Chronic Neurological Disease including Significant Learning Disorder

Coding system: SNOMED CT (UK Clinical Edition)
Coding system release: unknown
Organisation: PRIMIS Covid Vaccination Uptake Reporting
Codelist ID: primis-covid19-vacc-uptake/cns_cov
Version Tag: v1
Version ID: 3a82f99b
Number of codes included: 1,828

Versions

v2.5 Published
Created: 03 Jan 2024 at 14:38
v2.4 Published
Created: 20 Dec 2023 at 10:19
v.1.5.3 Published
Created: 16 Jun 2022 at 20:56
v1 Published
Created: 11 Feb 2021 at 19:59

Description

Taken from the `CNS_COV_COD` field in SARS-CoV2 COVID19 Vaccination Uptake Reporting Codes 20_21 v1, published by PRIMIS.

© PRIMIS - the University of Nottingham 2021

References

SARS-CoV2 (COVID-19) Vaccine Uptake Reporting Specification Collection

Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.

We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.

code	term
10007009	Coffin-Siris syndrome
100941000119100	Epilepsy in mother complicating pregnancy
101421000119107	Dementia due to Parkinson's disease
102831000119104	Paralytic syndrome of both lower limbs as sequela of stroke
10349009	Multi-infarct dementia with delirium
103761000119107	Paralytic syndrome of all four limbs as sequela of stroke
104461000119104	Ophthalmoplegia due to Graves disease
1055001	Stenosis of precerebral artery
106018006	Hereditary degenerative disease of central nervous system
106021000119105	Multi-infarct dementia due to atherosclerosis
10750951000119106	Epilepsy in mother complicating childbirth
108691000119102	Spasticity as sequela of stroke
10878002	Aneurysm of common carotid artery
1089411000000104	Cerebral infarction due to occlusion of cerebral artery
1089421000000105	Cerebral infarction due to stenosis of cerebral artery
1089501000000102	Presenile dementia with psychosis
1089521000000106	Predominantly cortical dementia
1089531000000108	Predominantly cortical vascular dementia
109478007	Kohlschutter's syndrome
109561000	Cerebrofacial dysplasia
109911004	Overlapping malignant neoplasm of brain and other parts of the central nervous system
109915008	Primary malignant neoplasm of meninges
111296006	Basilar artery embolism
111298007	Chronic cerebral ischemia
111299004	Atheroma of cerebral arteries
111337001	Dyke-Davidoff-Masson syndrome
111385000	Tay-Sachs disease
111480006	Psychoactive substance-induced organic dementia
111496009	Syringomyelia
111497000	Arterial thrombosis of spinal cord
111498005	Extratemporal epilepsy
111499002	Déjérine-Sottas disease
111500006	Muscular dystrophy-deafmutism syndrome
111501005	Congenital hereditary muscular dystrophy
111502003	Fukuyama congenital muscular dystrophy
111503008	Merosin deficient congenital muscular dystrophy
111505001	Muscle-eye-brain disease, congenital muscular dystrophy
111506000	Distal muscular dystrophy, Miyoshi type
111508004	Emery-Dreifuss muscular dystrophy
111527005	Partial optic atrophy
1131000119105	Sequela of cerebrovascular accident
11442006	Hereditary sensory neuropathy
11538006	Quadriplegia
116811000119106	Non-Hodgkin lymphoma of central nervous system metastatic to lymph node of lower limb
116821000119104	Non-Hodgkin lymphoma of central nervous system metastatic to lymph node of upper limb
11701009	Hemicephaly
119001000119108	Intractable simple partial epilepsy
12242711000119109	Weakness of left facial muscle due to and following cerebrovascular accident
12242751000119105	Weakness of right facial muscle due to and following cerebrovascular accident
12246008	Acute neuronopathic Gaucher's disease
12348006	Presenile dementia
123615007	Secondary optic atrophy
12367511000119101	Paraplegia due to and following cerebrovascular accident
1239331000000100	Significant intellectual disability
12454008	Cauda equina syndrome with neurogenic bladder
125081000119106	Cerebral infarction due to occlusion of precerebral artery
125501000119105	Fetus with complete trisomy 21 syndrome
125511000119108	Fetus with complete trisomy 18 syndrome
125521000119101	Fetus with complete trisomy 13 syndrome
126011000119107	Acquired caroticocavernous sinus fistula
126944002	Brain disorder resulting from a period of impaired oxygen delivery to the brain
126945001	Perinatal anoxic-ischemic brain injury
128171000119104	Spontaneous caroticocavernous sinus fistula
128190004	Inherited metabolic disorder of nervous system
128203003	Hereditary motor and sensory neuropathy with optic atrophy
128204009	Hereditary motor and sensory neuropathy with retinitis pigmentosa
128205005	Hereditary sensory and autonomic neuropathy
128206006	Congenital sensory neuropathy with selective loss of small myelinated fibers
128209004	Chronic inflammatory demyelinating polyradiculoneuropathy
128212001	Spinal muscular atrophy, type II
128213006	Neuromuscular junction disorder
128218002	Disorder of intracranial venous sinus
12853006	Embolism of torcular Herophili
128608001	Cerebral arterial aneurysm
128609009	Intracranial aneurysm
129583005	Paralysis of palate
129596006	Menopausal muscular dystrophy syndrome
129608008	Progressive pyramidopallidal degeneration
129614001	Paralysis of vagus, spinal accessory and hypoglossal nerves
129620000	Scapuloperoneal muscular dystrophy
129621001	Nemaline myopathy, early onset type
129622008	Nemaline myopathy, late onset type
130121000119104	Dementia due to Rett's syndrome
13092008	Pick's disease
133981000119106	Dysarthria as late effects of cerebrovascular disease
133991000119109	Fluency disorder as sequela of cerebrovascular disease
134771000119108	Alteration of sensation as late effect of stroke
13973009	Grand mal status
140281000119108	Hemiparesis as late effect of cerebrovascular disease
14070001	Multi-infarct dementia with depression
142031000119104	Visual field defect due to and following cerebrovascular accident
14210003	Lipofuscinosis
14246007	Embolism of intracranial venous sinus
14309005	Anterior choroidal artery syndrome
14401000119109	Partial frontal lobe epilepsy
147101000119108	Primary malignant astrocytoma of central nervous system
147131000119101	Glioblastoma multiforme of central nervous system
148871000119109	Weakness as a late effect of cerebrovascular accident
14977000	Multiple AND bilateral precerebral artery thrombosis
149821000119103	Cerebral infarction due to carotid artery occlusion
15080006	Myotubular myopathy with type I atrophy
15182000	Coffin-Lowry syndrome
15523002	Benign focal epilepsy of childhood
15632811000119100	Optic atrophy of right eye
15632851000119104	Optic atrophy of left eye
15648201000119100	Aneurysm of intracranial portion of right internal carotid artery
15648241000119103	Aneurysm of intracranial portion of left internal carotid artery
15648281000119108	Aneurysm of extracranial portion of right internal carotid artery
15648321000119103	Aneurysm of extracranial portion of left internal carotid artery
15648361000119108	Aneurysm of right internal carotid artery
15648401000119104	Aneurysm of left internal carotid artery
15648441000119102	Aneurysm of right common carotid artery
15648481000119107	Aneurysm of left common carotid artery
15648521000119107	Aneurysm of right carotid artery
15648561000119102	Aneurysm of left carotid artery
15662003	Senile dementia
15699121000119104	Hereditary right optic atrophy
15699161000119109	Hereditary left optic atrophy
15705007	Phlebitis of basilar sinus
15707961000119109	Dissection of bilateral carotid arteries
15708001000119106	Dissection of left carotid artery
15708041000119108	Dissection of right carotid artery
15710641000119100	Dissection of bilateral vertebral arteries
15710681000119105	Dissection of right vertebral artery
15710721000119104	Dissection of left vertebral artery
1591000119103	Dementia with behavioral disturbance
1593000	Infantile hemiplegia
15978431000119106	Thrombosis of right vertebral artery
15978471000119109	Thrombosis of left vertebral artery
15978631000119109	Occlusion of bilateral vertebral arteries
15982271000119104	Weakness of right facial muscle due to and following cerebrovascular disease
15982311000119104	Weakness of left facial muscle due to and following cerebrovascular disease
15988351000119101	Acquired right carotid cavernous fistula
15988391000119106	Acquired left carotid cavernous fistula
16218291000119100	Acute cerebral ischemia
16260551000119106	Dysphasia due to and following cerebrovascular accident
16276361000119109	Vascular dementia without behavioral disturbance
16279401000119108	Occlusion of right cilioretinal artery
16279441000119105	Occlusion of left cilioretinal artery
163594004	On examination - salaam attack
163601006	On examination - hemiplegia
163604003	On examination - paraplegia
163605002	On examination - quadriplegia
163606001	On examination - diplegia
16415361000119105	Radiologically isolated syndrome
16418006	Embolism of basilar sinus
16476641000119100	Acquired arteriovenous fistula of dura of cerebrum
16662331000119106	Aneurysm of right vertebral artery
16662371000119109	Aneurysm of left vertebral artery
1670004	Cerebral hemiparesis
16703551000119107	Memory deficit due to and following cerebrovascular disease
16703661000119105	Memory deficit due to and following cerebrovascular accident
16703761000119102	Memory deficit due to and following ischemic cerebrovascular accident
16703821000119101	Memory deficit due to and following hemorrhagic cerebrovascular accident
16709811000119106	Spontaneous hemorrhage of subarachnoid space from anterior communicating artery
16851005	Mitochondrial myopathy
171822009	Acute atrophic spinal paralysis
17409003	Facial hemiparesis
18058007	Phlebitis of intracranial venous sinus
18322005	Thrombosis of torcular Herophili
1845001	Paraparesis
186317009	Listerial cerebral arteritis
186476008	Acute paralytic non-bulbar poliomyelitis
186478009	Acute paralytic poliomyelitis, vaccine-associated
186479001	Acute paralytic poliomyelitis, wild virus, imported
186480003	Acute paralytic poliomyelitis, wild virus, indigenous
186831000119104	Apraxia due to and following cerebrovascular accident
186893003	Rupture of syphilitic cerebral aneurysm
18756002	Juvenile GM1 gangliosidosis
187931000119106	Atypical absence epilepsy
188312005	Malignant neoplasm of cerebral dura mater
188313000	Malignant neoplasm of cerebral arachnoid mater
188315007	Malignant neoplasm of cerebral pia mater
18927009	Niemann-Pick disease, type D
191449005	Uncomplicated senile dementia
191451009	Uncomplicated presenile dementia
191452002	Presenile dementia with delirium
191454001	Presenile dementia with paranoia
191455000	Presenile dementia with depression
191457008	Senile dementia with depressive or paranoid features
191458003	Senile dementia with paranoia
191459006	Senile dementia with depression
191461002	Senile dementia with delirium
191463004	Uncomplicated arteriosclerotic dementia
191464005	Arteriosclerotic dementia with delirium
191465006	Arteriosclerotic dementia with paranoia
191466007	Arteriosclerotic dementia with depression
191475009	Chronic alcoholic brain syndrome
191493005	Drug-induced dementia
191519005	Dementia associated with another disease
192673008	Sarcoid meningitis
192685000	Subacute sclerosing panencephalitis
192753009	Phlebitis and thrombophlebitis of intracranial sinuses
192754003	Embolism cavernous sinus
192755002	Embolism superior longitudinal sinus
192756001	Embolism lateral sinus
192757005	Embolism transverse sinus
192759008	Cerebral venous sinus thrombosis
192760003	Thrombosis of superior longitudinal sinus
192764007	Phlebitis cavernous sinus
192765008	Phlebitis of superior longitudinal sinus
192769002	Thrombophlebitis of central nervous system venous sinuses
192770001	Thrombophlebitis of cavernous sinus
192771002	Thrombophlebitis of superior longitudinal venous sinus
192781003	Leukodystrophy
192782005	Galactosylceramide beta-galactosidase deficiency
192787004	B variant hexosaminidase A deficiency
192788009	Retinal dystrophy in cerebroretinal lipidosis
192845009	Myoclonic encephalopathy
192904000	Myelopathy due to another disorder
192906003	Myelopathy due to neoplastic disease
192928003	Generalized multiple sclerosis
192929006	Exacerbation of multiple sclerosis
192949002	Congenital paraplegia
192964002	Flaccid tetraplegia
192965001	Spastic tetraplegia
192966000	Flaccid paraplegia
