ORPHA:444916
Pseudohypoaldosteronism
- 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Pseudohypoaldosteronism | |
| fr | Pseudohypoaldostéronisme | |
| de | Pseudohypoaldosteronismus | |
| es | Pseudohipoaldosteronismo | |
| it | Pseudoipoaldosteronismo | |
| nl | Pseudohypoaldosteronisme | PHA |
| pt | Pseudo-hiperaldosteronismo | |
| pl | Pseudohipoaldosteronizm | |
| cs | Pseudohypoaldosteronismus | |
| uk | Псевдогіпоальдостеронізм | |
| zh | 假性低醛固酮增多症 | |
| tr | Psödohipoaldosteronizm |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0018638 | E | validated | |
| MONDO | 18638 | E | validated | |
| MeSH | D011546 | E | validated | |
| UMLS | C0033805 | E | validated | |
| MedDRA | 10080593 | 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:93603Rare renal tubular disease
rare renal 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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/444916
- This record as JSON: /data/d/444916.json