM2 gangliosidosis, AB variant", "link_status": true, "children": [] } ] }, { "id": "DOID:3322", "label": "GM1 gangliosidosis", "link_status": true, "children": [ { "id": "DOID:0080489", "label": "GM1 gangliosidosis type 3", "link_status": true, "children": [] }, { "id": "DOID:0080501", "label": "GM1 gangliosidosis type 2", "link_status": true, "children": [] }, { "id": "DOID:0080502", "label": "GM1 gangliosidosis type 1", "link_status": true, "children": [] } ] } ] }, { "id": "DOID:2580", "label": "rhizomelic chondrodysplasia punctata", "link_status": true, "children": [ { "id": "DOID:0081243", "label": "rhizomelic chondrodysplasia punctate type 4", "link_status": true, "children": [] }, { "id": "DOID:0110851", "label": "rhizomelic chondrodysplasia punctata type 1", "link_status": true, "children": [] }, { "id": "DOID:0110852", "label": "rhizomelic chondrodysplasia punctata type 2", "link_status": true, "children": [] }, { "id": "DOID:0110853", "label": "rhizomelic chondrodysplasia punctata type 3", "link_status": true, "children": [] }, { "id": "DOID:0110854", "label": "rhizomelic chondrodysplasia punctata type 5", "link_status": true, "children": [] } ] }, { "id": "DOID:2717", "label": "Bloom syndrome", "link_status": true, "children": [] }, { "id": "DOID:2738", "label": "pseudoxanthoma elasticum", "link_status": true, "children": [] }, { "id": "DOID:2746", "label": "glycogen storage disease V", "link_status": true, "children": [] }, { "id": "DOID:2748", "label": "glycogen storage disease III", "link_status": true, "children": [] }, { "id": "DOID:2749", "label": "glycogen storage disease Ia", "link_status": true, "children": [] }, { "id": "DOID:2750", "label": "glycogen storage disease IV", "link_status": true, "children": [] }, { "id": "DOID:2752", "label": "glycogen storage disease II", "link_status": true, "children": [] }, { "id": "DOID:2754", "label": "glycogen storage disease VI", "link_status": true, "children": [] }, { "id": "DOID:2935", "label": "Chediak-Higashi syndrome", "link_status": true, "children": [] }, { "id": "DOID:2962", "label": "Cockayne syndrome", "link_status": true, "children": [ { "id": "DOID:0080907", "label": "Cockayne syndrome A", "link_status": true, "children": [] }, { "id": "DOID:0080908", "label": "Cockayne syndrome B", "link_status": true, "children": [] }, { "id": "DOID:0080910", "label": "cerebrooculofacioskeletal syndrome", "link_status": true, "children": [ { "id": "DOID:0080911", "label": "cerebrooculofacioskeletal syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0080912", "label": "cerebrooculofacioskeletal syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0080913", "label": "cerebrooculofacioskeletal syndrome 3", "link_status": true, "children": [] }, { "id": "DOID:0080914", "label": "cerebrooculofacioskeletal syndrome 4", "link_status": true, "children": [] } ] } ] }, { "id": "DOID:3389", "label": "Papillon-Lefevre disease", "link_status": true, "children": [] }, { "id": "DOID:3529", "label": "congenital myopathy 1A", "link_status": true, "children": [] }, { "id": "DOID:3534", "label": "Lafora disease", "link_status": true, "children": [] }, { "id": "DOID:3613", "label": "Canavan disease", "link_status": true, "children": [] }, { "id": "DOID:3753", "label": "Hermansky-Pudlak syndrome", "link_status": true, "children": [ { "id": "DOID:0060539", "label": "Hermansky-Pudlak syndrome 1", "link_status": true, "children": [] }, { "id": "DOID:0060540", "label": "Hermansky-Pudlak syndrome 2", "link_status": true, "children": [] }, { "id": "DOID:0060541", "label": "Hermansky-Pudlak syndrome 3", "link_status": true, "children": [] }, { "id": "DOID:0060542", "label": "Hermansky-Pudlak syndrome 4", "link_status": true, "children": [] }, { "id": "DOID:0060543", "label": "Hermansky-Pudlak syndrome 5", "link_status": true, "children": [] }, { "id": "DOID:0060544", "label": "Hermansky-Pudlak syndrome 6", "link_status": true, "children": [] }, { "id": "DOID:0060545", "label": "Hermansky-Pudlak syndrome 7", "link_status": true, "children": [] }, { "id": "DOID:0060546", "label": "Hermansky-Pudlak syndrome 8", "link_status": true, "children": [] }, { "id": "DOID:0060547", "label": "Hermansky-Pudlak syndrome 9", "link_status": true, "children": [] } ] }, { "id": "DOID:3755", "label": "antithrombin III deficiency", "link_status": true, "children": [] }, { "id": "DOID:3981", "label": "pantothenate kinase-associated neurodegeneration", "link_status": true, "children": [] }, { "id": "DOID:5325", "label": "Roberts syndrome", "link_status": true, "children": [] }, { "id": "DOID:5684", "label": "spondyloepimetaphyseal dysplasia, Sponastrime type", "link_status": true, "children": [] }, { "id": "DOID:5688", "label": "Werner syndrome", "link_status": true, "children": [] }, { "id": "DOID:5813", "label": "purine nucleoside phosphorylase deficiency", "link_status": true, "children": [] }, { "id": "DOID:6612", "label": "leukocyte adhesion deficiency", "link_status": true, "children": [ { "id": "DOID:0110910", "label": "leukocyte adhesion deficiency 1", "link_status": true, "children": [] }, { "id": "DOID:0110912", "label": "leukocyte adhesion deficiency 