ICD-10 Chapter VI: Diseases of the nervous system


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G00-G99 - Diseases of the nervous system

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

  • () Bacterial meningitis, not elsewhere classified
  • () Haemophilus meningitis
  • () Pneumococcal meningitis
  • () Streptococcal meningitis
  • () Staphylococcal meningitis
  • () Other bacterial meningitis
  • Meningitis due to Escherichia coli
  • Meningitis due to Friedländer bacillus
  • Meningitis due to Klebsiella
  • () Bacterial meningitis, unspecified
  • () Meningitis in bacterial diseases classified elsewhere
  • () Meningitis in other infectious and parasitic diseases classified elsewhere
  • () Meningitis due to other and unspecified causes
  • () Nonpyogenic meningitis
  • () Chronic meningitis
  • () Benign recurrent meningitis (Mollaret)
  • () Meningitis due to other specified causes
  • () Meningitis, unspecified
  • Arachnoiditis (spinal) NOS
  • () Encephalitis, myelitis and encephalomyelitis
  • () Acute disseminated encephalitis
  • () Tropical spastic paraplegia
  • () Bacterial meningoencephalitis and meningomyelitis, not elsewhere classified
  • () Other encephalitis, myelitis and encephalomyelitis
  • () Encephalitis, myelitis and encephalomyelitis, unspecified
  • () Encephalitis, myelitis and encephalomyelitis in diseases classified elsewhere
  • () Intracranial and intraspinal abscess and granuloma
  • () Intracranial and intraspinal abscess and granuloma in diseases classified elsewhere
  • () Intracranial and intraspinal phlebitis and thrombophlebitis
  • () Sequelae of inflammatory diseases of central nervous system
  • (G10-G13) Systemic atrophies primarily affecting the central nervous system

  • () Huntington's disease
  • () Hereditary ataxia
  • () Congenital nonprogressive ataxia
  • () 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
  • () Late-onset cerebellar ataxia
  • () Cerebellar ataxia with defective DNA repair
  • Ataxia telangiectasia (Louis-Bar)
  • () Hereditary spastic paraplegia
  • () Other hereditary ataxias
  • () Hereditary ataxia, unspecified
  • () Spinal muscular atrophy and related syndromes
  • () Werdnig-Hoffman disease (Type 1)
  • () Other inherited spinal muscular atrophy
  • Progressive bulbar palsy of childhood (Fazio-Londe)
  • Kugelberg-Welander disease (Type 3)
  • () Motor neuron disease
  • Familial motor neuron disease
  • Amyotrophic lateral sclerosis
  • Primary lateral sclerosis
  • Progressive bulbar palsy
  • Progressive spinal muscular atrophy
  • () Systemic atrophies primarily affecting central nervous system in diseases classified elsewhere
  • () Paraneoplastic neuromyopathy and neuropathy
  • () Other systemic atrophy primarily affecting central nervous system in neoplastic disease
  • Paraneoplastic limbic encephalopathy
  • () Systemic atrophy primarily affecting central nervous system in myxoedema
  • () Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere
  • (G20-G26) Extrapyramidal and movement disorders

  • () Parkinson's disease
  • () Secondary parkinsonism
  • () Malignant neuroleptic syndrome
  • () Postencephalitic parkinsonism
  • () Parkinsonism in diseases classified elsewhere
  • () Other degenerative diseases of basal ganglia
  • () Hallervorden-Spatz disease
  • () Progressive supranuclear ophthalmoplegia (Steele-Richardson-Olszewski)
  • () Striatonigral degeneration
  • () Other specified degenerative diseases of basal ganglia
  • () Degenerative disease of basal ganglia, unspecified
  • () Dystonia
  • () Drug-induced dystonia
  • () Idiopathic familial dystonia
  • () Idiopathic nonfamilial dystonia
  • () Spasmodic torticollis
  • () Idiopathic orofacial dystonia
  • Orofacial dyskinesia
  • () Blepharospasm
  • () Other dystonia
  • () Dystonia, unspecified
  • Dyskinesia NOS
  • () Other extrapyramidal and movement disorders
  • () Essential tremor
  • () Drug-induced tremor
  • () Other specified forms of tremor
  • () Myoclonus
  • () Drug-induced chorea
  • () Other chorea
  • () Drug-induced tics and other tics of organic origin
  • () Other specified extrapyramidal and movement disorders
  • Restless legs syndrome
  • Stiff-man syndrome
  • () Extrapyramidal and movement disorder, unspecified
  • () Extrapyramidal and movement disorders in diseases classified elsewhere
  • (G30-G32) Other degenerative diseases of the nervous system