192967009	Spastic paraplegia
192976002	Progressive supranuclear palsy
192979009	Generalized non-convulsive epilepsy
192990004	Benign myoclonic epilepsy in infancy
192999003	Partial epilepsy with impairment of consciousness
193000002	Temporal lobe epilepsy
193002005	Psychosensory epilepsy
193008009	Somatosensory epilepsy
193009001	Partial epilepsy with autonomic symptoms
193010006	Visual reflex epilepsy
193021002	Cursive (running) epilepsy
193022009	Localization-related(focal)(partial)idiopathic epilepsy and epileptic syndromes with seizures of localized onset
193165008	Neuropathy in association with hereditary ataxia
193195000	Sarcoid neuropathy
193207007	Juvenile or adult myasthenia gravis
193209005	Myasthenic syndrome due to another disorder
193212008	Myasthenic syndrome due to hypothyroidism
193213003	Myasthenic syndrome due to pernicious anemia
193214009	Myasthenic syndrome due to thyrotoxicosis
193216006	Congenital and developmental myasthenia
193225000	Hereditary progressive muscular dystrophy
193227008	Pelvic muscular dystrophy
193230001	Distal muscular dystrophy with juvenile onset
193237003	Myotonic disorder
193238008	Infantile myotonia
19373007	External ophthalmoplegia
194043004	Optic atrophy secondary to retinal disease
19448008	Optic atrophy associated with retinal dystrophy
195154000	Ruptured berry aneurysm
195155004	Subarachnoid hemorrhage from carotid siphon and bifurcation
195160000	Intracranial subarachnoid hemorrhage from vertebral artery
195180004	Basilar artery occlusion
195182007	Vertebral artery occlusion
195183002	Multiple and bilateral precerebral arterial occlusion
195185009	Cerebral infarct due to thrombosis of precerebral arteries
195186005	Cerebral infarction due to embolism of precerebral arteries
195189003	Cerebral infarction due to thrombosis of cerebral arteries
195190007	Cerebral infarction due to embolism of cerebral arteries
195199008	Vertebrobasilar artery syndrome
195229008	Non-pyogenic venous sinus thrombosis
195230003	Cerebral infarction due to cerebral venous thrombosis, non-pyogenic
195232006	Occlusion and stenosis of middle cerebral artery
195233001	Occlusion and stenosis of anterior cerebral artery
195234007	Occlusion and stenosis of posterior cerebral artery
195235008	Occlusion and stenosis of cerebellar arteries
195236009	Occlusion and stenosis of multiple and bilateral cerebral arteries
195239002	Late effects of cerebrovascular disease
195241001	Sequelae of intracerebral hemorrhage
195243003	Sequelae of cerebral infarction
19598007	Generalized epilepsy
199451000000106	Simple partial epileptic seizure
19972008	Postencephalitic parkinsonism
20022000	Hemiparesis
200258006	Obstetric cerebral venous thrombosis
200259003	Cerebral venous thrombosis in pregnancy
200260008	Cerebral venous thrombosis in the puerperium
200330000	Puerperal cerebrovascular disorder - delivered
200331001	Puerperal cerebrovascular disorder - delivered with postnatal complication
200332008	Puerperal cerebrovascular disorder with antenatal complication
200333003	Puerperal cerebrovascular disorder with postnatal complication
20059004	Occlusion of cerebral artery
20121000119105	Partial occipital lobe epilepsy
20305008	Congenital myotonia, autosomal recessive form
204036008	Lissencephaly
204040004	Agenesis of cerebrum
204052006	Cebocephaly
20447006	Plasma cell dyscrasia with polyneuropathy
204493007	Arteriovenous malformation of precerebral vessels
204497008	Cerebrovascular system anomalies
204501003	Congenital stricture of cerebral artery
204745000	Total intestinal aganglionosis
205615000	Trisomy 21- meiotic nondisjunction
205619006	Trisomy 13, meiotic nondisjunction
205620000	Trisomy 13 - mitotic nondisjunction mosaicism
205623003	Trisomy 18 - meiotic nondisjunction
205624009	Trisomy 18 - mitotic nondisjunction mosaicism
2065009	Dominant hereditary optic atrophy
20725005	Familial visceral neuropathy
21007002	Wernicke's disease
21086008	Cockayne syndrome
21098003	Primary optic atrophy
21111006	Complete trisomy 13 syndrome
213044006	Mechanical complication of carotid artery bypass
213208008	Anoxic brain damage complication
213209000	Cerebral anoxia complication
21361000119109	Paraneoplastic peripheral neuropathy
21391000119102	Partial parietal lobe epilepsy
21524000	Relaxation of diaphragm
2198002	Visceral epilepsy
22126005	Hereditary neuraxial edema
223176004	Cerebellar disorder
22381000119105	Primary degenerative dementia
22386003	Syphilitic optic atrophy
22811006	Leukoencephalopathy
22881000119100	Quadriplegia with quadriparesis
230156002	Malignant meningitis
230193008	Neurosarcoidosis
230220006	Intracranial septic embolism
230221005	Intracranial arterial septic embolism
230222003	Septic thrombophlebitis of straight sinus
230223008	Septic thrombophlebitis of sigmoid sinus
230224002	Septic thrombophlebitis of cortical vein
230226000	System disorder of the nervous system
230232005	Late onset cerebellar ataxia
230233000	Progressive cerebellar ataxia
230234006	Periodic ataxia
230237004	Progressive spinocerebellar ataxia with decreased tendon reflexes
230239001	Progressive cerebellar ataxia with palatal myoclonus
230240004	Progressive cerebellar ataxia with hypogonadism
230244008	Disorder primarily affecting the motor pathways
230247001	Distal spinal muscular atrophy
230248006	Scapuloperoneal spinal muscular atrophy
230249003	Facioscapulohumeral spinal muscular atrophy
230250003	Facioscapulohumeral spinal muscular atrophy with sensory loss
230251004	Scapulohumeral spinal muscular atrophy
230252006	Oculopharyngeal spinal muscular atrophy
230253001	Bulbospinal neuronopathy
230254007	Western Pacific motor neurone disease
230255008	Madras-type motor neurone disease
230257000	Paraneoplastic motor neurone disease
230258005	Amyotrophic lateral sclerosis with dementia
230264003	Troyer syndrome
230282000	Post-traumatic dementia
230283005	Punch drunk syndrome
230285003	Vascular dementia of acute onset
230286002	Subcortical vascular dementia
230287006	Mixed cortical and subcortical vascular dementia
230289009	Patchy dementia
230291001	Juvenile Parkinson's disease
230296006	Vascular parkinsonism
230297002	Multiple system atrophy
230298007	Disorder presenting primarily with chorea
230329009	Posthemiplegic dystonia
230363006	Progressive neuronal degeneration of childhood
230368002	Type III transitional Pelizaeus-Merzbacher disease
230369005	Type IV adult Pelizaeus-Merzbacher disease
230370006	Type V atypical Pelizaeus-Merzbacher disease
230371005	Type VI Cockayne Pelizaeus-Merzbacher disease
230372003	Acute relapsing multiple sclerosis
230373008	Chronic progressive multiple sclerosis
230375001	Subacute hemorrhagic leukoencephalitis
230380005	Balo concentric sclerosis
230381009	Localization-related epilepsy
230382002	Benign frontal epilepsy of childhood
230383007	Benign psychomotor epilepsy of childhood
230384001	Benign atypical partial epilepsy in childhood
230386004	Childhood epilepsy with occipital paroxysms
230387008	Benign occipital epilepsy of childhood - early onset variant
230388003	Benign occipital epilepsy of childhood - late onset variant
230389006	Primary inherited reading epilepsy
230390002	Localization-related symptomatic epilepsy
230393000	Lateral temporal epilepsy
230394006	Frontal lobe epilepsy
230395007	Supplementary motor epilepsy
230397004	Anterior frontopolar epilepsy
230398009	Orbitofrontal epilepsy
230399001	Dorsolateral epilepsy
230400008	Opercular epilepsy
230401007	Non-progressive Kozhevnikow syndrome
230403005	Parietal lobe epilepsy
230404004	Occipital lobe epilepsy
230406002	Localization-related symptomatic epilepsy with specific precipitant
230407006	Hemiplegia-hemiconvulsion-epilepsy syndrome
230408001	Localization-related cryptogenic epilepsy
230412007	Myoclonic epilepsy of early childhood
230413002	Juvenile absence epilepsy
230414008	Epilepsy with grand mal seizures on awakening
230415009	Cryptogenic generalized epilepsy
230416005	Cryptogenic West syndrome
230417001	Symptomatic West syndrome
230418006	Lennox-Gastaut syndrome
230419003	Cryptogenic Lennox-Gastaut syndrome
230420009	Symptomatic Lennox-Gastaut syndrome
230422001	Myoclonic absence epilepsy
230423006	Unverricht-Lundborg syndrome
230425004	Lafora disease
230427007	Cryptogenic myoclonic epilepsy
230428002	Idiopathic myoclonic epilepsy
230429005	Early infantile epileptic encephalopathy with suppression bursts
230430000	Symptomatic myoclonic epilepsy
230435005	Epilepsy undetermined whether focal or generalized
230437002	Severe myoclonic epilepsy in infancy
230438007	Acquired epileptic aphasia
230439004	Epilepsy with continuous spike wave during slow-wave sleep
230440002	Secondary reading epilepsy
230444006	Menstrual epilepsy
230445007	Nocturnal epilepsy
230447004	Eyelid myoclonus with absences
230448009	Writing epilepsy
230450001	Eating epilepsy
230452009	Toothbrushing epilepsy
230453004	Decision-making epilepsy
230454005	Aquagenic epilepsy
230456007	Status epilepticus
230457003	Non-convulsive status epilepticus with three per second spike wave
230458008	Non-convulsive status epilepticus without three per second spike wave
230459000	Non-convulsive simple partial status epilepticus
230460005	Complex partial status epilepticus
230466004	Alternating hemiplegia of childhood
230530003	Congenital nuclear ophthalmoplegia
230552007	X-linked hereditary motor and sensory neuropathy
230553002	Autosomal dominant sensory neuropathy
230556005	X-linked recessive sensory neuropathy
230557001	Hereditary dysautonomia with motor neuropathy
230558006	Hereditary liability to pressure palsies
230559003	Hereditary hypertrophic neuropathy with paraproteinemia
230561007	Congenital neuropathy with arthrogryposis multiplex congenita
230562000	Congenital hypomyelinating neuropathy
230564004	Chronic inflammatory demyelinating polyradiculoneuropathy with central nervous system demyelination
230586003	Neuropathy due to multiple myeloma
230594005	Critical illness polyneuropathy
230666006	Paraneoplastic autonomic dysfunction
230669004	Genetically determined myasthenia
230670003	Familial infantile myasthenia
230671004	Acetylcholine resynthesis deficiency
230672006	Congenital myasthenic syndrome
230673001	Congenital end-plate acetylcholine receptor deficiency
230674007	Pseudomyopathic myasthenia
230675008	Slow channel syndrome
230676009	Putative defect in acetylcholine synthesis or packaging
230677000	Congenital end-plate acetylcholinesterase deficiency
230678005	Decrease of motor end-plate potential amplitude without acetylcholine receptor deficiency
230679002	Abnormality of synaptic vesicles
230684008	Ocular myasthenia
230685009	Myasthenia gravis associated with thymoma
230686005	Generalized myasthenia
230687001	Myopathy in myasthenia gravis
230692004	Infarction - precerebral
230693009	Anterior cerebral circulation infarction
230694003	Total anterior cerebral circulation infarction
230695002	Partial anterior cerebral circulation infarction
230696001	Posterior cerebral circulation infarction
230698000	Lacunar infarction
230699008	Pure motor lacunar infarction
230700009	Pure sensory lacunar infarction
230701008	Pure sensorimotor lacunar infarction
230702001	Lacunar ataxic hemiparesis
230703006	Dysarthria-clumsy hand syndrome
230704000	Multi-infarct state
230706003	Hemorrhagic cerebral infarction
230707007	Anterior cerebral circulation hemorrhagic infarction
230708002	Posterior cerebral circulation hemorrhagic infarction
230720005	Cerebral venous thrombosis of straight sinus
230721009	Cerebral venous thrombosis of sigmoid sinus
230722002	Cerebral venous thrombosis of cortical vein
230724001	Cerebral amyloid angiopathy
230725000	Sporadic cerebral amyloid angiopathy
230730001	Dissection of vertebral artery
230731002	Cerebral arteritis in systemic vasculitis
230732009	Cerebral arteritis in giant cell arteritis
230735006	Syphilitic cerebral arteritis
230738008	Asymptomatic cerebrovascular disease
230739000	Spinal cord stroke
230745008	Hydrocephalus
232036006	Cilioretinal artery occlusion
232059000	Laurence-Moon syndrome
233718008	Pulmonary tuberous sclerosis
233964008	Internal carotid artery stenosis
233983001	Ruptured cerebral aneurysm
233988005	Carotid artery aneurysm
234005004	Vertebral artery rupture
