ICD-10 Chapter VI: Diseases of the nervous system

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Contents 1 G00-G99 - Diseases of the nervous system 1.1 (G00-G09) Inflammatory diseases of the central nervous system 1.2 (G10-G13) Systemic atrophies primarily affecting the central nervous system 1.3 (G20-G26) Extrapyramidal and movement disorders 1.4 (G30-G32) Other degenerative diseases of the nervous system 1.5 (G35-G37) Demyelinating diseases of the central nervous system 1.6 (G40-G47) Episodic and paroxysmal disorders 1.7 (G50-G59) Nerve, nerve root and plexus disorders 1.8 (G60-G64) Polyneuropathies and other disorders of the peripheral nervous system 1.9 (G70-G73) Diseases of myoneural junction and muscle 1.10 (G80-G83) Cerebral palsy and other paralytic syndromes 1.11 (G90-G99) Other disorders of the nervous system 2 See also

[edit] G00-G99 - Diseases of the nervous system

[edit] (G00-G09) Inflammatory diseases of the central nervous system

• (G00) Bacterial meningitis, not elsewhere classified
  • (G000) Haemophilus meningitis
  • (G001) Pneumococcal meningitis
  • (G002) Streptococcal meningitis
  • (G003) Staphylococcal meningitis
  • (G008) Other bacterial meningitis
    • Meningitis due to Escherichia coli
    • Meningitis due to Friedländer bacillus
    • Meningitis due to Klebsiella
  • (G009) Bacterial meningitis, unspecified

• (G01) Meningitis in bacterial diseases classified elsewhere
• (G02) Meningitis in other infectious and parasitic diseases classified elsewhere
• (G03) Meningitis due to other and unspecified causes
• (G04) Encephalitis, myelitis and encephalomyelitis
  • (G040) Acute disseminated encephalitis
  • (G041) Tropical spastic paraplegia
  • (G042) Bacterial meningoencephalitis and meningomyelitis, not elsewhere classified
  • (G048) Other encephalitis, myelitis and encephalomyelitis
  • (G049) Encephalitis, myelitis and encephalomyelitis, unspecified

• (G05) Encephalitis, myelitis and encephalomyelitis in diseases classified elsewhere
• (G06) Intracranial and intraspinal abscess and granuloma
• (G07) Intracranial and intraspinal abscess and granuloma in diseases classified elsewhere
• (G08) Intracranial and intraspinal phlebitis and thrombophlebitis
• (G09) Sequelae of inflammatory diseases of central nervous system

[edit] (G10-G13) Systemic atrophies primarily affecting the central nervous system

• (G10) Huntington's disease

• (G11) Hereditary ataxia
  • (G111) 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
  • (G112) Late-onset cerebellar ataxia
  • (G113) Cerebellar ataxia with defective DNA repair
    • Ataxia telangiectasia (Louis-Bar)
  • (G114) Hereditary spastic paraplegia

• (G12) Spinal muscular atrophy and related syndromes
  • (G120) Werdnig-Hoffman disease (Type 1)
  • (G121) Other inherited spinal muscular atrophy
    • Progressive bulbar palsy of childhood (Fazio-Londe)
    • Kugelberg-Welander disease (Type 3)
  • (G122) Motor neuron disease
    • Familial motor neuron disease
    • Amyotrophic lateral sclerosis
    • Primary lateral sclerosis
    • Progressive bulbar palsy
    • Progressive spinal muscular atrophy

• (G13) Systemic atrophies primarily affecting central nervous system in diseases classified elsewhere
  • (G130) Paraneoplastic neuromyopathy and neuropathy
  • (G131) Other systemic atrophy primarily affecting central nervous system in neoplastic disease
  • (G132) Systemic atrophy primarily affecting central nervous system in myxoedema
  • (G138) Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere

[edit] (G20-G26) Extrapyramidal and movement disorders

• (G20) Parkinson's disease

• (G21) Secondary parkinsonism
  • (G210) Malignant neuroleptic syndrome
  • (G213) Postencephalitic parkinsonism

• (G22) Parkinsonism in diseases classified elsewhere

• (G23) Other degenerative diseases of basal ganglia
  • (G230) Hallervorden-Spatz disease
  • (G231) Progressive supranuclear ophthalmoplegia (Steele-Richardson-Olszewski)
  • (G232) Striatonigral degeneration
  • (G238) Other specified degenerative diseases of basal ganglia
  • (G239) Degenerative disease of basal ganglia, unspecified