3", "link_status": true, "children": [] } ] }, { "id": "DOID:7400", "label": "Nijmegen breakage syndrome", "link_status": true, "children": [] }, { "id": "DOID:856", "label": "biotinidase deficiency", "link_status": true, "children": [] }, { "id": "DOID:905", "label": "Zellweger syndrome", "link_status": true, "children": [ { "id": "DOID:0080476", "label": "peroxisome biogenesis disorder 1A", "link_status": true, "children": [] }, { "id": "DOID:0080477", "label": "peroxisome biogenesis disorder 2A", "link_status": true, "children": [] }, { "id": "DOID:0080478", "label": "peroxisome biogenesis disorder 3A", "link_status": true, "children": [] }, { "id": "DOID:0080479", "label": "peroxisome biogenesis disorder 4A", "link_status": true, "children": [] }, { "id": "DOID:0080480", "label": "peroxisome biogenesis disorder 5A", "link_status": true, "children": [] }, { "id": "DOID:0080481", "label": "peroxisome biogenesis disorder 6A", "link_status": true, "children": [] }, { "id": "DOID:0080482", "label": "peroxisome biogenesis disorder 7A", "link_status": true, "children": [] }, { "id": "DOID:0080483", "label": "peroxisome biogenesis disorder 8A", "link_status": true, "children": [] }, { "id": "DOID:0080484", "label": "peroxisome biogenesis disorder 10A", "link_status": true, "children": [] }, { "id": "DOID:0080485", "label": "peroxisome biogenesis disorder 11A", "link_status": true, "children": [] }, { "id": "DOID:0080486", "label": "peroxisome biogenesis disorder 12A", "link_status": true, "children": [] }, { "id": "DOID:0080487", "label": "peroxisome biogenesis disorder 13A", "link_status": true, "children": [] } ] }, { "id": "DOID:9268", "label": "glycine encephalopathy", "link_status": true, "children": [ { "id": "DOID:0061001", "label": "glycine encephalopathy 2", "link_status": true, "children": [] }, { "id": "DOID:0070616", "label": "glycine encephalopathy 1", "link_status": true, "children": [] } ] }, { "id": "DOID:9280", "label": "carbamoyl phosphate synthetase I deficiency disease", "link_status": true, "children": [] }, { "id": "DOID:9521", "label": "Laron syndrome", "link_status": true, "children": [] } ], "id_list": [ "DOID:0050814", "DOID:0110854", "DOID:0110348", "DOID:0081241", "DOID:0080479", "DOID:0050335", "DOID:0080163", "DOID:0111948", "DOID:0110134", "DOID:0111127", "DOID:0070524", "DOID:0110294", "DOID:0060641", "DOID:0070179", "DOID:0070332", "DOID:0110849", "DOID:0111953", "DOID:0081009", "DOID:0051049", "DOID:0110123", "DOID:0051007", "DOID:0081141", "DOID:0110282", "DOID:0080289", "DOID:0061024", "DOID:0070413", "DOID:0080385", "DOID:0111807", "DOID:0111995", "DOID:0080327", "DOID:0080923", "DOID:0080262", "DOID:0110532", "DOID:0110131", "DOID:0112255", "DOID:0110368", "DOID:0080867", "DOID:0060589", "DOID:0112138", "DOID:0081215", "DOID:0111472", "DOID:3320", "DOID:0080754", "DOID:0060474", "DOID:0060266", "DOID:0090010", "DOID:0111594", "DOID:0060757", "DOID:0111335", "DOID:0061111", "DOID:0110521", "DOID:0081217", "DOID:0060796", "DOID:0061126", "DOID:0110005", "DOID:0070412", "DOID:0070578", "DOID:0110810", "DOID:0070177", "DOID:0111406", "DOID:0080065", "DOID:0070392", "DOID:0111449", "DOID:0110740", "DOID:0080953", "DOID:0080844", "DOID:0111677", "DOID:0050677", "DOID:0111274", "DOID:0080140", "DOID:0060559", "DOID:0061059", "DOID:0111848", "DOID:0070354", "DOID:0070502", "DOID:0080448", "DOID:0112083", "DOID:0110390", "DOID:0111278", "DOID:0060959", "DOID:0110283", "DOID:0110786", "DOID:0080785", "DOID:0080440", "DOID:0110095", "DOID:0061107", "DOID:0070568", "DOID:0060271", "DOID:0110840", "DOID:0110195", "DOID:0081425", "DOID:0081437", "DOID:0080107", "DOID:0110802", "DOID:0080464", "DOID:0110381", "DOID:0110401", "DOID:0080308", "DOID:0070503", "DOID:0070449", "DOID:12704", "DOID:0081334", "DOID:0070341", "DOID:0080059", "DOID:0110676", "DOID:0070284", "DOID:0110777", "DOID:0070218", "DOID:0070097", "DOID:0070100", "DOID:0111853", "DOID:0080453", "DOID:0060919", "DOID:0111959", "DOID:0112074", "DOID:0050450", "DOID:0080061", "DOID:0070450", "DOID:0110779", "DOID:0060241", "DOID:0060996", "DOID:0081193", "DOID:0060715", "DOID:0081346", "DOID:0110801", "DOID:0060655", "DOID:0070409", "DOID:0111667", "DOID:0070421", "DOID:0111871", "DOID:0060896", "DOID:0110399", "DOID:0112316", "DOID:0061131", "DOID:0080131", "DOID:0080055", "DOID:0111482", "DOID:0112324", "DOID:0110487", "DOID:0060364", "DOID:0081099", "DOID:0080133", "DOID:0110848", "DOID:0111258", "DOID:0050600", "DOID:0060861", "DOID:12177", "DOID:0090142", "DOID:0070499", "DOID:0112132", "DOID:0060265", "DOID:0081276", "DOID:0060983", "DOID:0060712", "DOID:0070592", "DOID:0110376", "DOID:0110204", "DOID:0111240", "DOID:0111149", "DOID:0111474", "DOID:0111870", "DOID:0112379", "DOID:0070581", "DOID:0060713", "DOID:0081137", "DOID:0110277", "DOID:0110127", "DOID:0111725", "DOID:0112249", "DOID:0111235", "DOID:0070289", "DOID:0081097", "DOID:0070463", "DOID:0080411", "DOID:0060781", "DOID:0112067", "DOID:0110515", "DOID:0070396", "DOID:0110803", "DOID:0080132", "DOID:0090059", "DOID:0112119", "DOID:0070201", "DOID:0111915", "DOID:0111699", "DOID:0111648", "DOID:0111590", "DOID:0111264", "DOID:0111857", "DOID:0081435", "DOID:0110838