G102026

Billable

Huntington's disease

Clinical Notes

FAQ

Related Codes
G10-G14Systemic atrophies primarily affecting the central nervous system (G10-G14)
G10Huntington's disease
G11Hereditary ataxia
G11.0Congenital nonprogressive ataxia
G11.1Early-onset cerebellar ataxia
G11.10unspecified
G11.11Friedreich ataxia
G11.19Other early-onset cerebellar ataxia
G11.2Late-onset cerebellar ataxia
G11.3Cerebellar ataxia with defective DNA repair
G11.4Hereditary spastic paraplegia
G11.5Hypomyelination - hypogonadotropic hypogonadism - hypodontia
G11.6Leukodystrophy with vanishing white matter disease
G11.8Other hereditary ataxias
G11.9unspecified
G12Spinal muscular atrophy and related syndromes
G12.0Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
G12.1Other inherited spinal muscular atrophy
G12.2Motor neuron disease
G12.20unspecified
G12.21Amyotrophic lateral sclerosis
G12.22Progressive bulbar palsy
G12.23Primary lateral sclerosis
G12.24Familial motor neuron disease
G12.25Progressive spinal muscle atrophy
G12.29Other motor neuron disease
G12.8Other spinal muscular atrophies and related syndromes
G12.9unspecified
G13affecting central nervous system in diseases classified elsewhere
G13.0Paraneoplastic neuromyopathy and neuropathy
G13.1Other systemic atrophy primarily affecting central nervous system in neoplastic disease
G13.2Systemic atrophy primarily affecting the central nervous system in myxedema
G13.8Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere
G14Postpolio syndrome