DisGeNET - a database of gene-disease associations

Source: LHGDN

Disease: Lymphoma ×

Gene: MSH2 ×

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:	4436
Gene Symbol:	MSH2

MSH2

CUI:	C0024299
Disease:	Lymphoma

Lymphoma

0.200

GeneticVariation

LHGDN

In this study, exon 13 of the hMSH2 gene was analyzed in different neoplasias, leukemias and lymphomas.

12688322

2003

Entrez Id:	4436
Gene Symbol:	MSH2

MSH2

CUI:	C0024299
Disease:	Lymphoma

Lymphoma

0.200

Biomarker

LHGDN

Early onset brain tumor and lymphoma in MSH2-deficient children.

12549480

2003