myocardial infarction Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Xref MGI. (Human Disease Ontology, DOID_5844)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001658
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Genes

11 genes associated with the myocardial infarction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCA1 ATP-binding cassette, sub-family A (ABC1), member 1
ABCC6 ATP-binding cassette, sub-family C (CFTR/MRP), member 6
CBS cystathionine-beta-synthase
CYP27A1 cytochrome P450, family 27, subfamily A, polypeptide 1
ENPP1 ectonucleotide pyrophosphatase/phosphodiesterase 1
GLA galactosidase, alpha
JAK2 Janus kinase 2
LMNA lamin A/C
LPL lipoprotein lipase
MYH9 myosin, heavy chain 9, non-muscle
SH2B3 SH2B adaptor protein 3