• Heart and skeletal muscle involvement, autosomal dominant includes 11 Gene(s)

• FSHD (FSHD1 phenocopies and FSHD2) includes 6 Gene(s)

• Congenital myasthenic syndrome (CMS) includes 34 Gene(s)

• Muscle weakness (myopathy, muscular dystrophy) - comprehensive panel includes 214 Gene(s)

• Duchenne / Becker-Kiener muscular dystrophy includes 1 Gene(s)

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

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

• Muscle weakness, early-onset, Floppy Infant includes 130 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 includes 29 Gene(s)

• Mitochondrial Myopathy, adult-onset includes 14 Gene(s)

• Muscle weakness, adult-onset includes 105 Gene(s)

• Myopathy, myofibrillar includes 9 Gene(s)

• Inclusion body myopathy/distal 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 30 Gene(s)

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

• RYR1 gene includes 1 Gene(s)

• Neonatal Apneas includes 13 Gene(s)

• Scapuloperoneal syndrome includes 9 Gene(s)

• SMN1 point mutation analysis includes 1 Gene(s)