G00–G99 – Diseases of the nervous system

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

 (G00) Bacterial meningitis, not elsewhere classified

o (G00.0) Haemophilus meningitis
o (G00.1) Pneumococcal meningitis
o (G00.2) Streptococcal meningitis
o (G00.3) Staphylococcal meningitis
o (G00.8) Other bacterial meningitis
 Meningitis due to Escherichia coli
 Meningitis due to Friedländer bacillus
 Meningitis due to Klebsiella
o (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
o (G03.0) Nonpyogenic meningitis
o (G03.1) Chronic meningitis
o (G03.2) Benign recurrent meningitis (Mollaret)
o (G03.8) Meningitis due to other specified causes
o (G03.9) Meningitis, unspecified
 Arachnoiditis (spinal) NOS
 (G04) Encephalitis, myelitis and encephalomyelitis
o (G04.0) Acute disseminated encephalitis
o (G04.1) Tropical spastic paraplegia
o (G04.2) Bacterial meningoencephalitis and meningomyelitis, not
elsewhere classified
o (G04.8) Other encephalitis, myelitis and encephalomyelitis
o (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
(G10–G13) Systemic atrophies primarily affecting the central nervous system

 (G10) Huntington's disease

 (G11) Hereditary ataxia
o (G11.0) Congenital nonprogressive ataxia
o (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
o (G11.2) Late-onset cerebellar ataxia
o (G11.3) Cerebellar ataxia with defective DNA repair
 Ataxia telangiectasia (Louis-Bar)
o (G11.4) Hereditary spastic paraplegia
o (G11.8) Other hereditary ataxias
o (G11.9) Hereditary ataxia, unspecified
 (G12) Spinal muscular atrophy and related syndromes
o (G12.0) Werdnig-Hoffman disease (Type 1)
o (G12.1) Other inherited spinal muscular atrophy
 Progressive bulbar palsy of childhood (Fazio-Londe)
 Kugelberg-Welander disease (Type 3)
o (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
o (G13.0) Paraneoplastic neuromyopathy and neuropathy
o (G13.1) Other systemic atrophy primarily affecting central nervous
system in neoplastic disease
 Paraneoplastic limbic encephalopathy
o (G13.2) Systemic atrophy primarily affecting central nervous system
in myxoedema
o (G13.8) Systemic atrophy primarily affecting central nervous system
in other diseases classified elsewhere
(G20–G26) Extrapyramidal and movement disorders

 (G20) Parkinson's disease

 (G21) Secondary parkinsonism
o (G21.0) Malignant neuroleptic syndrome
o (G21.3) Postencephalitic parkinsonism
 (G22) Parkinsonism in diseases classified elsewhere
 (G23) Other degenerative diseases of basal ganglia
o (G23.0) Hallervorden-Spatz disease
o (G23.1) Progressive supranuclear ophthalmoplegia (Steele-
Richardson-Olszewski)
o (G23.2) Striatonigral degeneration
o (G23.8) Other specified degenerative diseases of basal ganglia
o (G23.9) Degenerative disease of basal ganglia, unspecified
 (G24) Dystonia
o (G24.0) Drug-induced dystonia
o (G24.1) Idiopathic familial dystonia
o (G24.2) Idiopathic nonfamilial dystonia
o (G24.3) Spasmodic torticollis
o (G24.4) Idiopathic orofacial dystonia
 Orofacial dyskinesia
o (G24.5) Blepharospasm
o (G24.8) Other dystonia
o (G24.9) Dystonia, unspecified
 Dyskinesia NOS
 (G25) Other extrapyramidal and movement disorders
o (G25.0) Essential tremor
o (G25.1) Drug-induced tremor
o (G25.2) Other specified forms of tremor
o (G25.3) Myoclonus
o (G25.4) Drug-induced chorea
o (G25.5) Other chorea
o (G25.6) Drug-induced tics and other tics of organic origin
o (G25.8) Other specified extrapyramidal and movement disorders
 Restless legs syndrome
 Stiff-man syndrome
o (G25.9) Extrapyramidal and movement disorder, unspecified
 (G26) Extrapyramidal and movement disorders in diseases classified
elsewhere
(G30–G32) Other degenerative diseases of the nervous system

