Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 348
Gene Symbol: APOE
APOE
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II
0.060 GeneticVariation BEFREE The association study of lipid metabolism gene polymorphisms with AMD identifies a protective role for APOE-E2 allele in the wet form in a Northern Spanish population. 31654486

2019

Entrez Id: 348
Gene Symbol: APOE
APOE
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II
0.060 GeneticVariation BEFREE The current study was conducted to investigate the association of Apolipoprotein E (ApoE) polymorphism with the treatment response to ranibizumab for exudative AMD. 26398858

2016

Entrez Id: 348
Gene Symbol: APOE
APOE
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II
0.060 Biomarker BEFREE Apolipoprotein E Isoforms and AMD. 26427386

2016

Entrez Id: 348
Gene Symbol: APOE
APOE
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II
0.060 Biomarker BEFREE Other murine models target genes relevant to AMD, including inflammatory genes such as Cfh(-/-), Ccl2(-/-), Ccr2(-/-), Cx3cr1(-/-), and Ccl2(-/-)/cx3cr1(-/-), oxidative stress associated genes such as Sod1(-/-) and Sod2 knockdown, metabolic pathway genes such as neprilysin(-/-) (amyloid beta), transgenic mcd/mcd (cathepsin D), Cp(-/-)/Heph(-/Y) (ferroxidase ceruloplasmin/hepaestin, iron metabolism), and transgenic ApoE4 on high fat and high cholesterol diet (lipid metabolism). 20206286

2010

Entrez Id: 348
Gene Symbol: APOE
APOE
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II
0.060 Biomarker BEFREE No significant association was observed between neovascular AMD and APOE or ELOVL4. 17210851

2007

Entrez Id: 348
Gene Symbol: APOE
APOE
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II
0.060 GeneticVariation BEFREE To study the genotypes, allelic frequencies, and polymorphisms of apolipoprotein E (Apo E) in unrelated Japanese patients with polypoidal choroidal vasculopathy (PCV) or exudative age-related macular degeneration (AMD) and control subjects without macular degeneration. 15488782

2004