• (G24) Dystonia
  • (G240) Drug-induced dystonia
  • (G241) Idiopathic familial dystonia
  • (G242) Idiopathic nonfamilial dystonia
  • (G243) Spasmodic torticollis
  • (G244) Idiopathic orofacial dystonia
    • Orofacial dyskinesia
  • (G245) Blepharospasm
  • (G248) Other dystonia
  • (G249) Dystonia, unspecified
    • Dyskinesia NOS

• (G25) Other extrapyramidal and movement disorders
  • (G250) Essential tremor
  • (G251) Drug-induced tremor
  • (G252) Other specified forms of tremor
  • (G253) Myoclonus
  • (G254) Drug-induced chorea
  • (G255) Other chorea
  • (G256) Drug-induced tics and other tics of organic origin
  • (G258) Other specified extrapyramidal and movement disorders
    • Restless legs syndrome
    • Stiff-man syndrome
  • (G259) Extrapyramidal and movement disorder, unspecified

• (G26) Extrapyramidal and movement disorders in diseases classified elsewhere

[edit] (G30-G32) Other degenerative diseases of the nervous system

• (G30) Alzheimer's disease

• (G31) Other degenerative diseases of nervous system, not elsewhere classified
  • (G310) Circumscribed brain atrophy
  • (G311) Senile degeneration of brain, not elsewhere classified
  • (G312) Degeneration of nervous system due to alcohol
  • (G318) Other specified degenerative diseases of nervous system
    • Grey-matter degeneration (Alpers)
    • Lewy body dementia
    • Subacute necrotizing encephalopathy (Leigh)
  • (G319) Degenerative disease of nervous system, unspecified

• (G32) Other degenerative disorders of nervous system in diseases classified elsewhere

[edit] (G35-G37) Demyelinating diseases of the central nervous system

• (G35) Multiple sclerosis
• (G36) Other acute disseminated demyelination
• (G37) Other demyelinating diseases of central nervous system
  • (G370) Diffuse sclerosis
  • (G371) Central demyelination of corpus callosum
  • (G372) Central pontine myelinolysis
  • (G373) Acute transverse myelitis in demyelinating disease of central nervous system
  • (G374) Subacute necrotizing myelitis
  • (G375) Concentric sclerosis (Baló)
  • (G378) Other specified demyelinating diseases of central nervous system
  • (G379) Demyelinating disease of central nervous system, unspecified

[edit] (G40-G47) Episodic and paroxysmal disorders

• (G40) Epilepsy
  • (G400) Localization-related (focal)(partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset
  • (G401) Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures
  • (G402) Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures
  • (G403) Generalized idiopathic epilepsy and epileptic syndromes
    • Benign:
      • myoclonic epilepsy in infancy
      • neonatal convulsions (familial)
    • Childhood absence epilepsy (pyknolepsy)
    • Epilepsy with grand mal seizures on awakening
    • Juvenile:
      • absence epilepsy
      • myoclonic epilepsy (impulsive petit mal)
    • Nonspecific epileptic seizures:
      • atonic
      • clonic
      • myoclonic
      • tonic
      • tonic-clonic
  • (G404) Other generalized epilepsy and epileptic syndromes
    • Epilepsy with:
      • myoclonic absences
      • myoclonic-astatic seizures
    • Infantile spasms
    • Lennox-Gastaut syndrome
    • Salaam attacks
    • Symptomatic early myoclonic encephalopathy
    • West's syndrome
  • (G405) Special epileptic syndromes
    • Epilepsia partialis continua (Kozhevnikof)
  • (G406) Grand mal seizures, unspecified (with or without petit mal)
  • (G407) Petit mal, unspecified, without grand mal seizures
  • (G408) Other epilepsy
    • Epilepsies and epileptic syndromes undetermined as to whether they are focal or generalized
  • (G409) Epilepsy, unspecified

• (G41) Status epilepticus
  • (G410) Grand mal status epilepticus
  • (G411) Petit mal status epilepticus
  • (G412) Complex partial status epilepticus
  • (G418) Other status epilepticus
  • (G419) Status epilepticus, unspecified

