{"orpha":522556,"name":"Rare genetic 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-522556/","orphanet_url":"https://www.orpha.net/en/disease/detail/522556","names":{"fr":{"name":"Maladie génétique cornéenne rare"},"de":{"name":"Seltene genetische Erkrankung der Kornea"},"es":{"name":"Trastorno corneal genético raro"},"it":{"name":"Malattia genetica rara corneale"},"nl":{"name":"Zeldzame genetische aandoening van cornea","synonyms":["Zeldzame genetische aandoening van hoornvlies"]},"pt":{"name":"Doença da córnea genética rara"},"pl":{"name":"Rzadka choroba rogówki uwarunkowana genetycznie"},"cs":{"name":"Vzácná genetická porucha rohovky"},"uk":{"name":"Рідкісне генетично обумовлене захворювання рогівки"},"zh":{"name":"罕见遗传性角膜病"},"tr":{"name":"Nadir genetik kornea bozukluğu"}},"xrefs":[{"source":"UMLS","code":"C5681415","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":522538,"name":"Rare genetic disorder of the anterior segment of the eye","classifications":[156]}],"children":[{"orpha":53691,"name":"Congenital cornea plana","type":"Morphological anomaly"},{"orpha":98635,"name":"Corneodysgenesis","type":"Category"},{"orpha":522558,"name":"Rare genetic disorder with corneal involvement as a major feature","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}