Term Name: familial hyperaldosteronism II
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.
Ontology: Human Disease [DOID:0061249]   ( DOID:0061249 )

Relationships
is a type of: autosomal dominant disease familial hyperaldosteronism