All diseases

OMIM ID
610475
OMIM term:
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2; PPNAD2
Alternative terms:
PIGMENTED MICRONODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2
CUSHING SYNDROME, ADRENAL, DUE TO PPNAD2
(∗) Location:
2q31.2  
(†) Associated OMIM genes:
PDE11A  
(‡) Associated MGI genes:

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