 (G30) Alzheimer's disease

 (G31) Other degenerative diseases of nervous system, not elsewhere
classified
o (G31.0) Circumscribed brain atrophy
 Pick's disease
o (G31.1) Senile degeneration of brain, not elsewhere classified
o (G31.2) Degeneration of nervous system due to alcohol
o (G31.8) Other specified degenerative diseases of nervous system
 Grey-matter degeneration (Alpers)
 Lewy body dementia
 Subacute necrotizing encephalopathy (Leigh)
o (G31.9) Degenerative disease of nervous system, unspecified
 (G32) Other degenerative disorders of nervous system in diseases classified
elsewhere
o (G32.0) Subacute combined degeneration of spinal cord in diseases
classified elsewhere
o (G32.8) Other specified degenerative disorders of nervous system in
diseases classified elsewhere

(G35–G37) Demyelinating diseases of the central nervous system

 (G35) Multiple sclerosis

 (G36) Other acute disseminated demyelination
o (G36.0) Neuromyelitis optica (Devic)
o (G36.1) Acute and subacute haemorrhagic leukoencephalitis (Hurst)
o (G36.8) Other specified acute disseminated demyelination
o (G36.9) Acute disseminated demyelination, unspecified
 (G37) Other demyelinating diseases of central nervous system
o (G37.0) Diffuse sclerosis
o (G37.1) Central demyelination of corpus callosum
o (G37.2) Central pontine myelinolysis
o (G37.3) Acute transverse myelitis in demyelinating disease of central
nervous system
o (G37.4) Subacute necrotizing myelitis
o (G37.5) Concentric sclerosis (Baló)
o (G37.8) Other specified demyelinating diseases of central nervous
system
o (G37.9) Demyelinating disease of central nervous system, unspecified
(G40–G47) Episodic and paroxysmal disorders

Epilepsy

 (G40) Epilepsy
o (G40.0) Localization-related (focal)(partial) idiopathic epilepsy and
epileptic syndromes with seizures of localized onset
o (G40.1) Localization-related (focal)(partial) symptomatic epilepsy and
epileptic syndromes with simple partial seizures
o (G40.2) Localization-related (focal)(partial) symptomatic epilepsy and
epileptic syndromes with complex partial seizures
o (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
o (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
o (G40.5) Special epileptic syndromes
 Epilepsia partialis continua (Kozhevnikov)
o (G40.6) Grand mal seizures, unspecified (with or without petit mal)
o (G40.7) Petit mal, unspecified, without grand mal seizures
o (G40.8) Other epilepsy
  Epilepsies and epileptic syndromes undetermined as to whether
they are focal or generalized
o (G40.9) Epilepsy, unspecified
 (G41) Status epilepticus
o (G41.0) Grand mal status epilepticus
o (G41.1) Petit mal status epilepticus
o (G41.2) Complex partial status epilepticus
o (G41.8) Other status epilepticus
o (G41.9) Status epilepticus, unspecified

Headaches

 (G43) Migraine
o (G43.0) Migraine without aura (common migraine)
o (G43.1) Migraine with aura (classical migraine)
o (G43.2) Status migrainosus
o (G43.3) Complicated migraine
o (G43.8) Other migraine
o (G43.9) Migraine, unspecified
 (G44) Other headache syndromes
o (G44.0) Cluster headache syndrome
o (G44.1) Vascular headache, not elsewhere classified
o (G44.2) Tension-type headache
o (G44.3) Chronic post-traumatic headache
o (G44.4) Drug-induced headache, not elsewhere classified
o (G44.8) Other specified headache syndromes

Cerebrovascular

 (G45) Transient cerebral ischaemic attacks and related syndromes

o (G45.0) Vertebrobasilar artery syndrome
o (G45.1) Carotid artery syndrome (hemispheric)
o (G45.2) Multiple and bilateral precerebral artery syndromes
o (G45.3) Amaurosis fugax
o (G45.4) Transient global amnesia
o (G45.8) Other transient cerebral ischaemic attacks and related
syndromes
o (G45.9) Transient cerebral ischaemic attack, unspecified
 (G46) Vascular syndromes of brain in cerebrovascular diseases
o (G46.0) Middle cerebral artery syndrome
 o (G46.1) Anterior cerebral artery syndrome
o (G46.2) Posterior cerebral artery syndrome
o (G46.3) Brain stem stroke syndrome
 Benedikt syndrome
 Claude syndrome
 Foville syndrome
 Millard-Gubler syndrome
 Wallenberg syndrome
 Weber syndrome
o (G46.4) Cerebellar stroke syndrome
o (G46.5) Pure motor lacunar syndrome
o (G46.6) Pure sensory lacunar syndrome
o (G46.7) Other lacunar syndromes
o (G46.8) Other vascular syndromes of brain in cerebrovascular
diseases

