{"orpha":98623,"name":"Syndromic keratoconus","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-98623/","orphanet_url":"https://www.orpha.net/en/disease/detail/98623","names":{"fr":{"name":"Syndromes comprenant un kératocône"},"de":{"name":"Keratokonus, syndromaler"},"es":{"name":"Queratocono sindrómico"},"it":{"name":"Cheratocono sindromico"},"nl":{"name":"Syndromale keratoconus"},"pt":{"name":"Queratocone sindromático"},"pl":{"name":"Syndromiczny stożek rogówki"},"cs":{"name":"Syndromy s keratokonem"},"uk":{"name":"Синдромальний кератоконус"},"zh":{"name":"综合征性圆锥角膜"},"tr":{"name":"Sendromik keratokonus"}},"xrefs":[{"source":"UMLS","code":"C5681674","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":156071,"name":"OBSOLETE: Keratoconus","status":"inactive"}],"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":870,"name":"Down syndrome","type":"Malformation syndrome"},{"orpha":293936,"name":"EDICT syndrome","type":"Disease"},{"orpha":2067,"name":"GAPO syndrome","type":"Malformation syndrome"},{"orpha":558,"name":"Marfan syndrome","type":"Disease"},{"orpha":70476,"name":"Vernal keratoconjunctivitis","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}