{"orpha":93389,"name":"Brachydactyly type A5","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":[],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Brachydactyly type B","url":"https://raremap.alftech.space/d/ORPHA-93389/","orphanet_url":"https://www.orpha.net/en/disease/detail/93389","names":{"fr":{"name":"Brachydactylie type A5"},"de":{"name":"Brachydaktylie Typ A5"},"es":{"name":"Braquidactilia tipo A5"},"it":{"name":"Brachidattilia, tipo A5"},"nl":{"name":"Brachydactylie type A5"},"pt":{"name":"Braquidactilia tipo A5"},"pl":{"name":"Brachydaktylia typu A5"},"cs":{"name":"Brachydaktylie, typ A5"},"uk":{"name":"Брахідактилія, тип А5"},"zh":{"name":"短指（趾）畸形A5型"},"tr":{"name":"Brakidaktili tip A5"}},"xrefs":[{"source":"UMLS","code":"C1862138","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"982","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":93383,"name":"Brachydactyly type B"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}