MYOCD, myocardin, 93649

N. diseases: 79; N. variants: 7
Disease: Cardiomyopathies ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		0.300 Biomarker group GENOMICS_ENGLAND Loss-of-function variants in myocardin cause congenital megabladder in humans and mice. 31513549 2019
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		0.300 Biomarker group GENOMICS_ENGLAND Loss-of-function variants in myocardin cause congenital megabladder in humans and mice. 31513549 2019