234006003	Carotid artery rupture
234142008	Cerebral arteriovenous malformation
234149004	Congenital arteriovenous fistula of brain
23501004	Arginase deficiency
236529001	Prune belly syndrome with pulmonic stenosis, mental retardation and deafness
23671000119107	Sequela of ischemic cerebral infarction
23728006	Partial bilateral paralysis
23740006	Bilateral paralysis of tongue
237612000	Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction
237867001	Hereditary cerebrovascular amyloidosis
237960000	D-2-hydroxyglutaric aciduria
237961001	L-2-hydroxyglutaric aciduria
238018004	Total hexosaminidase deficiency - infantile
238019007	Total hexosaminidase deficiency - juvenile
238020001	Total hexosaminidase deficiency - adult
238021002	B variant hexosaminidase A deficiency - infantile
238022009	B variant hexosaminidase A deficiency - juvenile
238023004	B variant hexosaminidase A deficiency - adult
238024005	B1 variant hexosaminidase A deficiency
238025006	GM1 gangliosidosis
238026007	Infantile GM1 gangliosidosis
238027003	Adult GM1 gangliosidosis
238030005	Galactocerebroside beta-galactosidase deficiency - early onset
238031009	Arylsulfatase A deficiency
238048001	Alpha-N-acetylgalactosaminidase deficiency
23808003	Rolandic vein occlusion syndrome
23819000	Embolism of cavernous venous sinus
23849003	Sandhoff disease
238826008	de Barsy syndrome
23941000119108	Arnold Chiari type 2 without hydrocephalus
240046001	Muscular dystrophy with predominantly proximal limb girdle distribution
240047005	X-linked muscular dystrophy with limb girdle distribution
240048000	X-linked muscular dystrophy with abnormal dystrophin
240049008	Intermediate X-linked muscular dystrophy
240050008	Manifesting female carrier of X-linked muscular dystrophy
240051007	X-linked limb girdle muscular dystrophy with normal dystrophin
240052000	Ji muscular dystrophy
240053005	Hereditary myopathy limited to females
240054004	Autosomal recessive muscular dystrophy with limb girdle distribution
240055003	Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein
240056002	Severe autosomal recessive muscular dystrophy of childhood - North African type
240057006	Autosomal recessive muscular dystrophy with gene located at 15q
240058001	Reunion-Indiana Amish type muscular dystrophy
240059009	Congenital muscular dystrophy
240060004	Western type of congenital muscular dystrophy
240061000	Congenital muscular dystrophy with arthrogryposis multiplex congenita
240062007	Ullrich congenital muscular dystrophy
240063002	Eichsfeld type congenital muscular dystrophy
240064008	Hutterite type of muscular dystrophy
240065009	Adult onset autosomal recessive muscular dystrophy with normal dystrophin
240067001	Autosomal dominant muscular dystrophy with limb girdle distribution
240068006	Autosomal dominant muscular dystrophy with gene located at 5q31
240069003	Late onset proximal muscular dystrophy with dysarthria
240070002	Muscular dystrophy not predominantly limb girdle in distribution
240071003	X-linked muscular dystrophy not predominantly limb girdle
240072005	Benign scapuloperoneal muscular dystrophy with cardiomyopathy
240073000	Autosomal recessive muscular dystrophy not predominantly limb girdle
240074006	Scapulohumeral muscular dystrophy
240075007	Autosomal dominant muscular dystrophy not predominantly limb girdle
240076008	Benign scapuloperoneal muscular dystrophy
240077004	Severe scapuloperoneal muscular dystrophy with cardiomyopathy
240078009	Benign congenital muscular dystrophy with finger flexion contractures
240081004	Autosomal recessive centronuclear myopathy
240082006	Myopathy with abnormality of histochemical fiber type
240083001	Myopathy with type I hypotrophy
240084007	Congenital myopathy with fiber type disproportion
240085008	Congenital myopathy with uniform fiber type
240086009	Myopathy with cytoplasmic inclusions
240087000	Myopathy with tubular aggregates
240104008	Congenital myotonic dystrophy
240460008	Acute paralytic poliomyelitis
241006	Epilepsia partialis continua
2421000119107	Hallucinations co-occurrent and due to late onset dementia
24326000	Metachromatic leukodystrophy, adult type
24473007	Persistent vegetative state
24624008	Aneurysm of internal carotid artery
24700007	Multiple sclerosis
2495006	Congenital cerebral arteriovenous aneurysm
253098009	Neural tube defect
253116006	Fissured spine with hydrocephalus
253143001	Absence of septum pellucidum
253147000	Type 1 lissencephaly
253148005	Miller Dieker syndrome
253149002	Type 2 lissencephaly
253158009	Hydranencephaly with proliferative vasculopathy
253159001	Schizencephaly
253160006	Colpocephaly
253186001	Chiari malformation type III
25362006	Phytanic acid storage disease
253699002	Isolation of common carotid artery
254243001	Ash leaf spot, tuberous sclerosis
254775002	Bregeat's syndrome
254972008	Malignant tumor of optic nerve and sheath
254973003	Malignant astrocytoma of optic nerve
254974009	Malignant tumor of optic nerve sheath
254975005	Malignant meningioma of optic nerve sheath
256321009	Disorder of neuromuscular transmission
257277002	Combined disorder of muscle AND peripheral nerve
25772007	Multi-infarct dementia with delusions
2593002	Dubowitz's syndrome
26015003	Maroteaux-Lamy syndrome, intermediate form
26021000119107	Vertigo as sequela of cerebrovascular disease
262711004	Transection of cervical cord
26360005	Hereditary optic atrophy
26595007	Congenital absence of part of brain
266253001	Precerebral arterial occlusion
266254007	Occlusion of carotid artery
266257000	Transient ischemic attack
267581004	Progressive myoclonic epilepsy
267592003	Motor cortex epilepsy
267604001	Myasthenic syndrome due to diabetic mellitus
268612007	Senile and presenile organic psychotic conditions
26954004	Thrombophlebitis of superior sagittal sinus
27148008	Hereditary motor end-plate disease
271986005	Disorder of brain ventricular shunt
274100004	Cerebral hemorrhage
275363001	Rupture of superficial cerebral vein
276219001	Occipital cerebral infarction
276594006	Perinatal rupture of superficial cerebral vein
276599001	Cerebral leukomalacia
277196008	Berry aneurysm
277299009	Ruptured cerebral arteriovenous malformation
277315000	Ruptured aneurysm of anterior cerebral artery
277316004	Ruptured aneurysm of middle cerebral artery
277319006	Ruptured aneurysm of posterior cerebral artery
277320000	Ruptured aneurysm of anterior communicating artery
277322008	Ruptured aneurysm of posterior communicating artery
277324009	Ruptured aneurysm of basilar artery
277325005	Ruptured aneurysm of posterior inferior cerebellar artery
277328007	Ruptured internal carotid-anterior communicating artery zone aneurysm
277329004	Ruptured internal carotid-posterior communicating artery zone aneurysm
277330009	Ruptured internal carotid bifurcation aneurysm
277373000	Severe childhood autosomal recessive muscular dystrophy
277530005	Malignant melanoma of meninges
277922001	Aprosencephaly
277949001	Combined malformation of central nervous system and skeletal muscle
277950001	Muscle eye brain disease
278284007	Right hemiplegia
278285008	Left hemiplegia
278286009	Right hemiparesis
278287000	Left hemiparesis
278510009	Localization-related idiopathic epilepsy
28055006	West syndrome
281004	Dementia associated with alcoholism
281411007	Spastic diplegia
28366008	Cerebral arteritis
284811000119102	Aneurysm of extracranial portion of internal carotid artery
284821000119109	Aneurysm of intracranial portion of internal carotid artery
284861000119104	Atherosclerosis of bilateral carotid arteries
284871000119105	Atherosclerosis of left carotid artery
284881000119108	Atherosclerosis of right carotid artery
285161000119105	Occlusion of left carotid artery
285171000119104	Occlusion of right carotid artery
285191000119103	Stenosis of left carotid artery
285201000119100	Stenosis of right carotid artery
286742002	Impending cerebrovascular accident
287731003	Cerebral ischemia
28778005	Phrenic nerve paralysis as birth trauma
28790007	Obstruction of precerebral artery
288631000119104	Vascular dementia with behavioral disturbance
288723005	Acute ill-defined cerebrovascular disease
28978003	Progressive supranuclear ophthalmoplegia
290401000119108	Complete paraplegia
290411000119106	Incomplete paraplegia
290461000119109	Spastic hemiplegia of left dominant side
290471000119103	Spastic hemiplegia of left nondominant side
290481000119100	Spastic hemiplegia of right dominant side
290491000119102	Spastic hemiplegia of right nondominant side
290581000119101	Ataxia due to and following cerebrovascular accident
290631000119103	Dysarthria due to and following cerebrovascular accident
290641000119107	Dysphagia due to and following non-traumatic intracerebral hemorrhage
290671000119100	Status epilepticus due to complex partial epileptic seizure
290681000119102	Status epilepticus due to refractory complex partial seizures
290691000119104	Status epilepticus due to generalized idiopathic epilepsy
290711000119101	Status epilepticus due to intractable idiopathic generalized epilepsy
290721000119108	Status epilepticus due to refractory epilepsy
290741000119102	Intractable idiopathic partial epilepsy
290761000119103	Status epilepticus due to refractory simple partial epilepsy
290791000119105	Fluency disorder due to and following cerebrovascular accident
290871000119101	Infantile spasms co-occurrent with status epilepticus
290881000119103	Refractory infantile spasms co-occurrent with status epilepticus
29093005	Crossed hemiparesis
291311000119108	Status epilepticus in benign Rolandic epilepsy
291351000119109	Spontaneous hemorrhage of subarachnoid space from basilar artery
291371000119100	Spontaneous hemorrhage of subarachnoid space from intracranial artery
291411000119104	Spontaneous hemorrhage of subarachnoid space from left posterior communicating artery
291481000119105	Spontaneous haemorrhage of subarachnoid space from right posterior communicating artery
29159009	Familial dysautonomia
291721000119102	Aphasia due to and following non-traumatic intracerebral hemorrhage
29188005	Complete bilateral paralysis
292621000119100	Occlusion of right vertebral artery
292631000119102	Occlusion of left vertebral artery
292851000119109	Lacunar ataxic hemiparesis of right dominant side
292861000119106	Lacunar ataxic hemiparesis of left dominant side
292991000119106	Eaton Lambert syndrome without underlying malignancy
29322000	Acute cerebrovascular insufficiency
293811000119100	Cerebral infarction due to vertebral artery stenosis
293831000119105	Cerebral infarction due to stenosis of precerebral artery
294041000119107	Flaccid hemiplegia of left dominant side
294051000119109	Flaccid hemiplegia of left nondominant side
294061000119106	Flaccid hemiplegia of right dominant side
294071000119100	Flaccid hemiplegia of right nondominant side
294101000119109	Hemiplegia of left dominant side
294111000119107	Hemiplegia of left nondominant side
294121000119100	Hemiplegia of right dominant side
294131000119102	Hemiplegia of right nondominant side
29426003	Paralytic syndrome
297138001	Embolus of circle of Willis
297157005	Intracranial venous thrombosis
297176007	Vertebral artery aneurysm
297278001	Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator
29774004	Vascular myelopathy
298282001	Spastic quadriparesis
29941000119105	Ataxia as sequela of cerebrovascular disease
29951000119107	Ataxic hemiparesis
30023002	Hydranencephaly
300920004	Carotid atherosclerosis
302213007	Caroticocavernous sinus fistula
302878004	Intracranial septic thrombophlebitis
302879007	Septic thrombophlebitis of cavernous sinus
302880005	Septic thrombophlebitis of sagittal sinus
302887008	Neuropathy in secondary amyloidosis
302909007	Diffuse cerebrovascular disease
30400005	Middle meningeal hemorrhage following injury
305719002	Neuromyotonia
307356008	Motor epilepsy
307357004	Jacksonian, focal or motor epilepsy
307360006	Leucodystrophy without a known biochemical basis
307362003	Intracranial venous septic embolism
307363008	Multiple lacunar infarcts
307649006	Microglioma
307766002	Left sided cerebral infarction
307767006	Right sided cerebral infarction
30915001	Holoprosencephaly sequence
31076000	Congenital ischemic atrophy of central nervous system structure
