ORPHA:181419
Rare hypoaldosteronism
- 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 hypoaldosteronism | |
| fr | Hypoaldostéronisme rare | |
| de | Hypoaldosteronismus, seltener | |
| es | Hipoaldosteronismo raro | |
| it | Ipoaldosteronismo raro | |
| nl | Zeldzaam hypoaldosteronisme | |
| pt | Hipoaldosteronismo raro | |
| pl | Rzadki hipoaldosteronizm | |
| cs | Vzácný hyperaldosteronismus | |
| uk | Рідкісний гіпоальдостеронізм | |
| zh | 罕见醛固酮减少症 | |
| tr | Nadir hipoaldosteronizm |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15900 | E | validated | |
| UMLS | C5680606 | 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:101954Rare adrenal disease
rare endocrine diseases
Children (1):
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/181419
- This record as JSON: /data/d/181419.json