carney complex Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description An autosomal dominant disease characterized by myxomas, spotty pigmentation of the skin and endocrine overactivity. (Human Disease Ontology, DOID_0050471)
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Genes

1 genes involed in the disease carney complex from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

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