", "DOID:0051041", "DOID:0050774", "DOID:0112231", "DOID:0110491", "DOID:0111634", "DOID:0110923", "DOID:0111911", "DOID:0070253", "DOID:0111195", "DOID:0111259", "DOID:0110441", "DOID:0070141", "DOID:0111587", "DOID:0111582", "DOID:0080217", "DOID:0110722", "DOID:0070356", "DOID:0070435", "DOID:0080106", "DOID:0080614", "DOID:0111241", "DOID:0110918", "DOID:0110524", "DOID:0060027", "DOID:0060023", "DOID:0081203", "DOID:0112381", "DOID:0070429", "DOID:0080946", "DOID:0050682", "DOID:0112318", "DOID:0111937", "DOID:0080870", "DOID:0060718", "DOID:0070447", "DOID:0081431", "DOID:0111135", "DOID:0110476", "DOID:0050436", "DOID:0111394", "DOID:0080101", "DOID:0111592", "DOID:2746", "DOID:0090007", "DOID:0111456", "DOID:0110847", "DOID:0080786", "DOID:0080805", "DOID:0110009", "DOID:9521", "DOID:0112335", "DOID:0061109", "DOID:0080515", "DOID:0081144", "DOID:0080595", "DOID:0110332", "DOID:0112070", "DOID:0080571", "DOID:0112109", "DOID:0060653", "DOID:0080952", "DOID:0060247", "DOID:0081322", "DOID:0112254", "DOID:0070397", "DOID:0112354", "DOID:0110500", "DOID:0110523", "DOID:0110931", "DOID:0112235", "DOID:0081333", "DOID:0112378", "DOID:0110270", "DOID:0110721", "DOID:0112358", "DOID:0081383", "DOID:0070574", "DOID:0110245", "DOID:0110679", "DOID:0111238", "DOID:0081220", "DOID:0110852", "DOID:0061102", "DOID:0070521", "DOID:0111666", "DOID:0110192", "DOID:0111636", "DOID:0111929", "DOID:0111392", "DOID:0112115", "DOID:0112090", "DOID:0080735", "DOID:0080042", "DOID:0070591", "DOID:0061093", "DOID:0081149", "DOID:0070403", "DOID:0110085", "DOID:0081202", "DOID:0111515", "DOID:0081020", "DOID:0051033", "DOID:0110497", "DOID:0070352", "DOID:0111371", "DOID:0060934", "DOID:0080596", "DOID:0110910", "DOID:0090072", "DOID:0050949", "DOID:0080318", "DOID:0111230", "DOID:0111972", "DOID:0112347", "DOID:0111620", "DOID:0081335", "DOID:0080543", "DOID:14694", "DOID:0111116", "DOID:1099", "DOID:0050942", "DOID:0110281", "DOID:0112066", "DOID:0111698", "DOID:0111940", "DOID:0090088", "DOID:0080719", "DOID:0070280", "DOID:0110465", "DOID:0060556", "DOID:0111691", "DOID:0111138", "DOID:0110297", "DOID:0080459", "DOID:0111229", "DOID:0111471", "DOID:0081228", "DOID:0111445", "DOID:0110354", "DOID:0070255", "DOID:0061014", "DOID:0080913", "DOID:14775", "DOID:0060790", "DOID:0112108", "DOID:0081124", "DOID:0081224", "DOID:0070286", "DOID:0111668", "DOID:0080502", "DOID:0060540", "DOID:0061056", "DOID:0081236", "DOID:0081161", "DOID:0080802", "DOID:0080872", "DOID:0090117", "DOID:0110518", "DOID:0111920", "DOID:0090078", "DOID:0111990", "DOID:0061116", "DOID:0080081", "DOID:0111985", "DOID:0112092", "DOID:0110097", "DOID:0111277", "DOID:0070634", "DOID:0080026", "DOID:0090089", "DOID:0110719", "DOID:0111621", "DOID:0080460", "DOID:0070571", "DOID:0070585", "DOID:0110738", "DOID:0111481", "DOID:0050529", "DOID:0110063", "DOID:0061066", "DOID:0080197", "DOID:0080556", "DOID:0090004", "DOID:0110536", "DOID:0110936", "DOID:0110673", "DOID:1386", "DOID:0110384", "DOID:0081153", "DOID:0070132", "DOID:0080963", "DOID:0111591", "DOID:0080271", "DOID:0050883", "DOID:0081206", "DOID:0080071", "DOID:0080768", "DOID:0110812", "DOID:0111973", "DOID:0110632", "DOID:0051027", "DOID:0070256", "DOID:0081045", "DOID:0110506", "DOID:0080790", "DOID:0060960", "DOID:0061115", "DOID:0050816", "DOID:0110490", "DOID:0090127", "DOID:0110156", "DOID:0110924", "DOID:0081221", "DOID:0111448", "DOID:0070293", "DOID:0080590", "DOID:0110664", "DOID:0110250", "DOID:0070554", "DOID:0060752", "DOID:0080484", "DOID:0060484", "DOID:0110419", "DOID:0110658", "DOID:0111155", "DOID:0080250", "DOID:0111586", "DOID:0111084", "DOID:0060601", "DOID:0080980", "DOID:0111476", "DOID:0081394", "DOID:0110790", "DOID:0112334", "DOID:0050763", "DOID:0080673", "DOID:0060835", "DOID:0081175", "DOID:0112299", "DOID:0060638", "DOID:0110928", "DOID:0110959", "DOID:0080481", "DOID:0050530", "DOID:0090013", "DOID:0050797", "DOID:0111852", "DOID:0050950", "DOID:0110929", "DOID:0080485", "DOID:0112086", "DOID:0110670", "DOID:0080922", "DOID:0111589", "DOID:14497", "DOID:0110509", "DOID:0090050", "DOID:0110249", "DOID:0090008", "DOID:0111646", "DOID:0061090", "DOID:0081034", "DOID:0112338", "DOID:0061113", "DOID:0070331", "DOID:0081138", "DOID:0080414", "DOID:0112364", "DOID:0070371", "DOID:0111356", "DOID:0060490", "DOID:0110534", "DOID:0070307", "DOID:0070565", "DOID:0110215", "DOID:0060609", "DOID:0111643", "DOID:0070194", "DOID:0112198", "DOID:0051040", "DOID:0061019", "DOID:0060939", "DOID:0110839", "DOID:0110353", "DOID:0070451", "DOID:0080038", "DOID:0110078", "DOID:0080557", "DOID:0110731", "DOID:0111944", "DOID:0070264", "DOID:0070150", "DOID:0111999", "DOID:0060697", "DOID:0111981", "DOID:0080487", "DOID:0081200", "DOID:0050604", "DOID:0080871", "DOID:0070151", "DOID:0070576", "DOID:0080209", "DOID:0061074", "DOID:0081328", "DOID:0060654", "DOID:0070017", "DOID:0111265", "DOID:856", "DOID:0081433", "DOID:0070391", "DOID:0110674", "DOID:0112093", "DOID:0060968", "DOID:0050710", "DOID:0111213", "DOID:0081428", "DOID:0110296", "DOID:0111872", "DOID:0081434", "DOID:0060994", "DOID:0070146", "DOID:0080455", "DOID:0110293", "DOID:0111625", "DOID:0112062", "DOID:0111