31081000119101	Presenile dementia with delusions
31097004	Post poliomyelitis syndrome
31216003	Profound intellectual disability
312586003	Intracranial thrombophlebitis
312944002	Compressive optic atrophy
313434001	Residual hemiplegia
315608004	Cardiomyopathy in Duchenne muscular dystrophy
31839002	Myasthenia gravis, adult form
32162001	Facial hemiplegia
322112361000132104	Epilepsy due to scarring of brain
32875003	Inhalant-induced persisting dementia
329481000119106	Occlusion of right middle cerebral artery
329491000119109	Occlusion of left middle cerebral artery
329561000119101	Occlusion of right posterior cerebral artery
329571000119107	Occlusion of left posterior cerebral artery
330411000119109	Lacunar ataxic hemiparesis of left nondominant side
330421000119102	Lacunar ataxic hemiparesis of right nondominant side
33301000119105	Sequela of cardioembolic stroke
33316007	GM 2 gangliosidosis
33331000119103	Sequela of lacunar stroke
336191000119105	Occlusion of right central retinal artery
3371000119106	Refractory generalized convulsive epilepsy
341801000119101	Occlusion of left central retinal artery
34181000119102	Cerebral infarction due to occlusion of basilar artery
34191000119104	Cerebral infarction due to vertebral artery occlusion
347011000119102	Occlusion of bilateral central retinal arteries
34781003	Vertebral artery syndrome
352818000	Tonic-clonic epilepsy
35386004	Cavernous sinus syndrome
359683002	Complete optic atrophy
36025004	Fibrous skin tumor of tuberous sclerosis
361000119103	Paralytic syndrome on one side of the body as late effect of cerebrovascular accident
361123003	Psychomotor epilepsy
363235000	Hereditary disorder of nervous system
363474009	Malignant neoplasm of cerebral meninges
363497007	Malignant tumor of meninges
363498002	Malignant tumor of optic nerve
36803009	Idiopathic generalized epilepsy
3681008	Thrombophlebitis of torcular Herophili
371024007	Senile dementia with delusion
371026009	Senile dementia with psychosis
371029002	Ischemic disorder of spinal cord
371120001	Quadriplegic spinal paralysis
371129000	Paralysis from birth trauma
371158002	Disorder of basilar artery
371160000	Disorder of carotid artery
371313002	Congenital cerebellar cortical atrophy
372062007	Malignant neoplasm of central nervous system
372310001	Paralysis due to lesion of spinal cord
37340000	Motor neuron disease
373587001	Chiari malformation type II
37934003	Mitochondrial-lipid-glycogen storage myopathy
37943007	Multiple AND bilateral precerebral artery embolism
380941000000104	Progressive encephalopathy with oedema, hypsarrhythmia and optic atrophy syndrome
38228000	Paralysis of tongue
38523005	Syphilitic parkinsonism
38742007	Central retinal artery occlusion
387732009	Becker muscular dystrophy
389098007	Anoxic encephalopathy
389100007	Ischemic encephalopathy
390936003	Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
39390005	Niemann-Pick disease, type B
396338004	Metachromatic leucodystrophy
397734008	Hereditary sensory and autonomic neuropathy type I
398040009	Charcot-Marie-Tooth disease, type I
398100001	Hereditary motor and sensory neuropathy
398148000	Hereditary sensory and autonomic neuropathy type II
398187000	Charcot-Marie-Tooth disease, type II
398229007	Amyloid polyneuropathy type I
398432008	Bulbar weakness
399091004	Facioscapulohumeral muscular dystrophy
40161000119102	Weakness of face muscles as sequela of stroke
402460000	Familial amyloid polyneuropathy with cutaneous amyloidosis
40259002	Progressive sensory ataxia of Charolais
40276003	Embolism of precerebral artery
40354009	De Lange syndrome
403815003	Axillary freckling due to neurofibromatosis
403816002	Multiple café-au-lait macules due to neurofibromatosis
403817006	Multiple neurofibromas in neurofibromatosis
403819009	Elephantiasis neurofibromatosa
40425004	Postconcussion syndrome
40450001	Embolism of superior sagittal sinus
404664002	Malignant optic glioma
404689008	Alternating hemiplegia
40632002	Charcot-Marie-Tooth disease, type IA
4069002	Anoxic brain damage during AND/OR resulting from a procedure
40700009	Severe intellectual disability
40802007	Metachromatic leukodystrophy, congenital type
40816002	Retropulsion petit mal
408371000000100	[X]Cerebral palsy and other paralytic syndromes
408664007	Pontine artery occlusion
408665008	Pontine artery thrombosis
40980002	Spastic paralysis due to birth injury
410057002	Hereditary AND/OR degenerative disease of central nervous system
41040004	Complete trisomy 21 syndrome
41142009	Globoid cell leukodystrophy, late-onset
41283003	Cerebro-oculo-facio-skeletal syndrome
413101007	Stress-induced epilepsy
414927004	Ocular myasthenia with strabismus
41574007	Paramyotonia congenita
41590007	Familial amyloid polyneuropathy, Jewish type
4183003	Charcot-Marie-Tooth disease, type IC
42012007	Neuronal ceroid lipofuscinosis
420718004	Central nervous system demyelinating disease associated with acquired immunodeficiency syndrome
420788006	Intraocular non-Hodgkin malignant lymphoma
421998001	Central nervous disorder associated with acquired immunodeficiency syndrome
422474003	Partial absence of septum pellucidum
422513000	Epilepsy, not refractory
422724001	Refractory localization-related epilepsy
422873003	Refractory epilepsia partialis continua
42295001	Familial amyloid polyneuropathy
423144007	Multifactorial encephalopathy
423771003	Acquired neuromuscular ptosis
424795008	Non dystrophic myotonia
425054007	Refractory occipital lobe epilepsy
425219008	Progressive spinal ataxia
425237009	Refractory frontal lobe epilepsy
425349008	Refractory parietal lobe epilepsy
425390006	Dementia associated with Parkinson's Disease
425420004	Thrombosis of internal carotid artery
425500002	Secondary progressive multiple sclerosis
425687007	Spina bifida aperta of cervical spine
425882004	Paralytic syndrome as late effect of stroke
425932008	Thrombosis of posterior communicating artery
426033005	Dysphagia as a late effect of cerebrovascular accident
426107000	Acute lacunar infarction
4262001	Phlebitis of superior sagittal sinus
426373005	Relapsing remitting multiple sclerosis
426651005	Occlusion of bilateral carotid arteries
426788002	Vertigo as late effect of stroke
426814001	Transient cerebral ischemia due to atrial fibrillation
427020007	Cerebral vasculitis
427296003	Thalamic infarction
427432001	Paralytic syndrome as late effect of thalamic stroke
427943001	Ophthalmoplegia due to diabetes mellitus
428700003	Primary progressive multiple sclerosis
429458009	Dementia due to Creutzfeldt Jakob disease
429466000	Spina bifida aperta of lumbar spine
42970005	Nonpyogenic thrombosis of intracranial venous sinus
42986003	Charcot-Marie-Tooth disease, type IB
429998004	Vascular dementia
430947007	Paralytic syndrome of nondominant side as late effect of stroke
430959006	Paralytic syndrome of dominant side as late effect of stroke
43100002	Late cortical cerebellar atrophy
432504007	Cerebral infarction
433183000	Neurogenic bladder as late effect of cerebrovascular accident
434541000124109	Benign childhood epilepsy with centrotemporal spikes, refractory
434551000124106	Benign childhood epilepsy with centrotemporal spikes, non-refractory
43532007	Hereditary oculoleptomeningeal amyloid angiopathy
43658003	Vertebral artery obstruction
438511000	Benign multiple sclerosis
439567002	Malignant multiple sclerosis
44145005	Benign Rolandic epilepsy
441526008	Infarct of cerebrum due to iatrogenic cerebrovascular accident
441529001	Dysphasia as late effect of cerebrovascular disease
441630004	Aphasia as late effect of cerebrovascular disease
441678004	Refractory generalized nonconvulsive epilepsy
441688003	Incomplete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra
441705005	Complete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra
441717007	Hemiplegia of nondominant side
441722007	Spastic hemiplegia of nondominant side
441735003	Sensory disorder as a late effect of cerebrovascular disease
441759008	Abnormal vision as a late effect of cerebrovascular disease
441794001	Incomplete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra
441892008	Spastic hemiplegia of dominant side
441960006	Speech and language deficit as late effect of cerebrovascular accident
441980007	Complete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra
441991000	Hemiparesis as late effect of cerebrovascular accident
442020005	Flaccid hemiplegia of dominant side
442024001	Hemiplegia as late effect of cerebrovascular disease
442077006	Flaccid hemiplegia of nondominant side
442155009	Hemiplegia of dominant side
442344002	Dementia due to Huntington chorea
442481002	Epilepsy characterized by intractable complex partial seizures
442511009	Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome
442512002	Nonconvulsive status epilepticus
442617003	Aphasia as late effect of cerebrovascular accident
442668000	Hemiplegia of nondominant side as late effect of cerebrovascular disease
442676003	Hemiplegia of dominant side as late effect of cerebrovascular disease
442733008	Hemiplegia as late effect of cerebrovascular accident
44359008	Metachromatic leukodystrophy, juvenile type
443929000	Small vessel cerebrovascular disease
444024002	Multiple system atrophy, cerebellar variant
444172003	Recurrent transient cerebral ischemic attack
444197004	Multiple system atrophy, Parkinson variant
445109004	Isolation of left common carotid artery
445349004	Isolation of right common carotid artery
445355009	Refractory epilepsy
445475001	Paraneoplastic sensorimotor neuropathy
4463009	Familial amyloid polyneuropathy, type II
446311006	Acute bulbar poliomyelitis caused by Human poliovirus 2
446712002	Thromboembolus of precerebral artery
446957000	Acute bulbar poliomyelitis caused by Human poliovirus 1
446958005	Acute paralytic poliomyelitis caused by Human poliovirus 1
447262002	Acute paralytic poliomyelitis caused by Human poliovirus 2
447378002	Acute paralytic poliomyelitis caused by Human poliovirus 3
4477007	Juvenile myopathy AND lactate acidosis
448054001	Adult onset autosomal dominant leukodystrophy
448227009	X-linked periventricular heterotopia
448254007	Non-Hodgkin's lymphoma of central nervous system
448995000	Follicular non-Hodgkin's lymphoma of central nervous system
449221001	Diffuse non-Hodgkin's lymphoma of central nervous system
449305009	Paraneoplastic sensory neuropathy
45502001	Cerebrovascular amyloidosis
45853006	Roussy-Lévy syndrome
460307002	Systemic to pulmonary collateral artery from right carotid artery
460312001	Systemic to pulmonary collateral artery from left carotid artery
460890003	Anomalous common origin of brachiocephalic artery and left common carotid artery
460899002	Anomalous origin of left common carotid artery from brachiocephalic artery
461326001	Anomalous separate origins of internal carotid arteries and external carotid arteries from single aortic arch
46251005	Corticospinal motor disease
46252003	Progressive external ophthalmoplegia
46421000119102	Behavior disorder as sequela of cerebral infarction
46659004	Von Hippel-Lindau syndrome
46804001	Severe x-linked myotubular myopathy
472320005	Maternally inherited mitochondrial cardiomyopathy and myopathy
472746006	Cerebrovascular disorder due to paradoxical embolus
472916000	Toxic metabolic encephalopathy
47391000119107	Primary generalized absence epilepsy
47683004	Metachromatic leukodystrophy, late infantile type
48163001	Triparesis
48522003	Spinal cord disorder
48601000119107	Paralytic syndrome on one side of the body as effect of cerebrovascular accident
48601002	Thrombosis of precerebral artery
48662007	Cerebral paraplegia
49049000	Parkinson's disease
49562005	Adult chronic GM 2 gangliosidosis
49605003	Ophthalmoplegic migraine
49692006	Schilder's disease
49776008	Centrencephalic epilepsy
49793008	Hereditary motor neuron disease
49823009	Internuclear ophthalmoplegia
50582007	Hemiplegia
508171000000105	Severe learning disability
50866000	Childhood absence epilepsy
509341000000107	Petit-mal epilepsy
50967008	Gangliosidosis
5134006	Familial amyloid polyneuropathy, type VI
51500006	Complete trisomy 18 syndrome
52165006	Niemann-Pick disease, type A
52448006	Dementia
5262007	Spinal muscular atrophy
52677002	Deficiency of N-acetylgalactosamine-4-sulfatase
