Chronic Neurological Disease including Significant Learning Disorder
- Coding system
- SNOMED CT
- Coding system release
- unknown
- Organisation
- PRIMIS Covid Vaccination Uptake Reporting
- Codelist ID
- primis-covid19-vacc-uptake/cns_cov
- Version Tag
- v1
- Version ID
- 3a82f99b
Versions
Description
Taken from the CNS_COV_COD field in SARS-CoV2 COVID19 Vaccination Uptake Reporting Codes 20_21 v1, published by PRIMIS.
© PRIMIS - the University of Nottingham 2021
References
Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.
We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.
| code | term |
|---|---|
| 10007009 | Coffin-Siris syndrome |
| 100941000119100 | Epilepsy in mother complicating pregnancy |
| 101421000119107 | Dementia due to Parkinson's disease |
| 102831000119104 | Paralytic syndrome of both lower limbs as sequela of stroke |
| 10349009 | Multi-infarct dementia with delirium |
| 103761000119107 | Paralytic syndrome of all four limbs as sequela of stroke |
| 104461000119104 | Ophthalmoplegia due to Graves disease |
| 1055001 | Stenosis of precerebral artery |
| 106018006 | Hereditary degenerative disease of central nervous system |
| 106021000119105 | Multi-infarct dementia due to atherosclerosis |
| 10750951000119106 | Epilepsy in mother complicating childbirth |
| 108691000119102 | Spasticity as sequela of stroke |
| 10878002 | Aneurysm of common carotid artery |
| 1089411000000104 | Cerebral infarction due to occlusion of cerebral artery |
| 1089421000000105 | Cerebral infarction due to stenosis of cerebral artery |
| 1089501000000102 | Presenile dementia with psychosis |
| 1089521000000106 | Predominantly cortical dementia |
| 1089531000000108 | Predominantly cortical vascular dementia |
| 109478007 | Kohlschutter's syndrome |
| 109561000 | Cerebrofacial dysplasia |
| 109911004 | Overlapping malignant neoplasm of brain and other parts of the central nervous system |
| 109915008 | Primary malignant neoplasm of meninges |
| 111296006 | Basilar artery embolism |
| 111298007 | Chronic cerebral ischemia |
| 111299004 | Atheroma of cerebral arteries |
| 111337001 | Dyke-Davidoff-Masson syndrome |
| 111385000 | Tay-Sachs disease |
| 111480006 | Psychoactive substance-induced organic dementia |
| 111496009 | Syringomyelia |
| 111497000 | Arterial thrombosis of spinal cord |
| 111498005 | Extratemporal epilepsy |
| 111499002 | Déjérine-Sottas disease |
| 111500006 | Muscular dystrophy-deafmutism syndrome |
| 111501005 | Congenital hereditary muscular dystrophy |
| 111502003 | Fukuyama congenital muscular dystrophy |
| 111503008 | Merosin deficient congenital muscular dystrophy |
| 111505001 | Muscle-eye-brain disease, congenital muscular dystrophy |
| 111506000 | Distal muscular dystrophy, Miyoshi type |
| 111508004 | Emery-Dreifuss muscular dystrophy |
| 111527005 | Partial optic atrophy |
| 1131000119105 | Sequela of cerebrovascular accident |
| 11442006 | Hereditary sensory neuropathy |
| 11538006 | Quadriplegia |
| 116811000119106 | Non-Hodgkin lymphoma of central nervous system metastatic to lymph node of lower limb |
| 116821000119104 | Non-Hodgkin lymphoma of central nervous system metastatic to lymph node of upper limb |
| 11701009 | Hemicephaly |
| 119001000119108 | Intractable simple partial epilepsy |
| 12242711000119109 | Weakness of left facial muscle due to and following cerebrovascular accident |
| 12242751000119105 | Weakness of right facial muscle due to and following cerebrovascular accident |
| 12246008 | Acute neuronopathic Gaucher's disease |
| 12348006 | Presenile dementia |
| 123615007 | Secondary optic atrophy |
| 12367511000119101 | Paraplegia due to and following cerebrovascular accident |
| 1239331000000100 | Significant intellectual disability |
| 12454008 | Cauda equina syndrome with neurogenic bladder |
| 125081000119106 | Cerebral infarction due to occlusion of precerebral artery |
| 125501000119105 | Fetus with complete trisomy 21 syndrome |
| 125511000119108 | Fetus with complete trisomy 18 syndrome |
| 125521000119101 | Fetus with complete trisomy 13 syndrome |
| 126011000119107 | Acquired caroticocavernous sinus fistula |
| 126944002 | Brain disorder resulting from a period of impaired oxygen delivery to the brain |
| 126945001 | Perinatal anoxic-ischemic brain injury |
| 128171000119104 | Spontaneous caroticocavernous sinus fistula |
| 128190004 | Inherited metabolic disorder of nervous system |
| 128203003 | Hereditary motor and sensory neuropathy with optic atrophy |
| 128204009 | Hereditary motor and sensory neuropathy with retinitis pigmentosa |
| 128205005 | Hereditary sensory and autonomic neuropathy |
| 128206006 | Congenital sensory neuropathy with selective loss of small myelinated fibers |
| 128209004 | Chronic inflammatory demyelinating polyradiculoneuropathy |
| 128212001 | Spinal muscular atrophy, type II |
| 128213006 | Neuromuscular junction disorder |
| 128218002 | Disorder of intracranial venous sinus |
| 12853006 | Embolism of torcular Herophili |
| 128608001 | Cerebral arterial aneurysm |
| 128609009 | Intracranial aneurysm |
| 129583005 | Paralysis of palate |
| 129596006 | Menopausal muscular dystrophy syndrome |
| 129608008 | Progressive pyramidopallidal degeneration |
| 129614001 | Paralysis of vagus, spinal accessory and hypoglossal nerves |
| 129620000 | Scapuloperoneal muscular dystrophy |
| 129621001 | Nemaline myopathy, early onset type |
| 129622008 | Nemaline myopathy, late onset type |
| 130121000119104 | Dementia due to Rett's syndrome |
| 13092008 | Pick's disease |
| 133981000119106 | Dysarthria as late effects of cerebrovascular disease |
| 133991000119109 | Fluency disorder as sequela of cerebrovascular disease |
| 134771000119108 | Alteration of sensation as late effect of stroke |
| 13973009 | Grand mal status |
| 140281000119108 | Hemiparesis as late effect of cerebrovascular disease |
| 14070001 | Multi-infarct dementia with depression |
| 142031000119104 | Visual field defect due to and following cerebrovascular accident |
| 14210003 | Lipofuscinosis |
| 14246007 | Embolism of intracranial venous sinus |
| 14309005 | Anterior choroidal artery syndrome |
| 14401000119109 | Partial frontal lobe epilepsy |
| 147101000119108 | Primary malignant astrocytoma of central nervous system |
| 147131000119101 | Glioblastoma multiforme of central nervous system |
| 148871000119109 | Weakness as a late effect of cerebrovascular accident |
| 14977000 | Multiple AND bilateral precerebral artery thrombosis |
| 149821000119103 | Cerebral infarction due to carotid artery occlusion |
| 15080006 | Myotubular myopathy with type I atrophy |
| 15182000 | Coffin-Lowry syndrome |
| 15523002 | Benign focal epilepsy of childhood |
| 15632811000119100 | Optic atrophy of right eye |
| 15632851000119104 | Optic atrophy of left eye |
| 15648201000119100 | Aneurysm of intracranial portion of right internal carotid artery |
| 15648241000119103 | Aneurysm of intracranial portion of left internal carotid artery |
| 15648281000119108 | Aneurysm of extracranial portion of right internal carotid artery |
| 15648321000119103 | Aneurysm of extracranial portion of left internal carotid artery |
| 15648361000119108 | Aneurysm of right internal carotid artery |
| 15648401000119104 | Aneurysm of left internal carotid artery |
| 15648441000119102 | Aneurysm of right common carotid artery |
| 15648481000119107 | Aneurysm of left common carotid artery |
| 15648521000119107 | Aneurysm of right carotid artery |
| 15648561000119102 | Aneurysm of left carotid artery |
| 15662003 | Senile dementia |
| 15699121000119104 | Hereditary right optic atrophy |
| 15699161000119109 | Hereditary left optic atrophy |
| 15705007 | Phlebitis of basilar sinus |
| 15707961000119109 | Dissection of bilateral carotid arteries |
| 15708001000119106 | Dissection of left carotid artery |
| 15708041000119108 | Dissection of right carotid artery |
| 15710641000119100 | Dissection of bilateral vertebral arteries |
| 15710681000119105 | Dissection of right vertebral artery |
| 15710721000119104 | Dissection of left vertebral artery |
| 1591000119103 | Dementia with behavioral disturbance |
| 1593000 | Infantile hemiplegia |
| 15978431000119106 | Thrombosis of right vertebral artery |
| 15978471000119109 | Thrombosis of left vertebral artery |
| 15978631000119109 | Occlusion of bilateral vertebral arteries |
| 15982271000119104 | Weakness of right facial muscle due to and following cerebrovascular disease |
| 15982311000119104 | Weakness of left facial muscle due to and following cerebrovascular disease |
| 15988351000119101 | Acquired right carotid cavernous fistula |
| 15988391000119106 | Acquired left carotid cavernous fistula |
| 16218291000119100 | Acute cerebral ischemia |
| 16260551000119106 | Dysphasia due to and following cerebrovascular accident |
| 16276361000119109 | Vascular dementia without behavioral disturbance |
| 16279401000119108 | Occlusion of right cilioretinal artery |
| 16279441000119105 | Occlusion of left cilioretinal artery |
| 163594004 | On examination - salaam attack |
| 163601006 | On examination - hemiplegia |
| 163604003 | On examination - paraplegia |
| 163605002 | On examination - quadriplegia |
| 163606001 | On examination - diplegia |
| 16415361000119105 | Radiologically isolated syndrome |
| 16418006 | Embolism of basilar sinus |
| 16476641000119100 | Acquired arteriovenous fistula of dura of cerebrum |
| 16662331000119106 | Aneurysm of right vertebral artery |
| 16662371000119109 | Aneurysm of left vertebral artery |
| 1670004 | Cerebral hemiparesis |
| 16703551000119107 | Memory deficit due to and following cerebrovascular disease |
| 16703661000119105 | Memory deficit due to and following cerebrovascular accident |
| 16703761000119102 | Memory deficit due to and following ischemic cerebrovascular accident |
| 16703821000119101 | Memory deficit due to and following hemorrhagic cerebrovascular accident |
