{"orpha":520814,"name":"Rare disorder of the visual organs","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-520814/","orphanet_url":"https://www.orpha.net/en/disease/detail/520814","names":{"fr":{"name":"Maladie rare des organes visuels"},"de":{"name":"Seltene Krankheit des Sehorgans"},"es":{"name":"Trastorno raro de los órganos visuales"},"it":{"name":"Malattia rara dell'organo della vista"},"nl":{"name":"Zeldzame aandoening van visuele organen"},"pt":{"name":"Doença rara dos orgãos visuais"},"pl":{"name":"Rzadka choroba narządu wzroku"},"cs":{"name":"Vzácná porucha zrakových orgánů"},"uk":{"name":"Рідкісне захворювання органів зору"},"zh":{"name":"罕见的视觉器官病变"},"tr":{"name":"Görme organlarında görülen nadir bozukluk"}},"xrefs":[{"source":"UMLS","code":"C5681453","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":98702,"name":"OBSOLETE: Connective tissue disease with eye involvement","status":"inactive"},{"type":"Referred to","orpha":98709,"name":"OBSOLETE: Ectodermal malformation syndrome associated with ocular features","status":"inactive"}],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":97966,"name":"Rare ophthalmic disorder","classifications":[189]}],"children":[{"orpha":140653,"name":"Neuro-ophthalmological disease","type":"Category"},{"orpha":519329,"name":"Rare disorder involving multiple structures of the eye","type":"Category"},{"orpha":519284,"name":"Rare disorder of the anterior segment of the eye","type":"Category"},{"orpha":519266,"name":"Rare disorder of the ocular adnexa","type":"Category"},{"orpha":519311,"name":"Rare disorder of the posterior segment of the eye","type":"Category"},{"orpha":519298,"name":"Rare scleral disorder","type":"Category"},{"orpha":519272,"name":"Structural developmental eye defect","type":"Category"},{"orpha":98715,"name":"Uveitis","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}