{coronary artery disease} Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. (Human Disease Ontology, DOID_3393)
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Genes

1 genes associated with the {coronary artery disease} phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
TERT telomerase reverse transcriptase