| 16709811000119106 | Spontaneous hemorrhage of subarachnoid space from anterior communicating artery |
| 16851005 | Mitochondrial myopathy |
| 171822009 | Acute atrophic spinal paralysis |
| 17409003 | Facial hemiparesis |
| 18058007 | Phlebitis of intracranial venous sinus |
| 18322005 | Thrombosis of torcular Herophili |
| 1845001 | Paraparesis |
| 186317009 | Listerial cerebral arteritis |
| 186476008 | Acute paralytic non-bulbar poliomyelitis |
| 186478009 | Acute paralytic poliomyelitis, vaccine-associated |
| 186479001 | Acute paralytic poliomyelitis, wild virus, imported |
| 186480003 | Acute paralytic poliomyelitis, wild virus, indigenous |
| 186831000119104 | Apraxia due to and following cerebrovascular accident |
| 186893003 | Rupture of syphilitic cerebral aneurysm |
| 18756002 | Juvenile GM1 gangliosidosis |
| 187931000119106 | Atypical absence epilepsy |
| 188312005 | Malignant neoplasm of cerebral dura mater |
| 188313000 | Malignant neoplasm of cerebral arachnoid mater |
| 188315007 | Malignant neoplasm of cerebral pia mater |
| 18927009 | Niemann-Pick disease, type D |
| 191449005 | Uncomplicated senile dementia |
| 191451009 | Uncomplicated presenile dementia |
| 191452002 | Presenile dementia with delirium |
| 191454001 | Presenile dementia with paranoia |
| 191455000 | Presenile dementia with depression |
| 191457008 | Senile dementia with depressive or paranoid features |
| 191458003 | Senile dementia with paranoia |
| 191459006 | Senile dementia with depression |
| 191461002 | Senile dementia with delirium |
| 191463004 | Uncomplicated arteriosclerotic dementia |
| 191464005 | Arteriosclerotic dementia with delirium |
| 191465006 | Arteriosclerotic dementia with paranoia |
| 191466007 | Arteriosclerotic dementia with depression |
| 191475009 | Chronic alcoholic brain syndrome |
| 191493005 | Drug-induced dementia |
| 191519005 | Dementia associated with another disease |
| 192673008 | Sarcoid meningitis |
| 192685000 | Subacute sclerosing panencephalitis |
| 192753009 | Phlebitis and thrombophlebitis of intracranial sinuses |
| 192754003 | Embolism cavernous sinus |
| 192755002 | Embolism superior longitudinal sinus |
| 192756001 | Embolism lateral sinus |
| 192757005 | Embolism transverse sinus |
| 192759008 | Cerebral venous sinus thrombosis |
| 192760003 | Thrombosis of superior longitudinal sinus |
| 192764007 | Phlebitis cavernous sinus |
| 192765008 | Phlebitis of superior longitudinal sinus |
| 192769002 | Thrombophlebitis of central nervous system venous sinuses |
| 192770001 | Thrombophlebitis of cavernous sinus |
| 192771002 | Thrombophlebitis of superior longitudinal venous sinus |
| 192781003 | Leukodystrophy |
| 192782005 | Galactosylceramide beta-galactosidase deficiency |
| 192787004 | B variant hexosaminidase A deficiency |
| 192788009 | Retinal dystrophy in cerebroretinal lipidosis |
| 192845009 | Myoclonic encephalopathy |
| 192904000 | Myelopathy due to another disorder |
| 192906003 | Myelopathy due to neoplastic disease |
| 192928003 | Generalized multiple sclerosis |
| 192929006 | Exacerbation of multiple sclerosis |
| 192949002 | Congenital paraplegia |
| 192964002 | Flaccid tetraplegia |
| 192965001 | Spastic tetraplegia |
| 192966000 | Flaccid paraplegia |
| 192967009 | Spastic paraplegia |
| 192976002 | Progressive supranuclear palsy |
| 192979009 | Generalized non-convulsive epilepsy |
| 192990004 | Benign myoclonic epilepsy in infancy |
| 192999003 | Partial epilepsy with impairment of consciousness |
| 193000002 | Temporal lobe epilepsy |
| 193002005 | Psychosensory epilepsy |
| 193008009 | Somatosensory epilepsy |
| 193009001 | Partial epilepsy with autonomic symptoms |
| 193010006 | Visual reflex epilepsy |
| 193021002 | Cursive (running) epilepsy |
| 193022009 | Localization-related(focal)(partial)idiopathic epilepsy and epileptic syndromes with seizures of localized onset |
| 193165008 | Neuropathy in association with hereditary ataxia |
| 193195000 | Sarcoid neuropathy |
| 193207007 | Juvenile or adult myasthenia gravis |
| 193209005 | Myasthenic syndrome due to another disorder |
| 193212008 | Myasthenic syndrome due to hypothyroidism |
| 193213003 | Myasthenic syndrome due to pernicious anemia |
| 193214009 | Myasthenic syndrome due to thyrotoxicosis |
| 193216006 | Congenital and developmental myasthenia |
| 193225000 | Hereditary progressive muscular dystrophy |
| 193227008 | Pelvic muscular dystrophy |
| 193230001 | Distal muscular dystrophy with juvenile onset |
| 193237003 | Myotonic disorder |
| 193238008 | Infantile myotonia |
| 19373007 | External ophthalmoplegia |
| 194043004 | Optic atrophy secondary to retinal disease |
| 19448008 | Optic atrophy associated with retinal dystrophy |
| 195154000 | Ruptured berry aneurysm |
| 195155004 | Subarachnoid hemorrhage from carotid siphon and bifurcation |
| 195160000 | Intracranial subarachnoid hemorrhage from vertebral artery |
| 195180004 | Basilar artery occlusion |
| 195182007 | Vertebral artery occlusion |
| 195183002 | Multiple and bilateral precerebral arterial occlusion |
| 195185009 | Cerebral infarct due to thrombosis of precerebral arteries |
| 195186005 | Cerebral infarction due to embolism of precerebral arteries |
| 195189003 | Cerebral infarction due to thrombosis of cerebral arteries |
| 195190007 | Cerebral infarction due to embolism of cerebral arteries |
| 195199008 | Vertebrobasilar artery syndrome |
| 195229008 | Non-pyogenic venous sinus thrombosis |
| 195230003 | Cerebral infarction due to cerebral venous thrombosis, non-pyogenic |
| 195232006 | Occlusion and stenosis of middle cerebral artery |
| 195233001 | Occlusion and stenosis of anterior cerebral artery |
| 195234007 | Occlusion and stenosis of posterior cerebral artery |
| 195235008 | Occlusion and stenosis of cerebellar arteries |
| 195236009 | Occlusion and stenosis of multiple and bilateral cerebral arteries |
| 195239002 | Late effects of cerebrovascular disease |
| 195241001 | Sequelae of intracerebral hemorrhage |
| 195243003 | Sequelae of cerebral infarction |
| 19598007 | Generalized epilepsy |
| 199451000000106 | Simple partial epileptic seizure |
| 19972008 | Postencephalitic parkinsonism |
| 20022000 | Hemiparesis |
| 200258006 | Obstetric cerebral venous thrombosis |
| 200259003 | Cerebral venous thrombosis in pregnancy |
| 200260008 | Cerebral venous thrombosis in the puerperium |
| 200330000 | Puerperal cerebrovascular disorder - delivered |
| 200331001 | Puerperal cerebrovascular disorder - delivered with postnatal complication |
| 200332008 | Puerperal cerebrovascular disorder with antenatal complication |
| 200333003 | Puerperal cerebrovascular disorder with postnatal complication |
| 20059004 | Occlusion of cerebral artery |
| 20121000119105 | Partial occipital lobe epilepsy |
| 20305008 | Congenital myotonia, autosomal recessive form |
| 204036008 | Lissencephaly |
| 204040004 | Agenesis of cerebrum |
| 204052006 | Cebocephaly |
| 20447006 | Plasma cell dyscrasia with polyneuropathy |
| 204493007 | Arteriovenous malformation of precerebral vessels |
| 204497008 | Cerebrovascular system anomalies |
| 204501003 | Congenital stricture of cerebral artery |
| 204745000 | Total intestinal aganglionosis |
| 205615000 | Trisomy 21- meiotic nondisjunction |
| 205619006 | Trisomy 13, meiotic nondisjunction |
| 205620000 | Trisomy 13 - mitotic nondisjunction mosaicism |
| 205623003 | Trisomy 18 - meiotic nondisjunction |
| 205624009 | Trisomy 18 - mitotic nondisjunction mosaicism |
| 2065009 | Dominant hereditary optic atrophy |
| 20725005 | Familial visceral neuropathy |
| 21007002 | Wernicke's disease |
| 21086008 | Cockayne syndrome |
| 21098003 | Primary optic atrophy |
| 21111006 | Complete trisomy 13 syndrome |
| 213044006 | Mechanical complication of carotid artery bypass |
| 213208008 | Anoxic brain damage complication |
| 213209000 | Cerebral anoxia complication |
| 21361000119109 | Paraneoplastic peripheral neuropathy |
| 21391000119102 | Partial parietal lobe epilepsy |
| 21524000 | Relaxation of diaphragm |
| 2198002 | Visceral epilepsy |
| 22126005 | Hereditary neuraxial edema |
| 223176004 | Cerebellar disorder |
| 22381000119105 | Primary degenerative dementia |
| 22386003 | Syphilitic optic atrophy |
| 22811006 | Leukoencephalopathy |
| 22881000119100 | Quadriplegia with quadriparesis |
| 230156002 | Malignant meningitis |
| 230193008 | Neurosarcoidosis |
| 230220006 | Intracranial septic embolism |
| 230221005 | Intracranial arterial septic embolism |
| 230222003 | Septic thrombophlebitis of straight sinus |
| 230223008 | Septic thrombophlebitis of sigmoid sinus |
| 230224002 | Septic thrombophlebitis of cortical vein |
| 230226000 | System disorder of the nervous system |
| 230232005 | Late onset cerebellar ataxia |
| 230233000 | Progressive cerebellar ataxia |
| 230234006 | Periodic ataxia |
| 230237004 | Progressive spinocerebellar ataxia with decreased tendon reflexes |
| 230239001 | Progressive cerebellar ataxia with palatal myoclonus |
| 230240004 | Progressive cerebellar ataxia with hypogonadism |
| 230244008 | Disorder primarily affecting the motor pathways |
| 230247001 | Distal spinal muscular atrophy |
| 230248006 | Scapuloperoneal spinal muscular atrophy |
| 230249003 | Facioscapulohumeral spinal muscular atrophy |
| 230250003 | Facioscapulohumeral spinal muscular atrophy with sensory loss |
| 230251004 | Scapulohumeral spinal muscular atrophy |
| 230252006 | Oculopharyngeal spinal muscular atrophy |
| 230253001 | Bulbospinal neuronopathy |
| 230254007 | Western Pacific motor neurone disease |
| 230255008 | Madras-type motor neurone disease |
| 230257000 | Paraneoplastic motor neurone disease |
| 230258005 | Amyotrophic lateral sclerosis with dementia |
| 230264003 | Troyer syndrome |
| 230282000 | Post-traumatic dementia |
| 230283005 | Punch drunk syndrome |
| 230285003 | Vascular dementia of acute onset |
| 230286002 | Subcortical vascular dementia |
