{"orpha":431,"name":"Ichthyosis-male hypogonadism syndrome","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 Xp22.3 microdeletion syndrome","url":"https://raremap.alftech.space/d/ORPHA-431/","orphanet_url":"https://www.orpha.net/en/disease/detail/431","names":{"fr":{"name":"Syndrome d'hypogonadisme congénital-ichtyose"},"de":{"name":"Ichthyose und männlicher Hypogonadismus"},"es":{"name":"Síndrome de ictiosis-hipogonadismo masculino"},"it":{"name":"Ipogonadismo congenito con ittiosi"},"nl":{"name":"Ichthyosis - mannelijk hypogonadisme-syndroom"},"pt":{"name":"Síndrome de ictiose-hipogonadismo masculino"},"pl":{"name":"Rybia łuska - hipogonadyzm męski"},"cs":{"name":"Syndrom zahrnující ichtyózu a mužský hypogonadismus"},"uk":{"name":"Синдром іхтіозу - чоловічого гіпогонадизму"},"zh":{"name":"鱼鳞病-男性性腺功能减退综合征"},"tr":{"name":"İktiyoz-erkek hipogonadizm sendromu"}},"xrefs":[{"source":"OMIM","code":"308200","qualifier":"E","icd_relation":null,"validated":true},{"source":"MeSH","code":"C537365","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":1643,"name":"Xp22.3 microdeletion syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}