MYL4, myosin light chain 4, 4635

N. diseases: 26; N. variants: 5
Disease: ATRIAL FIBRILLATION, FAMILIAL, 18 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4310636
Disease: ATRIAL FIBRILLATION, FAMILIAL, 18
ATRIAL FIBRILLATION, FAMILIAL, 18 		0.500 GeneticVariation disease UNIPROT A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation. 27066836 2016
CUI: C4310636
Disease: ATRIAL FIBRILLATION, FAMILIAL, 18
ATRIAL FIBRILLATION, FAMILIAL, 18 		0.500 Biomarker disease CTD_human