| 230287006 | Mixed cortical and subcortical vascular dementia |
| 230289009 | Patchy dementia |
| 230291001 | Juvenile Parkinson's disease |
| 230296006 | Vascular parkinsonism |
| 230297002 | Multiple system atrophy |
| 230298007 | Disorder presenting primarily with chorea |
| 230329009 | Posthemiplegic dystonia |
| 230363006 | Progressive neuronal degeneration of childhood |
| 230368002 | Type III transitional Pelizaeus-Merzbacher disease |
| 230369005 | Type IV adult Pelizaeus-Merzbacher disease |
| 230370006 | Type V atypical Pelizaeus-Merzbacher disease |
| 230371005 | Type VI Cockayne Pelizaeus-Merzbacher disease |
| 230372003 | Acute relapsing multiple sclerosis |
| 230373008 | Chronic progressive multiple sclerosis |
| 230375001 | Subacute hemorrhagic leukoencephalitis |
| 230380005 | Balo concentric sclerosis |
| 230381009 | Localization-related epilepsy |
| 230382002 | Benign frontal epilepsy of childhood |
| 230383007 | Benign psychomotor epilepsy of childhood |
| 230384001 | Benign atypical partial epilepsy in childhood |
| 230386004 | Childhood epilepsy with occipital paroxysms |
| 230387008 | Benign occipital epilepsy of childhood - early onset variant |
| 230388003 | Benign occipital epilepsy of childhood - late onset variant |
| 230389006 | Primary inherited reading epilepsy |
| 230390002 | Localization-related symptomatic epilepsy |
| 230393000 | Lateral temporal epilepsy |
| 230394006 | Frontal lobe epilepsy |
| 230395007 | Supplementary motor epilepsy |
| 230397004 | Anterior frontopolar epilepsy |
| 230398009 | Orbitofrontal epilepsy |
| 230399001 | Dorsolateral epilepsy |
| 230400008 | Opercular epilepsy |
| 230401007 | Non-progressive Kozhevnikow syndrome |
| 230403005 | Parietal lobe epilepsy |
| 230404004 | Occipital lobe epilepsy |
| 230406002 | Localization-related symptomatic epilepsy with specific precipitant |
| 230407006 | Hemiplegia-hemiconvulsion-epilepsy syndrome |
| 230408001 | Localization-related cryptogenic epilepsy |
| 230412007 | Myoclonic epilepsy of early childhood |
| 230413002 | Juvenile absence epilepsy |
| 230414008 | Epilepsy with grand mal seizures on awakening |
| 230415009 | Cryptogenic generalized epilepsy |
| 230416005 | Cryptogenic West syndrome |
| 230417001 | Symptomatic West syndrome |
| 230418006 | Lennox-Gastaut syndrome |
| 230419003 | Cryptogenic Lennox-Gastaut syndrome |
| 230420009 | Symptomatic Lennox-Gastaut syndrome |
| 230422001 | Myoclonic absence epilepsy |
| 230423006 | Unverricht-Lundborg syndrome |
| 230425004 | Lafora disease |
| 230427007 | Cryptogenic myoclonic epilepsy |
| 230428002 | Idiopathic myoclonic epilepsy |
| 230429005 | Early infantile epileptic encephalopathy with suppression bursts |
| 230430000 | Symptomatic myoclonic epilepsy |
| 230435005 | Epilepsy undetermined whether focal or generalized |
| 230437002 | Severe myoclonic epilepsy in infancy |
| 230438007 | Acquired epileptic aphasia |
| 230439004 | Epilepsy with continuous spike wave during slow-wave sleep |
| 230440002 | Secondary reading epilepsy |
| 230444006 | Menstrual epilepsy |
| 230445007 | Nocturnal epilepsy |
| 230447004 | Eyelid myoclonus with absences |
| 230448009 | Writing epilepsy |
| 230450001 | Eating epilepsy |
| 230452009 | Toothbrushing epilepsy |
| 230453004 | Decision-making epilepsy |
| 230454005 | Aquagenic epilepsy |
| 230456007 | Status epilepticus |
| 230457003 | Non-convulsive status epilepticus with three per second spike wave |
| 230458008 | Non-convulsive status epilepticus without three per second spike wave |
| 230459000 | Non-convulsive simple partial status epilepticus |
| 230460005 | Complex partial status epilepticus |
| 230466004 | Alternating hemiplegia of childhood |
| 230530003 | Congenital nuclear ophthalmoplegia |
| 230552007 | X-linked hereditary motor and sensory neuropathy |
| 230553002 | Autosomal dominant sensory neuropathy |
| 230556005 | X-linked recessive sensory neuropathy |
| 230557001 | Hereditary dysautonomia with motor neuropathy |
| 230558006 | Hereditary liability to pressure palsies |
| 230559003 | Hereditary hypertrophic neuropathy with paraproteinemia |
| 230561007 | Congenital neuropathy with arthrogryposis multiplex congenita |
| 230562000 | Congenital hypomyelinating neuropathy |
| 230564004 | Chronic inflammatory demyelinating polyradiculoneuropathy with central nervous system demyelination |
| 230586003 | Neuropathy due to multiple myeloma |
| 230594005 | Critical illness polyneuropathy |
| 230666006 | Paraneoplastic autonomic dysfunction |
| 230669004 | Genetically determined myasthenia |
| 230670003 | Familial infantile myasthenia |
| 230671004 | Acetylcholine resynthesis deficiency |
| 230672006 | Congenital myasthenic syndrome |
| 230673001 | Congenital end-plate acetylcholine receptor deficiency |
| 230674007 | Pseudomyopathic myasthenia |
| 230675008 | Slow channel syndrome |
| 230676009 | Putative defect in acetylcholine synthesis or packaging |
| 230677000 | Congenital end-plate acetylcholinesterase deficiency |
| 230678005 | Decrease of motor end-plate potential amplitude without acetylcholine receptor deficiency |
| 230679002 | Abnormality of synaptic vesicles |
| 230684008 | Ocular myasthenia |
| 230685009 | Myasthenia gravis associated with thymoma |
| 230686005 | Generalized myasthenia |
| 230687001 | Myopathy in myasthenia gravis |
| 230692004 | Infarction - precerebral |
| 230693009 | Anterior cerebral circulation infarction |
| 230694003 | Total anterior cerebral circulation infarction |
| 230695002 | Partial anterior cerebral circulation infarction |
| 230696001 | Posterior cerebral circulation infarction |
| 230698000 | Lacunar infarction |
| 230699008 | Pure motor lacunar infarction |
| 230700009 | Pure sensory lacunar infarction |
| 230701008 | Pure sensorimotor lacunar infarction |
| 230702001 | Lacunar ataxic hemiparesis |
| 230703006 | Dysarthria-clumsy hand syndrome |
| 230704000 | Multi-infarct state |
| 230706003 | Hemorrhagic cerebral infarction |
| 230707007 | Anterior cerebral circulation hemorrhagic infarction |
| 230708002 | Posterior cerebral circulation hemorrhagic infarction |
| 230720005 | Cerebral venous thrombosis of straight sinus |
| 230721009 | Cerebral venous thrombosis of sigmoid sinus |
| 230722002 | Cerebral venous thrombosis of cortical vein |
| 230724001 | Cerebral amyloid angiopathy |
| 230725000 | Sporadic cerebral amyloid angiopathy |
| 230730001 | Dissection of vertebral artery |
| 230731002 | Cerebral arteritis in systemic vasculitis |
| 230732009 | Cerebral arteritis in giant cell arteritis |
| 230735006 | Syphilitic cerebral arteritis |
| 230738008 | Asymptomatic cerebrovascular disease |
| 230739000 | Spinal cord stroke |
| 230745008 | Hydrocephalus |
| 232036006 | Cilioretinal artery occlusion |
| 232059000 | Laurence-Moon syndrome |
| 233718008 | Pulmonary tuberous sclerosis |
| 233964008 | Internal carotid artery stenosis |
| 233983001 | Ruptured cerebral aneurysm |
| 233988005 | Carotid artery aneurysm |
| 234005004 | Vertebral artery rupture |
| 234006003 | Carotid artery rupture |
| 234142008 | Cerebral arteriovenous malformation |
| 234149004 | Congenital arteriovenous fistula of brain |
| 23501004 | Arginase deficiency |
| 236529001 | Prune belly syndrome with pulmonic stenosis, mental retardation and deafness |
| 23671000119107 | Sequela of ischemic cerebral infarction |
| 23728006 | Partial bilateral paralysis |
| 23740006 | Bilateral paralysis of tongue |
| 237612000 | Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction |
| 237867001 | Hereditary cerebrovascular amyloidosis |
| 237960000 | D-2-hydroxyglutaric aciduria |
| 237961001 | L-2-hydroxyglutaric aciduria |
| 238018004 | Total hexosaminidase deficiency - infantile |
| 238019007 | Total hexosaminidase deficiency - juvenile |
| 238020001 | Total hexosaminidase deficiency - adult |
| 238021002 | B variant hexosaminidase A deficiency - infantile |
| 238022009 | B variant hexosaminidase A deficiency - juvenile |
| 238023004 | B variant hexosaminidase A deficiency - adult |
| 238024005 | B1 variant hexosaminidase A deficiency |
| 238025006 | GM1 gangliosidosis |
| 238026007 | Infantile GM1 gangliosidosis |
| 238027003 | Adult GM1 gangliosidosis |
| 238030005 | Galactocerebroside beta-galactosidase deficiency - early onset |
| 238031009 | Arylsulfatase A deficiency |
| 238048001 | Alpha-N-acetylgalactosaminidase deficiency |
| 23808003 | Rolandic vein occlusion syndrome |
| 23819000 | Embolism of cavernous venous sinus |
| 23849003 | Sandhoff disease |
| 238826008 | de Barsy syndrome |
| 23941000119108 | Arnold Chiari type 2 without hydrocephalus |
| 240046001 | Muscular dystrophy with predominantly proximal limb girdle distribution |
| 240047005 | X-linked muscular dystrophy with limb girdle distribution |
| 240048000 | X-linked muscular dystrophy with abnormal dystrophin |
| 240049008 | Intermediate X-linked muscular dystrophy |
| 240050008 | Manifesting female carrier of X-linked muscular dystrophy |
| 240051007 | X-linked limb girdle muscular dystrophy with normal dystrophin |
| 240052000 | Ji muscular dystrophy |
| 240053005 | Hereditary myopathy limited to females |
| 240054004 | Autosomal recessive muscular dystrophy with limb girdle distribution |
| 240055003 | Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein |
| 240056002 | Severe autosomal recessive muscular dystrophy of childhood - North African type |
| 240057006 | Autosomal recessive muscular dystrophy with gene located at 15q |
| 240058001 | Reunion-Indiana Amish type muscular dystrophy |
| 240059009 | Congenital muscular dystrophy |
| 240060004 | Western type of congenital muscular dystrophy |
| 240061000 | Congenital muscular dystrophy with arthrogryposis multiplex congenita |
| 240062007 | Ullrich congenital muscular dystrophy |
| 240063002 | Eichsfeld type congenital muscular dystrophy |
| 240064008 | Hutterite type of muscular dystrophy |
| 240065009 | Adult onset autosomal recessive muscular dystrophy with normal dystrophin |