53633000	Peutz-Jeghers polyps of small bowel
53857003	Heredofamilial brachial plexus paralysis syndrome
54099005	Diplegia of upper limbs
54265003	Congenital anomaly of cerebral artery
54280009	Kugelberg-Welander disease
54364001	Lethal neonatal spasticity
54411001	Peutz-Jeghers syndrome
54519002	Basilar artery stenosis
55016009	Congenital muscular hypertrophy-cerebral syndrome
55051001	Myasthenia gravis, juvenile form
55382008	Cerebral atherosclerosis
55709000	Ethmocephalus
55734000	Endophlebitis of basilar sinus
56155002	Hemispheric cerebral agenesis
56267009	Multi-infarct dementia
56453003	Hereditary cerebral amyloid angiopathy, Dutch type
56989000	Eaton-Lambert syndrome
57938005	Congenital myotonia, autosomal dominant form
58263000	Maroteaux-Lamy syndrome, severe form
58459009	Sphingomyelin/cholesterol lipidosis
58557008	Spina bifida aperta
58610003	Leber's optic atrophy
58795000	Distal muscular dystrophy
590005	Congenital aneurysm of anterior communicating artery
5963005	Subacute neuronopathic Gaucher's disease
59636002	Pelizaeus-Merzbacher disease, connatal variant
60192008	Lethal multiple pterygium syndrome
60389000	Paraplegia
60706008	Phlebitis of torcular Herophili
608874000	Eaton Lambert syndrome with underlying malignancy
609553000	Paralytic syndrome of both lower limbs
609554006	Paralytic syndrome of all four limbs
609557004	Paralytic syndrome on one side of the body
61091005	Aneurysm of external carotid artery
6118003	Demyelinating disease of central nervous system
61200008	Pallidonigroluysian degeneration
62158001	Status marmoratus
62239001	Parkinson-dementia complex of Guam
62440002	Infantile GM 2 gangliosidosis
62702001	Cerebral vein occlusion
62914000	Cerebrovascular disease
62985007	Hereditary insensitivity to pain with anhidrosis
63081009	Acute infarction of spinal cord
63135006	Amyotonia congenita
63795001	Thrombosis of intracranial venous sinus of pregnancy AND/OR puerperium
64228003	Paralysis of diaphragm
64383006	Werdnig-Hoffmann disease
64586002	Carotid artery stenosis
64764001	Acute paralytic poliomyelitis, bulbar
64775002	Vertebral artery thrombosis
6481005	Diplegia
64855000	Pelizaeus-Merzbacher disease
65017003	Hereditary peripheral neuropathy
65084004	Vertebral artery embolism
65120008	Generalized convulsive epilepsy
65312002	Cerebral arteriosclerosis
65587001	Congenital anomaly of cerebrovascular system
65764006	Pseudo-Hurler polydystrophy
6594005	Cerebrovascular disorder in the puerperium
66521008	Deficiency of cerebroside-sulfatase
66751000	Niemann-Pick disease, type C
672441000119103	Hemiplegia of nondominant side due to and following ischemic cerebrovascular accident
672461000119104	Hemiplegia of dominant side due to and following ischemic cerebrovascular accident
672501000119104	Dysarthria due to and following ischemic cerebrovascular accident
672511000119101	Dysarthria due to and following hemorrhagic cerebrovascular accident
672521000119108	Dysphasia due to and following ischemic cerebrovascular accident
672531000119106	Dysphasia due to and following hemorrhagic cerebrovascular accident
672541000119102	Aphasia due to and following ischemic cerebrovascular accident
672551000119100	Aphasia due to and following hemorrhagic cerebrovascular accident
6729006	Cerebral-retinal arteriovenous aneurysm
674091000119108	Vertigo due to and following ischemic cerebrovascular accident
674111000119100	Ataxia due to and following ischemic cerebrovascular accident
674121000119107	Ataxia due to and following hemorrhagic cerebrovascular accident
674361000119104	Apraxia due to and following ischemic cerebrovascular accident
674381000119108	Weakness of facial muscle due to and following ischemic cerebrovascular accident
674391000119106	Speech and language deficit due to and following hemorrhagic cerebrovascular accident
674401000119108	Speech and language deficit due to and following ischemic cerebrovascular accident
67747009	Ocular muscular dystrophy
67854007	Maroteaux-Lamy syndrome, mild form
67855008	Niemann-Pick disease, type C, subacute form
67992007	Multiple AND bilateral precerebral artery obstruction
68186003	Congenital myopathy with abnormal subcellular organelles
68390005	Sphingolipid activator protein 1 deficiency
68618008	Rett's disorder
690171000119105	Weakness of facial muscle due to and following embolic cerebrovascular accident
690201000119109	Ataxia due to and following embolic cerebrovascular accident
690271000119104	Hemiplegia of nondominant side due to and following embolic cerebrovascular accident
690311000119104	Dysarthria due to and following embolic cerebrovascular accident
690321000119106	Aphasia due to and following embolic cerebrovascular accident
690331000119109	Speech and language deficit due to and following embolic cerebrovascular accident
690351000119103	Dysphasia due to and following embolic cerebrovascular accident
69131009	Spinal ataxia
69463008	Maroteaux-Lamy syndrome
69763009	Exophthalmic ophthalmoplegia
69798007	Carotid artery obstruction
697991001	Paralysis of uvula
698021005	Autosomal dominant nocturnal frontal lobe epilepsy
698291007	Acute paraplegia
698292000	Chronic paraplegia
698363002	Postoperative thromboembolus of precerebral artery
698624003	Dementia associated with cerebral lipidosis
698625002	Dementia associated with normal pressure hydrocephalus
698626001	Dementia associated with multiple sclerosis
698627005	Postoperative phlebitis and thrombophlebitis of intracranial sinuses
698687007	Post-traumatic dementia with behavioral change
698725008	Dementia associated with neurosyphilis
698726009	Dementia associated with viral encephalitis
698741009	Acute complete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra
698742002	Chronic incomplete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra
698743007	Acute complete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra
698744001	Chronic incomplete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra
698754002	Chronic paralysis due to lesion of spinal cord
698755001	Acute paralysis due to lesion of spinal cord
698760002	Generalized non-convulsive absence epilepsy
698762005	Refractory myoclonic epilepsy
698763000	Postoperative status epilepticus
698764006	Post infectious grand mal epilepsy
698767004	Post-cerebrovascular accident epilepsy
698781002	Dementia associated with cerebral anoxia
698846009	Tibial muscular dystrophy
698870008	2-hydroxyglutaric aciduria
698948009	Vascular dementia in remission
698949001	Dementia in remission
699184009	Perry syndrome
699190008	Paroxysmal extreme pain disorder
699688008	Generalized epilepsy with febrile seizures plus
699706000	Embolism of middle cerebral artery
700467001	Reversible cerebral vasoconstriction syndrome
70199000	I-cell disease
702326000	Progressive myoclonus epilepsy with ataxia
702327009	Monocarboxylate transporter 8 deficiency
702343002	Early onset myopathy with fatal cardiomyopathy
702363009	Cold-induced sweating syndrome
702382000	Inclusion body myopathy 2
702383005	Distal myopathy 2
702433001	Congenital cataracts, facial dysmorphism and neuropathy
702439002	Agenesis of corpus callosum with peripheral neuropathy
702441001	Fatal X-linked ataxia with deafness and loss of vision
702442008	Ataxia with vitamin E deficiency
702463005	Paralytic syndrome of two limbs
702464004	Paralytic syndrome of three limbs
702465003	Paralytic syndrome on both sides of the body
702575003	Retinocochleocerebral vasculopathy
702611008	Congenital brain aplasia
703163006	Secondary cerebrovascular disease
703166003	Dural arteriovenous fistula
703176000	Ruptured aneurysm of vertebral artery
703180005	Asymptomatic occlusion of extracranial carotid artery
703184001	Asymptomatic occlusion of intracranial carotid artery
703205008	Asymptomatic occlusion of posterior cerebral artery
703206009	Asymptomatic occlusion of basilar artery
703207000	Asymptomatic occlusion of anterior cerebral artery
703208005	Asymptomatic occlusion of middle cerebral artery
703218000	Cerebral vasoconstriction syndrome
703219008	Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
703221003	Congenital intracranial vascular malformation
703226008	Familial cerebral saccular aneurysm
703266007	Cerebrofacial arteriovenous metameric syndrome
703267003	Cerebrofacial arteriovenous metameric syndrome type 1
703268008	Cerebrofacial arteriovenous metameric syndrome type 3
703300001	Hypoxic ischemic encephalopathy
7033004	Petit mal status
703301002	Mild hypoxic ischemic encephalopathy
703302009	Moderate hypoxic ischemic encephalopathy
703303004	Severe hypoxic ischemic encephalopathy
703304005	Hypoxic ischemic encephalopathy due to strangulation
703305006	Hypoxic ischemic encephalopathy due to cardiac arrest
703311009	Cerebral arteritis due to infectious disease
703312002	Primary cerebral arteritis
703313007	Cerebral amyloid angiopathy associated with systemic amyloidosis
703429003	Malignant optic glioma of adulthood
70350007	Degenerative myelopathy
703524005	Spinal muscular atrophy with progressive myoclonic epilepsy
703535000	Mowat-Wilson syndrome
703544004	Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
705066004	Dissection of internal carotid artery
705128004	Cerebral infarction due to embolism of middle cerebral artery
705129007	Thrombosis of middle cerebral artery
705130002	Cerebral infarction due to thrombosis of middle cerebral artery
70528007	Mucolipidosis
70607008	Thrombosis of superior sagittal sinus
70694009	Diabetes mellitus AND insipidus with optic atrophy AND deafness
709281006	Rippling muscle disease
70936005	Multi-infarct dementia, uncomplicated
709415008	Mitochondrial membrane protein associated neurodegeneration
709469005	Periodontitis co-occurrent with Down syndrome
710046001	Refractory idiopathic generalized epilepsy
710575003	Transient ischemic attack due to embolism
711151004	Hypomagnesemia with secondary hypocalcemia
711406009	Autosomal recessive axonal neuropathy with neuromyotonia
711409002	3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome
711483003	Spinal muscular atrophy with respiratory distress type 1
71253000	Tay-Sachs disease, variant AB
712637001	Ribonucleic acid polymerase III-related leukodystrophy
713035000	Dissection of precerebral artery
713081000	Dissection of cerebral artery
713265001	Nontraumatic ruptured cerebral aneurysm
713327005	Malignant meningioma of meninges of brain
713401006	Combined D-2-hydroxyglutaric aciduria and L-2-hydroxyglutaric aciduria
713488003	Presenile dementia co-occurrent with human immunodeficiency virus infection
713543002	Demyelinating disease of central nervous system co-occurrent with human immunodeficiency virus infection
713844000	Dementia co-occurrent with human immunodeficiency virus infection
71444005	Cerebral arterial thrombosis
715317001	Proximal myotonic myopathy
715340002	Autosomal recessive limb girdle muscular dystrophy type 2D
715341003	Autosomal recessive limb girdle muscular dystrophy type 2A
715344006	Neurofibromatosis Noonan syndrome
715345007	Young onset Parkinson disease
715374003	Autosomal dominant optic atrophy plus syndrome
715406003	Isolated lissencephaly type 1 without known genetic defect
715419004	Lethal congenital contracture syndrome type 2
715422002	Craniotelencephalic dysplasia
715429006	Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome
715434005	Holoprosencephaly craniosynostosis syndrome
715565004	Lethal arthrogryposis co-occurrent with anterior horn cell disease
715624006	Chronic ataxic neuropathy, ophthalmoplegia, monoclonal immunoglobulin M protein, cold agglutinin and disialosyl antibody syndrome
715629001	Generalized epilepsy and paroxysmal dyskinesia syndrome
715645004	Hereditary thermosensitive neuropathy
715646003	Desmin related myopathy with Mallory body-like inclusions
715665006	Hereditary motor and sensory neuropathy Okinawa type
715666007	Charcot-Marie-Tooth disease type IE
715780008	Lissencephaly type 1 due to doublecortin gene mutation
715794009	Progressive encephalopathy with severe infantile anorexia
715795005	Charcot-Marie-Tooth disease type 4
715796006	Charcot-Marie-Tooth disease type 4A
715797002	Charcot-Marie-Tooth disease type 4C
715798007	Charcot-Marie-Tooth disease type 4D
715799004	Charcot-Marie-Tooth disease type 4G
