Pigmented nodular adrenocortical disease, primary, 1

Any primary pigmented nodular adrenocortical disease in which the cause of the disease is a mutation in the PRKAR1A gene.

Also known as: PRKAR1A primary pigmented nodular adrenocortical disease, pigmented nodular adrenocortical disease, primary, 1, pigmented nodular adrenocortical disease, primary, type 1, primary pigmented nodular adrenocortical disease caused by mutation in PRKAR1A, Cushing syndrome, adrenal, due to PPNAD1, PPNAD1, adrenocortical nodular dysplasia, primary, pigmented micronodular adrenocortical disease, primary, 1

3 clinical trials for this condition and its sub-types, 1 tagged with Pigmented nodular adrenocortical disease, primary, 1 itself.