- Muscular dystrophy, including
- autosomal recessive, childhood type
- benign [Becker]
- benign scapuloperoneal with early contractures [Emery-Dreifuss]
- distal
- facioscapulohumeral
- limb-girdle
- ocular
- oculopharyngeal
- scapuloperoneal
- Duchenne
- INCLUDES: congenital muscular dystrophy, congenital myopathy, including:
- central core disease
- minicore disease
- multicore disease
- Fibre-type disproportion
- myotubular (centronuclear)
- nemaline
- unspecified hereditary myopathy
- Drug-induced/Alcoholic/toxic agent/inflammatory myopathy
- Myopathy in infectious/parasitic disease
- Myopathy in endocrine disease
- hyperparathyroidism
- hypoparathyroidism
- Thyrotoxic myopathy
- Myopathy in metabolic disease
- glycogen storage disease
- lipid storage disorders
- Periodic paralysis, including:
- Periodic paralysis (familial)
- hyperkalaemic
- hypokalaemic
- myotonic
- normokalaemic
- Myopathy in other diseases:
- rheumatoid arthritis
- scleroderma
- sicca syndrome [Sjögren]
- systemic lupus erythematosus
- Paraneoplastic neuromyopathy
- Carcinomatous neuromyopathy