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"resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012094", "name": "prostate cancer, hereditary, type 4", "description": "" }, { "id": "MONDO:0012094", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012094", "name": "prostate cancer, susceptibility to, 4", "description": "" }, { "id": "MONDO:0012094", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012094", "name": "HPC4", "description": "" }, { "id": "MONDO:0012094", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012094", "name": "prostate cancer, hereditary, on chromosome 7", "description": "" }, { "id": "MONDO:0012244", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012244", "name": "prostate cancer, hereditary, 5", "description": "" }, { "id": "MONDO:0012244", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012244", "name": "prostate cancer, hereditary, 5", "description": "" }, { "id": "MONDO:0012244", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012244", "name": "prostate cancer, hereditary, type 5", "description": "" }, { "id": "MONDO:0012244", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012244", "name": "HPC5", "description": "" }, { "id": "MONDO:0012300", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012300", "name": "prostate cancer, hereditary, 6", "description": "" }, { "id": "MONDO:0012300", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012300", "name": "prostate cancer, hereditary, 6", "description": "" }, { "id": "MONDO:0012300", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012300", "name": "prostate cancer, hereditary, type 6", "description": "" }, { "id": "MONDO:0012300", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012300", "name": "HPC6", "description": "" }, { "id": "MONDO:0012300", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012300", "name": "prostate cancer, susceptibility to", "description": "" }, { "id": "MONDO:0012470", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012470", "name": "prostate cancer, hereditary, 7", "description": "" }, { "id": "MONDO:0012470", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012470", "name": "HPC7", "description": "" }, { "id": "MONDO:0012470", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012470", "name": "prostate cancer, hereditary, 7", "description": "" }, { "id": "MONDO:0012470", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012470", "name": "prostate cancer aggressiveness", "description": "" }, { "id": "MONDO:0012597", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012597", "name": "prostate cancer, hereditary, 9", "description": "" }, { "id": "MONDO:0012597", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012597", "name": "prostate cancer, hereditary, 9", "description": "" }, { "id": "MONDO:0012597", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012597", "name": "prostate cancer, hereditary, type 9", "description": "" }, { "id": "MONDO:0012597", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012597", "name": "HPC9", "description": "" }, { "id": "MONDO:0012620", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012620", "name": "prostate cancer, hereditary, 10", "description": "" }, { "id": "MONDO:0012620", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012620", "name": "HPC10", "description": "" }, { "id": "MONDO:0012620", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012620", "name": "prostate cancer, hereditary, 10", "description": "" }, { "id": "MONDO:0012741", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012741", "name": "prostate cancer, hereditary, 12", "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the EHBP1 gene." }, { "id": "MONDO:0012741", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012741", "name": "EHBP1 familial prostate cancer", "description": "" }, { "id": "MONDO:0012741", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012741", "name": "familial prostate cancer caused by mutation in EHBP1", "description": "" }, { "id": "MONDO:0012741", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012741", "name": "prostate cancer, hereditary, 12", "description": "" }, { "id": "MONDO:0012741", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012741", "name": "prostate cancer, hereditary, type 12", "description": "" }, { "id": "MONDO:0012741", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012741", "name": "HPC12", "description": "" }, { "id": "MONDO:0012758", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012758", "name": "prostate cancer, hereditary, 13", "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the MSMB gene." }, { "id": "MONDO:0012758", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012758", "name": "MSMB familial prostate cancer", "description": "" }, { "id": "MONDO:0012758", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012758", "name": "familial prostate cancer caused by mutation in MSMB", "description": "" }, { "id": "MONDO:0012758", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012758", "name": "prostate cancer, hereditary, 13", "description": "" }, { "id": "MONDO:0012758", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012758", "name": "prostate cancer, hereditary, type 13", "description": "" }, { "id": "MONDO:0012758", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012758", "name": "HPC13", "description": "" }, { "id": "MONDO:0012768", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012768", "name": "prostate cancer, hereditary, 11", "description": "" }, { "id": "MONDO:0012768", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012768", "name": "HPC11", "description": "" }, { "id": "MONDO:0012768", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012768", "name": "prostate cancer, hereditary, 11", "description": "" }, { "id": "MONDO:0012769", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012769", "name": "prostate cancer, hereditary, 14", "description": "" }, { "id": "MONDO:0012769", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012769", "name": "HPC14", "description": "" }, { "id": "MONDO:0012769", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012769", "name": "prostate cancer, hereditary, 14", "description": "" }, { "id": "MONDO:0012770", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012770", "name": "prostate cancer, hereditary, 15", "description": "" }, { "id": "MONDO:0012770", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012770", "name": "HPC15", "description": "" }, { "id": "MONDO:0012770", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012770", "name": "prostate cancer, hereditary, 15", "description": "" }, { "id": "MONDO:0700275", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0700275", "name": "prostate cancer, hereditary", "description": "An instance of prostate cancer that is caused by an inherited genomic modification in an individual. Familial prostate cancer (FPC) is a malignant tumor of the prostate with an early onset. FPC is either asymptomatic or causes mictionary symptoms, erectile dysfunction, bone pain, venous compression and infectious or inflammatory syndrome (for the metastatic forms). It is also characterized by familial antecedents." }, { "id": "MIM:601518", "resource": "MIM", "url": "https://www.omim.org/entry/601518", "name": "Prostate cancer, hereditary, 1", "description": "Prostate cancer, hereditary, 