angina pectoris Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Paroxysmal chest pain that occurs with exertion or stress and is related to myocardial ischemia. (Human Phenotype Ontology, HP_0001681)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001681
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Genes

6 genes associated with the angina pectoris phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCC6 ATP-binding cassette, sub-family C (CFTR/MRP), member 6
APOE apolipoprotein E
CYP27A1 cytochrome P450, family 27, subfamily A, polypeptide 1
GLA galactosidase, alpha
LIPC lipase, hepatic
LMNA lamin A/C