640", "DOID:0061085", "DOID:0110827", "DOID:0080607", "DOID:0060987", "DOID:0080119", "DOID:0111988", "DOID:0081352", "DOID:0060831", "DOID:0111134", "DOID:0112204", "DOID:0080562", "DOID:0060966", "DOID:0090130", "DOID:0111639", "DOID:0111975", "DOID:0070007", "DOID:0081181", "DOID:0060764", "DOID:0080715", "DOID:0080836", "DOID:0070506", "DOID:0111444", "DOID:0111405", "DOID:0110190", "DOID:0111436", "DOID:0051006", "DOID:0112087", "DOID:0080029", "DOID:0080738", "DOID:10923", "DOID:2580", "DOID:0110196", "DOID:0111242", "DOID:0090011", "DOID:0111051", "DOID:0111263", "DOID:0080512", "DOID:0112258", "DOID:0112351", "DOID:0111501", "DOID:0111974", "DOID:0060737", "DOID:0080501", "DOID:0111642", "DOID:0080283", "DOID:0112081", "DOID:0050560", "DOID:0090073", "DOID:0090112", "DOID:0111376", "DOID:0111485", "DOID:0081263", "DOID:0080239", "DOID:0061004", "DOID:0061020", "DOID:0111789", "DOID:0070302", "DOID:0081355", "DOID:0110033", "DOID:0112187", "DOID:0061060", "DOID:0080552", "DOID:0080898", "DOID:0090113", "DOID:0111077", "DOID:0070580", "DOID:0110483", "DOID:0111422", "DOID:0050585", "DOID:0110846", "DOID:0110713", "DOID:0110486", "DOID:0110336", "DOID:0080478", "DOID:0110016", "DOID:0111464", "DOID:0060698", "DOID:0111064", "DOID:0080330", "DOID:0080256", "DOID:0050569", "DOID:0080586", "DOID:0090068", "DOID:0060946", "DOID:0112224", "DOID:0081177", "DOID:0070167", "DOID:0070586", "DOID:0112346", "DOID:0060590", "DOID:0060779", "DOID:0070126", "DOID:0080274", "DOID:0070258", "DOID:0112304", "DOID:0112096", "DOID:0080255", "DOID:0112272", "DOID:0111616", "DOID:0110008", "DOID:0080358", "DOID:0111566", "DOID:0080066", "DOID:0111401", "DOID:0111858", "DOID:0110167", "DOID:0110927", "DOID:0110494", "DOID:0112356", "DOID:0070367", "DOID:0081396", "DOID:0110484", "DOID:0110505", "DOID:0112137", "DOID:0111414", "DOID:0111473", "DOID:0080387", "DOID:0111626", "DOID:0110176", "DOID:0111125", "DOID:0081234", "DOID:0111970", "DOID:0111797", "DOID:0080316", "DOID:0060849", "DOID:0111114", "DOID:0110735", "DOID:0080979", "DOID:0111656", "DOID:0110842", "DOID:0080060", "DOID:0070492", "DOID:0080126", "DOID:0111233", "DOID:0070559", "DOID:0110475", "DOID:0111261", "DOID:0112152", "DOID:0111588", "DOID:0070094", "DOID:0111774", "DOID:0111674", "DOID:0060547", "DOID:0110129", "DOID:0080761", "DOID:0081190", "DOID:0111477", "DOID:0110934", "DOID:0070191", "DOID:0080135", "DOID:0111864", "DOID:0051021", "DOID:0080051", "DOID:0110667", "DOID:0112298", "DOID:0112077", "DOID:0110519", "DOID:0112350", "DOID:0060793", "DOID:0080753", "DOID:0080124", "DOID:0110169", "DOID:0080142", "DOID:0061117", "DOID:0110768", "DOID:0111676", "DOID:0080678", "DOID:0080120", "DOID:0110533", "DOID:0111450", "DOID:0110263", "DOID:0111120", "DOID:0070437", "DOID:0111420", "DOID:0060950", "DOID:0111524", "DOID:0111187", "DOID:0110003", "DOID:0110462", "DOID:0080553", "DOID:0111941", "DOID:0081022", "DOID:0060240", "DOID:0081368", "DOID:0111480", "DOID:0112112", "DOID:0050754", "DOID:0080245", "DOID:0081230", "DOID:0110844", "DOID:0112078", "DOID:0111967", "DOID:0061023", "DOID:0050944", "DOID:0110831", "DOID:0110289", "DOID:0112323", "DOID:0110529", "DOID:0081218", "DOID:0110498", "DOID:0070430", "DOID:0110808", "DOID:0070613", "DOID:0081229", "DOID:0080573", "DOID:0070446", "DOID:0110124", "DOID:0081385", "DOID:0111732", "DOID:0111982", "DOID:0070579", "DOID:0051005", "DOID:0060370", "DOID:0070368", "DOID:0111580", "DOID:0112349", "DOID:0080806", "DOID:0110526", "DOID:0110184", "DOID:0110804", "DOID:0111618", "DOID:0050546", "DOID:0070006", "DOID:0061013", "DOID:0060535", "DOID:0110262", "DOID:0111978", "DOID:0060891", "DOID:0111912", "DOID:0080253", "DOID:0110266", "DOID:0051025", "DOID:0060940", "DOID:0070507", "DOID:0081231", "DOID:0060898", "DOID:0110488", "DOID:0110825", "DOID:0111415", "DOID:0070294", "DOID:0081446", "DOID:0080954", "DOID:0110869", "DOID:0110797", "DOID:0060993", "DOID:0080412", "DOID:0111654", "DOID:0112218", "DOID:905", "DOID:0110193", "DOID:0111637", "DOID:0111935", "DOID:0070376", "DOID:0111557", "DOID:0080482", "DOID:0112360", "DOID:0112273", "DOID:0060337", "DOID:0070199", "DOID:0080443", "DOID:0080621", "DOID:0080357", "DOID:0110639", "DOID:0080381", "DOID:0111468", "DOID:0110727", "DOID:0081007", "DOID:0112180", "DOID:0070493", "DOID:0080050", "DOID:0080254", "DOID:0060656", "DOID:0080732", "DOID:0111957", "DOID:0060789", "DOID:0111496", "DOID:0080908", "DOID:0111459", "DOID:0080417", "DOID:0081143", "DOID:0061112", "DOID:0060728", "DOID:0081270", "DOID:0051036", "DOID:0080052", "DOID:0080457", "DOID:0070544", "DOID:0061080", "DOID:0110832", "DOID:0111407", "DOID:0111996", "DOID:0051022", "DOID:0060947", "DOID:0110537", "DOID:0110828", "DOID:0112357", "DOID:0110530", "DOID:0070296", "DOID:0110704", "DOID:0080911", "DOID:0060642", "DOID:0060841", "DOID:0112141", "DOID:0110179", "DOID:0070254", "DOID:0081129", "DOID:0080434", "DOID:0111221", "DOID:0112329", "DOID:0070268", "DOID:0080939", "DOID:0080499", "DOID:0111950", "DOID:6612", "DOID:0080960", "DOID:0111379", "DOID:0110474", "DOID:0080359", "DOID:0070587", "DOID:0051035", "DOID:0070431", "DOID:0111905", "DOID:0112080", "DOID:0050857", "DOID:0070