| 240067001 | Autosomal dominant muscular dystrophy with limb girdle distribution |
| 240068006 | Autosomal dominant muscular dystrophy with gene located at 5q31 |
| 240069003 | Late onset proximal muscular dystrophy with dysarthria |
| 240070002 | Muscular dystrophy not predominantly limb girdle in distribution |
| 240071003 | X-linked muscular dystrophy not predominantly limb girdle |
| 240072005 | Benign scapuloperoneal muscular dystrophy with cardiomyopathy |
| 240073000 | Autosomal recessive muscular dystrophy not predominantly limb girdle |
| 240074006 | Scapulohumeral muscular dystrophy |
| 240075007 | Autosomal dominant muscular dystrophy not predominantly limb girdle |
| 240076008 | Benign scapuloperoneal muscular dystrophy |
| 240077004 | Severe scapuloperoneal muscular dystrophy with cardiomyopathy |
| 240078009 | Benign congenital muscular dystrophy with finger flexion contractures |
| 240081004 | Autosomal recessive centronuclear myopathy |
| 240082006 | Myopathy with abnormality of histochemical fiber type |
| 240083001 | Myopathy with type I hypotrophy |
| 240084007 | Congenital myopathy with fiber type disproportion |
| 240085008 | Congenital myopathy with uniform fiber type |
| 240086009 | Myopathy with cytoplasmic inclusions |
| 240087000 | Myopathy with tubular aggregates |
| 240104008 | Congenital myotonic dystrophy |
| 240460008 | Acute paralytic poliomyelitis |
| 241006 | Epilepsia partialis continua |
| 2421000119107 | Hallucinations co-occurrent and due to late onset dementia |
| 24326000 | Metachromatic leukodystrophy, adult type |
| 24473007 | Persistent vegetative state |
| 24624008 | Aneurysm of internal carotid artery |
| 24700007 | Multiple sclerosis |
| 2495006 | Congenital cerebral arteriovenous aneurysm |
| 253098009 | Neural tube defect |
| 253116006 | Fissured spine with hydrocephalus |
| 253143001 | Absence of septum pellucidum |
| 253147000 | Type 1 lissencephaly |
| 253148005 | Miller Dieker syndrome |
| 253149002 | Type 2 lissencephaly |
| 253158009 | Hydranencephaly with proliferative vasculopathy |
| 253159001 | Schizencephaly |
| 253160006 | Colpocephaly |
| 253186001 | Chiari malformation type III |
| 25362006 | Phytanic acid storage disease |
| 253699002 | Isolation of common carotid artery |
| 254243001 | Ash leaf spot, tuberous sclerosis |
| 254775002 | Bregeat's syndrome |
| 254972008 | Malignant tumor of optic nerve and sheath |
| 254973003 | Malignant astrocytoma of optic nerve |
| 254974009 | Malignant tumor of optic nerve sheath |
| 254975005 | Malignant meningioma of optic nerve sheath |
| 256321009 | Disorder of neuromuscular transmission |
| 257277002 | Combined disorder of muscle AND peripheral nerve |
| 25772007 | Multi-infarct dementia with delusions |
| 2593002 | Dubowitz's syndrome |
| 26015003 | Maroteaux-Lamy syndrome, intermediate form |
| 26021000119107 | Vertigo as sequela of cerebrovascular disease |
| 262711004 | Transection of cervical cord |
| 26360005 | Hereditary optic atrophy |
| 26595007 | Congenital absence of part of brain |
| 266253001 | Precerebral arterial occlusion |
| 266254007 | Occlusion of carotid artery |
| 266257000 | Transient ischemic attack |
| 267581004 | Progressive myoclonic epilepsy |
| 267592003 | Motor cortex epilepsy |
| 267604001 | Myasthenic syndrome due to diabetic mellitus |
| 268612007 | Senile and presenile organic psychotic conditions |
| 26954004 | Thrombophlebitis of superior sagittal sinus |
| 27148008 | Hereditary motor end-plate disease |
| 271986005 | Disorder of brain ventricular shunt |
| 274100004 | Cerebral hemorrhage |
| 275363001 | Rupture of superficial cerebral vein |
| 276219001 | Occipital cerebral infarction |
| 276594006 | Perinatal rupture of superficial cerebral vein |
| 276599001 | Cerebral leukomalacia |
| 277196008 | Berry aneurysm |
| 277299009 | Ruptured cerebral arteriovenous malformation |
| 277315000 | Ruptured aneurysm of anterior cerebral artery |
| 277316004 | Ruptured aneurysm of middle cerebral artery |
| 277319006 | Ruptured aneurysm of posterior cerebral artery |
| 277320000 | Ruptured aneurysm of anterior communicating artery |
| 277322008 | Ruptured aneurysm of posterior communicating artery |
| 277324009 | Ruptured aneurysm of basilar artery |
| 277325005 | Ruptured aneurysm of posterior inferior cerebellar artery |
| 277328007 | Ruptured internal carotid-anterior communicating artery zone aneurysm |
| 277329004 | Ruptured internal carotid-posterior communicating artery zone aneurysm |
| 277330009 | Ruptured internal carotid bifurcation aneurysm |
| 277373000 | Severe childhood autosomal recessive muscular dystrophy |
| 277530005 | Malignant melanoma of meninges |
| 277922001 | Aprosencephaly |
| 277949001 | Combined malformation of central nervous system and skeletal muscle |
| 277950001 | Muscle eye brain disease |
| 278284007 | Right hemiplegia |
| 278285008 | Left hemiplegia |
| 278286009 | Right hemiparesis |
| 278287000 | Left hemiparesis |
| 278510009 | Localization-related idiopathic epilepsy |
| 28055006 | West syndrome |
| 281004 | Dementia associated with alcoholism |
| 281411007 | Spastic diplegia |
| 28366008 | Cerebral arteritis |
| 284811000119102 | Aneurysm of extracranial portion of internal carotid artery |
| 284821000119109 | Aneurysm of intracranial portion of internal carotid artery |
| 284861000119104 | Atherosclerosis of bilateral carotid arteries |
| 284871000119105 | Atherosclerosis of left carotid artery |
| 284881000119108 | Atherosclerosis of right carotid artery |
| 285161000119105 | Occlusion of left carotid artery |
| 285171000119104 | Occlusion of right carotid artery |
| 285191000119103 | Stenosis of left carotid artery |
| 285201000119100 | Stenosis of right carotid artery |
| 286742002 | Impending cerebrovascular accident |
| 287731003 | Cerebral ischemia |
| 28778005 | Phrenic nerve paralysis as birth trauma |
| 28790007 | Obstruction of precerebral artery |
| 288631000119104 | Vascular dementia with behavioral disturbance |
| 288723005 | Acute ill-defined cerebrovascular disease |
| 28978003 | Progressive supranuclear ophthalmoplegia |
| 290401000119108 | Complete paraplegia |
| 290411000119106 | Incomplete paraplegia |
| 290461000119109 | Spastic hemiplegia of left dominant side |
| 290471000119103 | Spastic hemiplegia of left nondominant side |
| 290481000119100 | Spastic hemiplegia of right dominant side |
| 290491000119102 | Spastic hemiplegia of right nondominant side |
| 290581000119101 | Ataxia due to and following cerebrovascular accident |
| 290631000119103 | Dysarthria due to and following cerebrovascular accident |
| 290641000119107 | Dysphagia due to and following non-traumatic intracerebral hemorrhage |
| 290671000119100 | Status epilepticus due to complex partial epileptic seizure |
| 290681000119102 | Status epilepticus due to refractory complex partial seizures |
| 290691000119104 | Status epilepticus due to generalized idiopathic epilepsy |
| 290711000119101 | Status epilepticus due to intractable idiopathic generalized epilepsy |
| 290721000119108 | Status epilepticus due to refractory epilepsy |
| 290741000119102 | Intractable idiopathic partial epilepsy |
| 290761000119103 | Status epilepticus due to refractory simple partial epilepsy |
| 290791000119105 | Fluency disorder due to and following cerebrovascular accident |
| 290871000119101 | Infantile spasms co-occurrent with status epilepticus |
| 290881000119103 | Refractory infantile spasms co-occurrent with status epilepticus |
| 29093005 | Crossed hemiparesis |
| 291311000119108 | Status epilepticus in benign Rolandic epilepsy |
| 291351000119109 | Spontaneous hemorrhage of subarachnoid space from basilar artery |
| 291371000119100 | Spontaneous hemorrhage of subarachnoid space from intracranial artery |
| 291411000119104 | Spontaneous hemorrhage of subarachnoid space from left posterior communicating artery |
| 291481000119105 | Spontaneous haemorrhage of subarachnoid space from right posterior communicating artery |
| 29159009 | Familial dysautonomia |
| 291721000119102 | Aphasia due to and following non-traumatic intracerebral hemorrhage |
| 29188005 | Complete bilateral paralysis |
| 292621000119100 | Occlusion of right vertebral artery |
| 292631000119102 | Occlusion of left vertebral artery |
| 292851000119109 | Lacunar ataxic hemiparesis of right dominant side |
| 292861000119106 | Lacunar ataxic hemiparesis of left dominant side |
| 292991000119106 | Eaton Lambert syndrome without underlying malignancy |
| 29322000 | Acute cerebrovascular insufficiency |
| 293811000119100 | Cerebral infarction due to vertebral artery stenosis |
| 293831000119105 | Cerebral infarction due to stenosis of precerebral artery |
| 294041000119107 | Flaccid hemiplegia of left dominant side |
| 294051000119109 | Flaccid hemiplegia of left nondominant side |
| 294061000119106 | Flaccid hemiplegia of right dominant side |
| 294071000119100 | Flaccid hemiplegia of right nondominant side |
| 294101000119109 | Hemiplegia of left dominant side |
| 294111000119107 | Hemiplegia of left nondominant side |
| 294121000119100 | Hemiplegia of right dominant side |
| 294131000119102 | Hemiplegia of right nondominant side |
| 29426003 | Paralytic syndrome |
| 297138001 | Embolus of circle of Willis |
| 297157005 | Intracranial venous thrombosis |
| 297176007 | Vertebral artery aneurysm |
| 297278001 | Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator |
| 29774004 | Vascular myelopathy |
| 298282001 | Spastic quadriparesis |
| 29941000119105 | Ataxia as sequela of cerebrovascular disease |
| 29951000119107 | Ataxic hemiparesis |
| 30023002 | Hydranencephaly |
| 300920004 | Carotid atherosclerosis |
| 302213007 | Caroticocavernous sinus fistula |
| 302878004 | Intracranial septic thrombophlebitis |
| 302879007 | Septic thrombophlebitis of cavernous sinus |
| 302880005 | Septic thrombophlebitis of sagittal sinus |
| 302887008 | Neuropathy in secondary amyloidosis |
