ICD-10 Chapter VI: Diseases of the nervous system
This is a shortened version of the sixth chapter of the ICD-10: Diseases of the nervous system. It covers ICD codes G00.0 to G99. All versions of the ICD-10, including the most recent one (2019), can be browsed freely on the website of the World Health Organisation (WHO). The ICD-10 can also be downloaded in PDF-form.
Chapter | Block | Title |
---|---|---|
I | A00–B99 | Certain infectious and parasitic diseases |
II | C00–D48 | Neoplasms |
III | D50–D89 | Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism |
IV | E00–E90 | Endocrine, nutritional and metabolic diseases |
V | F00–F99 | Mental and behavioural disorders |
VI | G00–G99 | Diseases of the nervous system |
VII | H00–H59 | Diseases of the eye and adnexa |
VIII | H60–H95 | Diseases of the ear and mastoid process |
IX | I00–I99 | Diseases of the circulatory system |
X | J00–J99 | Diseases of the respiratory system |
XI | K00–K93 | Diseases of the digestive system |
XII | L00–L99 | Diseases of the skin and subcutaneous tissue |
XIII | M00–M99 | Diseases of the musculoskeletal system and connective tissue |
XIV | N00–N99 | Diseases of the genitourinary system |
XV | O00–O99 | Pregnancy, childbirth and the puerperium |
XVI | P00–P96 | Certain conditions originating in the perinatal period |
XVII | Q00–Q99 | Congenital malformations, deformations and chromosomal abnormalities |
XVIII | R00–R99 | Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified |
XIX | S00–T98 | Injury, poisoning and certain other consequences of external causes |
XX | V01–Y98 | External causes of morbidity and mortality |
XXI | Z00–Z99 | Factors influencing health status and contact with health services |
XXII | U00–U99 | Codes for special purposes |
Chapter VI covers such conditions as meningitis, Parkinson's disease, epilepsy and cerebral palsy. However, neoplastic conditions, such as meningiomas, are captured using codes from Chapter II: Neoplasms.
Inflammatory diseases of the central nervous system (G00–G09)
- 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
- G03.0 Nonpyogenic meningitis
- G03.1 Chronic meningitis
- G03.2 Benign recurrent meningitis (Mollaret)
- G03.8 Meningitis due to other specified causes
- G03.9 Meningitis, unspecified
- Arachnoiditis (spinal) NOS
- 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
Systemic atrophies primarily affecting the central nervous system (G10–G13)
- G10 Huntington's disease
- G11 Hereditary ataxia
- G11.0 Congenital nonprogressive 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
- G11.8 Other hereditary ataxias
- G11.9 Hereditary ataxia, unspecified
- G12 Spinal muscular atrophy and related syndromes
- 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)
- 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
- Paraneoplastic limbic encephalopathy
- 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
Extrapyramidal and movement disorders (G20–G26)
- G20 Parkinson's disease
- G21 Secondary parkinsonism
- G21.0 Malignant neuroleptic syndrome
- G21.3 Postencephalitic parkinsonism
- 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
- G24 Dystonia
- G24.0 Drug-induced dystonia
- G24.1 Idiopathic familial dystonia
- G24.2 Idiopathic nonfamilial dystonia
- G24.3 Spasmodic torticollis
- G24.4 Idiopathic orofacial dystonia
- Orofacial dyskinesia
- G24.5 Blepharospasm
- G24.8 Other dystonia
- G24.9 Dystonia, unspecified
- Dyskinesia NOS
- 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
- Restless legs syndrome
- Stiff-man syndrome
- G25.9 Extrapyramidal and movement disorder, unspecified
- G26 Extrapyramidal and movement disorders in diseases classified elsewhere
Other degenerative diseases of the nervous system (G30–G32)
- G30 Alzheimer's disease
- G31 Other degenerative diseases of nervous system, not elsewhere classified
- G31.0 Frontotemporal dementia
- G31.1 Senile degeneration of brain, not elsewhere classified
- G31.2 Degeneration of nervous system due to alcohol
- G31.8 Other specified degenerative diseases of nervous system
- Grey-matter degeneration (Alpers)
- Lewy body dementia
- Subacute necrotizing encephalopathy (Leigh)
- G31.9 Degenerative disease of nervous system, unspecified
- G32 Other degenerative disorders of nervous system in diseases classified elsewhere
- G32.0 Subacute combined degeneration of spinal cord in diseases classified elsewhere
- G32.8 Other specified degenerative disorders of nervous system in diseases classified elsewhere
Demyelinating diseases of the central nervous system (G35–G37)
- G35 Multiple sclerosis
- G36 Other acute disseminated demyelination
- G36.0 Neuromyelitis optica (Devic)
- G36.1 Acute and subacute haemorrhagic leukoencephalitis (Hurst)
- G36.8 Other specified acute disseminated demyelination
- G36.9 Acute disseminated demyelination, unspecified
- G37 Other demyelinating diseases of central nervous system
- G37.0 Diffuse sclerosis
- G37.1 Central demyelination of corpus callosum
