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G00-G99 - Diseases of the nervous system[]
(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
(G10-G13) Systemic atrophies primarily affecting the central nervous system[]
- (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
- (G111) Early-onset cerebellar ataxia
- (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
(G20-G26) Extrapyramidal and movement disorders[]
- (G21) Secondary parkinsonism
- (G210) Malignant neuroleptic syndrome
- (G213) Postencephalitic parkinsonism
- (G22) Parkinsonism in diseases classified elsewhere
- (G23) Other degenerative diseases of basal ganglia
- (G230) Pantothenate kinase-associated neurodegeneration
- (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
- (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
(G30-G32) Other degenerative diseases of the nervous system[]
- (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
(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
(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
- Benign:
- (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
- Epilepsy with:
- (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
- (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
(G50-G59) Nerve, nerve root and plexus disorders[]
- (G50) Disorders of trigeminal nerve
- (G51) Facial nerve disorders
- (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
- (G540) Brachial plexus disorders
- (G55) Nerve root and plexus compressions in diseases classified elsewhere
- (G56) Mononeuropathies of upper limb
- (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
(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
- (G600) Hereditary motor and sensory neuropathy
- (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
(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
- (G710) Muscular dystrophy
- (G72) Other myopathies
- (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
(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
- (G824) Spastic tetraplegia
- (G825) Tetraplegia, unspecified
- Quadriplegia NOS
(G90-G99) Other disorders of the nervous system[]
- (G90) Disorders of autonomic nervous system
- (G900) Idiopathic peripheral autonomic neuropathy
- (G901) Familial dysautonomia (Riley-Day)
- (G902) Horner's syndrome
- (G903) Multi-system degeneration
- (G908) Other disorders of autonomic nervous system
- (G909) Disorder of autonomic nervous system, unspecified
- (G91) Hydrocephalus
- (G92) Toxic encephalopathy
- (G95) Other diseases of spinal cord
- (G950) Syringomyelia and syringobulbia
- (G951) Vascular myelopathies
- (G952) Cord compression, unspecified
- (G958) Other specified diseases of spinal cord
- (G959) Disease of spinal cord, unspecified
- Myelopathy NOS
- (G96) Other disorders of central nervous system
- (G97) Postprocedural disorders of nervous system, not elsewhere classified
- (G98) Other disorders of nervous system, not elsewhere classified
- (G99) Other disorders of nervous system in diseases classified elsewhere
See also[]
- List of ICD-10 codes
- International Statistical Classification of Diseases and Related Health Problems
- nl:ICD10 Hoofdstuk VI
- ru:МКБ-10: Класс VI
- th:ICD-10 บท G: โรคระบบประสาท
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