{"orpha":98635,"name":"Corneodysgenesis","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Corneogoniodysgenesis"],"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-98635/","orphanet_url":"https://www.orpha.net/en/disease/detail/98635","names":{"fr":{"name":"Cornéo-dysgénésie","synonyms":["Cornéo-gonio-dysgénésie"]},"de":{"name":"Corneogoniodysgenesie"},"es":{"name":"Corneogoniodisgenesia"},"it":{"name":"Corneogoniodisgenesia"},"nl":{"name":"Corneogoniodysgenesie"},"pt":{"name":"Corneogoniodisgenesia"},"pl":{"name":"Korneogoniodysgeneza","synonyms":["Corneogoniodysgenesis"]},"cs":{"name":"Dysgeneze rohovky a komorového úhlu","synonyms":["Corneogoniodysgenesis"]},"uk":{"name":"Корнеодисгенез","synonyms":["Корнеогоніодисгенез"]},"zh":{"name":"角膜发育不全","synonyms":["角膜前房角发育不全"]},"tr":{"name":"Korneodisgenezi","synonyms":["Korneogoniodisgenezi"]}},"xrefs":[{"source":"UMLS","code":"C5680334","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":98553,"name":"Developmental defect of the eye","classifications":[147]},{"orpha":183557,"name":"Genetic developmental defect of the eye","classifications":[156]},{"orpha":519282,"name":"Rare corneal disorder","classifications":[189]},{"orpha":522556,"name":"Rare genetic corneal disorder","classifications":[156]}],"children":[{"orpha":91489,"name":"Isolated congenital megalocornea","type":"Morphological anomaly"},{"orpha":91490,"name":"Isolated congenital sclerocornea","type":"Morphological anomaly"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}