- G37.2 Central pontine myelinolysis
- G37.3 Acute transverse myelitis in demyelinating disease of central nervous system
- G37.4 Subacute necrotizing myelitis
- G37.5 Concentric sclerosis (Baló)
- G37.8 Other specified demyelinating diseases of central nervous system
- G37.9 Demyelinating disease of central nervous system, unspecified
Episodic and paroxysmal disorders (G40–G47)
Epilepsy
- 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
- 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
Headaches
Cerebrovascular
- G45 Transient cerebral ischaemic attacks and related syndromes
- G45.0 Vertebrobasilar 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
Sleep disorders
- 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
Nerve, nerve root and plexus disorders (G50–G59)
- G50 Disorders of trigeminal nerve (V)
- G51 Facial nerve disorders (VII)
- G51.0 Bell's palsy
- Facial palsy
- G51.1 Geniculate ganglionitis
- G51.2 Melkersson's syndrome
- Melkersson-Rosenthal syndrome
- G51.3 Clonic hemifacial spasm
- G51.4 Facial myokymia
- G51.8 Other disorders of facial nerve
- G51.9 Disorder of facial nerve, unspecified
- G51.0 Bell's palsy
- G52 Disorders of other cranial nerves
- G52.0 Disorders of olfactory nerve (I)
- G52.1 Disorders of glossopharyngeal nerve (IX)
- G52.2 Disorders of vagus nerve (X)
- G52.3 Disorders of hypoglossal nerve (XII)
- G52.7 Disorders of multiple cranial nerves
- G52.8 Disorders of other specified cranial nerves
- G52.9 Cranial nerve disorder, unspecified
- G53 Cranial nerve disorders in diseases classified elsewhere
- G54 Nerve root and plexus disorders
- G54.0 Brachial plexus disorders
- G54.1 Lumbosacral plexus disorders
- G54.2 Cervical root disorders, not elsewhere classified
- G54.3 Thoracic root disorders, not elsewhere classified
- G54.4 Lumbosacral root disorders, not elsewhere classified
- G54.5 Neuralgic Amyotrophy
- Parsonage-Aldren-Turner syndrome
- 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
- G57.0 Lesion of sciatic nerve
- G57.1 Meralgia paraesthetica
- G57.2 Lesion of femoral nerve
- G57.3 Lesion of lateral popliteal nerve
- G57.4 Lesion of medial popliteal nerve
- G57.5 Tarsal tunnel syndrome
- G57.6 Lesion of plantar nerve
- Morton's metatarsalgia
- G57.8 Other mononeuropathies of lower limb
- G57.9 Mononeuropathy of lower limb, unspecified
- G58 Other mononeuropathies
- G58.0 Intercostal neuropathy
- G58.7 Mononeuritis multiplex
- G58.8 Other specified mononeuropathies
- G58.9 Mononeuropathy, unspecified
- G59 Mononeuropathy in diseases classified elsewhere
Polyneuropathies and other disorders of the peripheral nervous system (G60–G64)
- G60 Hereditary and idiopathic neuropathy
- G60.0 Hereditary motor and sensory neuropathy
- Charcot–Marie–Tooth disease
- Dejerine–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
- G61 Inflammatory polyneuropathy
- G61.0 Guillain–Barré syndrome
- G61.1 Serum neuropathy
- G61.8 Other inflammatory polyneuropathies
- G61.9 Inflammatory polyneuropathy, unspecified
- 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
Diseases of myoneural junction and muscle (G70–G73)
- 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
Cerebral palsy and other paralytic syndromes (G80–G83)
- G80 Cerebral palsy
- G81 Hemiplegia
- G81.0 Flaccid hemiplegia
- G81.1 Spastic hemiplegia
- G81.9 Hemiplegia, 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
- Todd's paralysis (postepileptic)
- G83.9 Paralytic syndrome, unspecified
Other disorders of the nervous system (G90–G99)
- 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
- G91 Hydrocephalus
- G92 Toxic encephalopathy
- 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 (myalgic encephalomyelitis aka chronic fatigue syndrome)
- G93.4 Encephalopathy, unspecified
- G93.5 Compression of brain
- G93.6 Cerebral oedema
- G93.7 Reye's syndrome
- G93.8 Other specified disorders of brain
- Postradiation encephalopathy
- G93.9 Disorder of brain, unspecified
- G94 Other disorders of brain in diseases classified elsewhere
- 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
- G96.0 Cerebrospinal fluid leak
- G96.1 Disorders of meninges, not elsewhere classified
- Meningeal adhesions (cerebral)(spinal)
- G96.8 Other specified disorders of central nervous system
- G96.9 Disorder of central nervous system, unspecified
- 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
Excludes
- Certain conditions originating in the perinatal period (P04-P96)
- Certain infectious and parasitic diseases (A00-B99)
- Complications of pregnancy, childbirth and the puerperium (O00-O9A)
- Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- Endocrine, nutritional, and metabolic diseases (E00-E88)
- Injury, poisoning and certain other consequences of external causes (S00-T88)
- Neoplasms (C00-D49)
- Symptoms, signs, and abnormal clinical and laboratory findings, NEC (R00-R94)
See also
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