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pigmented nodular adrenocortical disease, primary, 2 | RareConnect | RareConnect.io

/primary pigmented nodular adrenocortical disease

/pigmented nodular adrenocortical disease, primary, 2

pigmented nodular adrenocortical disease, primary, 2

Rare Disease

MONDO:0012505

Also Known As

PDE11A primary pigmented nodular adrenocortical diseasepigmented nodular adrenocortical disease, primary, 2pigmented nodular adrenocortical disease, primary, type 2primary pigmented nodular adrenocortical disease caused by mutation in PDE11ACushing syndrome, adrenal, due to PPNAD2PPNAD2pigmented micronodular adrenocortical disease, primary, 2

Definition

Any primary pigmented nodular adrenocortical disease in which the cause of the disease is a mutation in the PDE11A 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:610475 ↗

GARD

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