ICD 10 Range Systemic atrophies primarily affecting the central nervous system

• 1 Huntington's disease( G10 )

• 2 Hereditary ataxia( G11 )

• 3 Congenital nonprogressive ataxia( G11.0 )

• 4 Early-onset cerebellar ataxia( G11.1 )

• 5 Early-onset cerebellar ataxia, unspecified( G11.10 )

• 6 Friedreich ataxia( G11.11 )

• 7 Other early-onset cerebellar ataxia( G11.19 )

• 8 Late-onset cerebellar ataxia( G11.2 )

• 9 Cerebellar ataxia with defective DNA repair( G11.3 )

• 10 Hereditary spastic paraplegia( G11.4 )

• 11 Hypomyelination - hypogonadotropic hypogonadism - hypodontia( G11.5 )

• 12 Leukodystrophy with vanishing white matter disease( G11.6 )

• 13 Other hereditary ataxias( G11.8 )

• 14 Hereditary ataxia, unspecified( G11.9 )

• 15 Spinal muscular atrophy and related syndromes( G12 )

• 16 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]( G12.0 )

• 17 Other inherited spinal muscular atrophy( G12.1 )

• 18 Motor neuron disease( G12.2 )

• 19 Motor neuron disease, unspecified( G12.20 )

• 20 Amyotrophic lateral sclerosis( G12.21 )

• 21 Progressive bulbar palsy( G12.22 )

• 22 Primary lateral sclerosis( G12.23 )

• 23 Familial motor neuron disease( G12.24 )

• 24 Progressive spinal muscle atrophy( G12.25 )

• 25 Other motor neuron disease( G12.29 )

• 26 Other spinal muscular atrophies and related syndromes( G12.8 )

• 27 Spinal muscular atrophy, unspecified( G12.9 )

• 28 Systemic atrophies primarily affecting central nervous system in diseases classified elsewhere( G13 )

• 29 Paraneoplastic neuromyopathy and neuropathy( G13.0 )

• 30 Other systemic atrophy primarily affecting central nervous system in neoplastic disease( G13.1 )

• 31 Systemic atrophy primarily affecting the central nervous system in myxedema( G13.2 )

• 32 Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere( G13.8 )

• 33 Postpolio syndrome( G14 )