{"orpha":3423,"name":"Vasquez-Hurst-Sotos syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["Hypogonadism-gynecomastia-X-linked intellectual disability syndrome"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Xq27.3q28 duplication syndrome","url":"https://raremap.alftech.space/d/ORPHA-3423/","orphanet_url":"https://www.orpha.net/en/disease/detail/3423","names":{"fr":{"name":"Syndrome de Vasquez-Hurst-Sotos","synonyms":["Syndrome d'hypogonadisme-gynécomastie-déficience intellectuelle lié à l'X"]},"de":{"name":"Vasquez-Hurst-Sotos-Syndrom"},"es":{"name":"Síndrome de Vasquez-Hurst-Sotos","synonyms":["Síndrome de hipogonadismo-ginecomastia-discapacidad intelectual ligada al cromosoma X"]},"it":{"name":"Sindrome di Vasquez-Hurst-Sotos","synonyms":["Sindrome ipogonadismo legato all'X-ginecomastia-disabilità intellettiva"]},"nl":{"name":"Syndroom van Vasquez-Hurst-Sotos","synonyms":["Hypogonadisme - gynaecomastie - X-gebonden intellectuele achterstand-syndroom"]},"pt":{"name":"Síndrome Vasquez-Hurst-Sotos","synonyms":["Síndrome de hipogonadismo-ginecomastia-perturbação do desenvolvimento intelectual ligada ao X"]},"pl":{"name":"Zespół Vasqueza, Hursta i Sotosa","synonyms":["Hipogonadyzm - ginekomastia - niepełnosprawnoś intelektualna sprzężona z chromosomem X"]},"cs":{"name":"Vasquezův-Hurstův-Sotosův syndrom","synonyms":["Syndrom zahrnující hypogonadismus, gynekomastii a X-vázanou mentální retardaci","Vasquez-Hurst-Sotosův syndrom"]},"uk":{"name":"Синдром Васкез-Херста-Сотоса","synonyms":["Х-зчеплений синдром гіпогонадизму-гінекомастії- інтелектуальної недостатності"]},"zh":{"name":"Vasquez-Hurst-Sotos综合征","synonyms":["性腺功能减退症-男子乳腺发育-X连锁智力障碍综合征"]},"tr":{"name":"Vasquez-Hurst-Sotos sendromu","synonyms":["Hipogonadizm-jinekomasti-X'e bağlı zihinsel yetersizlik sendromu"]}},"xrefs":[{"source":"MeSH","code":"C536533","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C2931231","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":261483,"name":"Xq27.3q28 duplication syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}