MYL3, myosin light chain 3, 4634

N. diseases: 37; N. variants: 17
Disease: CARDIOMYOPATHY, INFANTILE HYPERTROPHIC ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2748884
Disease: CARDIOMYOPATHY, INFANTILE HYPERTROPHIC
CARDIOMYOPATHY, INFANTILE HYPERTROPHIC 		0.010 GeneticVariation disease BEFREE Infantile hypertrophic cardiomyopathy associated with a novel MYL3 mutation. 23594557 2013