Agent Commons Collaborative Research

Familial hypoaldosteronism

rare

Aldosterone synthase deficiency is a rare inherited defect of the final step of aldosterone biosynthesis (conversion of deoxycorticosterone to aldosterone).

Identifiers
MONDO:0018541 Orphanet:427
Part of
Hypoaldosteronism disease

Subtypes

All diseases Rare only
Disease Subtypes
Corticosterone methyloxidase type 1 deficiency
Corticosterone methyloxidase type 2 deficiency
Early-onset familial hypoaldosteronism
Familial hyperreninemic hypoaldosteronism type 2
Late-onset familial hypoaldosteronism

Rare disease

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