Sleep disorders

 (G47) Sleep disorders

o (G47.0) Disorders of initiating and maintaining sleep (insomnias)
o (G47.1) Disorders of excessive somnolence (hypersomnias)
o (G47.2) Disruptions in circadian rhythm including jet lag
o (G47.3) Sleep apnoea
o (G47.4) Narcolepsy and cataplexy

(G50–G59) Nerve, nerve root and plexus disorders

 (G50) Disorders of trigeminal nerve (V)

o (G50.0) Trigeminal neuralgia
 (G51) Facial nerve disorders (VII)
o (G51.0) Bell's palsy
 Facial palsy
o (G51.1) Geniculate ganglionitis
o (G51.2) Melkersson's syndrome
 Melkersson-Rosenthal syndrome
o (G51.3) Clonic hemifacial spasm
o (G51.4) Facial myokymia
o (G51.8) Other disorders of facial nerve
o (G51.8) Disorder of facial nerve, unspecified
 (G52) Disorders of other cranial nerves
 o (G52.0) Disorders of olfactory nerve (I)
o (G52.1) Disorders of glossopharyngeal nerve (IX)
o (G52.2) Disorders of vagus nerve (X)
o (G52.3) Disorders of hypoglossal nerve (XII)
o (G52.7) Disorders of multiple cranial nerves
o (G52.8) Disorders of other specified cranial nerves
o (G52.9) Cranial nerve disorder, unspecified
 (G53) Cranial nerve disorders in diseases classified elsewhere
 (G54) Nerve root and plexus disorders
o (G54.0) Brachial plexus disorders
 Thoracic outlet syndrome
o (G54.1) Lumbosacral plexus disorders
o (G54.2) Cervical root disorders, not elsewhere classified
o (G54.3) Thoracic root disorders, not elsewhere classified
o (G54.4) Lumbosacral root disorders, not elsewhere classified
o (G54.5) Neuralgic Amyotrophy
 Parsonage-Aldren-Turner syndrome
o (G54.6) Phantom limb syndrome with pain
o (G54.7) Phantom limb syndrome without pain
 (G55) Nerve root and plexus compressions in diseases classified elsewhere
 (G56) Mononeuropathies of upper limb
o (G56.0) Carpal tunnel syndrome
o (G56.1) Other lesions of median nerve
o (G56.2) Lesion of ulnar nerve
 Tardy ulnar nerve palsy
o (G56.3) Lesion of radial nerve
o (G56.4) Causalgia
o (G56.8) Other mononeuropathies of upper limb
 Interdigital neuroma of upper limb
o (G56.9) Mononeuropathy of upper limb, unspecified
 (G57) Mononeuropathies of lower limb
o (G57.0) Lesion of sciatic nerve
o (G57.1) Meralgia paraesthetica
o (G57.2) Lesion of femoral nerve
o (G57.3) Lesion of lateral popliteal nerve
o (G57.4) Lesion of medial popliteal nerve
o (G57.5) Tarsal tunnel syndrome
o (G57.6) Lesion of plantar nerve
 Morton's metatarsalgia
o (G57.8) Other mononeuropathies of lower limb
 o (G57.9) Mononeuropathy of lower limb, unspecified
 (G58) Other mononeuropathies
o (G58.0) Intercostal neuropathy
o (G58.7) Mononeuritis multiplex
o (G58.8) Other specified mononeuropathies
o (G58.9) Mononeuropathy, unspecified
 (G59) Mononeuropathy in diseases classified elsewhere

(G60–G64) Polyneuropathies and other disorders of the peripheral nervous

system

 (G60) Hereditary and idiopathic neuropathy

o (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
o (G60.1) Refsum's disease
o (G60.2) Neuropathy in association with hereditary ataxia
o (G60.3) Idiopathic progressive neuropathy
o (G60.8) Other hereditary and idiopathic neuropathies
 Morvan's disease
 Nelaton's syndrome
 Sensory neuropathy
o (G60.9) Hereditary and idiopathic neuropathy, unspecified
 (G61) Inflammatory polyneuropathy
o (G61.0) Guillain-Barré syndrome
o (G61.1) Serum neuropathy
o (G61.8) Other inflammatory polyneuropathies
o (G61.9) Inflammatory polyneuropathy, unspecified
 (G62) Other polyneuropathies
o (G62.0) Drug-induced polyneuropathy
o (G62.1) Alcoholic polyneuropathy
o (G62.2) Polyneuropathy due to other toxic agents
o (G62.8) Other specified polyneuropathies
o (G62.9) 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

