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 2 Late-onset cerebellar ataxia
 * G11.3 Cerebellar ataxia with defective DNA repair
 * Ataxia telangiectasia [Louis-Bar]
 * Excludes2: Cockayne's syndrome (Q87.1)
 * other disorders of purine and pyrimidine metabolism (E79.-)
 * xeroderma pigmentosum (Q82.1)
 * G11.4 Hereditary spastic paraplegia
 * G11.8 Other hereditary ataxias
 * G11.9 Hereditary ataxia, unspecified
 * Hereditary cerebellar ataxia NOS
 * Hereditary cerebellar degeneration
 * Hereditary cerebellar disease
 * Hereditary cerebellar syndrome

G12 Spinal muscular atrophy and related syndromes

 * G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
 * G12.1 Other inherited spinal muscular atrophy
 * Adult form spinal muscular atrophy
 * Childhood form, type II spinal muscular atrophy
 * Distal spinal muscular atrophy
 * Juvenile form, type III spinal muscular atrophy [Kugelberg-Welander]
 * Progressive bulbar palsy of childhood [Fazio-Londe]
 * Scapuloperoneal form spinal muscular atrophy
 * G12.2 Motor neuron disease
 * G12.20 Motor neuron disease, unspecified
 * G12.21 Amyotrophic lateral sclerosis
 * Progressive spinal muscle atrophy
 * G12.22 Progressive bulbar palsy
 * G12.29 Other motor neuron disease
 * Familial motor neuron disease
 * Primary lateral sclerosis
 * G12.8 Other spinal muscular atrophies and related syndromes
 * G12.9 Spinal muscular atrophy, unspecified

G13 Systemic atrophies primarily affecting central nervous system in diseases classified elsewhere

 * G13.0 Paraneoplastic neuromyopathy and neuropathy
 * Carcinomatous neuromyopathy
 * Sensorial paraneoplastic neuropathy [Denny Brown]
 * Code first underlying neoplasm (C00-D48)
 * G13.1 Other systemic atrophy primarily affecting central nervous system in neoplastic disease
 * Paraneoplastic limbic encephalopathy
 * Code first underlying neoplasm (C00-D48)
 * G13.8 Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere
 * Code first underlying disease, such as:
 * cerebellar