raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:400025

Female infertility due to an implantation defect of genetic origin

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
enFemale infertility due to an implantation defect of genetic origin
frInfertilité féminine due à un défaut d'implantation d'origine génétique
deWeibliche Infertilität durch genetisch bedingten Implantations-Defekt
esInfertilidad femenina por un defecto en la implantación de origen genético
itSterilità femminile da difetto di impianto di origine genetica
nlVrouwelijke onvruchtbaarheid door implantatiedefect van genetische oorsprong
ptInfertilidade feminina por defeito de implantação de origem genética
plNiepłodność żeńska z powodu defektu implantacji pochodzenia genetycznego
csŽenská neplodnost způsobená poruchami implantace genetického původu
ukЖіноче безпліддя, зумовлене генетично обумовленим дефектом імплантації
zh遗传性植入缺陷导致的罕见女性不育
trGenetik kökenli implantasyon defektine bağlı kadın infertilitesi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO18414Evalidated
UMLSC5681136Evalidated

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 (1):

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