ORPHA:400022
Rare female infertility due to an anomaly of ovarian function 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| Lang | Name | Synonyms |
|---|---|---|
| en | Rare female infertility due to an anomaly of ovarian function of genetic origin | |
| fr | Infertilité féminine rare due à un dysfonctionnement ovarien d'origine génétique | |
| de | Seltene Form der weibliche Infertilität durch genetisch bedingte Funktionsstörung der Ovarien | |
| es | Infertilidad femenina rara por una anomalía de la función ovárica de origen genético | |
| it | Sterilità femminile rara da difetto della funzione ovarica di origine genetica | |
| nl | Zeldzame vrouwelijke onvruchtbaarheid door functiestoornis van ovarium van genetische oorsprong | |
| pt | Infertilidade feminina rara por anomalia da função ovariana de origem genética | |
| pl | Rzadka niepłodność żeńska z powodu nieprawidłowej funkcji jajników pochodzenia genetycznego | |
| cs | Vzácná ženská neplodnost způsobená anomáliemi ovariální funkce genetického původu | |
| uk | Рідкісне жіноче безпліддя, зумовлене генетично обумовленою аномалією функції яєчників | |
| zh | 遗传性卵巢功能异常导致的罕见女性不孕 | |
| tr | Genetik kökenli yumurtalık fonksiyonunun anomalisine bağlı nadir kadın infertilitesi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18413 | E | validated | |
| UMLS | C5681137 | 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):
Children (7):
- ORPHA:572354Blepharophimosis-ptosis-epicanthus inversus syndrome type 1
- ORPHA:79239Classic galactosemia
- ORPHA:2297Insulin-resistance syndrome type A
- ORPHA:75325Osteosclerosis-ichthyosis-premature ovarian failure syndrome
- ORPHA:9Tetrasomy X syndrome
- ORPHA:3375Trisomy X syndrome
- ORPHA:96201X small rings syndrome
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/400022
- This record as JSON: /data/d/400022.json