MYH1—autoimmune/inflammatory myopathies;MYH2—congenital myopathy with ophthalmoplegia;MYH3 → distal arthrogryposis syndromes;MYH7—cardiomyopathies and skeletal myopathies (Laing distal, myosin storage). This evidence concerns the gene MYH2 and Skeletal myopathy.