Pigmented nodular adrenocortical disease, primary, 2

Any primary pigmented nodular adrenocortical disease in which the cause of the disease is a mutation in the PDE11A gene.

Also known as: PDE11A primary pigmented nodular adrenocortical disease, pigmented nodular adrenocortical disease, primary, 2, pigmented nodular adrenocortical disease, primary, type 2, primary pigmented nodular adrenocortical disease caused by mutation in PDE11A, Cushing syndrome, adrenal, due to PPNAD2, PPNAD2, pigmented micronodular adrenocortical disease, primary, 2

8 clinical trials for this condition and its sub-types.