DisGeNET - a database of gene-disease associations

Source: LHGDN

Disease: Glycogen Storage Disease ×

Gene: PYGM ×

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:	5837
Gene Symbol:	PYGM

PYGM

CUI:	C0017919
Disease:	Glycogen Storage Disease

Glycogen Storage Disease

0.330

GeneticVariation

LHGDN

McArdle disease: molecular genetic update.

2007