M49
Details
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Charcot-Marie-Tooth disease
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Déjérine-Sottas disease
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Hereditary motor and sensory neuropathy, types I-IV
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Hypertrophic neuropathy of infancy
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Peroneal muscular atrophy (axonal type) (hypertrophic type)
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Roussy-Levy syndrome
- M49.8
Spondylopathy in diseases classified elsewhere
- M49.80
Spondylopathy in diseases classified elsewhere site unspecified
- M49.81
Spondylopathy in diseases classified elsewhere occipito-atlanto-axial region
- M49.82
Spondylopathy in diseases classified elsewhere cervical region
- M49.83
Spondylopathy in diseases classified elsewhere cervicothoracic region
- M49.84
Spondylopathy in diseases classified elsewhere thoracic region
- M49.85
Spondylopathy in diseases classified elsewhere thoracolumbar region
- M49.86
Spondylopathy in diseases classified elsewhere lumbar region
- M49.87
Spondylopathy in diseases classified elsewhere lumbosacral region
- M49.88
Spondylopathy in diseases classified elsewhere sacral and sacrococcygeal region
- M49.89
Spondylopathy in diseases classified elsewhere multiple sites in spine