  • () Alzheimer's disease
  • () Other degenerative diseases of nervous system, not elsewhere classified
  • () Circumscribed brain atrophy
  • Pick's disease
  • () Senile degeneration of brain, not elsewhere classified
  • () Degeneration of nervous system due to alcohol
  • () Other specified degenerative diseases of nervous system
  • Grey-matter degeneration (Alpers)
  • Lewy body dementia
  • Subacute necrotizing encephalopathy (Leigh)
  • () Degenerative disease of nervous system, unspecified
  • () Other degenerative disorders of nervous system in diseases classified elsewhere
  • (G35-G37) Demyelinating diseases of the central nervous system

  • () Multiple sclerosis
  • () Other acute disseminated demyelination
  • () Neuromyelitis optica (Devic)
  • () Acute and subacute haemorrhagic leukoencephalitis (Hurst)
  • () Other specified acute disseminated demyelination
  • () Acute disseminated demyelination, unspecified
  • () Other demyelinating diseases of central nervous system
  • () Diffuse sclerosis
  • () Central demyelination of corpus callosum
  • () Central pontine myelinolysis
  • () Acute transverse myelitis in demyelinating disease of central nervous system
  • () Subacute necrotizing myelitis
  • () Concentric sclerosis (Baló)
  • () Other specified demyelinating diseases of central nervous system
  • () Demyelinating disease of central nervous system, unspecified
  • (G40-G47) Episodic and paroxysmal disorders

  • () Epilepsy
  • () Localization-related (focal)(partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset
  • () Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures
  • () Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures
  • () 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
  • () 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
  • () Special epileptic syndromes
  • Epilepsia partialis continua (Kozhevnikof)
  • () Grand mal seizures, unspecified (with or without petit mal)
  • () Petit mal, unspecified, without grand mal seizures
  • () Other epilepsy
  • Epilepsies and epileptic syndromes undetermined as to whether they are focal or generalized
  • () Epilepsy, unspecified
  • () Status epilepticus
  • () Grand mal status epilepticus
  • () Petit mal status epilepticus
  • () Complex partial status epilepticus
  • () Other status epilepticus
  • () Status epilepticus, unspecified
  • () Migraine
  • () Migraine without aura (common migraine)
  • () Migraine with aura (classical migraine)
  • () Status migrainosus
  • () Complicated migraine
  • () Other migraine
  • () Migraine, unspecified
  • () Other headache syndromes
  • () Cluster headache syndrome
  • () Vascular headache, not elsewhere classified
  • () Tension-type headache
  • () Chronic post-traumatic headache
  • () Drug-induced headache, not elsewhere classified
  • () Other specified headache syndromes
  • () Transient cerebral ischaemic attacks and related syndromes
  • () Vertebro-basilar artery syndrome
  • () Carotid artery syndrome (hemispheric)
  • () Multiple and bilateral precerebral artery syndromes
  • () Amaurosis fugax
  • () Transient global amnesia
  • () Other transient cerebral ischaemic attacks and related syndromes
  • () Transient cerebral ischaemic attack, unspecified
  • () Vascular syndromes of brain in cerebrovascular diseases
  • () Middle cerebral artery syndrome
  • () Anterior cerebral artery syndrome
  • () Posterior cerebral artery syndrome
  • () Brain stem stroke syndrome
  • Benedikt syndrome
  • Claude syndrome
  • Foville syndrome
  • Millard-Gubler syndrome
  • Wallenberg syndrome
  • Weber syndrome
  • () Cerebellar stroke syndrome
  • () Pure motor lacunar syndrome
  • () Pure sensory lacunar syndrome
  • () Other lacunar syndromes
  • () Other vascular syndromes of brain in cerebrovascular diseases
  • () Sleep disorders
  • () Disorders of initiating and maintaining sleep (insomnias)
  • () Disorders of excessive somnolence (hypersomnias)
  • () Disruptions in circadian rhythm including jet lag
  • () Sleep apnoea
  • () Narcolepsy and cataplexy
  • (G50-G59) Nerve, nerve root and plexus disorders

