ORPHA:208596
Genetic hyperparathyroidism
- 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 | Genetic hyperparathyroidism | |
| fr | Hyperparathyroïdie génétique | |
| de | Hyperparathyreoidismus, genetisch bedingter | |
| es | Hiperparatiroidismo genético | |
| it | Iperparatiroidismo genetico | |
| nl | Genetische hyperparathyreoïdie | |
| pt | Hiperparatiroidismo genético | |
| pl | Nadczynność przytarczyc uwarunkowana genetycznie | |
| cs | Genetický hyperparathyreoidismus | |
| uk | Генетично обумовлений гіперпаратиреоз | |
| zh | 遗传性甲状旁腺机能亢进 | |
| tr | Genetik hiperparatiroidi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16166 | E | validated | |
| UMLS | C5680826 | 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:183634Rare genetic parathyroid disease and phosphocalcic metabolism disorder
rare genetic 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/208596
- This record as JSON: /data/d/208596.json