{"orpha":98341,"name":"OBSOLETE: Male infertility with normal virilization due to a systemic disease","type":"Category","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Rare male infertility","url":"https://raremap.alftech.space/d/ORPHA-98341/","orphanet_url":"https://www.orpha.net/en/disease/detail/98341","names":{"fr":{"name":"OBSOLETE : Infertilité masculine avec virilisation normale due à une maladie systémique"},"de":{"name":"OBSOLET: Männliche Infertilität bei testikulärer Funktionsstörung, assoziiert mit systemischer Krankheit, normale Virilisierung"},"es":{"name":"OBSOLETO: Infertilidad masculina con virilización normal debido a un defecto testicular adquirido asociado a enfermedad sistémica"},"it":{"name":"OBSOLETO: Sterilità maschile con virilizzazione normale da difetto testicolare associato a una malattia sistemica"},"nl":{"name":"OBSOLEET: Mannelijke onvruchtbaarheid met normale virilisatie als gevolg van een systemische ziekte"},"pt":{"name":"OBSOLETO: Infertilidade masculina com virilização normal por doença sistémica"},"pl":{"name":"NIEAKTUALNE: Nieplodnosc meska z prawidlowa wirylizacja z powodu choroby ukladowej"},"cs":{"name":"NEAKTUÁLNÍ: Mužská neplodnost s normální virilizací způsobená systémovým onemocněním"},"uk":{"name":"ЗАСТАРІЛО: Чоловіче безпліддя з нормальною вірилізацією внаслідок системного захворювання"},"zh":{"name":"弃用：系统性疾病所致男性不育症伴正常第二性征"},"tr":{"name":"Eski adı: Sistemik bir hastalığa bağlı normal virilizasyon ile seyreden erkek infertilitesi"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":98048,"name":"Rare male infertility"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}