{"orpha":1219,"name":"Aurocephalosyndactyly","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["Auralcephalosyndactyly","Kurczynski-Casperson syndrome"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Saethre-Chotzen syndrome","url":"https://raremap.alftech.space/d/ORPHA-1219/","orphanet_url":"https://www.orpha.net/en/disease/detail/1219","names":{"fr":{"name":"Auro-céphalo-syndactylie","synonyms":["Syndrome de Kurczynski-Casperson"]},"de":{"name":"Auro-Zephalo-Syndaktylie","synonyms":["Kurczynski-Casperson-Syndrom"]},"es":{"name":"Aurocefalosindactilia","synonyms":["Síndrome de Kurczynski-Casperson"]},"it":{"name":"Aurocefalosindattilia","synonyms":["Sindrome di Kurczynski-Casperson"]},"nl":{"name":"Aurocefalosyndactylie","synonyms":["Kurczynski-Caspersonsyndroom","Auralcefalosyndactylie"]},"pt":{"name":"Aurocefalossindactilia","synonyms":["Auralcefalossindactilia","Síndrome Kurczynski-Casperson"]},"pl":{"name":"Aurocefalosyndaktylia","synonyms":["Aurocefalosyndaktylia","Zespół Kurczynskiego i Caspersona"]},"cs":{"name":"Aurocefalosyndaktylie","synonyms":["Kurczynského-Caspersonové syndrom","Kurczynski-Caspersonové syndrom"]},"uk":{"name":"Ауроцефалосиндактилія","synonyms":["Ауралцефалосиндактилія","Синдром Курчинського-Касперсона"]},"zh":{"name":"尖头并趾畸形","synonyms":["Kurczynski-Casperson综合征"]},"tr":{"name":"Aurosefalosindaktili","synonyms":["Oralsefalosindaktili","Kurczynski-Casperson sendromu"]}},"xrefs":[{"source":"OMIM","code":"109050","qualifier":"E","icd_relation":null,"validated":true},{"source":"MeSH","code":"D000168","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C1862380","qualifier":"E","icd_relation":null,"validated":true},{"source":"MedDRA","code":"10000590","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":794,"name":"Saethre-Chotzen syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}