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