{"orpha":3215,"name":"OBSOLETE: Deafness-white hair-contractures-papillomas syndrome","type":"Disease","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Davenport-Donlan syndrome"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Syndromic genetic deafness","url":"https://raremap.alftech.space/d/ORPHA-3215/","orphanet_url":"https://www.orpha.net/en/disease/detail/3215","names":{"fr":{"name":"OBSOLETE : Syndrome de surdité-cheveux dépigmentés-contractures","synonyms":["OBSOLETE : Syndrome de Davenport-Donlan"]},"de":{"name":"OBSOLET: Taubheit-depigmentierte Haare-Kontrakturen-Papillom-Syndrom","synonyms":["OBSOLET: Davenport-Donlan-Syndrom"]},"es":{"name":"OBSOLETO: Síndrome de sordera-cabello blanco-contracturas-papilomas","synonyms":["OBSOLETO: Síndrome de Davenport-Donlan"]},"it":{"name":"OBSOLETO: Sindrome sordità-capelli bianchi-contratture-papillomi","synonyms":["OBSOLETO: Sindrome di Davenport-Donlan"]},"nl":{"name":"OBSOLEET: Doofheid - wit haar - contracturen - papillomen-syndroom","synonyms":["OBSOLEET: Syndroom van Davenport-Donlan"]},"pt":{"name":"OBSOLETO: Síndrome de surdez-piebaldismo-contracturas-papilomas","synonyms":["OBSOLETO: Síndrome Davenport-Donlan"]},"pl":{"name":"NIEAKTUALNE: Gluchota - biale wlosy - przykurcze - brodawczaki","synonyms":["NIEAKTUALNE: Zespół Davenporta i Donlana"]},"cs":{"name":"NEAKTUÁLNÍ: Syndrom zahrnující hluchotu, bílé vlasy, kontrakce a papilomy","synonyms":["OBSOLETE: Davenport-Donlan syndrome"]},"uk":{"name":"ЗАСТАРІЛО: Синдром глухоти-білого волосся-контрактур-папілом","synonyms":["ЗАСТАРІЛО: Синдром Девенпорта-Донлана"]},"zh":{"name":"弃用：耳聋-白发-挛缩-乳头状瘤综合征","synonyms":["Davenport-Donlan综合征"]},"tr":{"name":"Eski adı: Sağırlık-beyaz saç-kontraktür-papillom sendromu","synonyms":["Davenport-Donlan sendromu"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":90642,"name":"Rare syndromic genetic deafness"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}