| 302909007 | Diffuse cerebrovascular disease |
| 30400005 | Middle meningeal hemorrhage following injury |
| 305719002 | Neuromyotonia |
| 307356008 | Motor epilepsy |
| 307357004 | Jacksonian, focal or motor epilepsy |
| 307360006 | Leucodystrophy without a known biochemical basis |
| 307362003 | Intracranial venous septic embolism |
| 307363008 | Multiple lacunar infarcts |
| 307649006 | Microglioma |
| 307766002 | Left sided cerebral infarction |
| 307767006 | Right sided cerebral infarction |
| 30915001 | Holoprosencephaly sequence |
| 31076000 | Congenital ischemic atrophy of central nervous system structure |
| 31081000119101 | Presenile dementia with delusions |
| 31097004 | Post poliomyelitis syndrome |
| 31216003 | Profound intellectual disability |
| 312586003 | Intracranial thrombophlebitis |
| 312944002 | Compressive optic atrophy |
| 313434001 | Residual hemiplegia |
| 315608004 | Cardiomyopathy in Duchenne muscular dystrophy |
| 31839002 | Myasthenia gravis, adult form |
| 32162001 | Facial hemiplegia |
| 322112361000132104 | Epilepsy due to scarring of brain |
| 32875003 | Inhalant-induced persisting dementia |
| 329481000119106 | Occlusion of right middle cerebral artery |
| 329491000119109 | Occlusion of left middle cerebral artery |
| 329561000119101 | Occlusion of right posterior cerebral artery |
| 329571000119107 | Occlusion of left posterior cerebral artery |
| 330411000119109 | Lacunar ataxic hemiparesis of left nondominant side |
| 330421000119102 | Lacunar ataxic hemiparesis of right nondominant side |
| 33301000119105 | Sequela of cardioembolic stroke |
| 33316007 | GM 2 gangliosidosis |
| 33331000119103 | Sequela of lacunar stroke |
| 336191000119105 | Occlusion of right central retinal artery |
| 3371000119106 | Refractory generalized convulsive epilepsy |
| 341801000119101 | Occlusion of left central retinal artery |
| 34181000119102 | Cerebral infarction due to occlusion of basilar artery |
| 34191000119104 | Cerebral infarction due to vertebral artery occlusion |
| 347011000119102 | Occlusion of bilateral central retinal arteries |
| 34781003 | Vertebral artery syndrome |
| 352818000 | Tonic-clonic epilepsy |
| 35386004 | Cavernous sinus syndrome |
| 359683002 | Complete optic atrophy |
| 36025004 | Fibrous skin tumor of tuberous sclerosis |
| 361000119103 | Paralytic syndrome on one side of the body as late effect of cerebrovascular accident |
| 361123003 | Psychomotor epilepsy |
| 363235000 | Hereditary disorder of nervous system |
| 363474009 | Malignant neoplasm of cerebral meninges |
| 363497007 | Malignant tumor of meninges |
| 363498002 | Malignant tumor of optic nerve |
| 36803009 | Idiopathic generalized epilepsy |
| 3681008 | Thrombophlebitis of torcular Herophili |
| 371024007 | Senile dementia with delusion |
| 371026009 | Senile dementia with psychosis |
| 371029002 | Ischemic disorder of spinal cord |
| 371120001 | Quadriplegic spinal paralysis |
| 371129000 | Paralysis from birth trauma |
| 371158002 | Disorder of basilar artery |
| 371160000 | Disorder of carotid artery |
| 371313002 | Congenital cerebellar cortical atrophy |
| 372062007 | Malignant neoplasm of central nervous system |
| 372310001 | Paralysis due to lesion of spinal cord |
| 37340000 | Motor neuron disease |
| 373587001 | Chiari malformation type II |
| 37934003 | Mitochondrial-lipid-glycogen storage myopathy |
| 37943007 | Multiple AND bilateral precerebral artery embolism |
| 380941000000104 | Progressive encephalopathy with oedema, hypsarrhythmia and optic atrophy syndrome |
| 38228000 | Paralysis of tongue |
| 38523005 | Syphilitic parkinsonism |
| 38742007 | Central retinal artery occlusion |
| 387732009 | Becker muscular dystrophy |
| 389098007 | Anoxic encephalopathy |
| 389100007 | Ischemic encephalopathy |
| 390936003 | Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy |
| 39390005 | Niemann-Pick disease, type B |
| 396338004 | Metachromatic leucodystrophy |
| 397734008 | Hereditary sensory and autonomic neuropathy type I |
| 398040009 | Charcot-Marie-Tooth disease, type I |
| 398100001 | Hereditary motor and sensory neuropathy |
| 398148000 | Hereditary sensory and autonomic neuropathy type II |
| 398187000 | Charcot-Marie-Tooth disease, type II |
| 398229007 | Amyloid polyneuropathy type I |
| 398432008 | Bulbar weakness |
| 399091004 | Facioscapulohumeral muscular dystrophy |
| 40161000119102 | Weakness of face muscles as sequela of stroke |
| 402460000 | Familial amyloid polyneuropathy with cutaneous amyloidosis |
| 40259002 | Progressive sensory ataxia of Charolais |
| 40276003 | Embolism of precerebral artery |
| 40354009 | De Lange syndrome |
| 403815003 | Axillary freckling due to neurofibromatosis |
| 403816002 | Multiple café-au-lait macules due to neurofibromatosis |
| 403817006 | Multiple neurofibromas in neurofibromatosis |
| 403819009 | Elephantiasis neurofibromatosa |
| 40425004 | Postconcussion syndrome |
| 40450001 | Embolism of superior sagittal sinus |
| 404664002 | Malignant optic glioma |
| 404689008 | Alternating hemiplegia |
| 40632002 | Charcot-Marie-Tooth disease, type IA |
| 4069002 | Anoxic brain damage during AND/OR resulting from a procedure |
| 40700009 | Severe intellectual disability |
| 40802007 | Metachromatic leukodystrophy, congenital type |
| 40816002 | Retropulsion petit mal |
| 408371000000100 | [X]Cerebral palsy and other paralytic syndromes |
| 408664007 | Pontine artery occlusion |
| 408665008 | Pontine artery thrombosis |
| 40980002 | Spastic paralysis due to birth injury |
| 410057002 | Hereditary AND/OR degenerative disease of central nervous system |
| 41040004 | Complete trisomy 21 syndrome |
| 41142009 | Globoid cell leukodystrophy, late-onset |
| 41283003 | Cerebro-oculo-facio-skeletal syndrome |
| 413101007 | Stress-induced epilepsy |
| 414927004 | Ocular myasthenia with strabismus |
| 41574007 | Paramyotonia congenita |
| 41590007 | Familial amyloid polyneuropathy, Jewish type |
| 4183003 | Charcot-Marie-Tooth disease, type IC |
| 42012007 | Neuronal ceroid lipofuscinosis |
| 420718004 | Central nervous system demyelinating disease associated with acquired immunodeficiency syndrome |
| 420788006 | Intraocular non-Hodgkin malignant lymphoma |
| 421998001 | Central nervous disorder associated with acquired immunodeficiency syndrome |
| 422474003 | Partial absence of septum pellucidum |
| 422513000 | Epilepsy, not refractory |
| 422724001 | Refractory localization-related epilepsy |
| 422873003 | Refractory epilepsia partialis continua |
| 42295001 | Familial amyloid polyneuropathy |
| 423144007 | Multifactorial encephalopathy |
| 423771003 | Acquired neuromuscular ptosis |
| 424795008 | Non dystrophic myotonia |
| 425054007 | Refractory occipital lobe epilepsy |
| 425219008 | Progressive spinal ataxia |
| 425237009 | Refractory frontal lobe epilepsy |
| 425349008 | Refractory parietal lobe epilepsy |
| 425390006 | Dementia associated with Parkinson's Disease |
| 425420004 | Thrombosis of internal carotid artery |
| 425500002 | Secondary progressive multiple sclerosis |
| 425687007 | Spina bifida aperta of cervical spine |
| 425882004 | Paralytic syndrome as late effect of stroke |
| 425932008 | Thrombosis of posterior communicating artery |
| 426033005 | Dysphagia as a late effect of cerebrovascular accident |
| 426107000 | Acute lacunar infarction |
| 4262001 | Phlebitis of superior sagittal sinus |
| 426373005 | Relapsing remitting multiple sclerosis |
| 426651005 | Occlusion of bilateral carotid arteries |
| 426788002 | Vertigo as late effect of stroke |
| 426814001 | Transient cerebral ischemia due to atrial fibrillation |
| 427020007 | Cerebral vasculitis |
| 427296003 | Thalamic infarction |
| 427432001 | Paralytic syndrome as late effect of thalamic stroke |
| 427943001 | Ophthalmoplegia due to diabetes mellitus |
| 428700003 | Primary progressive multiple sclerosis |
| 429458009 | Dementia due to Creutzfeldt Jakob disease |
| 429466000 | Spina bifida aperta of lumbar spine |
| 42970005 | Nonpyogenic thrombosis of intracranial venous sinus |
| 42986003 | Charcot-Marie-Tooth disease, type IB |
| 429998004 | Vascular dementia |
| 430947007 | Paralytic syndrome of nondominant side as late effect of stroke |
| 430959006 | Paralytic syndrome of dominant side as late effect of stroke |
| 43100002 | Late cortical cerebellar atrophy |
| 432504007 | Cerebral infarction |
| 433183000 | Neurogenic bladder as late effect of cerebrovascular accident |
| 434541000124109 | Benign childhood epilepsy with centrotemporal spikes, refractory |
| 434551000124106 | Benign childhood epilepsy with centrotemporal spikes, non-refractory |
| 43532007 | Hereditary oculoleptomeningeal amyloid angiopathy |
| 43658003 | Vertebral artery obstruction |
| 438511000 | Benign multiple sclerosis |
| 439567002 | Malignant multiple sclerosis |
| 44145005 | Benign Rolandic epilepsy |
| 441526008 | Infarct of cerebrum due to iatrogenic cerebrovascular accident |
| 441529001 | Dysphasia as late effect of cerebrovascular disease |
| 441630004 | Aphasia as late effect of cerebrovascular disease |
| 441678004 | Refractory generalized nonconvulsive epilepsy |
| 441688003 | Incomplete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra |
| 441705005 | Complete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra |
| 441717007 | Hemiplegia of nondominant side |
| 441722007 | Spastic hemiplegia of nondominant side |
| 441735003 | Sensory disorder as a late effect of cerebrovascular disease |
| 441759008 | Abnormal vision as a late effect of cerebrovascular disease |
| 441794001 | Incomplete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra |
| 441892008 | Spastic hemiplegia of dominant side |
| 441960006 | Speech and language deficit as late effect of cerebrovascular accident |
| 441980007 | Complete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra |
| 441991000 | Hemiparesis as late effect of cerebrovascular accident |