098", "DOID:0111992", "DOID:0081350", "DOID:0060791", "DOID:0112145", "DOID:0112219", "DOID:0112236", "DOID:0081204", "DOID:0070287", "DOID:0111234", "DOID:0110945", "DOID:0110080", "DOID:0111266", "DOID:0111943", "DOID:0060368", "DOID:0081155", "DOID:0080335", "DOID:0051024", "DOID:0080360", "DOID:0110909", "DOID:0051044", "DOID:0080480", "DOID:0070489", "DOID:0070410", "DOID:0111614", "DOID:0050558", "DOID:0070588", "DOID:0061007", "DOID:0111395", "DOID:0060842", "DOID:0080129", "DOID:0081222", "DOID:0110280", "DOID:0110160", "DOID:2216", "DOID:0110774", "DOID:0080576", "DOID:0111486", "DOID:0070504", "DOID:0111081", "DOID:0110187", "DOID:0060979", "DOID:0060267", "DOID:0090009", "DOID:0070165", "DOID:3753", "DOID:10241", "DOID:0070277", "DOID:0090019", "DOID:0110535", "DOID:0110278", "DOID:0110329", "DOID:0050579", "DOID:0081179", "DOID:0070436", "DOID:0080136", "DOID:0110372", "DOID:0070543", "DOID:0070434", "DOID:0081386", "DOID:1485", "DOID:0070465", "DOID:0070582", "DOID:0111366", "DOID:0090074", "DOID:0081351", "DOID:0110843", "DOID:0111046", "DOID:0081156", "DOID:0111611", "DOID:0111218", "DOID:0090091", "DOID:0110672", "DOID:0110482", "DOID:0081237", "DOID:0110511", "DOID:0061025", "DOID:0060839", "DOID:0060902", "DOID:0111681", "DOID:0060714", "DOID:0080635", "DOID:0110940", "DOID:0080486", "DOID:0112365", "DOID:0110495", "DOID:0070433", "DOID:0112306", "DOID:0060941", "DOID:0112355", "DOID:0070583", "DOID:0070426", "DOID:0080731", "DOID:0110188", "DOID:0070174", "DOID:0112225", "DOID:0111391", "DOID:0060935", "DOID:0111355", "DOID:0111660", "DOID:2222", "DOID:0070269", "DOID:0112174", "DOID:0110358", "DOID:0070011", "DOID:0060374", "DOID:0080064", "DOID:0111475", "DOID:0081154", "DOID:0112348", "DOID:0061058", "DOID:0080382", "DOID:0060382", "DOID:0070166", "DOID:0110677", "DOID:0080349", "DOID:0080886", "DOID:0081361", "DOID:0110636", "DOID:0080212", "DOID:0111922", "DOID:0111113", "DOID:0060834", "DOID:0080379", "DOID:0111968", "DOID:0060696", "DOID:0080483", "DOID:0110480", "DOID:0080082", "DOID:0112015", "DOID:0050473", "DOID:0111914", "DOID:0060775", "DOID:0110815", "DOID:0111271", "DOID:0070454", "DOID:0070010", "DOID:0070462", "DOID:0110149", "DOID:0081232", "DOID:0111131", "DOID:0081233", "DOID:0080122", "DOID:0061061", "DOID:0111523", "DOID:0111270", "DOID:0112251", "DOID:0050427", "DOID:0111497", "DOID:0060238", "DOID:0110352", "DOID:0060545", "DOID:0061021", "DOID:0111919", "DOID:0081207", "DOID:0070181", "DOID:0112184", "DOID:0070282", "DOID:0081345", "DOID:0112220", "DOID:0111615", "DOID:0060717", "DOID:0060348", "DOID:0111337", "DOID:0112266", "DOID:0080261", "DOID:0111095", "DOID:0080380", "DOID:0080773", "DOID:0110002", "DOID:0080057", "DOID:0112068", "DOID:0070477", "DOID:0111119", "DOID:0080419", "DOID:0111118", "DOID:0112376", "DOID:0110298", "DOID:0110479", "DOID:0111527", "DOID:0110031", "DOID:0110841", "DOID:0111136", "DOID:0080628", "DOID:0110705", "DOID:0050807", "DOID:0080570", "DOID:0110816", "DOID:0110001", "DOID:0070448", "DOID:0081271", "DOID:0112188", "DOID:0112277", "DOID:0112283", "DOID:0112344", "DOID:0110795", "DOID:0111917", "DOID:0051053", "DOID:1930", "DOID:0110819", "DOID:0110128", "DOID:0070520", "DOID:0070369", "DOID:0110444", "DOID:0080394", "DOID:0112133", "DOID:0081213", "DOID:0060544", "DOID:0111619", "DOID:0080384", "DOID:0111093", "DOID:0060647", "DOID:0110275", "DOID:0111776", "DOID:0070140", "DOID:0070144", "DOID:0112082", "DOID:0050737", "DOID:0080730", "DOID:0080361", "DOID:2962", "DOID:0060733", "DOID:0111402", "DOID:0110477", "DOID:0051050", "DOID:0110800", "DOID:0110346", "DOID:0080121", "DOID:0110467", "DOID:0110807", "DOID:0112382", "DOID:0111998", "DOID:0111377", "DOID:0080415", "DOID:0060797", "DOID:0070232", "DOID:0060542", "DOID:0110292", "DOID:0080263", "DOID:0110380", "DOID:0070129", "DOID:0050790", "DOID:0111167", "DOID:0050711", "DOID:0110671", "DOID:0060639", "DOID:0050766", "DOID:0111703", "DOID:0090001", "DOID:0111451", "DOID:0061086", "DOID:0112267", "DOID:0110061", "DOID:0112223", "DOID:0111418", "DOID:0060778", "DOID:0070206", "DOID:0112075", "DOID:0111679", "DOID:0111089", "DOID:3323", "DOID:0080489", "DOID:0060269", "DOID:0111220", "DOID:0060773", "DOID:0110922", "DOID:0111645", "DOID:0070153", "DOID:4795", "DOID:0110247", "DOID:0080293", "DOID:0090141", "DOID:0081211", "DOID:0081188", "DOID:0111083", "DOID:0060958", "DOID:0080734", "DOID:0110916", "DOID:0112244", "DOID:0111483", "DOID:0110096", "DOID:0051001", "DOID:0061133", "DOID:0110276", "DOID:0112343", "DOID:0111495", "DOID:0110057", "DOID:0090116", "DOID:0080585", "DOID:0081395", "DOID:0111087", "DOID:0060759", "DOID:0111080", "DOID:0080592", "DOID:0112079", "DOID:0112212", "DOID:0070567", "DOID:0110194", "DOID:0111442", "DOID:0060571", "DOID:0070497", "DOID:0112211", "DOID:0070224", "DOID:0070584", "DOID:0080751", "DOID:0061077", "DOID:0081343", "DOID:0111044", "DOID:0110711", "DOID:0110267", "DOID:0080413", "DOID:0070494", "DOID:0080458", "DOID:0080273", "DOID:3613", "DOID:0060268", "DOID:0080594", "DOID:0112193", "DOID:0112117", "DOID:0050656", "DOID:0061088", "DOID:0111351", "DOID:0112332", "DOID:0060356", "DOID:0110338", "DOID:0110865", "DOID:0090043