• (G43) Migraine
  • (G430) Migraine without aura (common migraine)
  • (G431) Migraine with aura (classical migraine)
  • (G432) Status migrainosus
  • (G433) Complicated migraine
  • (G434) Other migraine
  • (G435) Migraine, unspecified

• (G44) Other headache syndromes
  • (G440) Cluster headache syndrome
  • (G441) Vascular headache, not elsewhere classified
  • (G442) Tension-type headache
  • (G443) Chronic post-traumatic headache
  • (G444) Drug-induced headache, not elsewhere classified
  • (G448) Other specified headache syndromes

• (G45) Transient cerebral ischaemic attacks and related syndromes
  • (G450) Vertebro-basilar artery syndrome
  • (G451) Carotid artery syndrome (hemispheric)
  • (G452) Multiple and bilateral precerebral artery syndromes
  • (G453) Amaurosis fugax
  • (G454) Transient global amnesia
  • (G458) Other transient cerebral ischaemic attacks and related syndromes
  • (G459) Transient cerebral ischaemic attack, unspecified

• (G46) Vascular syndromes of brain in cerebrovascular diseases
  • (G460) Middle cerebral artery syndrome
  • (G461) Anterior cerebral artery syndrome
  • (G462) Posterior cerebral artery syndrome
  • (G463) Brain stem stroke syndrome
    • Benedikt syndrome
    • Claude syndrome
    • Foville syndrome
    • Millard-Gubler syndrome
    • Wallenberg syndrome
    • Weber syndrome
  • (G464) Cerebellar stroke syndrome
  • (G465) Pure motor lacunar syndrome
  • (G466) Pure sensory lacunar syndrome
  • (G467) Other lacunar syndromes
  • (G468) Other vascular syndromes of brain in cerebrovascular diseases

• (G47) Sleep disorders
  • (G470) Disorders of initiating and maintaining sleep (insomnias)
  • (G471) Disorders of excessive somnolence (hypersomnias)
  • (G472) Disruptions in circadian rhythm including jet lag
  • (G473) Sleep apnoea
  • (G474) Narcolepsy and cataplexy

[edit] (G50-G59) Nerve, nerve root and plexus disorders

• (G50) Disorders of trigeminal nerve
  • (G500) Trigeminal neuralgia
• (G51) Facial nerve disorders
  • (G510) Bell's palsy
• (G52) Disorders of other cranial nerves
• (G53) Cranial nerve disorders in diseases classified elsewhere
• (G54) Nerve root and plexus disorders
  • (G540) Brachial plexus disorders
    • Thoracic outlet syndrome
  • (G546) Phantom limb syndrome with pain
  • (G547) Phantom limb syndrome without pain
• (G55) Nerve root and plexus compressions in diseases classified elsewhere
• (G56) Mononeuropathies of upper limb
  • (G560) Carpal tunnel syndrome
  • (G564) Causalgia
• (G57) Mononeuropathies of lower limb
  • (G570) Lesion of sciatic nerve
  • (G571) Meralgia paraesthetica
  • (G572) Lesion of femoral nerve
  • (G573) Lesion of lateral popliteal nerve
  • (G574) Lesion of medial popliteal nerve
  • (G575) Tarsal tunnel syndrome
  • (G576) Lesion of plantar nerve
  • (G578) Other mononeuropathies of lower limb
  • (G579) Mononeuropathy of lower limb, unspecified

• (G58) Other mononeuropathies
• (G59) Mononeuropathy in diseases classified elsewhere

[edit] (G60-G64) Polyneuropathies and other disorders of the peripheral nervous system

• (G60) Hereditary and idiopathic neuropathy
  • (G600) Hereditary motor and sensory neuropathy
    • Charcot-Marie-Tooth disease
    • Déjerine-Sottas disease
    • Hereditary motor and sensory neuropathy, types I-IV
    • Hypertrophic neuropathy of infancy
    • Peroneal muscular atrophy (axonal type)(hypertrophic type)
    • Roussy-Lévy syndrome
  • (G601) Refsum's disease
  • (G602) Neuropathy in association with hereditary ataxia
  • (G603) Idiopathic progressive neuropathy
  • (G608) Other hereditary and idiopathic neuropathies
    • Morvan's disease
    • Nelaton's syndrome
    • Sensory neuropathy
  • (G609) Hereditary and idiopathic neuropathy, unspecified