1" }, { "id": "MIM:610997", "resource": "MIM", "url": "https://www.omim.org/entry/610997", "name": "Prostate cancer, hereditary, 9", "description": "Prostate cancer, hereditary, 9" }, { "id": "MIM:611868", "resource": "MIM", "url": "https://www.omim.org/entry/611868", "name": "Prostate cancer, hereditary, 12", "description": "Prostate cancer, hereditary, 12" }, { "id": "MIM:611928", "resource": "MIM", "url": "https://www.omim.org/entry/611928", "name": "Prostate cancer, hereditary, 13", "description": "Prostate cancer, hereditary, 13" }, { "id": "MIM:611955", "resource": "MIM", "url": "https://www.omim.org/entry/611955", "name": "Prostate cancer, hereditary, 11", "description": "Prostate cancer, hereditary, 11" }, { "id": "MIM:176807", "resource": "MIM", "url": "https://www.omim.org/entry/176807", "name": "Prostate cancer", "description": "Prostate cancer" } ], "unlinked_id_list": [], "evidence": [ { "id": "10283", "database": "AGR", "url": "https://www.alliancegenome.org/disease/DOID:10283" } ] }, { "disease_id": "DOID:0080470", "recommended_name": { "id": "DOID:0080470", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0080470", "name": "developmental and epileptic encephalopathy 36", "description": "A developmental and epileptic encephalopathy characterized by X-linked dominant inheritance of infantile onset of seizures, delayed psychomotor development and in some patients dysmorphic features that has_material_basis_in heterozygous mutation in the ALG13 gene on chromosome Xq23." }, "synonyms": [ { "id": "DOID:0080470", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0080470", "name": "congenital disorder of glycosylation, type Is", "description": "" }, { "id": "DOID:0080470", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0080470", "name": "early infantile epileptic encephalopathy 36", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "developmental and epileptic encephalopathy, 36", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "ALG13-CDG", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "CDG syndrome type Is", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "CDG-Is", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "CDG1S", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", 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"MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "CDG Is", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "congenital disorder of glycosylation, type Is", "description": "" }, { "id": "MIM:300884", "resource": "MIM", "url": "https://www.omim.org/entry/300884", "name": "Developmental and epileptic encephalopathy 36", "description": "Developmental and epileptic encephalopathy 36" } ], "unlinked_id_list": [], "evidence": [ { "id": "0010472", "database": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472" }, { "id": "300884", "database": "MIM", "url": "https://www.omim.org/entry/300884" }, { "id": "79868", "database": "GlyCosmos", "url": "https://glycosmos.org/glycogenes/show/79868#disease" }, { "id": "0080470", "database": "AGR", "url": "https://www.alliancegenome.org/disease/DOID:0080470" } ] }, { "disease_id": "DOID:0080470", "recommended_name": { "id": "DOID:0080470", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0080470", "name": "developmental and epileptic encephalopathy 36", "description": "A developmental and epileptic encephalopathy characterized by X-linked dominant inheritance of infantile onset of seizures, delayed psychomotor development and in some patients dysmorphic features that has_material_basis_in heterozygous mutation in the ALG13 gene on chromosome Xq23." }, "synonyms": [ { "id": "DOID:0080470", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0080470", "name": "congenital disorder of glycosylation, type Is", "description": "" }, { "id": "DOID:0080470", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0080470", "name": "early infantile epileptic encephalopathy 36", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "developmental and epileptic encephalopathy, 36", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "ALG13-CDG", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "CDG syndrome type Is", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "CDG-Is", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "CDG1S", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "DEE36", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": 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"https://monarchinitiative.org/disease/MONDO:0010472", "name": "congenital disorder of glycosylation, type Is", "description": "" }, { "id": "MIM:300884", "resource": "MIM", "url": "https://www.omim.org/entry/300884", "name": "Developmental and epileptic encephalopathy 36", "description": "Developmental and epileptic encephalopathy 36" } ], "unlinked_id_list": [], "evidence": [ { "id": "0010472", "database": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472" }, { "id": "300884", "database": "MIM", "url": "https://www.omim.org/entry/300884" }, { "id": "79868", "database": "GlyCosmos", "url": "https://glycosmos.org/glycogenes/show/79868#disease" }, { "id": "0080470", "database": "AGR", "url": "https://www.alliancegenome.org/disease/DOID:0080470" } ] }, { "disease_id": "DOID:0080470", "recommended_name": { "id": "DOID:0080470", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0080470", "name": "developmental and epileptic encephalopathy 36", "description": "A developmental and epileptic encephalopathy characterized by X-linked dominant inheritance of infantile onset of seizures, delayed psychomotor development and in some patients dysmorphic features that has_material_basis_in heterozygous mutation in the ALG13 gene on chromosome Xq23." }, "synonyms": [ { "id": "DOID:0080470", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0080470", "name": "congenital disorder of glycosylation, type Is", "description": "" }, { "id": "DOID:0080470", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0080470", "name": "early infantile epileptic encephalopathy 36", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "developmental and epileptic encephalopathy, 36", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "ALG13-CDG", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "CDG syndrome type Is", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "CDG-Is", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "CDG1S", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "DEE36", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "EIEE36", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "congenital disorder of glycosylation type 1s", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "congenital disorder of glycosylation type Is", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "developmental and epileptic encephalopathy 36", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "epileptic encephalopathy, early infantile, 36", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "CDG Is", "description": "" }, { "id": "MONDO:0010472", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010472", "name": "congenital disorder of glycosylation, type Is", "description": "" }, { "id": "MIM:300884", "resource": "MIM", "url": "https://www.omim.org/entry/300884", "name": "Developmental and epileptic 