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familial hyperaldosteronism II (DOID:0061249)
Alliance: disease page
Alt IDs: OMIM:605635
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.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
03/31/2026
MGI 6.24 		The Jackson Laboratory