dementia; Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A cognitive disorder resulting from a loss of brain function affecting memory, thinking, language, judgement and behavior. (Human Disease Ontology, DOID_1307)
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7 genes associated with the disease dementia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
APOE apolipoprotein E
CCL2 chemokine (C-C motif) ligand 2
DCUN1D1 DCN1, defective in cullin neddylation 1, domain containing 1
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
VEGFA vascular endothelial growth factor A