Chronic Neurological Disease including Significant Learning Disorder



Coding system
SNOMED CT
Organisation
PRIMIS Covid Vaccination Uptake Reporting
Codelist ID
primis-covid19-vacc-uptake/cns_cov
Tag
v1
ID
3a82f99b

Versions
  • v1

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

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

Codes not in the full codelist are in faint grey.