715800000	Charcot-Marie-Tooth disease type 4B2
715801001	Charcot-Marie-Tooth disease type 4F
715802008	Charcot-Marie-Tooth disease type 4H
715803003	Charcot-Marie-Tooth disease type 4B1
715952000	Waardenburg syndrome co-occurrent with Hirschsprung disease
716091000	Holoprosencephaly and postaxial polydactyly syndrome
716107009	Early onset parkinsonism and intellectual disability syndrome
716169009	Holoprosencephaly sequence with hypokinesia and congenital joint contracture syndrome
716233007	Steinfeld syndrome
716243005	Deafness with malformation of ear and facial palsy syndrome
716278005	Jeavons syndrome
716662004	Autosomal dominant late onset Parkinson disease
716696006	Autosomal dominant centronuclear myopathy
716706009	Female restricted epilepsy with intellectual disability syndrome
716745004	Livedo reticularis and cerebrovascular accident syndrome
717008005	Autosomal dominant Charcot-Marie-Tooth disease type 2B
717010007	Autosomal dominant Charcot-Marie-Tooth disease type 2C
717011006	Autosomal dominant Charcot-Marie-Tooth disease type 2D
717012004	Autosomal dominant Charcot-Marie-Tooth disease type 2E
717013009	Autosomal dominant Charcot-Marie-Tooth disease type 2I
717014003	Autosomal dominant Charcot-Marie-Tooth disease type 2J
717016001	Autosomal dominant Charcot-Marie-Tooth disease type 2A1
717042001	Pelizaeus Merzbacher like disease
717223008	X-linked epilepsy with learning disability and behavior disorder syndrome
717266001	Sensory ataxic neuropathy with dysarthria and ophthalmoparesis syndrome
717336005	Autosomal dominant optic atrophy classic form
71779008	X-linked hydrocephalus syndrome
717812000	Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome
717825008	Hereditary sensory and autonomic neuropathy type 1B
717826009	Hereditary sensory and autonomic neuropathy with deafness and global delay
717943008	Brain malformation, congenital heart disease, postaxial polydactyly syndrome
717964007	Juvenile primary lateral sclerosis
717968005	Melanoma and neural system tumor syndrome
717975006	Autosomal dominant optic atrophy and peripheral neuropathy syndrome
717977003	Lissencephaly syndrome Norman Roberts type
718176005	Autosomal recessive limb girdle muscular dystrophy type 2C
718177001	Autosomal recessive limb girdle muscular dystrophy type 2F
718178006	Autosomal dominant limb girdle muscular dystrophy type 1B
718179003	Autosomal recessive limb girdle muscular dystrophy type 2B
718180000	Autosomal recessive limb girdle muscular dystrophy type 2I
718210003	Deficiency of monoamine oxidase A
718214007	Mitochondrial neurogastrointestinal encephalomyopathy syndrome
718221007	Behr syndrome
71831005	Symptomatic generalized epilepsy
718555006	Juvenile amyotrophic lateral sclerosis
718556007	Cranio-cerebello-cardiac dysplasia syndrome
718572004	Bethlem myopathy
718685006	Orthostatic hypotension co-occurrent and due to Parkinson's disease
718713000	Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome
718719001	Lissencephaly type 3 familial fetal akinesia sequence syndrome
718720007	Lissencephaly type 3 metacarpal bone dysplasia syndrome
718759003	Lissencephaly due to tubulin alpha 1A mutation
718847005	X-linked neurodegenerative syndrome Hamel type
718849008	X-linked neurodegenerative syndrome Bertini type
718850008	Autosomal recessive limb girdle muscular dystrophy type 2E
719069008	Shprintzen Goldberg craniosynostosis syndrome
719205008	Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome
719395001	Microcephalus facio-cardio-skeletal syndrome Hadziselimovic type
719430008	Leber plus disease
719510006	Autosomal dominant Charcot-Marie-Tooth disease type 2F
719511005	Autosomal dominant Charcot-Marie-Tooth disease type 2G
719512003	Autosomal dominant Charcot-Marie-Tooth disease type 2K
719513008	Autosomal dominant Charcot-Marie-Tooth disease type 2L
719514002	Autosomal dominant Charcot-Marie-Tooth disease type 2M
719515001	Autosomal dominant Charcot-Marie-Tooth disease type 2N
719517009	Autosomal dominant optic atrophy and cataract
719717006	Psychosis co-occurrent and due to Parkinson's disease
719815005	X-linked myopathy with excessive autophagy
719819004	Xeroderma pigmentosum and Cockayne syndrome complex
719836007	X-linked distal arthrogryposis multiplex congenita
719838008	X-linked hereditary sensory and autonomic neuropathy with deafness
7199000	Tuberous sclerosis syndrome
719979008	Charcot-Marie-Tooth disease type ID
719980006	Charcot-Marie-Tooth disease type IF
719981005	Charcot-Marie-Tooth disease type 2B2
719985001	Autosomal dominant limb girdle muscular dystrophy type 1A
719986000	Autosomal dominant limb girdle muscular dystrophy type 1C
719987009	Autosomal dominant limb girdle muscular dystrophy type 1D
719988004	Autosomal dominant limb girdle muscular dystrophy type 1E
719989007	Autosomal dominant limb girdle muscular dystrophy type 1F
719990003	Autosomal dominant limb girdle muscular dystrophy type 1G
720410001	Acrootoocular syndrome
720519003	Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome
720522001	Autosomal recessive limb girdle muscular dystrophy type 2G
720523006	Autosomal recessive limb girdle muscular dystrophy type 2K
720626009	Dissection of carotid artery
720634003	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome
720637005	Charcot-Marie-Tooth disease type 2H
720638000	Charcot-Marie-Tooth disease type 4J
720809000	Dissection of external carotid artery
720852000	Cervical hypertrichosis and peripheral neuropathy syndrome
720855003	Cerebrooculonasal syndrome
721088003	Developmental delay, epilepsy, neonatal diabetes syndrome
721200000	Early-onset X-linked optic atrophy
721221000	Hirschsprung disease with deafness and polydactyly syndrome
721222007	Hirschsprung disease with type D brachydactyly syndrome
721223002	Hirschsprung disease with nail hypoplasia and dysmorphism
721297008	Galloway Mowat syndrome
721843003	Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome
721979005	Lymphedema and cerebral arteriovenous anomaly syndrome
722004001	Agenesis of internal carotid artery
722006004	Isotretinoin embryopathy-like syndrome
722064003	Odontoleukodystrophy
722110003	Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome
722209002	Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome
722213009	Severe X-linked intellectual disability Gustavson type
722283003	Agnathia, holoprosencephaly, situs inversus syndrome
722294004	Autosomal dominant intermediate Charcot-Marie-Tooth disease type E
722377004	Paraganglioma and gastric stromal sarcoma syndrome
722389002	Congenital hereditary facial paralysis with variable hearing loss syndrome
722432000	Duane anomaly, myopathy, scoliosis syndrome
722456001	Intellectual disability, developmental delay, contracture syndrome
722599008	Parkinsonism due to hereditary spastic paraplegia
722671009	Metastatic malignant neoplasm of meninges
722718001	Primary malignant meningioma
722977005	Dementia co-occurrent and due to neurocysticercosis
722978000	Dementia caused by toxin
722979008	Dementia due to metabolic abnormality
722980006	Dementia due to chromosomal anomaly
722987009	Amyotrophic lateral sclerosis plus syndrome
722990003	Congenital atrophy of optic nerve
722997000	Inherited autonomic nervous system disorder
723082006	Silent cerebral infarct
723083001	Late effects of cerebral ischemic stroke
723084007	Sequela of non-traumatic intracerebral hemorrhage
723124007	Primary progressive apraxia of speech
723125008	Epileptic encephalopathy
723156000	Flaccid diplegia of upper limbs
723157009	Spastic diplegia of upper limbs
723158004	Diplegia of lower limbs
723304001	Microcephaly, seizure, intellectual disability, heart disease syndrome
723306004	Facial onset sensory and motor neuronopathy syndrome
723308003	Epidermolysis bullosa simplex with muscular dystrophy
723366001	Macrostomia, preauricular tag, external ophthalmoplegia syndrome
723390000	Rapidly progressive dementia
723405001	Microlissencephaly micromelia syndrome
723452007	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome
723497003	Peripheral neuropathy with sensorineural hearing impairment syndrome
723621000	Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome
723622007	X-linked spastic paraplegia type 2
723676007	Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome
723825006	Autosomal recessive spastic paraplegia type 55
723826007	Autosomal recessive spastic paraplegia type 57
723857007	Silent micro-hemorrhage of brain
724091002	Neuroectodermal melanolysosomal disease
724138007	Mitochondrial myopathy with sideroblastic anemia syndrome
724146008	Metaphyseal chondromatosis co-occurrent with D-2 hydroxyglutaric aciduria
724207001	Kleefstra syndrome
724349009	Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome
724357007	Hereditary cerebral hemorrhage with amyloidosis
724427002	Asymptomatic stenosis of intracranial artery
724428007	Asymptomatic stenosis of extracranial artery
724549005	Epilepsy due to infectious disease of central nervous system
724572007	Neuromuscular junction disorder caused by organic phosphorus compound ingestion
724576005	Pyridoxal 5-phosphate dependent epilepsy
724643004	Transient abnormal myelopoiesis co-occurrent with Down syndrome
724644005	Myeloid leukemia co-occurrent with Down syndrome
724761004	Sporadic Parkinson disease
724769002	Ataxia co-occurrent and due to phytanic acid storage disease
724776007	Dementia due to disorder of central nervous system
724777003	Dementia due to infectious disease
724778008	Progressive relapsing multiple sclerosis
724780002	Demyelination of central nervous system co-occurrent and due to neurosarcoidosis
724781003	Demyelination of central nervous system co-occurrent and due to systemic lupus erythematosus
724782005	Demyelination of central nervous system co-occurrent and due to Sjogren disease
724783000	Demyelination of central nervous system co-occurrent and due to Behcet disease
724784006	Demyelination of central nervous system co-occurrent and due to mitochondrial disease
724785007	Epilepsy due to perinatal stroke
724786008	Epilepsy due to perinatal anoxic-ischemic brain injury
724787004	Epilepsy due to cerebrovascular accident
724788009	Epilepsy due to and following traumatic brain injury
724789001	Epilepsy due to intracranial tumor
724813004	Autonomic nervous system disorder co-occurrent and due to neurodegenerative disorder
724819000	Functional paraparesis
724820006	Functional hemiparesis
72488000	Niemann-Pick disease, type C, chronic form
724990004	Epilepsy due to immune disorder
724991000	Epilepsy co-occurrent and due to demyelinating disorder
724992007	Epilepsy co-occurrent and due to dementia
724993002	Cerebral ischemic stroke due to occlusion of extracranial large artery
724994008	Cerebral ischemic stroke due to stenosis of extracranial large artery
724999003	Isolated optic nerve hypoplasia
725042001	Autosomal recessive limb girdle muscular dystrophy type 2J
725043006	Autosomal recessive limb girdle muscular dystrophy type 2O
725047007	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness
725048002	Charcot-Marie-Tooth disease type 2B1
725097006	Crisponi syndrome
725139005	Spastic paraplegia, optic atrophy, neuropathy syndrome
725146001	Atypical juvenile parkinsonism
725163002	X-linked spasticity, intellectual disability, epilepsy syndrome
725296006	Mucolipidosis type IV
725420009	Congenital muscular dystrophy Paradas type
725464001	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
725898002	Delirium co-occurrent with dementia
725907002	Autosomal recessive limb girdle muscular dystrophy type 2Y
726031001	Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome
726051002	Myotonia congenita
726107008	Distal myopathy Welander type
72655000	Alternating hypoglossal hemiplegia
726614009	Autosomal recessive limb girdle muscular dystrophy type 2P
726615005	Autosomal recessive limb girdle muscular dystrophy type 2Q
726616006	Autosomal recessive limb girdle muscular dystrophy type 2L
726617002	Autosomal recessive limb girdle muscular dystrophy type 2N
726618007	Autosomal recessive limb girdle muscular dystrophy type 2M
726669007	Central nervous system calcification, deafness, tubular acidosis, anemia syndrome
