familial hyperaldosteronism II

Term ID

DOID:0061249

Synonyms

Definition

A familial hyperaldosteronism characterized by hypertension due to increased aldosterone, often with hypokalemia that has_material_basis_in heterozygous mutation in the CLCN2 gene on chromosome 3q27. https://pubmed.ncbi.nlm.nih.gov/29403011/

References

• MIM:605635

Ontology

Human Disease   ( DOID:0061249 )