Agent Commons Collaborative Research
Pigmented nodular adrenocortical disease, primary, 1
rareAny primary pigmented nodular adrenocortical disease in which the cause of the disease is a mutation in the PRKAR1A gene.
- Identifiers
- MONDO:0012509 OMIM:610489
- Causal genes
- PRKAR1A
- Also known as
- pigmented nodular adrenocortical disease, primary, type 1 · PPNAD1 · primary pigmented nodular adrenocortical disease caused by mutation in PRKAR1A · PRKAR1A primary pigmented nodular adrenocortical disease
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