", "DOID:0060551", "DOID:0111635", "DOID:0110899", "DOID:0060978", "DOID:0080567", "DOID:0110944", "DOID:0081139", "DOID:0050462", "DOID:0081324", "DOID:0090003", "DOID:0110657", "DOID:0081341", "DOID:0081444", "DOID:0110941", "DOID:0061099", "DOID:0110139", "DOID:0080441", "DOID:0111112", "DOID:0111137", "DOID:0110264", "DOID:0070491", "DOID:2748", "DOID:0090106", "DOID:0110809", "DOID:0050946", "DOID:0110633", "DOID:12712", "DOID:0110539", "DOID:0112252", "DOID:0112189", "DOID:0070382", "DOID:0080260", "DOID:2231", "DOID:0070593", "DOID:0112303", "DOID:0070411", "DOID:0112185", "DOID:1064", "DOID:0081447", "DOID:0081180", "DOID:0061001", "DOID:0110845", "DOID:0070423", "DOID:0080718", "DOID:0060576", "DOID:0060949", "DOID:0110285", "DOID:0112336", "DOID:0080495", "DOID:0111928", "DOID:0080432", "DOID:0110851", "DOID:0070222", "DOID:0080433", "DOID:0081238", "DOID:0112333", "DOID:0111499", "DOID:0060449", "DOID:0112139", "DOID:0111378", "DOID:0070266", "DOID:0050941", "DOID:0080257", "DOID:0070468", "DOID:0070486", "DOID:0080424", "DOID:0060558", "DOID:0081136", "DOID:0081111", "DOID:0080386", "DOID:0050649", "DOID:0110726", "DOID:0070558", "DOID:0111939", "DOID:0070145", "DOID:0110402", "DOID:0060942", "DOID:0051028", "DOID:0081160", "DOID:0112259", "DOID:0080252", "DOID:0110799", "DOID:0060795", "DOID:0070002", "DOID:5325", "DOID:0070184", "DOID:0080329", "DOID:0081240", "DOID:0080561", "DOID:0112089", "DOID:0061132", "DOID:0070262", "DOID:0110850", "DOID:0060650", "DOID:0110290", "DOID:0060577", "DOID:0110822", "DOID:0070223", "DOID:0112271", "DOID:0051020", "DOID:0081272", "DOID:0060237", "DOID:0111465", "DOID:0111997", "DOID:0060539", "DOID:0110126", "DOID:0060967", "DOID:0110363", "DOID:0080765", "DOID:0110056", "DOID:0110383", "DOID:0111452", "DOID:0111638", "DOID:0111851", "DOID:0080389", "DOID:0112256", "DOID:0110926", "DOID:0080265", "DOID:0111516", "DOID:0111665", "DOID:0080435", "DOID:0070137", "DOID:0070024", "DOID:0111644", "DOID:0061003", "DOID:0111540", "DOID:0061062", "DOID:0110864", "DOID:0110066", "DOID:0081216", "DOID:0111994", "DOID:0110079", "DOID:0070572", "DOID:0112253", "DOID:0080950", "DOID:0111574", "DOID:0081274", "DOID:0112250", "DOID:0050634", "DOID:0051034", "DOID:0090115", "DOID:0111926", "DOID:0090071", "DOID:0081227", "DOID:0070424", "DOID:0110351", "DOID:0110930", "DOID:0070139", "DOID:0112095", "DOID:2749", "DOID:0060546", "DOID:0061081", "DOID:0110410", "DOID:0050540", "DOID:0060973", "DOID:0070594", "DOID:0080393", "DOID:0111491", "DOID:0080123", "DOID:0080259", "DOID:0060794", "DOID:14118", "DOID:0070193", "DOID:0060470", "DOID:0111214", "DOID:0110668", "DOID:0070291", "DOID:0110062", "DOID:0081011", "DOID:0112353", "DOID:0110000", "DOID:0112230", "DOID:0090126", "DOID:0112147", "DOID:0112233", "DOID:0060649", "DOID:0080914", "DOID:0112071", "DOID:0060481", "DOID:0070425", "DOID:0081134", "DOID:0070260", "DOID:0111043", "DOID:0080771", "DOID:0080579", "DOID:0060560", "DOID:0070476", "DOID:0111489", "DOID:0081235", "DOID:0070203", "DOID:0081146", "DOID:0110729", "DOID:0081354", "DOID:0081436", "DOID:0060375", "DOID:0110660", "DOID:0111453", "DOID:0111092", "DOID:0112173", "DOID:0060900", "DOID:0080272", "DOID:0112110", "DOID:14687", "DOID:0070404", "DOID:0070464", "DOID:0110088", "DOID:0110171", "DOID:0070443", "DOID:0111952", "DOID:0070219", "DOID:0070008", "DOID:0111918", "DOID:0070134", "DOID:0111065", "DOID:0111649", "DOID:0110093", "DOID:0070173", "DOID:0060787", "DOID:0112315", "DOID:0060491", "DOID:0110295", "DOID:0110830", "DOID:0061123", "DOID:0110861", "DOID:0111977", "DOID:0080476", "DOID:0050802", "DOID:0110198", "DOID:0060854", "DOID:0111216", "DOID:0060283", "DOID:0081344", "DOID:0070540", "DOID:0112307", "DOID:0111048", "DOID:2235", "DOID:0070398", "DOID:0080626", "DOID:0050719", "DOID:0110087", "DOID:0061051", "DOID:0111446", "DOID:0111397", "DOID:0070393", "DOID:0111332", "DOID:0080563", "DOID:0060711", "DOID:0111404", "DOID:0111222", "DOID:0112158", "DOID:0070009", "DOID:0110374", "DOID:0080580", "DOID:0110287", "DOID:0061067", "DOID:0070619", "DOID:14723", "DOID:0111254", "DOID:14502", "DOID:0110820", "DOID:0070261", "DOID:0110007", "DOID:0081440", "DOID:0080912", "DOID:0050588", "DOID:0080134", "DOID:0081265", "DOID:0080296", "DOID:0070172", "DOID:0070444", "DOID:0061091", "DOID:0110274", "DOID:0110349", "DOID:0110365", "DOID:0070183", "DOID:0070373", "DOID:0070577", "DOID:0070525", "DOID:0110201", "DOID:0081098", "DOID:0110724", "DOID:0111156", "DOID:0060346", "DOID:0110933", "DOID:0070143", "DOID:0111930", "DOID:0110867", "DOID:0111488", "DOID:0080516", "DOID:0070022", "DOID:0070283", "DOID:0081135", "DOID:0070531", "DOID:0060758", "DOID:0080496", "DOID:0112337", "DOID:0110725", "DOID:0110460", "DOID:0061063", "DOID:0080391", "DOID:0081427", "DOID:0081374", "DOID:0061002", "DOID:0080555", "DOID:0081150", "DOID:0090081", "DOID:0070456", "DOID:0110473", "DOID:0061052", "DOID:0060025", "DOID:0061124", "DOID:0110086", "DOID:0060720", "DOID:0070432", "DOID:0110279", "DOID:2738", "DOID:0080804", "DOID:0110635", "DOID:0080568", "DOID:0111641", "DOID:0070498", "DOID:0081147", "DOID:0070096", "DOID:0080105", "DOID:2368", "DOID:0111353", "DOID