DisGeNET - a database of gene-disease associations

Source: LHGDN

Disease: Fibrosis ×

Gene: MBL2 ×

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:	4153
Gene Symbol:	MBL2

MBL2

CUI:	C0016059
Disease:	Fibrosis

Fibrosis

0.020

GeneticVariation

LHGDN

Serum MBL levels were adversely associated with progression to fibrosis (p = 0.037).

2008

Entrez Id:	4153
Gene Symbol:	MBL2

MBL2

CUI:	C0016059
Disease:	Fibrosis

Fibrosis

0.020

GeneticVariation

LHGDN

Mannose-binding lectin in chronic hepatitis B virus infection.

2005