DisGeNET - a database of gene-disease associations

Source: LHGDN

Disease: Hypertrophic Cardiomyopathy ×

Gene: MYOZ2 ×

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:	51778
Gene Symbol:	MYOZ2

MYOZ2

CUI:	C0007194
Disease:	Hypertrophic Cardiomyopathy

Hypertrophic Cardiomyopathy

0.340

GeneticVariation

LHGDN

Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy.

2007