- OMIM ID
-
203400
- OMIM term:
- CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY
- Alternative terms:
-
CMO I DEFICIENCY
ALDOSTERONE DEFICIENCY I
HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1A
ALDOSTERONE DEFICIENCY DUE TO DEFECT IN STEROID 18-HYDROXYLASE
18-@HYDROXYLASE DEFICIENCY
STEROID 18-@HYDROXYLASE DEFICIENCY
- (∗) Location:
- 8q24.3
- (†) Associated OMIM genes:
- CYP11B2
- (‡) Associated MGI genes:
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