| 442020005 | Flaccid hemiplegia of dominant side |
| 442024001 | Hemiplegia as late effect of cerebrovascular disease |
| 442077006 | Flaccid hemiplegia of nondominant side |
| 442155009 | Hemiplegia of dominant side |
| 442344002 | Dementia due to Huntington chorea |
| 442481002 | Epilepsy characterized by intractable complex partial seizures |
| 442511009 | Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome |
| 442512002 | Nonconvulsive status epilepticus |
| 442617003 | Aphasia as late effect of cerebrovascular accident |
| 442668000 | Hemiplegia of nondominant side as late effect of cerebrovascular disease |
| 442676003 | Hemiplegia of dominant side as late effect of cerebrovascular disease |
| 442733008 | Hemiplegia as late effect of cerebrovascular accident |
| 44359008 | Metachromatic leukodystrophy, juvenile type |
| 443929000 | Small vessel cerebrovascular disease |
| 444024002 | Multiple system atrophy, cerebellar variant |
| 444172003 | Recurrent transient cerebral ischemic attack |
| 444197004 | Multiple system atrophy, Parkinson variant |
| 445109004 | Isolation of left common carotid artery |
| 445349004 | Isolation of right common carotid artery |
| 445355009 | Refractory epilepsy |
| 445475001 | Paraneoplastic sensorimotor neuropathy |
| 4463009 | Familial amyloid polyneuropathy, type II |
| 446311006 | Acute bulbar poliomyelitis caused by Human poliovirus 2 |
| 446712002 | Thromboembolus of precerebral artery |
| 446957000 | Acute bulbar poliomyelitis caused by Human poliovirus 1 |
| 446958005 | Acute paralytic poliomyelitis caused by Human poliovirus 1 |
| 447262002 | Acute paralytic poliomyelitis caused by Human poliovirus 2 |
| 447378002 | Acute paralytic poliomyelitis caused by Human poliovirus 3 |
| 4477007 | Juvenile myopathy AND lactate acidosis |
| 448054001 | Adult onset autosomal dominant leukodystrophy |
| 448227009 | X-linked periventricular heterotopia |
| 448254007 | Non-Hodgkin's lymphoma of central nervous system |
| 448995000 | Follicular non-Hodgkin's lymphoma of central nervous system |
| 449221001 | Diffuse non-Hodgkin's lymphoma of central nervous system |
| 449305009 | Paraneoplastic sensory neuropathy |
| 45502001 | Cerebrovascular amyloidosis |
| 45853006 | Roussy-Lévy syndrome |
| 460307002 | Systemic to pulmonary collateral artery from right carotid artery |
| 460312001 | Systemic to pulmonary collateral artery from left carotid artery |
| 460890003 | Anomalous common origin of brachiocephalic artery and left common carotid artery |
| 460899002 | Anomalous origin of left common carotid artery from brachiocephalic artery |
| 461326001 | Anomalous separate origins of internal carotid arteries and external carotid arteries from single aortic arch |
| 46251005 | Corticospinal motor disease |
| 46252003 | Progressive external ophthalmoplegia |
| 46421000119102 | Behavior disorder as sequela of cerebral infarction |
| 46659004 | Von Hippel-Lindau syndrome |
| 46804001 | Severe x-linked myotubular myopathy |
| 472320005 | Maternally inherited mitochondrial cardiomyopathy and myopathy |
| 472746006 | Cerebrovascular disorder due to paradoxical embolus |
| 472916000 | Toxic metabolic encephalopathy |
| 47391000119107 | Primary generalized absence epilepsy |
| 47683004 | Metachromatic leukodystrophy, late infantile type |
| 48163001 | Triparesis |
| 48522003 | Spinal cord disorder |
| 48601000119107 | Paralytic syndrome on one side of the body as effect of cerebrovascular accident |
| 48601002 | Thrombosis of precerebral artery |
| 48662007 | Cerebral paraplegia |
| 49049000 | Parkinson's disease |
| 49562005 | Adult chronic GM 2 gangliosidosis |
| 49605003 | Ophthalmoplegic migraine |
| 49692006 | Schilder's disease |
| 49776008 | Centrencephalic epilepsy |
| 49793008 | Hereditary motor neuron disease |
| 49823009 | Internuclear ophthalmoplegia |
| 50582007 | Hemiplegia |
| 508171000000105 | Severe learning disability |
| 50866000 | Childhood absence epilepsy |
| 509341000000107 | Petit-mal epilepsy |
| 50967008 | Gangliosidosis |
| 5134006 | Familial amyloid polyneuropathy, type VI |
| 51500006 | Complete trisomy 18 syndrome |
| 52165006 | Niemann-Pick disease, type A |
| 52448006 | Dementia |
| 5262007 | Spinal muscular atrophy |
| 52677002 | Deficiency of N-acetylgalactosamine-4-sulfatase |
| 53633000 | Peutz-Jeghers polyps of small bowel |
| 53857003 | Heredofamilial brachial plexus paralysis syndrome |
| 54099005 | Diplegia of upper limbs |
| 54265003 | Congenital anomaly of cerebral artery |
| 54280009 | Kugelberg-Welander disease |
| 54364001 | Lethal neonatal spasticity |
| 54411001 | Peutz-Jeghers syndrome |
| 54519002 | Basilar artery stenosis |
| 55016009 | Congenital muscular hypertrophy-cerebral syndrome |
| 55051001 | Myasthenia gravis, juvenile form |
| 55382008 | Cerebral atherosclerosis |
| 55709000 | Ethmocephalus |
| 55734000 | Endophlebitis of basilar sinus |
| 56155002 | Hemispheric cerebral agenesis |
| 56267009 | Multi-infarct dementia |
| 56453003 | Hereditary cerebral amyloid angiopathy, Dutch type |
| 56989000 | Eaton-Lambert syndrome |
| 57938005 | Congenital myotonia, autosomal dominant form |
| 58263000 | Maroteaux-Lamy syndrome, severe form |
| 58459009 | Sphingomyelin/cholesterol lipidosis |
| 58557008 | Spina bifida aperta |
| 58610003 | Leber's optic atrophy |
| 58795000 | Distal muscular dystrophy |
| 590005 | Congenital aneurysm of anterior communicating artery |
| 5963005 | Subacute neuronopathic Gaucher's disease |
| 59636002 | Pelizaeus-Merzbacher disease, connatal variant |
| 60192008 | Lethal multiple pterygium syndrome |
| 60389000 | Paraplegia |
| 60706008 | Phlebitis of torcular Herophili |
| 608874000 | Eaton Lambert syndrome with underlying malignancy |
| 609553000 | Paralytic syndrome of both lower limbs |
| 609554006 | Paralytic syndrome of all four limbs |
| 609557004 | Paralytic syndrome on one side of the body |
| 61091005 | Aneurysm of external carotid artery |
| 6118003 | Demyelinating disease of central nervous system |
| 61200008 | Pallidonigroluysian degeneration |
| 62158001 | Status marmoratus |
| 62239001 | Parkinson-dementia complex of Guam |
| 62440002 | Infantile GM 2 gangliosidosis |
| 62702001 | Cerebral vein occlusion |
| 62914000 | Cerebrovascular disease |
| 62985007 | Hereditary insensitivity to pain with anhidrosis |
| 63081009 | Acute infarction of spinal cord |
| 63135006 | Amyotonia congenita |
| 63795001 | Thrombosis of intracranial venous sinus of pregnancy AND/OR puerperium |
| 64228003 | Paralysis of diaphragm |
| 64383006 | Werdnig-Hoffmann disease |
| 64586002 | Carotid artery stenosis |
| 64764001 | Acute paralytic poliomyelitis, bulbar |
| 64775002 | Vertebral artery thrombosis |
| 6481005 | Diplegia |
| 64855000 | Pelizaeus-Merzbacher disease |
| 65017003 | Hereditary peripheral neuropathy |
| 65084004 | Vertebral artery embolism |
| 65120008 | Generalized convulsive epilepsy |
| 65312002 | Cerebral arteriosclerosis |
| 65587001 | Congenital anomaly of cerebrovascular system |
| 65764006 | Pseudo-Hurler polydystrophy |
| 6594005 | Cerebrovascular disorder in the puerperium |
| 66521008 | Deficiency of cerebroside-sulfatase |
| 66751000 | Niemann-Pick disease, type C |
| 672441000119103 | Hemiplegia of nondominant side due to and following ischemic cerebrovascular accident |
| 672461000119104 | Hemiplegia of dominant side due to and following ischemic cerebrovascular accident |
| 672501000119104 | Dysarthria due to and following ischemic cerebrovascular accident |
| 672511000119101 | Dysarthria due to and following hemorrhagic cerebrovascular accident |
| 672521000119108 | Dysphasia due to and following ischemic cerebrovascular accident |
| 672531000119106 | Dysphasia due to and following hemorrhagic cerebrovascular accident |
| 672541000119102 | Aphasia due to and following ischemic cerebrovascular accident |
| 672551000119100 | Aphasia due to and following hemorrhagic cerebrovascular accident |
| 6729006 | Cerebral-retinal arteriovenous aneurysm |
| 674091000119108 | Vertigo due to and following ischemic cerebrovascular accident |
| 674111000119100 | Ataxia due to and following ischemic cerebrovascular accident |
| 674121000119107 | Ataxia due to and following hemorrhagic cerebrovascular accident |
| 674361000119104 | Apraxia due to and following ischemic cerebrovascular accident |
| 674381000119108 | Weakness of facial muscle due to and following ischemic cerebrovascular accident |
| 674391000119106 | Speech and language deficit due to and following hemorrhagic cerebrovascular accident |
| 674401000119108 | Speech and language deficit due to and following ischemic cerebrovascular accident |
| 67747009 | Ocular muscular dystrophy |
| 67854007 | Maroteaux-Lamy syndrome, mild form |
| 67855008 | Niemann-Pick disease, type C, subacute form |
| 67992007 | Multiple AND bilateral precerebral artery obstruction |
| 68186003 | Congenital myopathy with abnormal subcellular organelles |
| 68390005 | Sphingolipid activator protein 1 deficiency |
| 68618008 | Rett's disorder |
| 690171000119105 | Weakness of facial muscle due to and following embolic cerebrovascular accident |
| 690201000119109 | Ataxia due to and following embolic cerebrovascular accident |
| 690271000119104 | Hemiplegia of nondominant side due to and following embolic cerebrovascular accident |
| 690311000119104 | Dysarthria due to and following embolic cerebrovascular accident |
| 690321000119106 | Aphasia due to and following embolic cerebrovascular accident |
| 690331000119109 | Speech and language deficit due to and following embolic cerebrovascular accident |
| 690351000119103 | Dysphasia due to and following embolic cerebrovascular accident |
| 69131009 | Spinal ataxia |
| 69463008 | Maroteaux-Lamy syndrome |
| 69763009 | Exophthalmic ophthalmoplegia |
| 69798007 | Carotid artery obstruction |
| 697991001 | Paralysis of uvula |
| 698021005 | Autosomal dominant nocturnal frontal lobe epilepsy |
