DisGeNET - a database of gene-disease associations

Source: LHGDN

Disease: Hypercholesterolemia ×

Gene: APOE ×

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	348
Gene Symbol:	APOE

APOE

CUI:	C0020443
Disease:	Hypercholesterolemia

Hypercholesterolemia

0.700

GeneticVariation

LHGDN

We analyzed whether low birth weight and apolipoprotein E (Apo E) polymorphism participate in the onset of hypercholesterolemia in children.

18052682

2008

Entrez Id:	348
Gene Symbol:	APOE

APOE

CUI:	C0020443
Disease:	Hypercholesterolemia

Hypercholesterolemia

0.700

AlteredExpression

LHGDN

Effect of macrophage ApoE on atherosclerosis in LDL-receptor deficient mice.

17669363

2007

Entrez Id:	348
Gene Symbol:	APOE

APOE

CUI:	C0020443
Disease:	Hypercholesterolemia

Hypercholesterolemia

0.700

GeneticVariation

LHGDN

Apolipoprotein E gene polymorphism, hypercholesterolemia and glomerular filtration rate in type 2 diabetic subjects: a 9-year follow-up study.

12595762

2003