:0110481", "DOID:0070519", "DOID:0110527", "DOID:0070505", "DOID:0110337", "DOID:0111085", "DOID:0090060", "DOID:0110125", "DOID:0110060", "DOID:0080331", "DOID:0112182", "DOID:0112317", "DOID:0080363", "DOID:0081330", "DOID:0110116", "DOID:0111951", "DOID:3529", "DOID:0111398", "DOID:0081219", "DOID:0081046", "DOID:0080062", "DOID:0110094", "DOID:0111115", "DOID:0111629", "DOID:0111479", "DOID:0070363", "DOID:0070135", "DOID:0080498", "DOID:0110501", "DOID:0081223", "DOID:0080865", "DOID:0070279", "DOID:0090076", "DOID:0111467", "DOID:0111487", "DOID:0060065", "DOID:0080981", "DOID:0081010", "DOID:0080717", "DOID:5813", "DOID:0110133", "DOID:0080477", "DOID:0070496", "DOID:0112194", "DOID:0110470", "DOID:0070556", "DOID:0111923", "DOID:0070170", "DOID:0111494", "DOID:0061089", "DOID:0110288", "DOID:2211", "DOID:0050812", "DOID:0080565", "DOID:2012", "DOID:0080127", "DOID:0110805", "DOID:0080672", "DOID:0080587", "DOID:0110513", "DOID:0070225", "DOID:0111961", "DOID:0070263", "DOID:0110939", "DOID:0110730", "DOID:0112222", "DOID:0080427", "DOID:12705", "DOID:0110089", "DOID:0050632", "DOID:0110136", "DOID:0070575", "DOID:0070562", "DOID:0110946", "DOID:0070147", "DOID:0112091", "DOID:0061114", "DOID:0110796", "DOID:0111662", "DOID:0060708", "DOID:0070395", "DOID:0111500", "DOID:2752", "DOID:0111236", "DOID:0080452", "DOID:0110238", "DOID:12241", "DOID:0060988", "DOID:0110183", "DOID:0081163", "DOID:0111121", "DOID:0111354", "DOID:0070458", "DOID:0112094", "DOID:0110728", "DOID:0110342", "DOID:0070523", "DOID:0080125", "DOID:0061134", "DOID:0110140", "DOID:0111437", "DOID:0110675", "DOID:0110525", "DOID:0070478", "DOID:0060672", "DOID:0112340", "DOID:0112113", "DOID:0070537", "DOID:7400", "DOID:0060580", "DOID:0111773", "DOID:0080558", "DOID:0080497", "DOID:0080663", "DOID:0080560", "DOID:0111522", "DOID:0111498", "DOID:0080092", "DOID:0112216", "DOID:0110463", "DOID:0111991", "DOID:0070500", "DOID:0080581", "DOID:0111680", "DOID:0060270", "DOID:0080195", "DOID:0112118", "DOID:0110712", "DOID:0111063", "DOID:0111237", "DOID:0060021", "DOID:0081178", "DOID:0081326", "DOID:0112136", "DOID:0110678", "DOID:0081205", "DOID:0111197", "DOID:0110137", "DOID:0111722", "DOID:0061105", "DOID:0080569", "DOID:0080769", "DOID:0080058", "DOID:0111980", "DOID:0080559", "DOID:0051023", "DOID:0060889", "DOID:0111984", "DOID:0111389", "DOID:0081133", "DOID:0112163", "DOID:0070138", "DOID:2754", "DOID:0070541", "DOID:0110065", "DOID:0080343", "DOID:0061078", "DOID:0080181", "DOID:0111268", "DOID:0112217", "DOID:0112279", "DOID:0081208", "DOID:0081226", "DOID:0060915", "DOID:0061016", "DOID:0110186", "DOID:0070259", "DOID:0070005", "DOID:0060856", "DOID:0070226", "DOID:0081210", "DOID:0080622", "DOID:0081008", "DOID:0112257", "DOID:0112300", "DOID:0061083", "DOID:0111873", "DOID:0110135", "DOID:0112142", "DOID:5684", "DOID:0110242", "DOID:0070569", "DOID:0070387", "DOID:0110367", "DOID:0112362", "DOID:0070192", "DOID:0081214", "DOID:2750", "DOID:0111669", "DOID:0110764", "DOID:0070490", "DOID:0060557", "DOID:0050603", "DOID:0111627", "DOID:0112097", "DOID:3321", "DOID:0050943", "DOID:0070163", "DOID:0112321", "DOID:0110119", "DOID:0112129", "DOID:0060837", "DOID:0070495", "DOID:0080554", "DOID:0110092", "DOID:0110389", "DOID:0112331", "DOID:0112073", "DOID:0070015", "DOID:0080736", "DOID:0070133", "DOID:0081130", "DOID:0111934", "DOID:0060689", "DOID:0080063", "DOID:0080884", "DOID:0060948", "DOID:0051052", "DOID:0110471", "DOID:0110661", "DOID:0111416", "DOID:0080054", "DOID:0081448", "DOID:0060308", "DOID:0070374", "DOID:0112327", "DOID:0112171", "DOID:0070364", "DOID:0110347", "DOID:0070473", "DOID:0081168", "DOID:0061103", "DOID:0080390", "DOID:0080036", "DOID:0060020", "DOID:0060916", "DOID:0080866", "DOID:0112006", "DOID:0061065", "DOID:0080426", "DOID:14699", "DOID:0081182", "DOID:0110826", "DOID:0081243", "DOID:0112088", "DOID:0081387", "DOID:0070372", "DOID:0111168", "DOID:0111633", "DOID:0080514", "DOID:0080632", "DOID:0090014", "DOID:2236", "DOID:0060296", "DOID:3755", "DOID:0110361", "DOID:0112201", "DOID:0081349", "DOID:0112269", "DOID:0080246", "DOID:0110130", "DOID:0060694", "DOID:0080128", "DOID:0090118", "DOID:0110138", "DOID:0060225", "DOID:0081047", "DOID:0080564", "DOID:0061098", "DOID:0111232", "DOID:0111855", "DOID:2935", "DOID:0112319", "DOID:0110217", "DOID:0112116", "DOID:0070013", "DOID:0110004", "DOID:0111983", "DOID:0070292", "DOID:0070539", "DOID:1935", "DOID:0110132", "DOID:0070095", "DOID:0061130", "DOID:0111583", "DOID:0070215", "DOID:0112192", "DOID:0051032", "DOID:0111333", "DOID:0061079", "DOID:0110395", "DOID:0110834", "DOID:0050602", "DOID:0080350", "DOID:0070388", "DOID:0110630", "DOID:0111262", "DOID:0111989", "DOID:0081159", "DOID:0061069", "DOID:5688", "DOID:0110030", "DOID:0081384", "DOID:0080869", "DOID:0110853", "DOID:0070123", "DOID:0112072", "DOID:0070408", "DOID:0070427", "DOID:0080312", "DOID:0060833", "DOID:0081438", "DOID:0070510", "DOID:0111239", "DOID:0110464", "DOID:0081148", "DOID:0090143", "DOID:0050528", "DOID:0060236", "DOID:0112186", "DOID:0060541", "DOID:0110243", "DOID:0070019", "DOID:0050470", "DOID:0111955", "DOID:0110821", "DOID:0070248", "DOID:0060832