Carney complex, type 1 Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An autosomal dominant disease characterized by myxomas, spotty pigmentation of the skin and endocrine overactivity. (Human Disease Ontology, DOID_0050471)
External Link http://www.omim.org/entry/160980
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Genes

1 genes associated with the Carney complex, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha