ORPHA:650070
Rare central precocious puberty in female
Synonyms: Rare CPP in female · Rare central precocious puberty in girl
- Type
- Clinical group
- 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
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare central precocious puberty in female | Rare CPP in female · Rare central precocious puberty in girl |
| fr | Puberté précoce centrale rare de la femme | Puberté précoce centrale rare de la fille |
| de | Seltene zentrale vorzeitige Pubertät bei Mädchen | Pubertas praecox, zentrale, weibliche Form |
| es | Pubertad precoz central rara en la mujer | PPC rara en la mujer · Pubertad precoz central rara en la niña |
| it | Pubertà femminile precoce centrale rara | CPP rara femminile · Pubertà precoce centrale rara nella ragazza |
| nl | Zeldzame centrale pubertas praecox bij vrouw | Zeldzame CPP bij vrouw · Zeldzame centrale pubertas praecox bij meisje · Zeldzame centrale vroegtijdige puberteit bij vrouw |
| pt | Puberdade precoce central rara no indivíduo feminino | CPP em indivíduo feminino rara · CPP genética em indivíduo feminino · Puberdade precoce central rara na rapariga |
| pl | Przedwczesne dojrzewanie płciowe pochodzenia ośrodkowego u kobiety | Rzadkie ośrodkowe przedwczesne dojrzewanie płciowe u kobi |
| cs | Vzácná centrální předčasná puberta u žen | = en |
| uk | Рідкісне центральне передчасне статеве дозрівання у дівчат | Рідкісне центральне передчасне статеве дозрівання у дівчинки · Рідкісне CPP у жінок |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5816764 | 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 (2):
- ORPHA:650063Rare central precocious puberty
rare endocrine diseases - ORPHA:435561Rare precocious puberty in female
rare gynecological and obstetric diseases
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Genes
0 directOrphanet records no gene directly on this code.
5
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/650070
- This record as JSON: /data/d/650070.json