726704006	Cataract, congenital heart disease, neural tube defect syndrome
73173006	Spasm of cerebral arteries
73192008	Multiple AND bilateral precerebral artery stenosis
732245008	Pure mitochondrial myopathy
732261005	Cyprus facial neuromusculoskeletal syndrome
732264002	Coenzyme A synthase protein associated neurodegeneration
732929002	Autosomal recessive limb girdle muscular dystrophy type 2S
732930007	Autosomal recessive limb girdle muscular dystrophy type 2T
732931006	Autosomal recessive limb girdle muscular dystrophy type 2R
732951005	Mitochondrial myopathy, lactic acidosis, deafness syndrome
732959007	Beta-propeller protein-associated neurodegeneration
73297009	Muscular dystrophy
733028000	Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome
733032006	Epilepsy telangiectasia syndrome
733044009	Dermatoleukodystrophy
733068001	Absent tibia, polydactyly, arachnoid cyst syndrome
733071009	Deafness, small bowel diverticulosis, neuropathy syndrome
733082001	Early-onset Lafora body disease
733091002	Isolated hereditary congenital facial paralysis
733184002	Dementia caused by heavy metal exposure
733185001	Dementia following injury caused by exposure to ionizing radiation
733190003	Dementia due to primary malignant neoplasm of brain
733191004	Dementia due to chronic subdural hematoma
733192006	Dementia due to herpes encephalitis
733194007	Dementia co-occurrent and due to Down syndrome
733195008	Epilepsy of infancy with migrating focal seizures
733199002	Multifocal cerebral infarction due to and following procedure on cardiovascular system
733469003	Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome
733489002	Distal myopathy with posterior leg and anterior hand involvement
733599009	Adult-onset multiple mitochondrial deoxyribonucleic acid deletion syndrome due to deoxyguanosine kinase deficiency
733623005	Autism spectrum disorder, epilepsy, arthrogryposis syndrome
733630004	Deficiency of alpha-ketoglutarate dehydrogenase
733636005	3-phosphoglycerate dehydrogenase deficiency juvenile form
733650000	Adult familial nephronophthisis with spastic quadriparesia syndrome
73390009	Endophlebitis of cavernous venous sinus
733926004	Ganglioneuroblastoma of central nervous system
734017008	Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome
734022008	Wolfram-like syndrome
734066005	Diffuse large B-cell lymphoma of central nervous system
734099007	Neuroblastoma of central nervous system
734326000	Stenosis of left vertebral artery
734327009	Stenosis of right vertebral artery
734374000	Thrombosis of left carotid artery
734382000	Thrombosis of right carotid artery
734383005	Thrombosis of left middle cerebral artery
734384004	Thrombosis of right middle cerebral artery
734396006	Spontaneous rupture of left posterior communicating artery
734397002	Spontaneous rupture of right posterior communicating artery
734434007	Pyridoxine-dependent epilepsy
734879002	Ruptured aneurysm of right posterior communicating artery
734880004	Ruptured aneurysm of left posterior communicating artery
734959006	Embolus of left cerebellar artery
734960001	Embolus of right cerebellar artery
734961002	Embolus of left posterior cerebral artery
734963004	Embolus of right posterior cerebral artery
734964005	Embolus of left middle cerebral artery
734965006	Embolus of right middle cerebral artery
735114006	Occlusion of right pontine artery
735115007	Occlusion of left pontine artery
735131004	Occlusion of left cerebellar artery
735132006	Occlusion of right cerebellar artery
73663008	Neurologic xeroderma pigmentosum
737159004	Aneurysm of basilar artery
737160009	Dissection of basilar artery
7379000	Pseudobulbar palsy
74073002	Cerebellar hemangioblastomatosis
75023009	Post-traumatic epilepsy
75046006	Combined pyramidal-extrapyramidal syndrome
75072002	Nemaline myopathy
75111000	Painful ophthalmoplegia
751371000000107	Personal history of transient ischaemic attack
75138007	Endophlebitis of superior sagittal sinus
75299005	Spastic spinal syphilitic paralysis
75491005	Amyotrophia congenita
75543006	Cerebral embolism
76043009	Hereditary sensory-motor neuropathy, type V
762350007	Dementia due to prion disease
762351006	Dementia due to and following injury of head
762352004	Demyelination due to systemic vasculitis
762629007	Occlusion of right middle cerebral artery by embolus
762630002	Occlusion of left middle cerebral artery by embolus
762632005	Occlusion of left cerebellar artery by embolus
762633000	Occlusion of right cerebellar artery by embolus
762648006	Stenosis of right cerebellar artery
762649003	Stenosis of left cerebellar artery
762651004	Occlusion of right posterior cerebral artery by embolus
762652006	Occlusion of left posterior cerebral artery by embolus
762707000	Subcortical dementia
763067000	Autosomal dominant congenital benign spinal muscular atrophy
763135001	Charcot-Marie-Tooth disease type 4E
763136000	Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome
763314009	Congenital muscular dystrophy with hyperlaxity
763315005	Congenital myopathy with myasthenic-like onset
763345008	Charcot-Marie-Tooth disease type 4B3
763347000	X-linked Charcot-Marie-Tooth disease type 6
763400005	X-linked Charcot-Marie-Tooth disease type 4
763455008	X-linked Charcot-Marie-Tooth disease type 1
763457000	X-linked Charcot-Marie-Tooth disease type 2
763458005	X-linked Charcot-Marie-Tooth disease type 3
763460007	X-linked Charcot-Marie-Tooth disease type 5
763533003	Distal hereditary motor neuropathy Jerash type
763534009	Hot water reflex epilepsy
763622006	Thinking epilepsy
763632004	Startle epilepsy
763669001	Spastic ataxia with congenital miosis
763718009	Finnish upper limb onset distal myopathy
763743003	Intellectual disability, spasticity, ectrodactyly syndrome
763776004	Kelch like family member 9 related early-onset distal myopathy
763802009	Micturition induced epilepsy
763827002	Orgasm induced epilepsy
763829004	Oculopharyngodistal myopathy
763895001	Myosclerosis
76402003	Carotid artery insufficiency syndrome
764453009	Action myoclonus renal failure syndrome
764522009	Familial focal epilepsy with variable foci
764525006	Cylindrical spirals myopathy
764730007	Autosomal dominant Charcot-Marie-Tooth disease type 2 due to kinesin family member 5A mutation
764733009	Progressive external ophthalmoplegia, myopathy, emaciation syndrome
764812008	Autosomal recessive myogenic arthrogryposis multiplex congenita
764850002	Autosomal dominant Charcot-Marie-Tooth disease type 2A2
764854006	Autosomal dominant slowed nerve conduction velocity
764859001	Laing early-onset distal myopathy
764944006	Congenital muscular dystrophy type 1B
764945007	Congenital myopathy with internal nuclei and atypical cores
765046002	Autosomal dominant Charcot-Marie-Tooth disease type 2U
765047006	SURF1, cytochrome c oxidase assembly factor related Charcot-Marie-Tooth disease type 4
765093009	Rolandic epilepsy, speech dyspraxia syndrome
765170001	Sodium voltage-gated channel alpha subunit 8-related epilepsy with encephalopathy
765197008	Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier
765202001	Familial multiple benign meningioma
765216006	Audiogenic epilepsy
765325002	Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease
765331004	Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
765434008	Human immunodeficiency virus type I enhancer binding protein 2 related intellectual disability
765744006	Autosomal dominant intermediate Charcot-Marie-Tooth disease type A
765745007	Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
765746008	Autosomal dominant intermediate Charcot-Marie-Tooth disease type C
765747004	Autosomal dominant intermediate Charcot-Marie-Tooth disease type D
765758008	Microcephalic primordial dwarfism Montreal type
766032007	Holoprosencephaly, ectrodactyly, cleft lip, cleft palate syndrome
766044005	Acute encephalopathy with biphasic seizures and late reduced diffusion
766251006	Lethal infantile mitochondrial myopathy
76670001	Duchenne muscular dystrophy
766752000	Neurolymphomatosis
766753005	Nijmegen breakage syndrome-like disorder
766764008	X-linked distal spinal muscular atrophy type 3
766815007	Perioral myoclonia with absences
766931003	Hypomyelination neuropathy arthrogryposis syndrome
766977007	Severe early-onset axonal neuropathy due to mitofusin 2 deficiency
766987006	Moebius syndrome
768473009	Purine rich element binding protein A syndrome
768555009	5q31.3 microdeletion syndrome
768666006	Syntaxin binding protein 1 encephalopathy with epilepsy
76880004	Angelman syndrome
769065000	Tubulin beta 4A class IVa related leukodystrophy
77015008	Crossed hemiplegia
770430000	Autosomal recessive distal spinal muscular atrophy type 3
770431001	Early-onset epileptic encephalopathy and intellectual disability due to glutamate receptor, ionotropic, N-methyl-D-aspartate, subunit 2A mutation
770438007	Infantile spasm and broad thumb syndrome
770560008	Lissencephaly due to LIS1 mutation
770596007	Rippling muscle disease with myasthenia gravis
770623004	Benign occipital lobe epilepsy
770624005	Benign partial epilepsy of infancy with complex partial seizures
770625006	Combined immunodeficiency with faciooculoskeletal anomalies syndrome
770626007	Congenital Horner syndrome
770627003	Desmin-related myofibrillar myopathy
770630005	Distal hereditary motor neuropathy type 1
770655004	Microcephalus, brain defect, spasticity, hypernatremia syndrome
770723007	Optic atrophy, intellectual disability syndrome
770727008	Spinal muscular atrophy with respiratory distress type 2
770758009	New-onset refractory status epilepticus
770759001	Autosomal dominant intermediate Charcot-Marie-Tooth disease type F
770786001	Hereditary inclusion body myopathy type 4
770792007	Adult-onset distal myopathy due to valosin containing protein mutation
77097004	Oculopharyngeal muscular dystrophy
771081007	Distal hereditary motor neuropathy type 7
771141002	Benign partial epilepsy with secondarily generalized seizures in infancy
771143004	Hereditary motor and sensory neuropathy type 5
771144005	Hereditary motor and sensory neuropathy with acrodystrophy
771147003	Isolated arhinencephaly
771238004	Spinal atrophy, ophthalmoplegia, pyramidal syndrome
771261002	Digital extensor muscle aplasia with polyneuropathy
771263004	Ptosis and vocal cord paralysis syndrome
771267003	Congenital muscular dystrophy with integrin alpha-7 deficiency
771272007	Congenital muscular dystrophy due to lamin A/C mutation
771302009	Autosomal recessive lower motor neuron disease with childhood onset
771304005	Benign nocturnal alternating hemiplegia of childhood
771307003	Charcot-Marie-Tooth disease type 2B5
771334000	Autosomal dominant limb-girdle muscular dystrophy type 1H
771336003	Polymicrogyria with optic nerve hypoplasia
771448004	Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency
771471002	Optic nerve edema, splenomegaly syndrome
771475006	Young adult-onset distal hereditary motor neuropathy
771509001	Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial deoxyribonucleic acid mutation
771514002	Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome
772129007	Autosomal dominant childhood-onset proximal spinal muscular atrophy
773230003	Cyclin-dependent kinase-like 5 deficiency
773306002	Congenital lethal myopathy Compton North type
773308001	Autosomal recessive intermediate Charcot-Marie-Tooth disease type A
773330000	Autosomal recessive intermediate Charcot-Marie-Tooth disease type B
773393001	Autosomal dominant Charcot-Marie-Tooth disease type 2Q
773398005	Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome
773414009	Autosomal recessive intermediate Charcot-Marie-Tooth disease type C
773415005	Contiguous ABCD1 DXS1357E deletion syndrome
773421009	Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
773492007	Childhood-onset spasticity with hyperglycinemia
773555005	Severe neurodegenerative syndrome with lipodystrophy
773643006	Multiple congenital anomalies, hypotonia, seizures syndrome type 2
773648002	Congenital cataract, hearing loss, severe developmental delay syndrome
773737004	Nephrocystin 3-related Meckel-like syndrome
774069007	Protein kinase cAMP-dependent type I regulatory subunit beta-related neurodegenerative dementia with intermediate filaments
