{"orpha":1011,"name":"Alopecia-hypogonadism-extrapyramidal syndrome","type":"Disease","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["Devriendt-Legius-Fryns syndrome"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Woodhouse-Sakati syndrome","url":"https://raremap.alftech.space/d/ORPHA-1011/","orphanet_url":"https://www.orpha.net/en/disease/detail/1011","names":{"fr":{"name":"Syndrome extrapyramidal-alopécie-hypogonadisme","synonyms":["Syndrome de Devriendt-Legius-Fryns"]},"de":{"name":"Alopezie-Hypogonadismus-extrapyramidale Störung-Syndrom","synonyms":["Devriendt-Legius-Fryns-Syndrom"]},"es":{"name":"Síndrome de alopecia-hipogonadismo-trastorno extrapiramidal","synonyms":["Síndrome de Devriendt-Legius-Fryns"]},"it":{"name":"Sindrome alopecia-ipogonadismo-disturbo extrapiramidale","synonyms":["Sindrome di Devriendt-Legius-Fryns"]},"nl":{"name":"Alopecie - hypogonadisme - extrapiramidale stoornis-syndroom","synonyms":["Syndroom van Devriendt-Legius-Fryns"]},"pt":{"name":"Alopecia-hipogonadismo-síndrome extrapiramidal"},"pl":{"name":"Zespół łysienia, hipogonadyzmu i zaburzeń pozapiramidowych","synonyms":["Zespół Devrienda, Legiusa i Frynsa"]},"cs":{"name":"Syndrom zahrnující alopecii, hypogonadismus a extrapyramidální poruchu","synonyms":["Devriendtův-Legiusův-Frynsův syndrom","Devriendt-Legius-Frynsův syndrom"]},"uk":{"name":"Алопеція-гіпогонадизм-екстрапірамідний синдром","synonyms":["Синдром Девріндта-Легіуса-Фрінса"]},"zh":{"name":"脱发-性腺功能减退-锥体外系综合征","synonyms":["Devriendt-Legius-Fryns综合征"]},"tr":{"name":"Alopesi-hipogonadizm-ekstrapiramidal sendrom","synonyms":["Devriendt-Legius-Fryns sendromu"]}},"xrefs":[{"source":"MeSH","code":"C537053","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C2931406","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":3464,"name":"Woodhouse-Sakati syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}