raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:399839

Rare female infertility due to a congenital hypogonadotropic hypogonadism

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 a congenital hypogonadotropic hypogonadism
frInfertilité féminine rare due à un hypogonadisme hypogonadotrope congénital
deSeltene Form der weibliche Infertilität durch kongenitalen hypogonadotropen Hypogonadismus
esInfertilidad femenina rara por hipogonadismo hipogonadotrópico congénito
itSterilità femminile rara da ipogonadismo ipogonadotropo congenito
nlZeldzame vrouwelijke onvruchtbaarheid door congenitaal hypogonadotroop hypogonadisme
ptInfertilidade feminina rara devido a um hipogonadismo hipogonadotrópico congénito
plRzadka niepłodność żeńska z powodu wrodzonego hipogonadyzmu hipogonadotropowego
csVzácná porucha ženské plodnosti způsobená vrozeným hypogonadotropním hypogonadismem
ukРідкісне жіноче безпліддя, зумовлене вродженим гіпогонадотропним гіпогонадизмом
zh先天性低促性腺素性腺功能减退症所致罕见女性不育
trDoğumsal hipogonadotropik hipogonadizme bağlı nadir kadın infertilitesi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO18398Evalidated
UMLSC5681158Evalidated

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 (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