• Glycogen storage disease type II - GAA includes 1 Gene(s)

• McArdle Disease I PYGM includes 1 Gene(s)

• FSHD2 and phenocopies includes 7 Gene(s)

• Congenital myasthenic syndrome (CMS) includes 36 Gene(s)

• Muscle weakness (myopathy, muscular dystrophy) - comprehensive panel includes 222 Gene(s)

• CPEO (Chronic progressive external ophthalmoplegia), nuclear includes 12 Gene(s)

• Muscular dystrophy, Duchenne / Becker (Dystrophinopathy) includes 1 Gene(s)

• Muscular dystrophy, congenital, dystroglycanopathy includes 14 Gene(s)

• Muscular dystrophy, type Emery-Dreifuss includes 4 Gene(s)

• Muscle weakness, early-onset, Floppy Infant includes 131 Gene(s)

• Muscular dystrophy, limb-girdle - core panel includes 9 Gene(s)

• Muscular dystrophy, congenital, collagen-associated (Bethlem/Ullrich and phenocopies) includes 7 Gene(s)

• Muscular dystrophy, congenital, entire panel includes 29 Gene(s)

• CK-elevation, isolated includes 9 Gene(s)

• Myopathy, mitochondrial, nuclear genes includes 20 Gene(s)

• Myalgia, muscle cramps includes 9 Gene(s)

• Muscle weakness, adult-onset includes 106 Gene(s)

• Myopathy, myofibrillar includes 9 Gene(s)

• Myopathy, distal / Inclusion body myopathy includes 9 Gene(s)

• Muscle disease with contractures and/or rigid spine includes 26 Gene(s)

• Myopathy, congenital - nemaline / core / centronuclear includes 19 Gene(s)

• Myopathy, congenital - centronuclear includes 5 Gene(s)

• Metabolic myopathy and rhabdomyolysis includes 31 Gene(s)

• CPEO (Chronic progressive external ophthalmoplegia), nuclear genes and phenocopies includes 35 Gene(s)

• Apneas, neonatal includes 13 Gene(s)

• Muscular dystrophy, scapuloperoneal syndrome includes 9 Gene(s)