| 698291007 | Acute paraplegia |
| 698292000 | Chronic paraplegia |
| 698363002 | Postoperative thromboembolus of precerebral artery |
| 698624003 | Dementia associated with cerebral lipidosis |
| 698625002 | Dementia associated with normal pressure hydrocephalus |
| 698626001 | Dementia associated with multiple sclerosis |
| 698627005 | Postoperative phlebitis and thrombophlebitis of intracranial sinuses |
| 698687007 | Post-traumatic dementia with behavioral change |
| 698725008 | Dementia associated with neurosyphilis |
| 698726009 | Dementia associated with viral encephalitis |
| 698741009 | Acute complete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra |
| 698742002 | Chronic incomplete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra |
| 698743007 | Acute complete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra |
| 698744001 | Chronic incomplete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra |
| 698754002 | Chronic paralysis due to lesion of spinal cord |
| 698755001 | Acute paralysis due to lesion of spinal cord |
| 698760002 | Generalized non-convulsive absence epilepsy |
| 698762005 | Refractory myoclonic epilepsy |
| 698763000 | Postoperative status epilepticus |
| 698764006 | Post infectious grand mal epilepsy |
| 698767004 | Post-cerebrovascular accident epilepsy |
| 698781002 | Dementia associated with cerebral anoxia |
| 698846009 | Tibial muscular dystrophy |
| 698870008 | 2-hydroxyglutaric aciduria |
| 698948009 | Vascular dementia in remission |
| 698949001 | Dementia in remission |
| 699184009 | Perry syndrome |
| 699190008 | Paroxysmal extreme pain disorder |
| 699688008 | Generalized epilepsy with febrile seizures plus |
| 699706000 | Embolism of middle cerebral artery |
| 700467001 | Reversible cerebral vasoconstriction syndrome |
| 70199000 | I-cell disease |
| 702326000 | Progressive myoclonus epilepsy with ataxia |
| 702327009 | Monocarboxylate transporter 8 deficiency |
| 702343002 | Early onset myopathy with fatal cardiomyopathy |
| 702363009 | Cold-induced sweating syndrome |
| 702382000 | Inclusion body myopathy 2 |
| 702383005 | Distal myopathy 2 |
| 702433001 | Congenital cataracts, facial dysmorphism and neuropathy |
| 702439002 | Agenesis of corpus callosum with peripheral neuropathy |
| 702441001 | Fatal X-linked ataxia with deafness and loss of vision |
| 702442008 | Ataxia with vitamin E deficiency |
| 702463005 | Paralytic syndrome of two limbs |
| 702464004 | Paralytic syndrome of three limbs |
| 702465003 | Paralytic syndrome on both sides of the body |
| 702575003 | Retinocochleocerebral vasculopathy |
| 702611008 | Congenital brain aplasia |
| 703163006 | Secondary cerebrovascular disease |
| 703166003 | Dural arteriovenous fistula |
| 703176000 | Ruptured aneurysm of vertebral artery |
| 703180005 | Asymptomatic occlusion of extracranial carotid artery |
| 703184001 | Asymptomatic occlusion of intracranial carotid artery |
| 703205008 | Asymptomatic occlusion of posterior cerebral artery |
| 703206009 | Asymptomatic occlusion of basilar artery |
| 703207000 | Asymptomatic occlusion of anterior cerebral artery |
| 703208005 | Asymptomatic occlusion of middle cerebral artery |
| 703218000 | Cerebral vasoconstriction syndrome |
| 703219008 | Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy |
| 703221003 | Congenital intracranial vascular malformation |
| 703226008 | Familial cerebral saccular aneurysm |
| 703266007 | Cerebrofacial arteriovenous metameric syndrome |
| 703267003 | Cerebrofacial arteriovenous metameric syndrome type 1 |
| 703268008 | Cerebrofacial arteriovenous metameric syndrome type 3 |
| 703300001 | Hypoxic ischemic encephalopathy |
| 7033004 | Petit mal status |
| 703301002 | Mild hypoxic ischemic encephalopathy |
| 703302009 | Moderate hypoxic ischemic encephalopathy |
| 703303004 | Severe hypoxic ischemic encephalopathy |
| 703304005 | Hypoxic ischemic encephalopathy due to strangulation |
| 703305006 | Hypoxic ischemic encephalopathy due to cardiac arrest |
| 703311009 | Cerebral arteritis due to infectious disease |
| 703312002 | Primary cerebral arteritis |
| 703313007 | Cerebral amyloid angiopathy associated with systemic amyloidosis |
| 703429003 | Malignant optic glioma of adulthood |
| 70350007 | Degenerative myelopathy |
| 703524005 | Spinal muscular atrophy with progressive myoclonic epilepsy |
| 703535000 | Mowat-Wilson syndrome |
| 703544004 | Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia |
| 705066004 | Dissection of internal carotid artery |
| 705128004 | Cerebral infarction due to embolism of middle cerebral artery |
| 705129007 | Thrombosis of middle cerebral artery |
| 705130002 | Cerebral infarction due to thrombosis of middle cerebral artery |
| 70528007 | Mucolipidosis |
| 70607008 | Thrombosis of superior sagittal sinus |
| 70694009 | Diabetes mellitus AND insipidus with optic atrophy AND deafness |
| 709281006 | Rippling muscle disease |
| 70936005 | Multi-infarct dementia, uncomplicated |
| 709415008 | Mitochondrial membrane protein associated neurodegeneration |
| 709469005 | Periodontitis co-occurrent with Down syndrome |
| 710046001 | Refractory idiopathic generalized epilepsy |
| 710575003 | Transient ischemic attack due to embolism |
| 711151004 | Hypomagnesemia with secondary hypocalcemia |
| 711406009 | Autosomal recessive axonal neuropathy with neuromyotonia |
| 711409002 | 3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome |
| 711483003 | Spinal muscular atrophy with respiratory distress type 1 |
| 71253000 | Tay-Sachs disease, variant AB |
| 712637001 | Ribonucleic acid polymerase III-related leukodystrophy |
| 713035000 | Dissection of precerebral artery |
| 713081000 | Dissection of cerebral artery |
| 713265001 | Nontraumatic ruptured cerebral aneurysm |
| 713327005 | Malignant meningioma of meninges of brain |
| 713401006 | Combined D-2-hydroxyglutaric aciduria and L-2-hydroxyglutaric aciduria |
| 713488003 | Presenile dementia co-occurrent with human immunodeficiency virus infection |
| 713543002 | Demyelinating disease of central nervous system co-occurrent with human immunodeficiency virus infection |
| 713844000 | Dementia co-occurrent with human immunodeficiency virus infection |
| 71444005 | Cerebral arterial thrombosis |
| 715317001 | Proximal myotonic myopathy |
| 715340002 | Autosomal recessive limb girdle muscular dystrophy type 2D |
| 715341003 | Autosomal recessive limb girdle muscular dystrophy type 2A |
| 715344006 | Neurofibromatosis Noonan syndrome |
| 715345007 | Young onset Parkinson disease |
| 715374003 | Autosomal dominant optic atrophy plus syndrome |
| 715406003 | Isolated lissencephaly type 1 without known genetic defect |
| 715419004 | Lethal congenital contracture syndrome type 2 |
| 715422002 | Craniotelencephalic dysplasia |
| 715429006 | Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome |
| 715434005 | Holoprosencephaly craniosynostosis syndrome |
| 715565004 | Lethal arthrogryposis co-occurrent with anterior horn cell disease |
| 715624006 | Chronic ataxic neuropathy, ophthalmoplegia, monoclonal immunoglobulin M protein, cold agglutinin and disialosyl antibody syndrome |
| 715629001 | Generalized epilepsy and paroxysmal dyskinesia syndrome |
| 715645004 | Hereditary thermosensitive neuropathy |
| 715646003 | Desmin related myopathy with Mallory body-like inclusions |
| 715665006 | Hereditary motor and sensory neuropathy Okinawa type |
| 715666007 | Charcot-Marie-Tooth disease type IE |
| 715780008 | Lissencephaly type 1 due to doublecortin gene mutation |
| 715794009 | Progressive encephalopathy with severe infantile anorexia |
| 715795005 | Charcot-Marie-Tooth disease type 4 |
| 715796006 | Charcot-Marie-Tooth disease type 4A |
| 715797002 | Charcot-Marie-Tooth disease type 4C |
| 715798007 | Charcot-Marie-Tooth disease type 4D |
| 715799004 | Charcot-Marie-Tooth disease type 4G |
| 715800000 | Charcot-Marie-Tooth disease type 4B2 |
| 715801001 | Charcot-Marie-Tooth disease type 4F |
| 715802008 | Charcot-Marie-Tooth disease type 4H |
| 715803003 | Charcot-Marie-Tooth disease type 4B1 |
| 715952000 | Waardenburg syndrome co-occurrent with Hirschsprung disease |
| 716091000 | Holoprosencephaly and postaxial polydactyly syndrome |
| 716107009 | Early onset parkinsonism and intellectual disability syndrome |
| 716169009 | Holoprosencephaly sequence with hypokinesia and congenital joint contracture syndrome |
| 716233007 | Steinfeld syndrome |
| 716243005 | Deafness with malformation of ear and facial palsy syndrome |
| 716278005 | Jeavons syndrome |
| 716662004 | Autosomal dominant late onset Parkinson disease |
| 716696006 | Autosomal dominant centronuclear myopathy |
| 716706009 | Female restricted epilepsy with intellectual disability syndrome |
| 716745004 | Livedo reticularis and cerebrovascular accident syndrome |
| 717008005 | Autosomal dominant Charcot-Marie-Tooth disease type 2B |
| 717010007 | Autosomal dominant Charcot-Marie-Tooth disease type 2C |
| 717011006 | Autosomal dominant Charcot-Marie-Tooth disease type 2D |
| 717012004 | Autosomal dominant Charcot-Marie-Tooth disease type 2E |
| 717013009 | Autosomal dominant Charcot-Marie-Tooth disease type 2I |
| 717014003 | Autosomal dominant Charcot-Marie-Tooth disease type 2J |
| 717016001 | Autosomal dominant Charcot-Marie-Tooth disease type 2A1 |
| 717042001 | Pelizaeus Merzbacher like disease |
| 717223008 | X-linked epilepsy with learning disability and behavior disorder syndrome |
| 717266001 | Sensory ataxic neuropathy with dysarthria and ophthalmoparesis syndrome |
| 717336005 | Autosomal dominant optic atrophy classic form |
| 71779008 | X-linked hydrocephalus syndrome |
| 717812000 | Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome |
| 717825008 | Hereditary sensory and autonomic neuropathy type 1B |
| 717826009 | Hereditary sensory and autonomic neuropathy with deafness and global delay |
