ORPHA:399846
Rare disorder with 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare disorder with female infertility due to a congenital hypogonadotropic hypogonadism | |
| fr | Maladie rare avec Infertilité féminine due à un hypogonadisme hypogonadotrope congénital | |
| de | Seltene Störung mit weiblicher Infertilität durch kongenitalen hypogonadotropen Hypogonadismus | |
| es | Trastorno raro con infertilidad femenina por hipogonadismo hipogonadotrópico congénito | |
| it | Disturbo raro con sterilità femminile da ipogonadismo ipogonadotropo congenito | |
| nl | Zeldzame aandoening met vrouwelijke onvruchtbaarheid door congenitaal hypogonadotroop hypogonadisme | |
| pt | Doença rara com infertilidade feminina devido a hipogonadismo hipogonadotrópico congénito | |
| pl | Rzadkie zaburzenie z niepłodnością żeńską z powodu wrodzonego hipogonadyzmu hipogonadotropowego | |
| cs | Vzácná porucha doprovázená ženskou neplodností, způsobená vrozeným hypogonadotropním hypogonadismem | |
| uk | Рідкісне захворювання з жіночим безпліддям, зумовленим вродженим гіпогонадотропним гіпогонадизмом | |
| zh | Rare disorder with female infertility due to a congenital hypogonadotropic hypogonadism | |
| tr | Doğumsal hipogonadotropik hipogonadizme bağlı kadın infertilitesi ile seyreden nadir bozukluk |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681161 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:399839Rare female infertility due to a congenital hypogonadotropic hypogonadism
rare genetic diseases; rare infertility disorders
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/399846
- This record as JSON: /data/d/399846.json