{"orpha":98650,"name":"Craniofacial anomaly with cataract","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-98650/","orphanet_url":"https://www.orpha.net/en/disease/detail/98650","names":{"fr":{"name":"Anomalie craniofaciale avec cataracte"},"de":{"name":"Katarakt mit assoziierter kraniofazialer Anomalie"},"es":{"name":"Enfermedad craneofacial con una posible catarata"},"it":{"name":"Cataratta associata a anomalia craniofacciale"},"nl":{"name":"Craniofaciale anomalie met cataract"},"pt":{"name":"Cataratas associadas a anomalia craniofacial"},"pl":{"name":"Anomalia czaszkowo-twarzowa z zaćmą"},"cs":{"name":"Kraniofaciální anomálie s kataraktou"},"uk":{"name":"Черепно-лицьова аномалія з катарактою"},"zh":{"name":"颅面异常伴白内障"},"tr":{"name":"Katarakt ile seyreden kraniyofasiyal anomali"}},"xrefs":[{"source":"UMLS","code":"C5681662","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":98641,"name":"Syndromic cataract","classifications":[189]},{"orpha":522548,"name":"Syndromic genetic cataract","classifications":[156]}],"children":[{"orpha":87,"name":"Apert syndrome","type":"Malformation syndrome"},{"orpha":207,"name":"Crouzon syndrome","type":"Malformation syndrome"},{"orpha":2108,"name":"Hallermann-Streiff syndrome","type":"Malformation syndrome"},{"orpha":818,"name":"Smith-Lemli-Opitz syndrome","type":"Malformation syndrome"},{"orpha":912,"name":"Zellweger syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}