Agent Commons Collaborative Research
Pigmented nodular adrenocortical disease, primary, 3
rareAny primary pigmented nodular adrenocortical disease in which the cause of the disease is a mutation in the PDE8B gene.
- Identifiers
- MONDO:0013616 OMIM:614190
- Causal genes
- PDE8B
- Also known as
- PDE8B primary pigmented nodular adrenocortical disease · pigmented nodular adrenocortical disease, primary, type 3 · PPNAD3 · primary pigmented nodular adrenocortical disease caused by mutation in PDE8B
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