G10-G14
Systemic atrophies primarily affecting the central nervous system
- G10Huntington's disease
- G11.0Congenital nonprogressive ataxia
- G11.1Early-onset cerebellar ataxia
- G11.2Late-onset cerebellar ataxia
- G11.3Cerebellar ataxia with defective DNA repair
- G11.4Hereditary spastic paraplegia
- G11.8Other hereditary ataxias
- G11.9Hereditary ataxia, unspecified
- G12.0Infantile spinal muscular atrophy, Type I [Werdnig-Hoffman]
- G12.1Other inherited spinal muscular atrophy
- G12.2Motor neuron disease
- G12.8Other spinal muscular atrophies and related syndromes
- G12.9Spinal muscular atrophy, unspecified
- G13.0Paraneoplastic neuromyopathy and neuropathy
- G13.1Other systemic atrophy primarily affecting central nervous system in neoplastic disease
- G13.2Systemic atrophy primarily affecting central nervous system in myxoedema (E00.1+, E03.-+)
- G13.8Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere
- G14Postpolio syndrome