{"orpha":202,"name":"Crandall syndrome","type":"Disease","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["Alopecia-deafness-hypogonadism syndrome","Alopecia-hearing loss-hypogonadism syndrome","Alopecia-sensorineural deafness-hypogonadism syndrome","Alopecia-sensorineural hearing loss-hypogonadism syndrome"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Björnstad syndrome","url":"https://raremap.alftech.space/d/ORPHA-202/","orphanet_url":"https://www.orpha.net/en/disease/detail/202","names":{"fr":{"name":"Syndrome de Crandall","synonyms":["Syndrome d'alopécie-surdité neurosensorielle-hypogonadisme","Syndrome d'alopécie-surdité-hypogonadisme"]},"de":{"name":"Crandall-Syndrom","synonyms":["Alopezie-Schwerhörigkeit-Hypogonadismus-Syndrom","Alopezie-sensorineurale Schwerhörigkeit-Hypogonadismus-Syndrom"]},"es":{"name":"Síndrome de Crandall","synonyms":["Síndrome de alopecia-hipoacusia neurosensorial-hipogonadismo","Síndrome de alopecia-hipoacusia-hipogonadismo","Síndrome de alopecia-sordera neurosensorial-hipogonadismo","Síndrome de alopecia-sordera-hipogonadismo"]},"it":{"name":"Sindrome di Crandall","synonyms":["Sindrome alopecia-sordità-ipogonadismo"]},"nl":{"name":"Syndroom van Crandall","synonyms":["Alopecie - doofheid - hypogonadisme-syndroom","Alopecie - gehoorverlies - hypogonadisme-syndroom","Alopecie - sensorineuraal gehoorverlies - hypogonadisme-syndroom","Alopecie - sensorineurale doofheid - hypogonadisme-syndroom"]},"pt":{"name":"Síndrome Crandall"},"pl":{"name":"Zespół Crandalla","synonyms":["Zespół łysienia, głuchoty i hipogonadyzmu"]},"cs":{"name":"Crandallův syndrom","synonyms":["Syndrom zahrnující alopecii, hluchotu a hypogonadismus"]},"uk":{"name":"Синдром Крендалла","synonyms":["Синдром алопеції-глухоти-гіпогонадизму","Синдром алопеції-глухоти-гіпогонадизму","Синдром алопеції-сенсоневральної глухоти-гіпогонадизму","Алопеція-сенсоневральна туговухість-гіпогонадизм"],"definition":"Crandall syndrome is characterized by progressive sensorineural deafness, alopecia and hypogonadism with LH and GH deficiencies. It has been described in three brothers. It resembles Björnstad's syndrome (see this term) that combines irregular pili torti and deafness. It is probably inherited as and autosomal recessive disorder."},"zh":{"name":"Crandall综合征","synonyms":["脱发-感音神经性听力丧失-性腺功能减退综合征"]},"tr":{"name":"Crandall sendromu","synonyms":["Alopesi-sağırlık-hipogonadizm sendromu","Alopesi-işitme kaybı-hipogonadizm sendromu","Alopesi-sensörinöral sağırlık-hipogonadizm sendromu","Alopesi-sensörinöral işitme kaybı-hipogonadizm sendromu"]}},"xrefs":[{"source":"MONDO","code":"0016067","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0432348","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"1561","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":123,"name":"Björnstad syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}