raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98313

Male infertility due to gonadal dysgenesis

Synonyms: Male infertility due to testicular dysgenesis

Type
Category
Group
Group of disorders
Status
active

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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enMale infertility due to gonadal dysgenesisMale infertility due to testicular dysgenesis
frInfertilité masculine due à une dysgénésie gonadiqueInfertilité masculine due à une dysgénésie testiculaire
deMännliche Infertilität durch Gonadendysgenesie
esInfertilidad masculina por disgenesia gonadalInfertilidad masculina por disgenesia testicular
itSterilità maschile da disgenesia gonadicaSterilità maschile da disgenesia testicolare
nlMannelijke onvruchtbaarheid als gevolg van gonadale dysgenesieMannelijke onvruchtbaarheid als gevolg van testiculaire dysgenesie
ptInfertilidade masculina devida a disgenesia gonadalInfertilidade masculina com compromisso da virilização por anomalia do desenvolvimento e estrutura testicular
plNiepłodność męska z powodu dysgenezji gonadNiepłodność męska z powodu dysgenezji jąder
csMužská neplodnost způsobená gonadální dysgenezíMužská neplodnost způsobená testikulární dysgenezí
ukЧоловіче безпліддя внаслідок дисгенезії гонадЧоловіче безпліддя через дисгенезію яєчок
zh性腺发育不全所致男性不育症睾丸发育不全所致男性不育症
trGonadal disgeneze bağlı erkek infertilitesiTestis disgenezine bağlı erkek infertilitesi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC5680350Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

Children (8):

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