memory impairment Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An impairment of memory as manifested by a reduced ability to remember things such as dates and names, and increased forgetfulness. (Human Phenotype Ontology, HP_0002354)
Similar Terms
Downloads & Tools

Genes

7 genes associated with the disease memory impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
APOE apolipoprotein E
AR androgen receptor
BDNF brain-derived neurotrophic factor
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
KL klotho
NOS3 nitric oxide synthase 3 (endothelial cell)
PRNP prion protein