Pigmented nodular adrenocortical disease, primary, 3

MONDO:0013616

Any primary pigmented nodular adrenocortical disease in which the cause of the disease is a mutation in the PDE8B gene.

Also known as: PDE8B primary pigmented nodular adrenocortical disease, pigmented nodular adrenocortical disease, primary, 3, pigmented nodular adrenocortical disease, primary, type 3, primary pigmented nodular adrenocortical disease caused by mutation in PDE8B, Cushing syndrome, adrenal, due to PPNAD3, PPNAD3

2 clinical trials for this condition and its sub-types, 0 tagged with Pigmented nodular adrenocortical disease, primary, 3 itself.

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↑ Primary pigmented nodular adrenocortical disease (2)

Including sub-types (2) Tagged with Pigmented nodular adrenocortical disease, primary, 3 (0)

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