raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98330

OBSOLETE: Male infertility with normal virilization due to androgen administration

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

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Male infertility with normal virilization due to androgen administration
frOBSOLETE : Infertilité masculine avec virilisation normale due à la prise d'andrognes
deOBSOLET: Männliche Infertilität bei Androgensubstitution, normale Virilisierung
esOBSOLETO: Infertilidad masculina con virilización normal debido a la administración de andrógenos
itOBSOLETO: Sterilità maschile con virilizzazione normale da somministrazione di androgeni
nlOBSOLEET: Mannelijke onvruchtbaarheid met normale virilisatie als gevolg van androgeentoediening
ptOBSOLETO: Infertilidade masculina com virilização normal por administração de androgénio
plNIEAKTUALNE: Nieplodnosc meska z prawidlowa wirylizacja z powodu podania androgenów
csNEAKTUÁLNÍ: Mužská neplodnost s normální virilizací způsobená podávání androgenů
ukЗАСТАРІЛО: чоловіче безпліддя з нормальною вірилізацією внаслідок прийому андрогенів
zh弃用:雄激素使用所致男性不育症伴正常第二性征
trEski adı: Androjen uygulamasına bağlı normal virilizasyon ile seyreden erkek infertilitesi
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card