raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:399764

Male infertility due to gonadal dysgenesis or sperm disorder

Synonyms: Male infertility due to testicular dysgenesis or sperm disorder

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 dysgenesis or sperm disorderMale infertility due to testicular dysgenesis or sperm disorder
frInfertilité masculine due à une dysgénésie gonadique ou anomalie du spermeInfertilité masculine due à une dysgénésie testiculaire ou anomalie du sperme
deMännliche Infertilität durch Gonadendysgenesie oder Spermienstörung
esInfertilidad masculina por disgenesia gonadal o un trastorno del espermaInfertilidad masculina por disgenesia testicular o un trastorno del esperma
itSterilità maschile da disgenesia gonadica o anomalie spermaticheSterilità maschile da disgenesia testicolare o anomalie spermatiche
nlMannelijke onvruchtbaarheid door gonadale dysgenesie of spermastoornisMannelijke onvruchtbaarheid door testiculaire dysgenesie of spermastoornis
ptInfertilidade masculina devida a disgenesia gonadal ou alteração espermática
plNiepłodność męska spowodowana dysgenezją gonad lub nieprawidłowym nasieniemNiepłodność męska spowodowana dysgenezją jąder lub nieprawidłowym nasieniem
csMužská neplodnost způsobená gonadální dysgenezí nebo abnormalitami spermatuMužská neplodnost způsobená testikulární dysgenezí nebo abnormalitami spermatu
ukЧоловіче безпліддя, зумовлене дисгенезією гонад або порушенням сперматогенезуЧоловіче безпліддя через дисгенезію яєчок або порушення сперматогенезу
zh性腺发育不全或精子异常所致男性不育睾丸发育不良或精子障碍所致男性不育
trGonadal disgenezi veya sperm bozukluğuna bağlı erkek infertilitesiTestis disgenezi veya sperm bozukluğuna bağlı erkek infertilitesi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO18389Evalidated
UMLSC5680033Evalidated

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 (2):

Children (2):

Codes that Orphanet moved or referred to this one:

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