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"N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G89141ZC", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89143RS", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89144TN", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89153EV", "type": "N-linked", "subtype": "High mannose" }, { "glytoucan_ac": "G89159EV", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89168IV", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89168LM", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89170GQ", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G89177YT", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89181JW", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89186VO", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89194QY", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89202HP", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89205LT", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89206JP", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89206MS", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89222FP", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G89233TP", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89241QS", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G89253ZV", "type": "N-linked", "subtype": "High mannose" }, { "glytoucan_ac": "G89255EP", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89261EQ", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89264TR", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89264ZR", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G89279QH", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G89282EC", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G89283LM", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G89285HT", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89285QP", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G89290XU", "type": "N-linked", "subtype": "Paucimannose" }, { "glytoucan_ac": "G89295QX", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G89307HV", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89317SY", "type": "N-linked", "subtype": "Other" }, { "glytoucan_ac": "G89319AW", "type": "N-linked", "subtype": "Hybrid" }, { "glytoucan_ac": "G89323TE", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89325VN", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89333YV", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G89343RJ", "type": "N-linked", "subtype": "Hybrid" }, { "glytoucan_ac": "G89345GA", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89353OJ", "type": "N-linked", "subtype": "High mannose" }, { "glytoucan_ac": "G89362MU", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89364NG", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G89365KN", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89366NN", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89370FG", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G89375LQ", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89378FW", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89378UY", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89395YL", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G89398CR", "type": "N-linked", "subtype": "Hybrid" }, { "glytoucan_ac": "G89404LS", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G89414BZ", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G89417VQ", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G89425XZ", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89446MD", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89451OH", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89455DQ", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89463XE", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G89466MK", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89494ET", "type": "N-linked", "subtype": "High mannose" }, { "glytoucan_ac": "G89496HB", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89498BT", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89522MV", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89532GI", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89532UK", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G89547PG", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G89561DW", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G89584RR", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89587BP", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89602QT", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89602RY", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89615SV", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G89615VR", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89619KY", "type": "N-linked", "subtype": "High mannose" }, { "glytoucan_ac": "G89620UQ", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89623PK", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89624LF", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89632SS", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89637WE", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G89641ZV", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89654YT", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89658RO", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G89663TB", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G89664KV", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89669IB", "type": "N-linked", "subtype": "Hybrid" }, { "glytoucan_ac": "G89669MO", "type": "N-linked", "subtype": "Other" }, { "glytoucan_ac": "G89685ZW", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89701XL", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89714WN", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G89720ZS", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G89722NR", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G89722OZ", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G89729ZG", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G89736EE", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89738LW", "type": "N-linked", "subtype": "High mannose" }, { "glytoucan_ac": "G89738UT", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G89749WS", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89756YF", "type": "N-linked", "subtype": "Hybrid" }, { "glytoucan_ac": "G89794YL", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89799OK", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89803GR", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89808TP", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G89814XX", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89826GE", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89835HT", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89838LO", "type": "N-linked", "subtype": "Other" }, { "glytoucan_ac": "G89839UI", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89841WS", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89845CN", "type": "N-linked", "subtype": "Bisected" }, { "glytoucan_ac": "G89846HT", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G89857VC", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G89858HW", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G89864BN", "type": "N-linked", "subtype": "High mannose" }, { "glytoucan_ac": "G89865CB", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89868JS", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G89870WK", "type": "N-linked", "subtype": "High