{"orpha":522578,"name":"Rare genetic disorder involving multiple structures of the eye","type":"Category","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-522578/","orphanet_url":"https://www.orpha.net/en/disease/detail/522578","names":{"fr":{"name":"Maladie génétique rare avec atteinte de multiples structures de l'oeil"},"de":{"name":"Seltene genetische Krankheit mit Beteiligung multipler Strukturen des Auges"},"es":{"name":"Trastorno genético raro con afectación de múltiples estructuras del ojo"},"it":{"name":"Malattia genetica rara coinvolgente strutture multiple dell'occhio"},"nl":{"name":"Zeldzame genetische aandoening met betrokkenheid van multipele oogstructuren"},"pt":{"name":"Doença genética rara com envolvimento de múltiplas estruturas do olho"},"pl":{"name":"Rzadka choroba obejmująca liczne struktury oka uwarunkowana genetycznie"},"cs":{"name":"Vzácná genetická porucha postihující více očních struktur"},"uk":{"name":"Рідкісне генетично обумовлене захворювання, що охоплює кілька структур ока"},"zh":{"name":"罕见涉及眼睛多个结构的遗传性疾病"},"tr":{"name":"Gözün birden çok yapısını içeren nadir genetik bozukluk"}},"xrefs":[{"source":"UMLS","code":"C5681403","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":522504,"name":"Rare genetic disorder of the visual organs","classifications":[156]}],"children":[{"orpha":617449,"name":"Congenital aphakia-iris hypoplasia-microphthalmia-microcornea syndrome","type":"Disease"},{"orpha":314555,"name":"Facial dysmorphism-ocular anomalies-osteopenia-intellectual disability-dental anomalies syndrome","type":"Malformation syndrome"},{"orpha":98706,"name":"Oculocutaneous or ocular albinism","type":"Category"},{"orpha":359,"name":"Pediatric-onset glaucoma of genetic origin","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}