  • () Disorders of trigeminal nerve (V)
  • () Trigeminal neuralgia
  • () Facial nerve disorders (VII)
  • () Bell's palsy
  • Facial palsy
  • () Geniculate ganglionitis
  • () Melkersson's syndrome
  • Melkersson-Rosenthal syndrome
  • () Clonic hemifacial spasm
  • () Facial myokymia
  • () Other disorders of facial nerve
  • () Disorder of facial nerve, unspecified
  • () Disorders of other cranial nerves
  • () Disorders of olfactory nerve (I)
  • () Disorders of glossopharyngeal nerve (IX)
  • () Disorders of vagus nerve (X)
  • () Disorders of hypoglossal nerve (XII)
  • () Disorders of multiple cranial nerves
  • () Disorders of other specified cranial nerves
  • () Cranial nerve disorder, unspecified
  • () Cranial nerve disorders in diseases classified elsewhere
  • () Nerve root and plexus disorders
  • () Brachial plexus disorders
  • Thoracic outlet syndrome
  • () Lumbosacral plexus disorders
  • () Cervical root disorders, not elsewhere classified
  • () Thoracic root disorders, not elsewhere classified
  • () Lumbosacral root disorders, not elsewhere classified
  • () Neuralgic amyotrophy
  • Parsonage-Aldren-Turner syndrome
  • () Phantom limb syndrome with pain
  • () Phantom limb syndrome without pain
  • () Nerve root and plexus compressions in diseases classified elsewhere
  • () Mononeuropathies of upper limb
  • () Carpal tunnel syndrome
  • () Causalgia
  • () Mononeuropathies of lower limb
  • () Lesion of sciatic nerve
  • () Meralgia paraesthetica
  • () Lesion of femoral nerve
  • () Lesion of lateral popliteal nerve
  • () Lesion of medial popliteal nerve
  • () Tarsal tunnel syndrome
  • () Lesion of plantar nerve
  • Morton's metatarsalgia
  • () Other mononeuropathies of lower limb
  • () Mononeuropathy of lower limb, unspecified
  • () Other mononeuropathies
  • () Intercostal neuropathy
  • () Mononeuritis multiplex
  • () Other specified mononeuropathies
  • () Mononeuropathy, unspecified
  • () Mononeuropathy in diseases classified elsewhere
  • (G60-G64) Polyneuropathies and other disorders of the peripheral nervous system

  • () Hereditary and idiopathic neuropathy
  • () 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
  • () Refsum's disease
  • () Neuropathy in association with hereditary ataxia
  • () Idiopathic progressive neuropathy
  • () Other hereditary and idiopathic neuropathies
  • Morvan's disease
  • Nelaton's syndrome
  • Sensory neuropathy
  • () Hereditary and idiopathic neuropathy, unspecified
  • () Inflammatory polyneuropathy
  • () Guillain-Barré syndrome
  • () Serum neuropathy
  • () Other inflammatory polyneuropathies
  • () Inflammatory polyneuropathy, unspecified
  • () Other polyneuropathies
  • () Drug-induced polyneuropathy
  • () Alcoholic polyneuropathy
  • () Polyneuropathy due to other toxic agents
  • () Other specified polyneuropathies
  • () Polyneuropathy, unspecified
  • Neuropathy NOS
  • () Polyneuropathy in diseases classified elsewhere
  • () Other Disorders of peripheral nervous system
  • (G70-G73) Diseases of myoneural junction and muscle