mannose" }, { "glytoucan_ac": "G89877QI", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89878ZY", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89891DR", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G89895CK", "type": "N-linked", "subtype": "Hybrid" }, { "glytoucan_ac": "G89905SH", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89908RT", "type": "N-linked", "subtype": "Other" }, { "glytoucan_ac": "G89911NQ", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G89920YU", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G89923TD", "type": "N-linked", "subtype": "High mannose" }, { "glytoucan_ac": "G89932GS", "type": "N-linked", "subtype": "Hybrid" }, { "glytoucan_ac": "G89941FZ", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G89948KF", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89949WN", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89950AZ", "type": "N-linked", "subtype": "High mannose" }, { "glytoucan_ac": "G89950GK", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89955WO", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G89970IY", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G89978EP", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G89982KK", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G89982OT", "type": "N-linked", "subtype": "Bisected" }, { "glytoucan_ac": "G89993FE", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G89999GG", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G90000WS", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G90017UO", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G90023TN", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G90028HY", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G90033AN", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G90052RE", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G90065BD", "type": "N-linked", "subtype": "Hybrid" }, { "glytoucan_ac": "G90081OR", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G90091ZQ", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G90099GV", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G90107JW", "type": "N-linked", "subtype": "Other" }, { "glytoucan_ac": "G90111MD", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G90119WQ", "type": "N-linked", "subtype": "Hybrid" }, { "glytoucan_ac": "G90125QJ", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G90130AG", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G90133BE", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G90163GT", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G90172SA", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G90175OT", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G90192JZ", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G90192ZU", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G90193GR", "type": "N-linked", "subtype": "Hybrid" }, { "glytoucan_ac": "G90197OV", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G90202LF", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G90204HK", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G90206GU", "type": "N-linked", "subtype": "High mannose" }, { "glytoucan_ac": "G90208CJ", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G90223GH", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G90223PU", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G90238QO", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G90241LW", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G90244AZ", "type": "N-linked", "subtype": "Other" }, { "glytoucan_ac": "G90249RX", "type": "N-linked", "subtype": "Other" }, { "glytoucan_ac": "G90260XX", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G90263JN", "type": "N-linked", "subtype": "High mannose" }, { "glytoucan_ac": "G90267TS", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G90290ME", "type": "N-linked", "subtype": "Arm-fucosylated" }, { "glytoucan_ac": "G90304FZ", "type": "N-linked", "subtype": "Tetraantennary" }, { 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"type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G99647DZ", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G99651QK", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G99669MJ", "type": "N-linked", "subtype": "High mannose" }, { "glytoucan_ac": "G99675NK", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G99676LZ", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G99683ND", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G99684PD", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G99689NZ", "type": "N-linked", "subtype": "Other" }, { "glytoucan_ac": "G99691HE", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G99707FV", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G99714FV", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G99729IU", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G99732NX", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G99770NO", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G99777VA", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G99783ON", "type": "N-linked", "subtype": "Other" }, { "glytoucan_ac": "G99796NW", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G99797PH", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G99801SM", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G99801VV", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G99808VS", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G99829YW", "type": "N-linked", "subtype": "Bisected" }, { "glytoucan_ac": "G99831DA", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G99844CS", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G99846PG", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G99848OC", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G99853JR", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G99858XP", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G99866WK", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G99873PN", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G99876AH", "type": "N-linked", "subtype": "High mannose" }, { "glytoucan_ac": "G99883ZA", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G99891PR", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G99896CG", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G99897FQ", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G99902FH", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G99927HL", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G99935CU", "type": "N-linked", "subtype": "Hybrid" }, { "glytoucan_ac": "G99943EE", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G99950SF", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G99952ON", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G99954GW", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G99954ZJ", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G99956MJ", "type": "N-linked", "subtype": "Tetraantennary" }, { "glytoucan_ac": "G99969SS", "type": "N-linked", "subtype": "Hybrid" }, { "glytoucan_ac": "G99980WG", "type": "N-linked", "subtype": "Hybrid" }, { "glytoucan_ac": "G99981ST", "type": "N-linked", "subtype": "Triantennary" }, { "glytoucan_ac": "G99981ZK", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G99992LL", "type": "N-linked", "subtype": "Complex" }, { "glytoucan_ac": "G99996FL", "type": "N-linked", "subtype": "Core-fucosylated" }, { "glytoucan_ac": "G99997WS", "type": "N-linked", "subtype": "Complex" } ] } }