{"orpha":1767,"name":"Familial progressive vestibulocochlear dysfunction","type":"Disease","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 Autosomal dominant non-syndromic sensorineural deafness type DFNA","url":"https://raremap.alftech.space/d/ORPHA-1767/","orphanet_url":"https://www.orpha.net/en/disease/detail/1767","names":{"fr":{"name":"Dysfonctionnement vestibulo-cochléaire progressif familial"},"de":{"name":"Vestibulocochleäre Dysfunktion, progressive, familiärer Typ"},"es":{"name":"Disfunción vestibulococlear progresiva familiar"},"it":{"name":"Disfunzione vestibolo-cocleare progressiva familiare"},"nl":{"name":"Familiale progressieve vestibulocochleaire disfunctie"},"pt":{"name":"Disfunção vestibulo-coclear progressiva familiar"},"pl":{"name":"Rodzinna postępująca dysfunkcja przedsionkowo-ślimakowa"},"cs":{"name":"Familiární progresivní vestibulokochleární dysfunkce"},"uk":{"name":"Сімейна прогресуюча вестибулокохлеарна дисфункція"},"zh":{"name":"家族性进行性前庭耳蜗功能障碍"},"tr":{"name":"Ailesel ilerleyici vestibülokoklear disfonksiyon"}},"xrefs":[{"source":"OMIM","code":"193005","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":90635,"name":"Autosomal dominant non-syndromic genetic deafness"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}