{"orpha":519290,"name":"Rare inflammatory/autoimmune corneal disorder","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-519290/","orphanet_url":"https://www.orpha.net/en/disease/detail/519290","names":{"fr":{"name":"Maladie cornéenne auto-inflammatoire ou auto-immune"},"de":{"name":"Seltene entzündliche/autoimmune Krankheit der Kornea"},"es":{"name":"Trastorno raro corneal inflamatorio/autoinmune"},"it":{"name":"Patologia rara corneale infiammatoria/autoimmune"},"nl":{"name":"Zeldzame inflammatoire/auto-immune aandoening van cornea","synonyms":["Zeldzame inflammatoire/auto-immune aandoening van hoornvlies"]},"pt":{"name":"Doença da córnea inflamatória/autoimune rara"},"pl":{"name":"Rzadka choroba zapalna/autoimmunologiczna rogówki"},"cs":{"name":"Vzácná zánětlivá/autoimunitní porucha rohovky"},"uk":{"name":"Рідкісне запальне/аутоімунне захворювання рогівки"},"zh":{"name":"罕见的炎症/自身免疫性角膜疾病"},"tr":{"name":"Nadir inflamatuar/otoimmün kornea bozukluğu"}},"xrefs":[{"source":"UMLS","code":"C5681389","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":519288,"name":"Rare disorder with corneal involvement as a major feature","classifications":[189]}],"children":[{"orpha":2334,"name":"Autosomal dominant keratitis","type":"Disease"},{"orpha":1467,"name":"Cogan syndrome","type":"Disease"},{"orpha":314017,"name":"Idiopathic linear interstitial keratitis","type":"Disease"},{"orpha":519278,"name":"Infective keratitis","type":"Category"},{"orpha":477,"name":"KID syndrome","type":"Disease"},{"orpha":519406,"name":"Thygeson superficial punctate keratitis","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}