• (G61) Inflammatory polyneuropathy
  • (G610) Guillain-Barré syndrome
  • (G611) Serum neuropathy
  • (G618) Other inflammatory polyneuropathies
  • (G619) Inflammatory polyneuropathy, unspecified

• (G62) Other polyneuropathies
  • (G620) Drug-induced polyneuropathy
  • (G621) Alcoholic polyneuropathy
  • (G622) Polyneuropathy due to other toxic agents
  • (G628) Other specified polyneuropathies
  • (G629) Polyneuropathy, unspecified
    • Neuropathy NOS

• (G63) Polyneuropathy in diseases classified elsewhere
• (G64) Other Disorders of peripheral nervous system

[edit] (G70-G73) Diseases of myoneural junction and muscle

• (G70) Myasthenia gravis and other myoneural disorders
  • (G700) Myasthenia gravis
  • (G701) Toxic myoneural disorders
  • (G702) Congenital and developmental myasthenia
• (G71) Primary disorders of muscles
  • (G710) Muscular dystrophy
    • benign muscular dystrophy (Becker muscular dystrophy)
    • benign scapuloperoneal muscular dystrophy with early contractures (Emery-Dreifuss muscular dystrophy)
    • distal muscular dystrophy
    • facioscapulohumeral muscular dystrophy
    • limb-girdle muscular dystrophy
    • ocular muscular dystrophy
    • oculopharyngeal muscular dystrophy
    • scapuloperoneal muscular dystrophy
    • severe muscular dystrophy (Duchenne muscular dystrophy)
  • (G711) Myotonic disorders
    • Dystrophia myotonica (Steinert)
    • chondrodystrophic myotonia
    • drug-induced myotonia
    • symptomatic myotonia
    • Myotonia congenita - NOS:
    • Myotonia congenita - dominant (Thomsen)
    • Myotonia congenita - recessive (Becker)
    • Neuromyotonia (Isaacs)
    • Paramyotonia congenita
    • Pseudomyotonia
  • (G712) Congenital myopathies, including:
    • Central core disease
    • Congenital muscular dystrophy
    • Centronuclear myopathy
    • Fibre-type disproportion
    • Minicore disease
    • Multicore disease
    • Myotubular myopathy
    • Nemaline myopathy
  • (G713) Mitochondrial myopathy, not elsewhere classified
• (G72) Other myopathies
  • (G720) Drug-induced myopathy
  • (G721) Alcoholic myopathy
  • (G722) Myopathy due to other toxic agents
  • (G723) Periodic paralysis
    • Hypokalemic periodic paralysis
    • Hyperkalemic periodic paralysis
• (G73) Disorders of myoneural junction and muscle in diseases classified elsewhere
  • (G730) Myasthenic syndromes in endocrine diseases
  • (G731) Eaton-Lambert syndrome
  • (G732) Other myasthenic syndromes in neoplastic disease
  • (G733) Myasthenic syndromes in other diseases classified elsewhere
  • (G734) Myopathy in infectious and parasitic diseases classified elsewhere
  • (G735) Myopathy in endocrine diseases
  • (G736) Myopathy in metabolic diseases
  • (G737) Myopathy in other diseases classified elsewhere

[edit] (G80-G83) Cerebral palsy and other paralytic syndromes

• (G80) Cerebral palsy
  • (G800) Spastic quadriplegic cerebral palsy
  • (G801) Spastic diplegic cerebral palsy
  • (G802) Spastic hemiplegic cerebral palsy
  • (G803) Dyskinetic cerebral palsy
  • (G804) Ataxic cerebral palsy
  • (G808) Other cerebral palsy
  • (G809) Cerebral palsy, unspecified

• (G81) Hemiplegia
  • (G810) Flaccid hemiplegia
  • (G811) Spastic hemiplegia
  • (G819) Hemiplegia, unspecified

• (G82) Paraplegia and tetraplegia
  • (G820) Flaccid paraplegia
  • (G821) Spastic paraplegia
  • (G822) Paraplegia, unspecified
    • Paralysis of both lower limbs NOS
    • Paraplegia (lower) NOS
  • (G823) Flaccid tetraplegia
  • (