ORPHA:208593
Genetic hypoparathyroidism
- 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Genetic hypoparathyroidism | |
| fr | Hypoparathyroïdie génétique | |
| de | Hypoparathyreoidismus, genetisch bedingter | |
| es | Hipoparatiroidismo genético | |
| it | Ipoparatiroidismo genetico | |
| nl | Genetische hypoparathyreoïdie | |
| pt | Hipoparatiroidismo genético | |
| pl | Niedoczynność przytarczyc uwarunkowana genetycznie | |
| cs | Genetický hypoparathyreoidismus | |
| uk | Генетично обумовлений гіпопаратиреоз | |
| zh | 遗传性甲状旁腺机能减退 | |
| tr | Genetik hipoparatiroidi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16165 | E | validated | |
| UMLS | C5680825 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
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/208593
- This record as JSON: /data/d/208593.json