", "DOID:0111628", "DOID:0111257", "DOID:0112084", "DOID:0110540", "DOID:0050997", "DOID:0110723", "DOID:0080572", "DOID:0112111", "DOID:0111942", "DOID:0070300", "DOID:0080138", "DOID:0110669", "DOID:0060852", "DOID:0080689", "DOID:0110268", "DOID:0111650", "DOID:0061057", "DOID:0081151", "DOID:0080513", "DOID:0112181", "DOID:0080770", "DOID:0081269", "DOID:0111057", "DOID:0090048", "DOID:0070453", "DOID:0111124", "DOID:0080762", "DOID:0112164", "DOID:0111361", "DOID:0111493", "DOID:0112162", "DOID:0081331", "DOID:0080172", "DOID:0110493", "DOID:0110942", "DOID:0111455", "DOID:0051030", "DOID:0080791", "DOID:0060372", "DOID:0050755", "DOID:9268", "DOID:0050577", "DOID:0110375", "DOID:0080623", "DOID:0080962", "DOID:0111393", "DOID:0081183", "DOID:0060350", "DOID:0080887", "DOID:0111976", "DOID:0111122", "DOID:0060738", "DOID:0081061", "DOID:0110662", "DOID:0110189", "DOID:0111096", "DOID:0112268", "DOID:0070616", "DOID:0051031", "DOID:0080098", "DOID:0112361", "DOID:0070000", "DOID:0080518", "DOID:0110732", "DOID:0070182", "DOID:0060777", "DOID:0060294", "DOID:0050712", "DOID:0070479", "DOID:0070566", "DOID:0050559", "DOID:0110330", "DOID:2215", "DOID:0111585", "DOID:0060868", "DOID:0112153", "DOID:0111470", "DOID:0112342", "DOID:3981", "DOID:0112345", "DOID:0080737", "DOID:0111927", "DOID:0112325", "DOID:0110141", "DOID:0111458", "DOID:2717", "DOID:0111490", "DOID:0070012", "DOID:0060981", "DOID:0111390", "DOID:0080251", "DOID:0112290", "DOID:0111658", "DOID:0111255", "DOID:0070407", "DOID:0112069", "DOID:0110396", "DOID:0090032", "DOID:0111993", "DOID:0111117", "DOID:0051047", "DOID:0060369", "DOID:0111836", "DOID:0060974", "DOID:0070231", "DOID:0112175", "DOID:0112207", "DOID:0050779", "DOID:0111924", "DOID:0110868", "DOID:9280", "DOID:0060955", "DOID:0080392", "DOID:0080575", "DOID:0110118", "DOID:0070570", "DOID:0112248", "DOID:0050439", "DOID:0111059", "DOID:0060719", "DOID:0111345", "DOID:0112352", "DOID:0111123", "DOID:0050441", "DOID:0080141", "DOID:0112134", "DOID:0110682", "DOID:0080258", "DOID:0090144", "DOID:0081353", "DOID:0110064", "DOID:0111904", "DOID:0050474", "DOID:0080449", "DOID:0111276", "DOID:0070155", "DOID:0110912", "DOID:0060769", "DOID:0112004", "DOID:0060193", "DOID:0080292", "DOID:14671", "DOID:0060692", "DOID:0111555", "DOID:0111469", "DOID:0050999", "DOID:2217", "DOID:0090005", "DOID:0110680", "DOID:0081162", "DOID:0081439", "DOID:0090017", "DOID:0110814", "DOID:0080493", "DOID:0112377", "DOID:0112200", "DOID:0070336", "DOID:0080907", "DOID:0112246", "DOID:0110717", "DOID:0070589", "DOID:0080613", "DOID:0060543", "DOID:0112264", "DOID:0111651", "DOID:0112213", "DOID:0110798", "DOID:0070290", "DOID:0110714", "DOID:0081209", "DOID:0061094", "DOID:3322", "DOID:0061073", "DOID:0111678", "DOID:0061075", "DOID:0070563", "DOID:0080778", "DOID:0070542", "DOID:0110920", "DOID:0051039", "DOID:0110191", "DOID:0110161", "DOID:0061082", "DOID:0080566", "DOID:0080758", "DOID:0110407", "DOID:0111938", "DOID:0112326", "DOID:0090012", "DOID:0112196", "DOID:0060961", "DOID:0080803", "DOID:0110665", "DOID:0111484", "DOID:0110299", "DOID:0051026", "DOID:0060938", "DOID:0111126", "DOID:0070526", "DOID:0080910", "DOID:0080337", "DOID:0111559", "DOID:0110520", "DOID:0111849", "DOID:0060575", "DOID:0110090", "DOID:0060911", "DOID:0070267", "DOID:0110718", "DOID:0050684", "DOID:0111466", "DOID:0110637", "DOID:0090026", "DOID:0112076", "DOID:0111082", "DOID:0090038", "DOID:0111854", "DOID:0061026", "DOID:0080410", "DOID:0111478", "DOID:0080729", "DOID:0090067", "DOID:11721", "DOID:0050576", "DOID:0080624", "DOID:0081429", "DOID:0090024", "DOID:0070557", "DOID:0080733", "DOID:0070590", "DOID:0110203", "DOID:0110284", "DOID:0110517", "DOID:0112260", "DOID:0060956", "DOID:0060862", "DOID:0081419", "DOID:0070511", "DOID:0070573", "DOID:0081426", "DOID:0112104", "DOID:0110813", "DOID:0080295", "DOID:0080388", "DOID:0081016", "DOID:0110371", "DOID:0060943", "DOID:0111231", "DOID:0112278", "DOID:0081145", "DOID:13777", "DOID:0080542", "DOID:0081131", "DOID:0110736", "DOID:12714", "DOID:0111971", "DOID:0061092", "DOID:0060756", "DOID:0080978", "DOID:0112270", "DOID:0081152", "DOID:0110703", "DOID:0050886", "DOID:0070485", "DOID:0080309", "DOID:0112380", "DOID:0112176", "DOID:0110866", "DOID:0111913", "DOID:0060776", "DOID:0110091", "DOID:0110716", "DOID:0060990", "DOID:0111492", "DOID:0112114", "DOID:0111613", "DOID:0110357", "DOID:0081212", "DOID:0110185", "DOID:0060744", "DOID:0110629", "DOID:14501", "DOID:0080612", "DOID:0060710", "DOID:0070452", "DOID:0070278", "DOID:0090124", "DOID:0061005", "DOID:0070285", "DOID:0070288", "DOID:0110943", "DOID:0112085", "DOID:0110806", "DOID:0080925", "DOID:0111869", "DOID:0051004", "DOID:3534", "DOID:0060788", "DOID:0060999", "DOID:0070501", "DOID:0111091", "DOID:0111916", "DOID:0070399", "DOID:0050565", "DOID:0060962", "DOID:0112330", "DOID:0070555", "DOID:3389", "DOID:0081339", "DOID:0110489", "DOID:0080451", "DOID:0060707", "DOID:0060792", "DOID:0070257", "DOID:0110512", "DOID:0111334", "DOID:0050553", "DOID:0080722", "DOID:0081225", "DOID:0070281" ], "unlinked_id_list": [ "DOID:0110003", "DOID:0112317", "DOID:0070144", "DOID:0070141", "DOID:2368" ] }