- OMIM ID
-
202110
- OMIM term:
- ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 17-ALPHA-HYDROXYLASE DEFICIENCY
- Alternative terms:
-
ADRENAL HYPERPLASIA V
17-@ALPHA-HYDROXYLASE DEFICIENCY 17,20-@LYASE DEFICIENCY, ISOLATED, INCLUDED
17-@ALPHA-HYDROXYLASE/17,20-LYASE DEFICIENCY, COMBINED COMPLETE, INCLUDED
17-@ALPHA-HYDROXYLASE/17,20-LYASE DEFICIENCY, COMBINED PARTIAL, INCLUDED
- (∗) Location:
- 10q24.32
- (†) Associated OMIM genes:
- CYP17A1
- (‡) Associated MGI genes:
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