- OMIM ID
-
610600
- OMIM term:
- CORTICOSTERONE METHYLOXIDASE TYPE II DEFICIENCY
- Alternative terms:
-
CMO II DEFICIENCY
ALDOSTERONE DEFICIENCY II
HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1B
ALDOSTERONE DEFICIENCY DUE TO DEFICIENCY OF STEROID 18-OXIDASE
STEROID 18-OXIDASE DEFICIENCY
18-@OXIDASE DEFICIENCY
- (∗) Location:
- 8q24.3
- (†) Associated OMIM genes:
- CYP11B2
- (‡) Associated MGI genes:
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