o (G70.0) Myasthenia gravis
o (G70.1) Toxic myoneural disorders
o (G70.2) Congenital and developmental myasthenia
 (G71) Primary disorders of muscles
o (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)
o (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
o (G71.2) Congenital myopathies, including:
 Central core disease
 Congenital muscular dystrophy
 Centronuclear myopathy
 Fibre-type disproportion
 Minicore disease
 Multicore disease
 Myotubular myopathy
 Nemaline myopathy
 o (G71.3) Mitochondrial myopathy, not elsewhere classified
 (G72) Other myopathies
o (G72.0) Drug-induced myopathy
o (G72.1) Alcoholic myopathy
o (G72.2) Myopathy due to other toxic agents
o (G72.3) Periodic paralysis
 Hypokalemic periodic paralysis
 Hyperkalemic periodic paralysis
 (G73) Disorders of myoneural junction and muscle in diseases classified
elsewhere
o (G73.0) Myasthenic syndromes in endocrine diseases
o (G73.1) Eaton-Lambert syndrome
o (G73.2) Other myasthenic syndromes in neoplastic disease
o (G73.3) Myasthenic syndromes in other diseases classified elsewhere
o (G73.4) Myopathy in infectious and parasitic diseases classified
elsewhere
o (G73.5) Myopathy in endocrine diseases
o (G73.6) Myopathy in metabolic diseases
o (G73.7) Myopathy in other diseases classified elsewhere

(G80–G83) Cerebral palsy and other paralytic syndromes

 (G80) Cerebral palsy

o (G80.0) Spastic quadriplegic cerebral palsy
o (G80.1) Spastic diplegic cerebral palsy
o (G80.2) Spastic hemiplegic cerebral palsy
o (G80.3) Dyskinetic cerebral palsy
o (G80.4) Ataxic cerebral palsy
o (G80.8) Other cerebral palsy
o (G80.9) Cerebral palsy, unspecified
 (G81) Hemiplegia
o (G81.0) Flaccid hemiplegia
o (G81.1) Spastic hemiplegia
o (G81.9) Hemiplegia, unspecified
 (G82) Paraplegia and tetraplegia
o (G82.0) Flaccid paraplegia
o (G82.1) Spastic paraplegia
o (G82.2) Paraplegia, unspecified
 Paralysis of both lower limbs NOS
 Paraplegia (lower) NOS
 o (G82.3) Flaccid tetraplegia
o (G82.4) Spastic tetraplegia
o (G82.5) Tetraplegia, unspecified
 Quadriplegia NOS
 (G83) Other paralytic syndromes
o (G83.0) Diplegia of upper limbs
o (G83.1) Monoplegia of lower limb
o (G83.2) Monoplegia of upper limb
o (G83.3) Monoplegia, unspecified
o (G83.4) Cauda equina syndrome
o (G83.8) Other specified paralytic syndromes
 Todd's paralysis (postepileptic)
o (G83.9) Paralytic syndrome, unspecified

(G90–G99) Other disorders of the nervous system

 (G90) Disorders of autonomic nervous system

o (G90.0) Idiopathic peripheral autonomic neuropathy
o (G90.1) Familial dysautonomia (Riley-Day)
o (G90.2) Horner's syndrome
o (G90.3) Multi-system degeneration
o (G90.8) Other disorders of autonomic nervous system
o (G90.9) Disorder of autonomic nervous system, unspecified
 (G91) Hydrocephalus
 (G92) Toxic encephalopathy
 (G93) Other disorders of brain
o (G93.0) Cerebral cysts
o (G93.1) Anoxic brain damage, not elsewhere classified
o (G93.2) Benign intracranial hypertension
o (G93.3) Postviral fatigue syndrome
o (G93.4) Encephalopathy, unspecified
o (G93.5) Compression of brain
o (G93.6) Cerebral oedema
o (G93.7) Reye's syndrome
o (G93.8) Other specified disorders of brain
 Postradiation encephalopathy
o (G93.9) Disorder of brain, unspecified
 (G94) Other disorders of brain in diseases classified elsewhere
 (G95) Other diseases of spinal cord
o (G95.0) Syringomyelia and syringobulbia
 o (G95.1) Vascular myelopathies
o (G95.2) Cord compression, unspecified
o (G95.8) Other specified diseases of spinal cord
o (G95.9) Disease of spinal cord, unspecified
 Myelopathy NOS
 (G96) Other disorders of central nervous system
o (G96.0) Cerebrospinal fluid leak
o (G96.1) Disorders of meninges, not elsewhere classified
 Meningeal adhesions (cerebral)(spinal)
o (G96.8) Other specified disorders of central nervous system
o (G96.9) Disorder of central nervous system, unspecified
 (G97) Postprocedural disorders of nervous system, not elsewhere classified
o (G97.0) Cerebrospinal fluid leak from spinal puncture
o (G97.1) Other reaction to spinal and lumbar puncture
o (G97.2) Intracranial hypotension following ventricular shunting
o (G97.8) Other postprocedural disorders of nervous system
o (G97.9) Postprocedural disorder of nervous system, unspecified
 (G98) Other disorders of nervous system, not elsewhere classified
 (G99) Other disorders of nervous system in diseases classified elsewhere

