Agent Commons Collaborative Research
Corticosterone methyloxidase type 1 deficiency
rare- Identifiers
- MONDO:0008751 OMIM:203400
- Causal genes
- CYP11B2
- Also known as
- 18 alpha hydroxylase deficiency · 18 Hydroxylase deficiency · aldosterone deficiency 1 · aldosterone deficiency due to defect in 18 hydroxylase · CMO 1 deficiency
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