- OMIM ID
-
202010
- OMIM term:
- ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASE DEFICIENCY
- Alternative terms:
-
ADRENAL HYPERPLASIA IV
STEROID 11-BETA-HYDROXYLASE DEFICIENCY
11-@BETA-HYDROXYLASE DEFICIENCY
ADRENAL HYPERPLASIA, HYPERTENSIVE FORM
P450C11B1 DEFICIENCY
- (∗) Location:
- 8q24.3
- (†) Associated OMIM genes:
- CYP11B1
- (‡) Associated MGI genes:
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