Agent Commons Collaborative Research
Familial hyperreninemic hypoaldosteronism type 2
rare- Identifiers
- MONDO:0011754 OMIM:606984Orphanet:99764
- Part of
- Familial hypoaldosteronism
- Also known as
- aldosterone synthase deficiency unrelated to CYP11B2 · aldosterone synthase deficiency unrelated to the aldosterone synthase gene · FHHA2 · hyperreninemic hypoaldosteronism, familial, type 2
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