774070008	Fibulin 1-related developmental delay, central nervous system anomaly, syndactyly syndrome
774147002	Charcot-Marie-Tooth disease type 2R
774149004	Severe intellectual disability, progressive postnatal microcephaly, midline stereotypic hand movements syndrome
774150004	Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome
774205007	Growth and developmental delay, hypotonia, vision impairment, lactic acidosis syndrome
77461000119109	Myasthenia gravis with exacerbation
77471000119103	Myasthenia gravis without exacerbation
77659000	Paraneoplastic neuropathy
777999008	Hypomyelination with brain stem and spinal cord involvement and leg spasticity
778001003	Potassium voltage-gated channel subfamily Q member 2 related epileptic encephalopathy
778003000	Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain
778021002	Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome
778027003	Primary CD59 deficiency
778047006	Myoclonic epilepsy in non-progressive encephalopathy
778063003	Cryptogenic late-onset epileptic spasms
77835008	Ophthalmoplegia plus syndrome
77956009	Steinert myotonic dystrophy syndrome
780827006	Synaptic Ras GTPase activating protein 1- related intellectual disability
78097002	Total ophthalmoplegia
782675008	Distal myopathy with anterior tibial onset
782723007	Severe intellectual disability, progressive spastic diplegia syndrome
782739000	Male emopamil-binding protein disorder with neurological defect
782742006	Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons
782744007	Lipoic acid synthetase deficiency
782752005	Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome
782754006	Foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis syndrome
782822006	Infantile cerebellar and retinal degeneration
782824007	Sodium channelopathy-related small fiber neuropathy
782826009	Charcot-Marie-Tooth disease type 2P
782829002	Autosomal dominant Charcot-Marie-Tooth disease type 2O
782881002	Hereditary sensorimotor neuropathy with hyperelastic skin
782886007	Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome
782887003	Inherited congenital spastic tetraplegia
782941005	Richieri Costa-da Silva syndrome
782945001	Ophthalmoplegia, intellectual disability, lingua scrotalis syndrome
783057002	DNA replication helicase/nuclease 2-related mitochondrial deoxyribonucleic acid deletion syndrome
78306007	Epidural ascending spinal paralysis
783065004	Autosomal recessive optic atrophy type 7
783091003	46,XY gonadal dysgenesis, motor and sensory neuropathy syndrome
783148005	Distal nebulin myopathy
783160006	Hereditary gelsolin amyloidosis
783166000	Distal anoctaminopathy
783175003	Congenital muscular dystrophy without intellectual disability
783413008	Multiple aneurysms of cerebral artery
783415001	Aneurysm of internal carotid bifurcation
783416000	Aneurysm of anterior cerebral artery
783417009	Aneurysm of posterior inferior cerebellar artery
783418004	Aneurysm of anterior communicating artery
783419007	Aneurysm of posterior cerebral artery
783420001	Aneurysm of middle cerebral artery
783421002	Aneurysm of posterior communicating artery
783422009	Aneurysm of internal carotid-anterior communicating artery zone
783423004	Aneurysm of internal carotid-posterior communicating artery zone
783550006	Hereditary sensory and autonomic neuropathy type 7
783554002	Autosomal recessive limb girdle muscular dystrophy type 2U
783558004	Combined oxidative phosphorylation defect type 11
783618006	Lower motor neuron syndrome with late-adult onset
783629005	Congenital aneurysm of cerebral artery
783630000	Congenital aneurysm of precerebral artery
783707003	Cerebral aneurysm due to dissection of cerebral artery
783716004	Acquired aneurysm of cerebral artery
783722008	Myopathy and diabetes mellitus
783731008	Fibromuscular dysplasia of wall of carotid artery
783733006	Fibromuscular dysplasia of wall of bilateral carotid arteries
783739005	Familial temporal lobe epilepsy
784341001	Amyotrophic lateral sclerosis type 4
784346006	Navajo neurohepatopathy
784347002	Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome
784352007	X-linked scapuloperoneal muscular dystrophy
784370005	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
784372002	Familial mesial temporal lobe epilepsy with febrile seizures
784377008	Autosomal dominant epilepsy with auditory features
784391002	Autosomal dominant adult-onset proximal spinal muscular atrophy
78468005	Erb's muscular dystrophy
785299009	Cobblestone lissencephaly without muscular or ocular involvement
785809005	Mills syndrome
785810000	Synucleinopathy
78689005	Chronic brain syndrome
787037000	Congenital muscular dystrophy type 1A
787044009	Stenosis of bilateral carotid arteries
787172004	Childhood-onset autosomal recessive myopathy with external ophthalmoplegia
788417006	Alopecia, epilepsy, intellectual disability syndrome Moynahan type
788454002	Stenosis of bilateral vertebral arteries
788455001	Occlusion of bilateral pontine arteries
788898005	Dementia caused by volatile inhalant
789005009	Paralysis of uvula after diphtheria
789674008	Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder
791000124107	2-methyl-3-hydroxybutyric aciduria
7931000119101	Anterior choroidal artery thrombosis
79633009	Spastic hemiplegia
79745005	Reflex epilepsy
80328002	Progressive cone-rod dystrophy
80544005	Spongy degeneration of central nervous system
80606009	Carotid artery embolism
80690008	Degenerative disease of the central nervous system
80901002	Endophlebitis of torcular Herophili
80935004	Flaccid hemiplegia
80976008	Myasthenic crisis
81211007	Primary lateral sclerosis
81308009	Disorder of brain
8166000	Thrombophlebitis of basilar sinus
816984002	Progressive multiple sclerosis
81854007	Alexander's disease
818967003	Medulloepithelioma of central nervous system
82077006	Myotubular myopathy
82361000119107	Altered behavior in dementia due to Huntington chorea
82371000119101	Dementia due to multiple sclerosis with altered behavior
82381000119103	Epileptic dementia with behavioral disturbance
82501000119102	Anaplastic astrocytoma of central nervous system
8269002	Cerebrospinal angiopathy
827115000	Autosomal dominant progressive external ophthalmoplegia
827117008	Autosomal recessive progressive external ophthalmoplegia
8291000119107	Atonic epilepsy
838275008	Stenosis of cerebral artery
838307002	Childhood-onset autosomal dominant optic atrophy
838308007	Fibromuscular dysplasia of wall of intracranial artery
838309004	Cerebrovascular abnormality due to Takayasu disease
83832001	Metachromatic leukodystrophy without arylsulfatase deficiency
838345001	Autosomal recessive optic atrophy type 6
840419005	Dissection of extracranial carotid artery
840420004	Dissection of extracranial vertebral artery
840422007	Dissection of anterior cerebral artery
840434004	Dissection of posterior cerebral artery
840436002	Dissection of middle cerebral artery
840437006	Dissection of multiple cerebral arteries
840438001	Dissection of intracranial vertebral artery
840439009	Dissection of intracranial carotid artery
840441005	Dissection of intracranial artery
840464007	Dementia due to carbon monoxide poisoning
840505007	Down syndrome co-occurrent with leukemoid reaction associated transient neonatal pustulosis
84160009	Laryngeal hemiplegia
84161000119100	Partial epileptic seizure of parietal lobe with impairment of consciousness
84171000119106	Partial epileptic seizure of frontal lobe with impairment of consciousness
84181000119109	Partial epileptic seizure of occipital lobe with impairment of consciousness
84191000119107	Partial epileptic seizure of temporal lobe with impairment of consciousness
84201000119105	Intractable partial temporal lobe epilepsy with impairment of consciousness
84211000119108	Intractable partial parietal lobe epilepsy with impairment of consciousness
84216001	Cerebral venous thrombosis of pregnancy AND/OR puerperium
84221000119101	Intractable partial frontal lobe epilepsy with impairment of consciousness
84231000119103	Intractable partial occipital lobe epilepsy with impairment of consciousness
84455002	Spinal paraplegia
84590007	Lower motor neuron disease
84757009	Epilepsy
85102008	Cerebellar ataxia
85505000	Adult spinal muscular atrophy
8563000	Cholinergic crisis
85641006	Hemianencephaly
85672005	Anterior horn cell disease
86003009	Carotid artery thrombosis
86044005	Amyotrophic lateral sclerosis
860804005	Epilepsy due to infectious encephalitis
860806007	Epilepsy due to infectious meningitis
860807003	Hereditary autonomic neuropathy
860809000	Hereditary sensory autonomic neuropathy type IIA
860810005	Hereditary sensory autonomic neuropathy type IIB
860811009	Hereditary sensory autonomic neuropathy type ID
860812002	Hereditary sensory autonomic neuropathy type IE
860813007	Hereditary sensory autonomic neuropathy type IA
860814001	Hereditary sensory autonomic neuropathy type IC
860815000	Epilepsy due to neonatal central nervous system infection
860881004	Flaccid diplegia of lower extremities
86444004	Niemann-Pick disease, type C, acute form
866050001	Mixed germ cell neoplasm of central nervous system
866051002	Motor neuron disease due to lead intoxication
870284000	Pelizaeus Merzbacher like disease due to HSPD1 mutation
870285004	Pelizaeus Merzbacher like disease due to SLC16A2 mutation
870286003	Pelizaeus Merzbacher like disease due to AIMP1 mutation
870287007	Pelizaeus Merzbacher like disease due to GJC2 mutation
870319003	Optic atrophy due to late syphilis
870544005	Occlusion of distal basilar artery
870566003	Occlusion of anterior choroidal artery
870579007	Occlusion of branch of basilar artery
870637009	Dissection of cervical artery
87151000119105	Malignant glioma of central nervous system
871637001	Thrombosis of multiple cerebral veins
87551000119101	Visual disturbance as sequela of cerebrovascular disease
87607002	Pelizaeus-Merzbacher disease, classic form
87842000	Generalized neuromuscular exhaustion syndrome
87937009	Endophlebitis of intracranial venous sinus
88174006	Basilar artery thrombosis
88922007	Thrombosis of basilar sinus
88923002	Progressive muscular atrophy
89142007	Progressive intracranial arterial occlusion
89437009	Cerebral paraparesis
89980009	Thrombosis of cavernous venous sinus
903741000000102	Uhthoff phenomenon
90520006	Vertebral artery stenosis
91327001	Quadriparesis
9133005	Familial amyloid polyneuropathy, Iowa type
91502009	Spinocerebellar disease
91601000119109	Sequela of thrombotic stroke
91637004	Myasthenia gravis
92341000119107	Weakness of extremities as sequela of stroke
92503002	Neurofibromatosis type 2
92824003	Neurofibromatosis type 1
92962004	Congenital absence of carotid artery
92997002	Congenital anomaly of carotid artery
93054001	Congenital dilatation of carotid artery
93153005	Limb-girdle muscular dystrophy
93312006	Congenital malposition of carotid artery
93396008	Congenital stenosis of carotid artery
936271000000100	Congenital anomaly of precerebral vessel
93744007	Primary malignant neoplasm of central nervous system
93747000	Primary malignant neoplasm of cerebral meninges
93931007	Primary malignant neoplasm of optic nerve
94243009	Secondary malignant neoplasm of central nervous system
94246001	Secondary malignant neoplasm of cerebral meninges
943181000000103	Degenerative disease of basal ganglia
94452002	Secondary malignant neoplasm of optic nerve
95208000	Photogenic epilepsy
95235009	Retroesophageal carotid artery
9537004	Juvenile GM 2 gangliosidosis
95455008	Thrombosis of cerebral veins
95458005	Cerebellar artery occlusion
95461006	Thrombophlebitis of cerebral vein
95477007	Congenital degeneration of nervous system
95610008	Congenital brain damage
95647008	Upper motor neuron disease
95650006	Transient hemiplegia
95651005	Chronic progressive paraparesis
95774001	Atrophy of optic disc
95775000	Retrobulbar optic nerve atrophy
9611000119107	Symptomatic carotid artery stenosis
97381000119100	Neurogenic bladder due to quadriplegia
97391000119102	Paraplegia with neurogenic bladder
9753004	Triplegia
984681000000101	Profound learning disability
99451000119105	Cerebral infarction due to stenosis of carotid artery

Chronic Neurological Disease including Significant Learning Disorder

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