Diseases of the nervous system
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(G00–G99) Diseases of the nervous system |
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(G00–G09) Inflammatory diseases of the central nervous system |
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G00 |
Bacterial meningitis, not elsewhere classified |
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G00.0 |
Haemophilus meningitis |
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G00.1 |
Pneumococcal meningitis |
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G00.2 |
Streptococcal meningitis |
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G00.3 |
Staphylococcal meningitis |
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G00.8 |
Other bacterial meningitis Meningitis due to Escherichia coli Meningitis due to Friedländer bacillus Meningitis due to Klebsiella |
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G00.9 |
Bacterial meningitis, unspecified |
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G01 |
Meningitis in bacterial diseases classified elsewhere |
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G02 |
Meningitis in other infectious and parasitic diseases classified elsewhere |
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G03 |
Meningitis due to other and unspecified causes |
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G03.0 |
Nonpyogenic meningitis |
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G03.1 |
Chronic meningitis |
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G03.2 |
Benign recurrent meningitis (Mollaret) |
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G03.8 |
Meningitis due to other specified causes |
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G03.9 |
Meningitis, unspecified Arachnoiditis (spinal) NOS |
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G04 |
Encephalitis, myelitis and encephalomyelitis |
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G04.0 |
Acute disseminated encephalitis |
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G04.1 |
Tropical spastic paraplegia |
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G04.2 |
Bacterial meningoencephalitis and meningomyelitis, not elsewhere classified |
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G04.8 |
Other encephalitis, myelitis and encephalomyelitis |
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G04.9 |
Encephalitis, myelitis and encephalomyelitis, unspecified |
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G05 |
Encephalitis, myelitis and encephalomyelitis in diseases classified elsewhere |
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G06 |
Intracranial and intraspinal abscess and granuloma |
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G07 |
Intracranial and intraspinal abscess and granuloma in diseases classified elsewhere |
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G08 |
Intracranial and intraspinal phlebitis and thrombophlebitis |
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G09 |
Sequelae of inflammatory diseases of central nervous system |
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(G10–G13) Systemic atrophies primarily affecting the central nervous system |
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G10 |
Huntington's disease |
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G11 |
Hereditary ataxia |
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G11.0 |
Congenital nonprogressive ataxia |
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G11.1 |
Early-onset cerebellar ataxia Early-onset cerebellar ataxia with essential tremor Early-onset cerebellar ataxia with myoclonus (Hunt's ataxia) Early-onset cerebellar ataxia with retained tendon reflexes Friedreich's ataxia (autosomal recessive) X-linked recessive spinocerebellar ataxia |
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G11.2 |
Late-onset cerebellar ataxia |
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G11.3 |
Cerebellar ataxia with defective DNA repair Ataxia telangiectasia (Louis-Bar) |
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G11.4 |
Hereditary spastic paraplegia |
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G11.8 |
Other hereditary ataxias |
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G11.9 |
Hereditary ataxia, unspecified |
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G12 |
Spinal muscular atrophy and related syndromes |
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G12.0 |
Werdnig–Hoffmann disease (spinal muscular atrophy type 1) (G12.1) Other inherited spinal muscular atrophy Progressive bulbar palsy of childhood (Fazio–Londe disease) Kugelberg–Welander disease (spinal muscular atrophy type 3) |
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G12.2 |
Motor neuron disease Familial motor neuron disease Amyotrophic lateral sclerosis Primary lateral sclerosis Progressive bulbar palsy Progressive spinal muscular atrophy |
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G13 |
Systemic atrophies primarily affecting central nervous system in diseases classified elsewhere |
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G13.0 |
Paraneoplastic neuromyopathy and neuropathy |
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G13.1 |
Other systemic atrophy primarily affecting central nervous system in neoplastic disease Paraneoplastic limbic encephalopathy |
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G13.2 |
Systemic atrophy primarily affecting central nervous system in myxoedema |
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G13.8 |
Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere |
