peripheral vascular disease Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A vascular disease that is characterized by obstruction of larger arteries not within the coronary, aortic arch vasculature, or brain. (Human Disease Ontology, DOID_341)
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12 genes involed in the disease peripheral vascular disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ABCA1 ATP-binding cassette, sub-family A (ABC1), member 1
APOA1 apolipoprotein A-I
APOB apolipoprotein B
APOBR apolipoprotein B receptor
CETP cholesteryl ester transfer protein, plasma
F12 coagulation factor XII (Hageman factor)
ITPKC inositol-trisphosphate 3-kinase C
LDLRAP1 low density lipoprotein receptor adaptor protein 1
LPA lipoprotein, Lp(a)
RSAD2 radical S-adenosyl methionine domain containing 2
SCN9A sodium channel, voltage gated, type IX alpha subunit
SERPING1 serpin peptidase inhibitor, clade G (C1 inhibitor), member 1