Hyperreninemic hypoaldosteronism, familial, 2

Preferred Label : Hyperreninemic hypoaldosteronism, familial, 2;

CISMeF acronym : FHHA2;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : FHHA2;

Prefixed ID : %606984;

Details

Origin ID

606984;

UMLS CUI

C1846990;

Automatic exact mappings (from CISMeF team)
- Familial hypoaldosteronism [ORDO Disease]
Currated CISMeF NLP mapping
- Familial hyperreninaemic hypoaldosteronism type 2 [ICD-11 More detail]
- Familial hyperreninemic hypoaldosteronism type 2 [ORDO Disease]
- Familial hyperreninemic hypoaldosteronism type 2 (disorder) [SNOMED CT concept]
- hyperreninemic hypoaldosteronism, familial, 2 [MeSH concept]
- hyperreninemic hypoaldosteronism, familial, 2 [MeSH Supplementary Concept]
ORDO concept(s)
- Familial hyperreninemic hypoaldosteronism type 2 [ORDO Disease]
- Familial hypoaldosteronism [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial hyperreninemic hypoaldosteronism type 2 [ORDO Disease]
- hyperreninemic hypoaldosteronism, familial, 2 [MeSH Supplementary Concept]
- hyperreninemic hypoaldosteronism, familial, 2 [MeSH concept]

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