ORPHA:435561
Rare precocious puberty in female
- 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 precocious puberty in female | |
| fr | Puberté précoce rare de la femme | |
| de | Pubertas praecox bei Mädchen | Vorzeitige weibliche Pubertät |
| es | Pubertad precoz rara en la mujer | |
| it | Pubertà precoce rara nelle femmine | |
| nl | Zeldzame pubertas praecox bij vrouw | Zeldzame vroegtijdige puberteit bij vrouw |
| pt | Puberdade precoce em indivíduos femininos | |
| pl | Przedwczesne dojrzewanie płciowe u kobiet | Rzadkie przedwczesne dojrzewanie płciowe u kobiety |
| cs | Předčasná puberta u dívek | |
| uk | Рідкісне передчасне статеве дозрівання у жінок | |
| zh | 女性性早熟 | |
| tr | Kadınlarda erken ergenlik |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18561 | E | validated | |
| UMLS | C5816689 | 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:180208Anomaly of puberty or/and menstrual cycle
rare gynecological and obstetric diseases
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/435561
- This record as JSON: /data/d/435561.json