ORPHA:95709
Rare acquired premature ovarian failure
- 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 acquired premature ovarian failure | |
| fr | Insuffisance ovarienne précoce acquise rare | |
| de | Seltene vorzeitige erworbene Ovarialinsuffizienz | |
| es | Insuficiencia ovárica precoz rara adquirida | |
| it | Insufficienza ovarica precoce acquisita rara | |
| nl | Zeldzaam verworven prematuur ovariumfalen | Zeldzaam verworven prematuur ovarieel falen |
| pt | Falência ovárica prematura rara adquirida | |
| pl | Rzadka nabyta przedwczesna niewydolność jajników | |
| cs | Získané předčasné selhání vaječníků | |
| uk | Рідкісна набута передчасна оваріальна недостатність | |
| zh | 获得性卵巢早衰 | |
| tr | Edinsel prematüre over yetmezliği |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | E28.8 | E | specific | validated |
| UMLS | C5925051 | 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 (3):
- ORPHA:180208Anomaly of puberty or/and menstrual cycle
rare gynecological and obstetric diseases - ORPHA:156643Genetic endocrine growth disease
rare genetic diseases - ORPHA:90692Rare endocrine growth disease
rare endocrine diseases
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/95709
- This record as JSON: /data/d/95709.json