raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:399813

Male infertility due to sperm motility disorder

Synonyms: Male infertility due to asthenozoospermia

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 sperm motility disorderMale infertility due to asthenozoospermia
frInfertilité masculine due à un défaut de motilité
deMännliche Infertilität durch Störung der SpermienmotilitätMännliche Infertilität durch Asthenozoospermie
esInfertilidad masculina por un trastorno de motilidad del espermaInfertilidad masculina por astenozoospermia
itSterilità maschile da difetto della motilità spermaticaSterilità maschile da astenozoospermia
nlMannelijke onvruchtbaarheid door stoornis van spermamotiliteitMannelijke onvruchtbaarheid door asthenozoöspermie
ptInfertilidade masculina por alteração da motilidade espermática
plNiepłodność męska z powodu zaburzeń ruchliwości plemnikówNiepłodność męska z powodu astenozoospermii
csMužská neplodnost způsobená nedostatečnou pohyblivostí spermiíMužská neplodnost způsobená astenozoospermií
ukЧоловіче безпліддя, зумовлене порушенням рухливості сперматозоїдівЧоловіче безпліддя через астенозооспермію
zh精子运动障碍导致的男性不育弱精子症所致男性不育
trSperm motilite bozukluğuna bağlı erkek infertilitesiAstenozoospermiye bağlı erkek infertilitesi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO18395Evalidated
UMLSC5680032Evalidated

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 (3):

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