Familial hyperaldosteronism type 3 is an autosomal dominant disorder caused by mutations of the calcium channel genes, CACNA1D and CACNA1H.
Hyperaldosteronism | ||||
Conn syndrome | ||||
Glucocorticoid triggered hypertension | ||||
Hyperaldosteronism type 1 | ||||
Hyperaldosteronism type 2 | ||||
Hyperaldosteronism type 3 | ||||
Hyperaldosteronism type 4 | ||||
CACNA1D | ||||
CACNA1H | ||||
1. |
Scholl UI et al. (2013) Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism. |
2. |
OMIM.ORG article Omim 615474 |