raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98323

OBSOLETE: Male infertility with impaired virilization due to a testicular disorder associated with a hepatic disease

inactive · referred to ORPHA:98048Rare male infertility

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

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Male infertility with impaired virilization due to a testicular disorder associated with a hepatic disease
frOBSOLETE : Infertilité masculine avec défaut de virilisation d'origine testiculaire associé à une insuffisance hépatique
deOBSOLET: Männliche Infertilität mit gestörter Virilisierung bei testikulärer Funktionsstörung, assoziiert mit Leberkrankheit
esOBSOLETO: Infertilidad masculina con deficiencia de virilización por trastorno testicular asociado a enfermedad hepática
itOBSOLETO: Sterilità maschile con virilizzazione anomala da disturbo testicolare associato a malattia epatica
nlOBSOLEET: Mannelijke onvruchtbaarheid met verminderde virilisatie door testiculaire aandoening geassocieerd met leverziekte
ptOBSOLETO: Infertilidade masculina com compromisso da virilização por anomalia testicular, associada a doença hepática
plNIEAKTUALNE: Nieplodnosc meska z uposledzona wirylizacja z powodu wady jader spowodowanej choroba watroby
csNEAKTUÁLNÍ: Mužská neplodnost s poruchou virilizace způsobená poruchou varlat spojená s jaterním onemocněním
ukЗАСТАРІЛО: Чоловіче безпліддя з порушенням вірилізації через розлад яєчок, повязаний із захворюванням печінки.
zh弃用:肝病相关睾丸异常所致男性不育症伴男性第二性征缺陷
trEski adı: Hepatik bir hastalık ilişkili bir testis bozukluğuna bağlı virilizasyon bozukluğu 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