{"orpha":519329,"name":"Rare 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-519329/","orphanet_url":"https://www.orpha.net/en/disease/detail/519329","names":{"fr":{"name":"Maladie rare avec atteinte de multiples structures de l'oeil"},"de":{"name":"Seltene Krankheit mit Beteiligung multipler Strukturen des Auges"},"es":{"name":"Trastorno raro con afectación de múltiples estructuras del ojo"},"it":{"name":"Malattia rara coinvolgente strutture oculari multiple"},"nl":{"name":"Zeldzame stoornis met betrokkenheid van multipele oogstructuren"},"pt":{"name":"Doença rara com envolvimento de múltiplas estruturas oculares"},"pl":{"name":"Rzadka choroba obejmująca liczne struktury gałki ocznej"},"cs":{"name":"Vzácná porucha zahrnující více očních struktur"},"uk":{"name":"Рідкісне захворювання, що охоплює кілька структур ока"},"zh":{"name":"罕见累及眼部多个结构的病变"},"tr":{"name":"Gözün birden çok yapısını içeren nadir bozukluk"}},"xrefs":[{"source":"UMLS","code":"C5681352","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":520814,"name":"Rare disorder of the visual organs","classifications":[189]}],"children":[{"orpha":617449,"name":"Congenital aphakia-iris hypoplasia-microphthalmia-microcornea syndrome","type":"Disease"},{"orpha":141132,"name":"Craniofacial microsomia","type":"Malformation syndrome"},{"orpha":199323,"name":"Endophthalmitis","type":"Disease"},{"orpha":466682,"name":"Euthyroid Graves orbitopathy","type":"Disease"},{"orpha":314555,"name":"Facial dysmorphism-ocular anomalies-osteopenia-intellectual disability-dental anomalies syndrome","type":"Malformation syndrome"},{"orpha":636950,"name":"Glaucomatocyclitic crisis disease","type":"Disease"},{"orpha":728633,"name":"Idiopathic orbital inflammation syndrome","type":"Disease"},{"orpha":449563,"name":"IgG4-related ophthalmic disease","type":"Clinical subtype"},{"orpha":647815,"name":"Keratitis fugax hereditaria","type":"Disease"},{"orpha":98706,"name":"Oculocutaneous or ocular albinism","type":"Category"},{"orpha":523000,"name":"Pediatric-onset glaucoma","type":"Category"},{"orpha":1214,"name":"Progressive hemifacial atrophy","type":"Disease"},{"orpha":90080,"name":"Scarring in glaucoma filtration surgical procedures","type":"Particular clinical situation in a disease or syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}