ORPHA:178040
Rare peripheral precocious puberty
- 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 peripheral precocious puberty | |
| fr | Puberté précoce périphérique rare | |
| de | Pubertät, periphere vorzeitige | |
| es | Pubertad precoz periférica rara | |
| it | Pubertà precoce periferica | |
| nl | Zeldzame perifere pubertas praecox | Zeldzame perifere vroegtijdige puberteit |
| pt | Puberdade precoce periférica | |
| pl | Przedwczesne dojrzewanie pochodzenia obwodowego | |
| cs | Periferní předčasná puberta | Periferní pubertas praecox · Pseudopuberta |
| uk | Рідкісне периферичне передчасне статеве дозрівання | |
| zh | 罕见外周性性早熟 | |
| tr | Nadir periferik erken ergenlik |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 5A92 | E | specific | validated |
| MONDO | 15791 | E | validated | |
| UMLS | C5680513 | 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:435554Genetic precocious puberty
rare genetic diseases - ORPHA:95708Rare precocious puberty
rare endocrine 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/178040
- This record as JSON: /data/d/178040.json