ORPHA:231637
Rare surgically correctable form of primary aldosteronism
- Type
- Category
- Group
- Group of disorders
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
A rare primary hyperaldosteronism characterized by unilateral aldosterone hypersecretion and renin suppression, associated with varying degrees of hypertension and hypokalemia.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare surgically correctable form of primary aldosteronism | |
| fr | Hyperaldostéronisme primitif rare traitable chirurgicalement | |
| de | Seltene chirurgisch korrigierbar Formen des primären Hyperaldosteronismus | |
| es | Hiperaldosteronismo primario raro corregible por cirugía | |
| it | Iperaldosteronismo primitivo raro corregibile chirurgicamente | |
| nl | Zeldzame chirurgisch corrigeerbare vorm van primair aldosteronisme | |
| pt | Hiperaldosteronismo primário raro corrigível cirurgicamente | |
| pl | Rzadka forma pierwotnego aldosteronizmu możliwa do korekcji chirurgicznej | |
| cs | Vzácná chirurgicky odstranitelná forma primárního aldosteronismu | |
| uk | Рідкісна форма первинного альдостеронізму, що піддається хірургічній корекції | |
| zh | 罕见手术可纠正型原发性醛固酮症 | |
| tr | Primer aldosteronizmin nadir cerrahi olarak düzeltilebilir formu |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16507 | E | validated | |
| UMLS | C5680925 | 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:181415Rare primary hyperaldosteronism
rare endocrine diseases
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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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/231637
- This record as JSON: /data/d/231637.json