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pigmented nodular adrenocortical disease, primary, 4 | RareConnect | RareConnect.io

/primary pigmented nodular adrenocortical disease

/pigmented nodular adrenocortical disease, primary, 4

pigmented nodular adrenocortical disease, primary, 4

Rare Disease

MONDO:0014359

Also Known As

Cushing syndrome, ACTH-independent adrenal, somaticPRKACA primary pigmented nodular adrenocortical diseasepigmented nodular adrenocortical disease, primary, 4pigmented nodular adrenocortical disease, primary, type 4primary pigmented nodular adrenocortical disease caused by mutation in PRKACAACTH-independent adrenal Cushing syndrome, somaticCushing syndrome, adrenal, due to Ppnad4PPNAD4chromosome 19P13 Duplication syndrome

Definition

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

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:615830 ↗

GARD

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