Version May 2024
| Myopathies |
| Muscular dystrophies |
| Dystrophinopathies - Duchenne and Becker dystrophies |
| Limb-girdle, Emery-Dreifuss, facioscapulohumeral, congenital, autosomal recessive, and myotonic muscular dystrophies |
| Congenital and metabolic myopathies (eg, acid maltase deficiency, alpha glucosidase deficiency) |
| Inflammatory myopathies (eg, polymyositis) |
| Diseases of myoneural junction (eg, myasthenia gravis) |
| Neurological disorders |
| Spinal muscular atrophies |
| Motor neuron diseases (eg, amyotrophic lateral sclerosis, poliomyelitis, postpoliomyelitis) |
| Hereditary sensory motor neuropathies |
| Neuropathies (eg, phrenic neuropathies, Guillain-Barré syndrome) |
| Multiple sclerosis |
| Toxic tetraplegia (eg, pancuronium bromide, botulism) |
| Traumatic and other myelopathies (eg, spinal cord injury) |
| Congenital hypoventilation syndromes |
| Other pathology |
| Kyphoscoliosis |
| Osteogenesis imperfecta |
| Morbid obesity hypoventilation |
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