DisGeNET - a database of gene-disease associations

Source: LHGDN

Disease: Inclusion Body Myositis (disorder) ×

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:	C0238190
Disease:	Inclusion Body Myositis (disorder)

Inclusion Body Myositis (disorder)

0.040

GeneticVariation

LHGDN

Apolipoprotein epsilon alleles in sporadic inclusion body myositis: a reappraisal.

2008