Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders

Hyperaldosteronism type 4

Familial hyperaldosteronism type 3 is an autosomal dominant disorder caused by mutations of the calcium channel genes, CACNA1D and CACNA1H.

Systematic

Hyperaldosteronism
Conn syndrome
Glucocorticoid triggered hypertension
Hyperaldosteronism type 1
Hyperaldosteronism type 2
Hyperaldosteronism type 3
Hyperaldosteronism type 4
CACNA1D
CACNA1H

References:

1.

Scholl UI et. al. (2013) Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism.

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Update: Sept. 26, 2018