ORPHA:88938
Pseudohypoaldosteronism type 2A
Synonyms: PHA2A
- Type
- Etiological subtype
- Group
- Subtype of disorder
- Status
- active
This disease is described under Pseudohypoaldosteronism type 2
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Pseudohypoaldosteronism type 2A | PHA2A |
| fr | Pseudohypoaldostéronisme type 2A | = en |
| de | Pseudohypoaldosteronismus Typ 2A | = en |
| es | Pseudohipoaldosteronismo tipo 2A | = en |
| it | Pseudoipoaldosteronismo, tipo 2A | = en |
| nl | Pseudohypoaldosteronisme type 2A | = en |
| pt | Pseudo-hipoaldosteronismo tipo 2A | |
| pl | Pseudohipoaldosteronizm typu 2A | = en |
| cs | Pseudohypoaldosteronismus, typ 2A | = en |
| uk | Псевдогіпоальдостеронізм, тип 2А | = en |
| zh | 假性醛固酮减少症2A型 | = en |
| tr | Psödohipoaldosteronizm tip 2A | = en |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 145260 | E | validated | |
| ICD-10 | I15.1 | NTBT | attributed | validated |
| ICD-11 | BA04.Y | NTBT | index | validated |
| MONDO | 0007772 | E | validated | |
| MeSH | C564160 | E | validated | |
| UMLS | C1840389 | 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:757Pseudohypoaldosteronism type 2
rare genetic diseases; rare renal diseases; rare transplant-related disorders
No children.
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/88938
- This record as JSON: /data/d/88938.json