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Taxonomy Codes
Diseases of the nervous system
Systemic atrophies primarily affecting the central nervous system (G10-G14)
Huntington's disease (G10)
G10
- Huntington's disease
Hereditary ataxia (G11)
G11
- Hereditary ataxia
G11.0
- Congenital nonprogressive ataxia
G11.1
- Early-onset cerebellar ataxia
G11.10
- Early-onset cerebellar ataxia, unspecified
G11.11
- Friedreich ataxia
G11.19
- Other early-onset cerebellar ataxia
G11.2
- Late-onset cerebellar ataxia
G11.3
- Cerebellar ataxia with defective DNA repair
G11.4
- Hereditary spastic paraplegia
G11.5
- Hypomyelination - hypogonadotropic hypogonadism - hypodontia
G11.6
- Leukodystrophy with vanishing white matter disease
G11.8
- Other hereditary ataxias
G11.9
- Hereditary ataxia, unspecified
Spinal muscular atrophy and related syndromes (G12)
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
G12.20
- Motor neuron disease, unspecified
G12.21
- Amyotrophic lateral sclerosis
G12.22
- Progressive bulbar palsy
G12.23
- Primary lateral sclerosis
G12.24
- Familial motor neuron disease
G12.25
- Progressive spinal muscle atrophy
G12.29
- Other motor neuron disease
G12.8
- Other spinal muscular atrophies and related syndromes
G12.9
- Spinal muscular atrophy, unspecified
Systemic atrophies primarily affecting central nervous system in diseases classified elsewhere (G13)
G13
- Systemic atrophies aff cnsl in diseases classd elswhr
G13.0
- Paraneoplastic neuromyopathy and neuropathy
G13.1
- Oth systemic atrophy aff cnsl in neoplastic disease
G13.2
- Systemic atrophy primarily affecting the cnsl in myxedema
G13.8
- Systemic atrophy aff cnsl in oth diseases classd elswhr
Postpolio syndrome (G14)
G14
- Postpolio syndrome