Pigmented nodular adrenocortical disease, primary, 4
MONDO:0014359Any primary pigmented nodular adrenocortical disease in which the cause of the disease is a mutation in the PRKACA gene.
Also known as: Cushing syndrome, ACTH-independent adrenal, somatic, PRKACA primary pigmented nodular adrenocortical disease, pigmented nodular adrenocortical disease, primary, 4, pigmented nodular adrenocortical disease, primary, type 4, primary pigmented nodular adrenocortical disease caused by mutation in PRKACA, ACTH-independent adrenal Cushing syndrome, somatic, Cushing syndrome, adrenal, due to Ppnad4, PPNAD4
8 clinical trials for this condition and its sub-types.
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