{"orpha":284804,"name":"Ocular albinism","type":"Clinical group","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-284804/","orphanet_url":"https://www.orpha.net/en/disease/detail/284804","names":{"fr":{"name":"Albinisme oculaire"},"de":{"name":"Albinismus, okulärer"},"es":{"name":"Albinismo ocular"},"it":{"name":"Albinismo oculare"},"nl":{"name":"Oculair albinisme"},"pt":{"name":"Albinismo ocular"},"pl":{"name":"Albinizm oczny"},"cs":{"name":"Oční albinismus","synonyms":["Okulární albinismus"]},"uk":{"name":"Очний альбінізм"},"zh":{"name":"眼白化病"},"tr":{"name":"Oküler albinizm"}},"xrefs":[{"source":"ICD-11","code":"9E1Y","qualifier":"NTBT","icd_relation":"index","validated":true,"icd11_uri":"1147926040"},{"source":"MONDO","code":"0017304","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"17304","qualifier":"E","icd_relation":null,"validated":true},{"source":"MeSH","code":"D016117","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0078917","qualifier":"E","icd_relation":null,"validated":true},{"source":"MedDRA","code":"10065276","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":352728,"name":"Disorder of melanin metabolism","classifications":[150,156]},{"orpha":98706,"name":"Oculocutaneous or ocular albinism","classifications":[156,189]}],"children":[{"orpha":1000,"name":"Ocular albinism with late-onset sensorineural deafness","type":"Disease"},{"orpha":54,"name":"X-linked recessive ocular albinism","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}