{"orpha":90649,"name":"Orofaciodigital syndrome type 7","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["OFD7","Oral-facial-digital syndrome type 7","Whelan syndrome"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Orofaciodigital syndrome type 1","url":"https://raremap.alftech.space/d/ORPHA-90649/","orphanet_url":"https://www.orpha.net/en/disease/detail/90649","names":{"fr":{"name":"Syndrome oro-facio-digital de type 7","synonyms":["OFD7","Syndrome de Whelan","Syndrome orofaciodigital de type 7"]},"de":{"name":"Oro-fazio-digitales Syndrom Typ 7","synonyms":["OFD7","Whelan-Syndrom"]},"es":{"name":"Síndrome orofaciodigital tipo 7","synonyms":["OFD7","Síndrome de Whelan"]},"it":{"name":"Sindrome orofaciodigitale, tipo 7","synonyms":["OFD7","Sindrome di Whelan","Sindrome oro-facio-digitale, tipo 7"]},"nl":{"name":"Orofaciodigitaal syndroom type 7","synonyms":["OFD7","Oraal-faciaal-digitaal syndroom type 7","Syndroom van Whelan"]},"pt":{"name":"Síndrome orofaciodigital tipo 7"},"pl":{"name":"Zespół ustno-twarzowo-palcowy typu 7","synonyms":["Zespół ustno-twarzowo-palcowy typu 7","OFD7","Zespół Whelana"]},"cs":{"name":"Orofaciodigitální syndrom, typ 7","synonyms":["OFD7","Orální-faciální-digitální syndrom, typ 7","Whelanův syndrom"]},"uk":{"name":"Орофаціодигітальний синдром, тип 7","synonyms":["OFD7","Орально-лицево-пальцевий синдром, тип 7","Синдром Вілана"]},"zh":{"name":"口面指综合征7型","synonyms":["口-面-指综合征7型"]},"tr":{"name":"Orofasiyodijital sendromu tip 7","synonyms":["OFD7","Whelan sendromu","Oral-fasiyal-dijital sendromu tip 7"]}},"xrefs":[{"source":"OMIM","code":"608518","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0796100","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":2750,"name":"Orofaciodigital syndrome type 1"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}