familial hyperreninemic hypoaldosteronism type 1 (Q56014440)
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human disease
- FHHA1
- CMO I
- Aldosterone synthase deficiency
- CMO II
- Corticosterone methyloxidase deficiency type I
- 18-hydroxylase deficiency
- 18-oxidase deficiency
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | familial hyperreninemic hypoaldosteronism type 1 |
human disease |
|
Statements
1 reference
Identifiers
1 reference
1 reference
1 reference