{"orpha":98312,"name":"OBSOLETE: Male infertility with impaired virilization due to a testicular disorder","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 due to testicular endocrine disorder","url":"https://raremap.alftech.space/d/ORPHA-98312/","orphanet_url":"https://www.orpha.net/en/disease/detail/98312","names":{"fr":{"name":"OBSOLETE : Infertilité masculine avec défaut de virilisation d'origine testiculaire"},"de":{"name":"OBSOLET: Männliche Infertilität mit gestörter Virilisierung bei testikulärer Funktionsstörung"},"es":{"name":"OBSOLETO: Infertilidad masculina con deficiencia de virilización por defecto testicular"},"it":{"name":"OBSOLETO: Sterilità maschile con virilizzazione anomala da difetto testicolare"},"nl":{"name":"OBSOLEET: Mannelijke onvruchtbaarheid met verminderde virilisatie als gevolg van een testiculaire stoornis"},"pt":{"name":"OBSOLETO: Infertilidade masculina com compromisso da virilização por doença testicular"},"pl":{"name":"NIEAKTUALNE: Nieplodnosc meska z uposledzona wirylizacja z powodu zaburzen w jadrach"},"cs":{"name":"NEAKTUÁLNÍ: Mužská neplodnost s poruchou virilizace způsobená poruchou varlat"},"uk":{"name":"ЗАСТАРІЛО: Чоловіче безпліддя з порушенням вірилізації через захворювання яєчок"},"zh":{"name":"弃用：睾丸异常所致男性不育症伴男性第二性征缺陷"},"tr":{"name":"Eski adı: Testis bozukluğuna bağlı olarak virilizasyon bozukluğu ile seyreden erkek infertilitesi"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":399685,"name":"Rare male infertility due to testicular endocrine disorder"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}