cerebrovascular disease Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An artery disease that is characterized by dysfunction of the blood vessels supplying the brain. (Human Disease Ontology, DOID_6713)
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11 genes associated with the disease cerebrovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
APOE apolipoprotein E
C4B complement component 4B (Chido blood group)
CYBA cytochrome b-245, alpha polypeptide
FABP2 fatty acid binding protein 2, intestinal
GP1BA glycoprotein Ib (platelet), alpha polypeptide
KRIT1 KRIT1, ankyrin repeat containing
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
NPPA natriuretic peptide A
PON1 paraoxonase 1
SELPLG selectin P ligand
SERPINA3 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 3