raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:399882

Rare female infertility due to an implantation defect

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 an implantation defect
frInfertilité féminine rare due à un défaut d'implantation
deSeltene weibliche Infertilität durch Implantationsdefekt
esInfertilidad femenina rara por un defecto en la implantación
itSterilità femminile da difetto di impianto
nlZeldzame vrouwelijke onvruchtbaarheid door implantatiedefect
ptInfertilidade feminina por defeito de implantação
plNiepłodność żeńska z powodu nieprawidłowej implantacji
csŽenská neplodnost způsobená poruchou implantace
ukРідкісне жіноче безпліддя, зумовлене дефектом імплантації
zh植入缺陷所致罕见女性不育
trİmplantasyon defektine bağlı nadir kadın infertilitesi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO18403Evalidated
UMLSC5681135Evalidated

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 (5):

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