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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