ICD-10 Chapter VI: Diseases of the nervous system
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[edit] G00-G99 - Diseases of the nervous system
[edit] (G00-G09) Inflammatory diseases of the central nervous system
- (G00.) Bacterial meningitis, not elsewhere classified
- (G00.0) Haemophilus meningitis
- (G00.1) Pneumococcal meningitis
- (G00.2) Streptococcal meningitis
- (G00.3) Staphylococcal meningitis
- (G00.8) Other bacterial meningitis
- Meningitis due to Escherichia coli
- Meningitis due to Friedländer bacillus
- Meningitis due to Klebsiella
- (G00.9) 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
- (G04.0) Acute disseminated encephalitis
- (G04.1) Tropical spastic paraplegia
- (G04.2) Bacterial meningoencephalitis and meningomyelitis, not elsewhere classified
- (G04.8) Other encephalitis, myelitis and encephalomyelitis
- (G04.9) 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
- (G11.) Hereditary ataxia
- (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
- (G11.2) Late-onset cerebellar ataxia
- (G11.3) Cerebellar ataxia with defective DNA repair
- Ataxia telangiectasia (Louis-Bar)
- (G11.4) Hereditary spastic paraplegia
- (G11.1) Early-onset cerebellar ataxia
- (G12.) Spinal muscular atrophy and related syndromes
- (G12.0) Werdnig-Hoffman disease (Type 1)
- (G12.1) Other inherited spinal muscular atrophy
- (G12.2) 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
- (G13.0) Paraneoplastic neuromyopathy and neuropathy
- (G13.1) Other systemic atrophy primarily affecting central nervous system in neoplastic disease
- (G13.2) Systemic atrophy primarily affecting central nervous system in myxoedema
- (G13.8) Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere
[edit] (G20-G26) Extrapyramidal and movement disorders
- (G22.) Parkinsonism in diseases classified elsewhere
- (G23.) Other degenerative diseases of basal ganglia
- (G23.0) Hallervorden-Spatz disease
- (G23.1) Progressive supranuclear ophthalmoplegia (Steele-Richardson-Olszewski)
- (G23.2) Striatonigral degeneration
- (G23.8) Other specified degenerative diseases of basal ganglia
- (G23.9) Degenerative disease of basal ganglia, unspecified
- (G25.) Other extrapyramidal and movement disorders
- (G25.0) Essential tremor
- (G25.1) Drug-induced tremor
- (G25.2) Other specified forms of tremor
- (G25.3) Myoclonus
- (G25.4) Drug-induced chorea
- (G25.5) Other chorea
- (G25.6) Drug-induced tics and other tics of organic origin
- (G25.8) Other specified extrapyramidal and movement disorders
- (G25.9) Extrapyramidal and movement disorder, unspecified
- (G26.) Extrapyramidal and movement disorders in diseases classified elsewhere
[edit] (G30-G32) Other degenerative diseases of the nervous system
[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
[edit] (G40-G47) Episodic and paroxysmal disorders
- (G40.) Epilepsy
- (G40.0) Localization-related (focal)(partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset
- (G40.1) Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures
- (G40.2) Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures
- (G40.3) 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:
- (G40.4) 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:
- (G40.5) Special epileptic syndromes
- Epilepsia partialis continua (Kozhevnikof)
- (G40.6) Grand mal seizures, unspecified (with or without petit mal)
- (G40.7) Petit mal, unspecified, without grand mal seizures
- (G40.8) Other epilepsy
- Epilepsies and epileptic syndromes undetermined as to whether they are focal or generalized
- (G40.9) Epilepsy, unspecified
- (G41.) Status epilepticus
- (G41.0) Grand mal status epilepticus
- (G41.1) Petit mal status epilepticus
- (G41.2) Complex partial status epilepticus
- (G41.8) Other status epilepticus
- (G41.9) Status epilepticus, unspecified
- (G44.) Other headache syndromes
- (G44.0) Cluster headache syndrome
- (G44.1) Vascular headache, not elsewhere classified
- (G44.2) Tension-type headache
- (G44.3) Chronic post-traumatic headache
- (G44.4) Drug-induced headache, not elsewhere classified
- (G44.8) Other specified headache syndromes
- (G45.) Transient cerebral ischaemic attacks and related syndromes
- (G45.0) Vertebro-basilar artery syndrome
- (G45.1) Carotid artery syndrome (hemispheric)
- (G45.2) Multiple and bilateral precerebral artery syndromes
- (G45.3) Amaurosis fugax
- (G45.4) Transient global amnesia
- (G45.8) Other transient cerebral ischaemic attacks and related syndromes
- (G45.9) Transient cerebral ischaemic attack, unspecified
- (G46.) Vascular syndromes of brain in cerebrovascular diseases
- (G46.0) Middle cerebral artery syndrome
- (G46.1) Anterior cerebral artery syndrome
- (G46.2) Posterior cerebral artery syndrome
- (G46.3) Brain stem stroke syndrome
- Benedikt syndrome