I60–I69) Cerebrovascular diseases

 (I60) Subarachnoid hemorrhage

o (I60.0) Subarachnoid haemorrhage from carotid siphon and
bifurcation
o (I60.1) Subarachnoid haemorrhage from middle cerebral artery
o (I60.2) Subarachnoid haemorrhage from anterior communicating
artery
o (I60.3) Subarachnoid haemorrhage from posterior communicating
artery
o (I60.4) Subarachnoid haemorrhage from basilar artery
o (I60.5) Subarachnoid haemorrhage from vertebral artery
o (I60.6) Subarachnoid haemorrhage from other intracranial arteries
o (I60.7) Subarachnoid haemorrhage from intracranial artery,
unspecified
 (I61) Intracerebral haemorrhage
o (I61.0) Intracerebral haemorrhage in hemisphere, subcortical
o (I61.1) Intracerebral haemorrhage in hemisphere, cortical
o (I61.2) Intracerebral haemorrhage in hemisphere, unspecified
o (I61.3) Intracerebral haemorrhage in brain stem
 o (I61.4) Intracerebral haemorrhage in cerebellum
o (I61.5) Intracerebral haemorrhage, intraventricular
o (I61.6) Intracerebral haemorrhage, multiple localized
 (I62) Other nontraumatic intracranial haemorrhage
o (I62.0) Subdural haemorrhage (acute)(nontraumatic)
o (I62.1) Nontraumatic extradural haemorrhage
 Nontraumatic epidural haemorrhage
 (I63) Cerebral infarction
o (I63.0) Cerebral infarction due to thrombosis of precerebral arteries
o (I63.1) Cerebral infarction due to embolism of precerebral arteries
o (I63.2) Cerebral infarction due to unspecified occlusion or stenosis of
precerebral arteries
o (I63.3) Cerebral infarction due to thrombosis of cerebral arteries
o (I63.4) Cerebral infarction due to embolism of cerebral arteries
o (I63.5) Cerebral infarction due to unspecified occlusion or stenosis of
cerebral arteries
o (I63.6) Cerebral infarction due to cerebral venous thrombosis,
nonpyogenic
 (I64) Stroke, not specified as hemorrhage or infarction
 (I65) Occlusion and stenosis of precerebral arteries, not resulting in cerebral
infarction
o (I65.0) Occlusion and stenosis of vertebral artery
o (I65.1) Occlusion and stenosis of basilar artery
o (I65.2) Occlusion and stenosis of carotid artery
o (I65.3) Occlusion and stenosis of multiple and bilateral precerebral
arteries
o (I65.8) Occlusion and stenosis of other precerebral artery
o (I65.9) Occlusion and stenosis of unspecified precerebral artery
 (I66) Occlusion and stenosis of cerebral arteries, not resulting in cerebral
infarction
o (I66.0) Occlusion and stenosis of middle cerebral artery
o (I66.1) Occlusion and stenosis of anterior cerebral artery
o (I66.2) Occlusion and stenosis of posterior cerebral artery
o (I66.3) Occlusion and stenosis of cerebellar arteries
o (I66.4) Occlusion and stenosis of multiple and bilateral cerebral
arteries
o (I66.5) Occlusion and stenosis of other cerebral artery
o (I66.6) Occlusion and stenosis of unspecified cerebral artery
 (I67) Other cerebrovascular diseases
o (I67.1) Cerebral aneurysm, nonruptured
 o (I67.2) Cerebral atherosclerosis
o (I67.3) Progressive vascular leukoencephalopathy
 Binswanger's disease
o (I67.4) Hypertensive encephalopathy
o (I67.5) Moyamoya disease
o (I67.6) Nonpyogenic thrombosis of intracranial venous system
o (I67.7) Cerebral arteritis, not elsewhere classified
 (I68) Cerebrovascular disorders in diseases classified elsewhere
 (I69) Sequelae of cerebrovascular disease