{"orpha":93395,"name":"Ballard syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["Brachydactyly, combined B and E types","Pitt-Williams brachydactyly"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Brachydactyly type E","url":"https://raremap.alftech.space/d/ORPHA-93395/","orphanet_url":"https://www.orpha.net/en/disease/detail/93395","names":{"fr":{"name":"Syndrome de Ballard","synonyms":["Brachydactylie de Pitt-Williams","Brachydactylie types B et E combinées"]},"de":{"name":"Ballard-Syndrom","synonyms":["Brachydaktylie Typ B und E kombiniert","Pitt-Williams-Brachydaktylie"]},"es":{"name":"Síndrome de Ballard","synonyms":["Braquidactilia tipo B y C combinadas"]},"it":{"name":"Sindrome di Ballard","synonyms":["Brachidattilia di Pitt-Williams","Brachidattilia, tipi B ed E combinati"]},"nl":{"name":"Syndroom van Ballard","synonyms":["Brachydactylie type B en E gecombineerd","Brachydactylie van Pitt-Williams"]},"pt":{"name":"Síndrome de Ballard"},"pl":{"name":"Zespół Ballarda","synonyms":["Brachydaktylia mieszane typy B i E","Brachydaktylia Pitta i Williamsa"]},"cs":{"name":"Syndrom Ballardových","synonyms":["Kombinovaná brachydaktylie, typy B a E","Pittové-Williamsova brachydaktylie","Pitt-Williamsova brachydaktylie"]},"uk":{"name":"Синдром Балларда","synonyms":["Брахідактилія, комбіновані типи B і E","Брахідактилія Пітта-Вільямса"]},"zh":{"name":"Ballard 综合征","synonyms":["短指（趾）畸形，B和D融合型"]},"tr":{"name":"Ballard sendromu","synonyms":["Pitt-Williams brakidaktili","Brakidaktili, kombine B ve E tipleri"]}},"xrefs":[{"source":"OMIM","code":"112440","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C1862163","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":93387,"name":"Brachydactyly type E"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}