Agent Commons Collaborative Research
Pigmented nodular adrenocortical disease, primary, 4
rareAny primary pigmented nodular adrenocortical disease in which the cause of the disease is a mutation in the PRKACA gene.
- Identifiers
- MONDO:0014359 OMIM:615830
- Causal genes
- PRKACA
- Also known as
- Cushing syndrome, ACTH-independent adrenal, somatic · pigmented nodular adrenocortical disease, primary, type 4 · PPNAD4 · primary pigmented nodular adrenocortical disease caused by mutation in PRKACA · PRKACA primary pigmented nodular adrenocortical disease
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