{"orpha":1894,"name":"Ectrodactyly-spina bifida-cardiopathy syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["Kasznica-Carlson-Coppedge syndrome"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Acrocardiofacial syndrome","url":"https://raremap.alftech.space/d/ORPHA-1894/","orphanet_url":"https://www.orpha.net/en/disease/detail/1894","names":{"fr":{"name":"Syndrome d'ectrodactylie-spina bifida-cardiopathie","synonyms":["Syndrome de Kasznica-Carlson-Coppedge"]},"de":{"name":"Ektrodaktylie-Spina bifida-Kardiopathie-Syndrom","synonyms":["Kasznica-Carlson-Coppedge-Syndrom"]},"es":{"name":"Síndrome de ectrodactilia-espina bífida-cardiopatía","synonyms":["Síndrome de Kasznica-Carlson-Coppedge"]},"it":{"name":"Ectrodattilia - spina bifida - cardiopatia","synonyms":["Sindrome di Kasznica-Carlson-Coppedge"]},"nl":{"name":"Ectrodactylie - spina bifida - cardiopathie-syndroom","synonyms":["Syndroom van Kasznica-Carlson-Coppedge"]},"pt":{"name":"Síndrome de ectrodactilia-espinha bífida-cardiopatia","synonyms":["Síndrome Kasznica-Carlson-Coppedge"]},"pl":{"name":"Ektrodaktylia - rozszczep kręgosłupa - kardiopatia","synonyms":["Zespół Kasznica, Carlsona i Coppedge'a"]},"cs":{"name":"Syndrom zahrnující ektrodaktylii, spina bifida a kardiomyopatii","synonyms":["Kasznicaův-Carlsonův-Coppedgeův syndrom","Kasznica-Carlson-Coppedgeův syndrom"]},"uk":{"name":"Синдром ектродактилії-spina bifida-кардіопатії","synonyms":["Синдром Кашніца-Карлсона-Коппеджа"]},"zh":{"name":"缺指畸形-脊柱裂-心脏病综合征","synonyms":["Kasznica-Carlson-Coppedge 综合征"]},"tr":{"name":"Ektrodaktili-spina bifida-kardiyopati sendromu","synonyms":["Kasznica-Carlson-Coppedge sendromu"]}},"xrefs":[{"source":"UMLS","code":"C2931393","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":2008,"name":"Acrocardiofacial syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}