|Dataset||ClinVar Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||An autosomal dominant disease characterized by myxomas, spotty pigmentation of the skin and endocrine overactivity. (Human Disease Ontology, DOID_0050471)|
|Downloads & Tools|
1 genes associated with the Carney complex, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
|PRKAR1A||protein kinase, cAMP-dependent, regulatory, type I, alpha|