raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98343

Male infertility due to obstructive azoospermia

Synonyms: Male infertility due to impaired sperm transport

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 obstructive azoospermiaMale infertility due to impaired sperm transport
frInfertilité masculine due à une azoospermie obstructiveInfertilité masculine due à une azoospermie excrétoire
deMännliche Infertilität durch obstruktive AzoospermieMännliche Infertilität durch gestörten Spermientransport
esInfertilidad masculina por azoospermia obstructivaInfertilidad masculina por problemas en el transporte del esperma
itSterilità maschile da azoospermia ostruttivaSterilità maschile da anomalie del trasporto dello sperma
nlMannelijke onvruchtbaarheid als gevolg van obstructieve azoöspermieMannelijke onvruchtbaarheid als gevolg van verstoord spermatransport
ptInfertilidade masculina com virilização normal por compromisso do transporte do esperma
plNiepłodność męska z powodu azoospermii obstrukcyjnejNiepłodność męska z powodu upośledzonego transportu spermy
csMužská neplodnost způsobená obstruktivní azoospermiíMužská neplodnost způsobená poškozeným transportem spermií
ukЧоловіче безпліддя внаслідок обструктивної азоосперміїЧоловіче безпліддя через порушення транспортування сперматозоїдів
zh梗阻性无精子症所致男性不育症精子运输障碍所致男性不育症
trObstrüktif azospermiye bağlı erkek infertilitesiSperm aktarımının bozulmasına bağlı erkek kısırlığı
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC5680348Evalidated

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 (2):

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