  • () Myasthenia gravis and other myoneural disorders
  • () Myasthenia gravis
  • () Toxic myoneural disorders
  • () Congenital and developmental myasthenia
  • () Primary disorders of muscles
  • () 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)
  • () 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
  • () Congenital myopathies, including:
  • Central core disease
  • Congenital muscular dystrophy
  • Centronuclear myopathy
  • Fibre-type disproportion
  • Minicore disease
  • Multicore disease
  • Myotubular myopathy
  • Nemaline myopathy
  • () Mitochondrial myopathy, not elsewhere classified
  • () Other myopathies
  • () Drug-induced myopathy
  • () Alcoholic myopathy
  • () Myopathy due to other toxic agents
  • () Periodic paralysis
  • Hypokalemic periodic paralysis
  • Hyperkalemic periodic paralysis
  • () Disorders of myoneural junction and muscle in diseases classified elsewhere
  • () Myasthenic syndromes in endocrine diseases
  • () Eaton-Lambert syndrome
  • () Other myasthenic syndromes in neoplastic disease
  • () Myasthenic syndromes in other diseases classified elsewhere
  • () Myopathy in infectious and parasitic diseases classified elsewhere
  • () Myopathy in endocrine diseases
  • () Myopathy in metabolic diseases
  • () Myopathy in other diseases classified elsewhere
  • (G80-G83) Cerebral palsy and other paralytic syndromes

  • () Cerebral palsy
  • () Spastic quadriplegic cerebral palsy
  • () Spastic diplegic cerebral palsy
  • () Spastic hemiplegic cerebral palsy
  • () Dyskinetic cerebral palsy
  • () Ataxic cerebral palsy
  • () Other cerebral palsy
  • () Cerebral palsy, unspecified
  • () Hemiplegia
  • () Flaccid hemiplegia
  • () Spastic hemiplegia
  • () Hemiplegia, unspecified
  • () Paraplegia and tetraplegia
  • () Flaccid paraplegia
  • () Spastic paraplegia
  • () Paraplegia, unspecified
  • Paralysis of both lower limbs NOS
  • Paraplegia (lower) NOS
  • () Flaccid tetraplegia
  • () Spastic tetraplegia
  • () Tetraplegia, unspecified
  • Quadriplegia NOS
  • () Other paralytic syndromes
  • () Diplegia of upper limbs
  • () Monoplegia of lower limb
  • () Monoplegia of upper limb
  • () Monoplegia, unspecified
  • () Cauda equina syndrome
  • () Other specified paralytic syndromes
  • () Paralytic syndrome, unspecified
  • (G90-G99) Other disorders of the nervous system

  • () Disorders of autonomic nervous system
  • () Idiopathic peripheral autonomic neuropathy
  • () Familial dysautonomia (Riley-Day)
  • () Horner's syndrome
  • () Multi-system degeneration
  • () Other disorders of autonomic nervous system
  • () Disorder of autonomic nervous system, unspecified
  • () Hydrocephalus
  • () Toxic encephalopathy
  • () Other disorders of brain
  • () Cerebral cysts
  • () Anoxic brain damage, not elsewhere classified
  • () Benign intracranial hypertension
  • () Postviral fatigue syndrome
  • () Encephalopathy, unspecified
  • () Compression of brain
  • () Cerebral oedema
  • () Reye's syndrome
  • () Other disorders of brain in diseases classified elsewhere
  • () Other diseases of spinal cord
  • () Syringomyelia and syringobulbia
  • () Vascular myelopathies
  • () Cord compression, unspecified
  • () Other specified diseases of spinal cord
  • () Disease of spinal cord, unspecified
  • Myelopathy NOS
  • () Other disorders of central nervous system
  • () Postprocedural disorders of nervous system, not elsewhere classified
  • () Other disorders of nervous system, not elsewhere classified
  • () Other disorders of nervous system in diseases classified elsewhere



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