- OMIM ID
-
201910
- OMIM term:
- ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY
- Alternative terms:
-
ADRENAL HYPERPLASIA III
21-@HYDROXYLASE DEFICIENCY
CYP21 DEFICIENCY
CONGENITAL ADRENAL HYPERPLASIA 1; CAH1 HYPERANDROGENISM, NONCLASSIC TYPE, DUE TO 21-HYDROXYLASE DEFICIENCY, INCLUDED
- (∗) Location:
- 6p21.33
- (†) Associated OMIM genes:
- CYP21A2
- (‡) Associated MGI genes:
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