- Claude syndrome
- Foville syndrome
- Millard-Gubler syndrome
- Wallenberg syndrome
- Weber syndrome
- (G46.4) Cerebellar stroke syndrome
- (G46.5) Pure motor lacunar syndrome
- (G46.6) Pure sensory lacunar syndrome
- (G46.7) Other lacunar syndromes
- (G46.8) Other vascular syndromes of brain in cerebrovascular diseases
- (G47.) Sleep disorders
- (G47.0) Disorders of initiating and maintaining sleep (insomnias)
- (G47.1) Disorders of excessive somnolence (hypersomnias)
- (G47.2) Disruptions in circadian rhythm including jet lag
- (G47.3) Sleep apnoea
- (G47.4) Narcolepsy and cataplexy
[edit] (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
- (G54.0) Brachial plexus disorders
- (G54.6) Phantom limb syndrome with pain
- (G54.7) Phantom limb syndrome without pain
- (G55.) Nerve root and plexus compressions in diseases classified elsewhere
- (G56.) Mononeuropathies of upper limb
- (G57.) Mononeuropathies of lower limb
- (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
- (G60.0) 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
- (G60.1) Refsum's disease
- (G60.2) Neuropathy in association with hereditary ataxia
- (G60.3) Idiopathic progressive neuropathy
- (G60.8) Other hereditary and idiopathic neuropathies
- Morvan's disease
- Nelaton's syndrome
- Sensory neuropathy
- (G60.9) Hereditary and idiopathic neuropathy, unspecified
- (G60.0) Hereditary motor and sensory neuropathy
- (G62.) Other polyneuropathies
- (G62.0) Drug-induced polyneuropathy
- (G62.1) Alcoholic polyneuropathy
- (G62.2) Polyneuropathy due to other toxic agents
- (G62.8) Other specified polyneuropathies
- (G62.9) 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
- (G70.0) Myasthenia gravis
- (G70.1) Toxic myoneural disorders
- (G70.2) Congenital and developmental myasthenia
- (G71.) Primary disorders of muscles
- (G71.0) 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)
- (G71.1) 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
- (G71.2) Congenital myopathies, including:
- Central core disease
- Congenital muscular dystrophy
- Centronuclear myopathy
- Fibre-type disproportion
- Minicore disease
- Multicore disease
- Myotubular myopathy
- Nemaline myopathy
- (G71.3) Mitochondrial myopathy, not elsewhere classified
- (G71.0) Muscular dystrophy
- (G72.) Other myopathies
- (G73.) Disorders of myoneural junction and muscle in diseases classified elsewhere
- (G73.0) Myasthenic syndromes in endocrine diseases
- (G73.1) Eaton-Lambert syndrome
- (G73.2) Other myasthenic syndromes in neoplastic disease
- (G73.3) Myasthenic syndromes in other diseases classified elsewhere
- (G73.4) Myopathy in infectious and parasitic diseases classified elsewhere
- (G73.5) Myopathy in endocrine diseases
- (G73.6) Myopathy in metabolic diseases
- (G73.7) Myopathy in other diseases classified elsewhere
[edit] (G80-G83) Cerebral palsy and other paralytic syndromes
- (G80.) Cerebral palsy
- (G80.0) Spastic quadriplegic cerebral palsy
- (G80.1) Spastic diplegic cerebral palsy
- (G80.2) Spastic hemiplegic cerebral palsy
- (G80.3) Dyskinetic cerebral palsy
- (G80.4) Ataxic cerebral palsy
- (G80.8) Other cerebral palsy
- (G80.9) Cerebral palsy, unspecified
- (G82.) Paraplegia and tetraplegia
- (G82.0) Flaccid paraplegia
- (G82.1) Spastic paraplegia
- (G82.2) Paraplegia, unspecified
- Paralysis of both lower limbs NOS
- Paraplegia (lower) NOS
- (G82.3) Flaccid tetraplegia
- (G82.4) Spastic tetraplegia
- (G82.5) Tetraplegia, unspecified
- Quadriplegia NOS
- (G83.) Other paralytic syndromes
- (G83.0) Diplegia of upper limbs
- (G83.1) Monoplegia of lower limb
- (G83.2) Monoplegia of upper limb
- (G83.3) Monoplegia, unspecified
- (G83.4) Cauda equina syndrome
- (G83.8) Other specified paralytic syndromes
- (G83.9) Paralytic syndrome, unspecified
[edit] (G90-G99) Other disorders of the nervous system
- (G90.) Disorders of autonomic nervous system
- (G90.0) Idiopathic peripheral autonomic neuropathy
- (G90.1) Familial dysautonomia (Riley-Day)
- (G90.2) Horner's syndrome
- (G90.3) Multi-system degeneration
- (G90.8) Other disorders of autonomic nervous system
- (G90.9) Disorder of autonomic nervous system, unspecified
- (G93.) Other disorders of brain
- (G93.0) Cerebral cysts
- (G93.1) Anoxic brain damage, not elsewhere classified
- (G93.2) Benign intracranial hypertension
- (G93.3) Postviral fatigue syndrome
- (G93.4) Encephalopathy, unspecified
- (G93.5) Compression of brain
- (G93.6) Cerebral oedema
- (G93.7) Reye's syndrome
- (G95.) Other diseases of spinal cord
- (G95.0) Syringomyelia and syringobulbia
- (G95.1) Vascular myelopathies
- (G95.2) Cord compression, unspecified
- (G95.8) Other specified diseases of spinal cord
- (G95.9) 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
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