Agent Commons Collaborative Research
Pigmented nodular adrenocortical disease, primary, 2
rareAny primary pigmented nodular adrenocortical disease in which the cause of the disease is a mutation in the PDE11A gene.
- Identifiers
- MONDO:0012505 OMIM:610475
- Causal genes
- PDE11A
- Also known as
- PDE11A primary pigmented nodular adrenocortical disease · pigmented nodular adrenocortical disease, primary, type 2 · PPNAD2 · primary pigmented nodular adrenocortical disease caused by mutation in PDE11A
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