MeSH Treeview
Query OMIM entry list
160790
MYL3
MYOSIN, LIGHT CHAIN 3, ALKALI, VENTRICULAR, SKELETAL, SLOW
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Musculoskeletal Diseases
Muscular Diseases
Nervous System Diseases
Neuromuscular Diseases
Muscular Diseases
Cardiovascular Diseases
Heart Diseases
Cardiomyopathies
Cardiomyopathy, Hypertrophic
Cardiomyopathy, Hypertrophic, Familial
Heart Valve Diseases
Aortic Valve Stenosis
Aortic Stenosis, Subvalvular
Cardiomyopathy, Hypertrophic
Ventricular Dysfunction
Ventricular Dysfunction, Left
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Cardiomyopathy, Hypertrophic, Familial
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