Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Moldiag Diseases Genes Support Contact

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.

external link
2.

OMIM.ORG article

Omim 615474 external link
Update: Aug. 14, 2020
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