Myopathy
Centronuclear myopathy
Congenital myopathy
Mitochondrial myopathy
Nemaline myopathy
Hereditary inclusion body myopathy
Distal myopathy
Bethlem myopathy
Multi/minicore myopathy
X-linked myotubular myopathy
Statin-associated autoimmune myopathy
Desmin-related myofibrillar myopathy
Inflammatory myopathy
Brody myopathy
Metabolic myopathy
Thyrotoxic myopathy
Sporadic late-onset nemaline myopathy
Acquired non-inflammatory myopathy
Oculopharyngodistal myopathy
Autophagic vacuolar myopathy
Equine polysaccharide storage myopathy
Myopathy, X-linked, with excessive autophagy
Equine atypical myopathy
Compton-North congenital myopathy
Hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis
ISCU
Ullrich congenital muscular dystrophy
Critical illness polyneuropathy
MELAS syndrome
STAC3
Myositis
Inclusion body myositis
Myosin-heavy chain myopathy
Desmin
Carey Fineman Ziter syndrome
Neutral lipid storage disease
Central core disease
Megaduodenum
Nutritional muscular dystrophy
Titin
Sengers syndrome
Marinesco–Sjögren syndrome
Exercise therapy for idiopathic inflammatory myopathies
Glycogen storage disease type V
Mitochondrial disease
Myotonic dystrophy
Limb–girdle muscular dystrophy
Carnitine palmitoyltransferase II deficiency
Primrose syndrome
Barth syndrome
Dilated cardiomyopathy
Short-chain acyl-coenzyme A dehydrogenase deficiency
Diabetes