ORPHA:98331
OBSOLETE: Male infertility with normal virilization due to a testicular defect
inactive · referred to ORPHA:399685Rare male infertility due to testicular endocrine disorder
- Type
- Category
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
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
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Male infertility with normal virilization due to a testicular defect | |
| fr | OBSOLETE : Infertilité masculine avec virilisation normale d'origine testiculaire | |
| de | OBSOLET: Männliche Infertilität bei testikulärer Funktionsstörung, normale Virilisierung | |
| es | OBSOLETO: Infertilidad masculina con virilización normal debido a un defecto testicular | |
| it | OBSOLETO: Sterilità maschile con virilizzazione normale da difetti testicolari | |
| nl | OBSOLEET: Mannelijke onvruchtbaarheid met normale virilisatie als gevolg van een testiculair defect | |
| pt | OBSOLETO: Infertilidade masculina com virilização normal por anomalia testicular | |
| pl | NIEAKTUALNE: Nieplodnosc meska z prawidlowa wirylizacja z powodu wady jader | |
| cs | NEAKTUÁLNÍ: Mužská neplodnost s normální virilizací způsobená defektem varlat | |
| uk | ЗАСТАРІЛО: Чоловіче безпліддя з нормальною вірилізацією внаслідок дефекту яєчок | |
| zh | 弃用：睾丸缺失所致男性不育症伴正常第二性征 | |
| tr | Eski adı: Testis defektine bağlı normal virilizasyon ile seyreden erkek infertilitesi |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98331
- This record as JSON: /data/d/98331.json