Hyperaldosteronism, familial, type iv

Preferred Label : Hyperaldosteronism, familial, type iv;

Symbol : HALD4;

CISMeF acronym : HALD4;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Fh iv; Aldosteronism, primary, and hypertension;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the calcium channel, voltage-dependent, T type, alpha-1H subunit gene (CACNA1H, 607904.0007);

Laboratory abnormalities : Low renin levels; Elevated aldosterone levels;

Prefixed ID : #617027;

Details

Origin ID

617027;

UMLS CUI

C4310756;

Genes related to phenotype
- Calcium channel, voltage-dependent, t type, alpha-1h subunit [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Hypertension [HPO term]
ORDO concept(s)
- Familial hyperaldosteronism type IV [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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