DisGeNET - a database of gene-disease associations

Source: GENOMICS_ENGLAND

Disease: Cardiomyopathies ×

Gene: MYOCD ×

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:	93649
Gene Symbol:	MYOCD

MYOCD

CUI:	C0878544
Disease:	Cardiomyopathies

Cardiomyopathies

0.300

Biomarker

GENOMICS_ENGLAND

Loss-of-function variants in myocardin cause congenital megabladder in humans and mice.

31513549

2019

Entrez Id:	93649
Gene Symbol:	MYOCD