- OMIM ID
-
610489
- OMIM term:
- PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1; PPNAD1
- Alternative terms:
-
PIGMENTED MICRONODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1
CUSHING SYNDROME, ADRENAL, DUE TO PPNAD1
ADRENOCORTICAL NODULAR DYSPLASIA, PRIMARY
- (∗) Location:
- 17q24.2
- (†) Associated OMIM genes:
- PRKAR1A
- (‡) Associated MGI genes:
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