Also Known As
LGMD1AMYOT autosomal dominant distal myopathyMYOT autosomal dominant limb-girdle muscular dystrophyautosomal dominant distal myopathy caused by mutation in MYOTautosomal dominant limb-girdle muscular dystrophy caused by mutation in MYOTautosomal dominant limb-girdle muscular dystrophy type 1Adistal myotilinopathylimb-girdle muscular dystrophy due to myotilin deficiencymuscular dystrophy limb-girdle type 1Amyofibrillar myopathy type 3myopathy, myofibrillar, type 3myotilinopathyproximal muscular dystrophy type 1Aspheroid body myopathyLGMD1MFM3autosomal dominant spheroid body myopathylimb-girdle muscular dystrophy type 1Amuscular dystrophy, limb-girdle, type 1Amuscular dystrophy, proximal, type 1Amyopathy, myofibrillar, 3myopathy, myofibrillar, myotilin-relatedmyopathy, spheroid body