G10-G14
Systemic atrophies primarily affecting the central nervous system
G10
Popular lookup
Primary diagnosis candidate
Huntington disease
G11
Hereditary ataxia
G11.0
Primary diagnosis candidate
Congenital nonprogressive ataxia
G11.1
Primary diagnosis candidate
Early-onset cerebellar ataxia
G11.2
Primary diagnosis candidate
Late-onset cerebellar ataxia
G11.3
Primary diagnosis candidate
Cerebellar ataxia with defective DNA repair
G11.4
Primary diagnosis candidate
Hereditary spastic paraplegia
G11.8
Primary diagnosis candidate
Other hereditary ataxias
G11.9
Primary diagnosis candidate
Hereditary ataxia, unspecified
G12
Spinal muscular atrophy and related syndromes
G12.0
Primary diagnosis candidate
Infantile spinal muscular atrophy, type I [Werdnig- Hoffman]
G12.1
Primary diagnosis candidate
Other inherited spinal muscular atrophy
G12.2
Primary diagnosis candidate
Motor neuron disease
G12.8
Primary diagnosis candidate
Other spinal muscular atrophies and related syndromes
G12.9
Primary diagnosis candidate
Spinal muscular atrophy, unspecified
G13*
Systemic atrophies primarily affecting central nervous system in diseases classified elsewhere
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 nervous system in myxoedema (E00.1, E03.-)
G13.8*
Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere
G14
Primary diagnosis candidate
Postpolio syndrome
