raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:399877

Rare female infertility due to gonadal dysgenesis

Synonyms: Rare female infertility due to ovarian 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
enRare female infertility due to gonadal dysgenesisRare female infertility due to ovarian dysgenesis
frInfertilité féminine rare due à une dysgénésie gonadique
deSeltene weibliche Infertilität durch GonadendysgenesieSeltene weibliche Infertilität durch Ovarialdysgenesie · Weibliche Infertilität durch Ovarialdysgenesie
esInfertilidad femenina rara por disgenesia gonadalInfertilidad femenina rara por disgenesia ovárica
itSterilità femminile da disgenesia gonadicaSterilità femminile da disgenesia ovarica
nlZeldzame vrouwelijke onvruchtbaarheid door gonadale dysgenesieZeldzame vrouwelijke onvruchtbaarheid door ovariële dysgenesie
ptInfertilidade feminina rara devida a disgenesia gonadal
plNiepłodność żeńska z powodu dysgenezji gonadNiepłodność żeńska z powodu dysgenezji jajników
csŽenská neplodnost způsobená gonadální dysgenezíŽenská neplodnost způsobená ovariální dysgenezí
ukРідкісне жіноче безпліддя, зумовлене дисгенезією гонадРідкісне жіноче безпліддя через дисгенезію яєчників
zh性腺发育不全所致罕见女性不育卵巢发育不全所致罕见女性不孕
trGonadal disgeneze bağlı nadir kadın infertilitesiYumurtalık disgenezine bağlı nadir kadın infertilitesi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO18402Evalidated
UMLSC5680010Evalidated

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 (6):

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