Systemic atrophies primarily affecting the central nervous system

G10 Huntington's disease

• G10 Huntington's disease

G11 Hereditary ataxia

• G11 Hereditary ataxia
• G11.0 Congenitial nonprogressive ataxia
• G11.1 Early-onset cerebellar ataxia
• G11.2 Late-onset celebellar ataxia
• G11.3 Celebellar ataxia with defective DNA repair
• G11.4 Hereditary spastic paraplegia
• G11.8 Other hereditary ataxias
• G11.9 Hereditary ataxia, unspecified

G12 Spinal muscular atrophy and related syndromes

• G12 Spinal muscular atrophy and related syndromes
• G12.0 Infantile spinal muscular atrophy, type I [werdnig-Hoffman]
• G12.1 Other inherited spinal muscular atrophy
• G12.2 Motor neuron disease
• G12.8 Other spinal muscular atrophies and related syndromes
• G12.9 Spinal muscular atrophy, unspecified

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

• G13 Systemic atrophies primarily affecting central nerovous system in diseases classified elsewhere
• G13.0 Paraneoplastic neuromyopathy and neuropathy
• G13.0 Paraneoplastic neuromyopathy and neuropathy
• G13.1 Other systemic atrophy primarily affecting central nervous system in neoplastic disease
• G13.2 Systemic atrophy primarily affecting central nerovous system in myxoedema [E00.1*, E03.-*]
• G13.8 Systemic atrophy primarily affecting central nerovous system in other diseases classified elsewhere