| 717943008 | Brain malformation, congenital heart disease, postaxial polydactyly syndrome |
| 717964007 | Juvenile primary lateral sclerosis |
| 717968005 | Melanoma and neural system tumor syndrome |
| 717975006 | Autosomal dominant optic atrophy and peripheral neuropathy syndrome |
| 717977003 | Lissencephaly syndrome Norman Roberts type |
| 718176005 | Autosomal recessive limb girdle muscular dystrophy type 2C |
| 718177001 | Autosomal recessive limb girdle muscular dystrophy type 2F |
| 718178006 | Autosomal dominant limb girdle muscular dystrophy type 1B |
| 718179003 | Autosomal recessive limb girdle muscular dystrophy type 2B |
| 718180000 | Autosomal recessive limb girdle muscular dystrophy type 2I |
| 718210003 | Deficiency of monoamine oxidase A |
| 718214007 | Mitochondrial neurogastrointestinal encephalomyopathy syndrome |
| 718221007 | Behr syndrome |
| 71831005 | Symptomatic generalized epilepsy |
| 718555006 | Juvenile amyotrophic lateral sclerosis |
| 718556007 | Cranio-cerebello-cardiac dysplasia syndrome |
| 718572004 | Bethlem myopathy |
| 718685006 | Orthostatic hypotension co-occurrent and due to Parkinson's disease |
| 718713000 | Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome |
| 718719001 | Lissencephaly type 3 familial fetal akinesia sequence syndrome |
| 718720007 | Lissencephaly type 3 metacarpal bone dysplasia syndrome |
| 718759003 | Lissencephaly due to tubulin alpha 1A mutation |
| 718847005 | X-linked neurodegenerative syndrome Hamel type |
| 718849008 | X-linked neurodegenerative syndrome Bertini type |
| 718850008 | Autosomal recessive limb girdle muscular dystrophy type 2E |
| 719069008 | Shprintzen Goldberg craniosynostosis syndrome |
| 719205008 | Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome |
| 719395001 | Microcephalus facio-cardio-skeletal syndrome Hadziselimovic type |
| 719430008 | Leber plus disease |
| 719510006 | Autosomal dominant Charcot-Marie-Tooth disease type 2F |
| 719511005 | Autosomal dominant Charcot-Marie-Tooth disease type 2G |
| 719512003 | Autosomal dominant Charcot-Marie-Tooth disease type 2K |
| 719513008 | Autosomal dominant Charcot-Marie-Tooth disease type 2L |
| 719514002 | Autosomal dominant Charcot-Marie-Tooth disease type 2M |
| 719515001 | Autosomal dominant Charcot-Marie-Tooth disease type 2N |
| 719517009 | Autosomal dominant optic atrophy and cataract |
| 719717006 | Psychosis co-occurrent and due to Parkinson's disease |
| 719815005 | X-linked myopathy with excessive autophagy |
| 719819004 | Xeroderma pigmentosum and Cockayne syndrome complex |
| 719836007 | X-linked distal arthrogryposis multiplex congenita |
| 719838008 | X-linked hereditary sensory and autonomic neuropathy with deafness |
| 7199000 | Tuberous sclerosis syndrome |
| 719979008 | Charcot-Marie-Tooth disease type ID |
| 719980006 | Charcot-Marie-Tooth disease type IF |
| 719981005 | Charcot-Marie-Tooth disease type 2B2 |
| 719985001 | Autosomal dominant limb girdle muscular dystrophy type 1A |
| 719986000 | Autosomal dominant limb girdle muscular dystrophy type 1C |
| 719987009 | Autosomal dominant limb girdle muscular dystrophy type 1D |
| 719988004 | Autosomal dominant limb girdle muscular dystrophy type 1E |
| 719989007 | Autosomal dominant limb girdle muscular dystrophy type 1F |
| 719990003 | Autosomal dominant limb girdle muscular dystrophy type 1G |
| 720410001 | Acrootoocular syndrome |
| 720519003 | Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome |
| 720522001 | Autosomal recessive limb girdle muscular dystrophy type 2G |
| 720523006 | Autosomal recessive limb girdle muscular dystrophy type 2K |
| 720626009 | Dissection of carotid artery |
| 720634003 | Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome |
| 720637005 | Charcot-Marie-Tooth disease type 2H |
| 720638000 | Charcot-Marie-Tooth disease type 4J |
| 720809000 | Dissection of external carotid artery |
| 720852000 | Cervical hypertrichosis and peripheral neuropathy syndrome |
| 720855003 | Cerebrooculonasal syndrome |
| 721088003 | Developmental delay, epilepsy, neonatal diabetes syndrome |
| 721200000 | Early-onset X-linked optic atrophy |
| 721221000 | Hirschsprung disease with deafness and polydactyly syndrome |
| 721222007 | Hirschsprung disease with type D brachydactyly syndrome |
| 721223002 | Hirschsprung disease with nail hypoplasia and dysmorphism |
| 721297008 | Galloway Mowat syndrome |
| 721843003 | Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome |
| 721979005 | Lymphedema and cerebral arteriovenous anomaly syndrome |
| 722004001 | Agenesis of internal carotid artery |
| 722006004 | Isotretinoin embryopathy-like syndrome |
| 722064003 | Odontoleukodystrophy |
| 722110003 | Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome |
| 722209002 | Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome |
| 722213009 | Severe X-linked intellectual disability Gustavson type |
| 722283003 | Agnathia, holoprosencephaly, situs inversus syndrome |
| 722294004 | Autosomal dominant intermediate Charcot-Marie-Tooth disease type E |
| 722377004 | Paraganglioma and gastric stromal sarcoma syndrome |
| 722389002 | Congenital hereditary facial paralysis with variable hearing loss syndrome |
| 722432000 | Duane anomaly, myopathy, scoliosis syndrome |
| 722456001 | Intellectual disability, developmental delay, contracture syndrome |
| 722599008 | Parkinsonism due to hereditary spastic paraplegia |
| 722671009 | Metastatic malignant neoplasm of meninges |
| 722718001 | Primary malignant meningioma |
| 722977005 | Dementia co-occurrent and due to neurocysticercosis |
| 722978000 | Dementia caused by toxin |
| 722979008 | Dementia due to metabolic abnormality |
| 722980006 | Dementia due to chromosomal anomaly |
| 722987009 | Amyotrophic lateral sclerosis plus syndrome |
| 722990003 | Congenital atrophy of optic nerve |
| 722997000 | Inherited autonomic nervous system disorder |
| 723082006 | Silent cerebral infarct |
| 723083001 | Late effects of cerebral ischemic stroke |
| 723084007 | Sequela of non-traumatic intracerebral hemorrhage |
| 723124007 | Primary progressive apraxia of speech |
| 723125008 | Epileptic encephalopathy |
| 723156000 | Flaccid diplegia of upper limbs |
| 723157009 | Spastic diplegia of upper limbs |
| 723158004 | Diplegia of lower limbs |
| 723304001 | Microcephaly, seizure, intellectual disability, heart disease syndrome |
| 723306004 | Facial onset sensory and motor neuronopathy syndrome |
| 723308003 | Epidermolysis bullosa simplex with muscular dystrophy |
| 723366001 | Macrostomia, preauricular tag, external ophthalmoplegia syndrome |
| 723390000 | Rapidly progressive dementia |
| 723405001 | Microlissencephaly micromelia syndrome |
| 723452007 | Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome |
| 723497003 | Peripheral neuropathy with sensorineural hearing impairment syndrome |
| 723621000 | Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome |
| 723622007 | X-linked spastic paraplegia type 2 |
| 723676007 | Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome |
| 723825006 | Autosomal recessive spastic paraplegia type 55 |
| 723826007 | Autosomal recessive spastic paraplegia type 57 |
| 723857007 | Silent micro-hemorrhage of brain |
| 724091002 | Neuroectodermal melanolysosomal disease |
| 724138007 | Mitochondrial myopathy with sideroblastic anemia syndrome |
| 724146008 | Metaphyseal chondromatosis co-occurrent with D-2 hydroxyglutaric aciduria |
| 724207001 | Kleefstra syndrome |
| 724349009 | Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome |
| 724357007 | Hereditary cerebral hemorrhage with amyloidosis |
| 724427002 | Asymptomatic stenosis of intracranial artery |
| 724428007 | Asymptomatic stenosis of extracranial artery |
| 724549005 | Epilepsy due to infectious disease of central nervous system |
| 724572007 | Neuromuscular junction disorder caused by organic phosphorus compound ingestion |
| 724576005 | Pyridoxal 5-phosphate dependent epilepsy |
| 724643004 | Transient abnormal myelopoiesis co-occurrent with Down syndrome |
| 724644005 | Myeloid leukemia co-occurrent with Down syndrome |
| 724761004 | Sporadic Parkinson disease |
| 724769002 | Ataxia co-occurrent and due to phytanic acid storage disease |
| 724776007 | Dementia due to disorder of central nervous system |
| 724777003 | Dementia due to infectious disease |
| 724778008 | Progressive relapsing multiple sclerosis |
| 724780002 | Demyelination of central nervous system co-occurrent and due to neurosarcoidosis |
| 724781003 | Demyelination of central nervous system co-occurrent and due to systemic lupus erythematosus |
| 724782005 | Demyelination of central nervous system co-occurrent and due to Sjogren disease |
| 724783000 | Demyelination of central nervous system co-occurrent and due to Behcet disease |
| 724784006 | Demyelination of central nervous system co-occurrent and due to mitochondrial disease |
| 724785007 | Epilepsy due to perinatal stroke |
| 724786008 | Epilepsy due to perinatal anoxic-ischemic brain injury |
| 724787004 | Epilepsy due to cerebrovascular accident |
| 724788009 | Epilepsy due to and following traumatic brain injury |
| 724789001 | Epilepsy due to intracranial tumor |
| 724813004 | Autonomic nervous system disorder co-occurrent and due to neurodegenerative disorder |
| 724819000 | Functional paraparesis |
| 724820006 | Functional hemiparesis |
| 72488000 | Niemann-Pick disease, type C, chronic form |
| 724990004 | Epilepsy due to immune disorder |
| 724991000 | Epilepsy co-occurrent and due to demyelinating disorder |
| 724992007 | Epilepsy co-occurrent and due to dementia |
| 724993002 | Cerebral ischemic stroke due to occlusion of extracranial large artery |
| 724994008 | Cerebral ischemic stroke due to stenosis of extracranial large artery |
| 724999003 | Isolated optic nerve hypoplasia |
| 725042001 | Autosomal recessive limb girdle muscular dystrophy type 2J |
| 725043006 | Autosomal recessive limb girdle muscular dystrophy type 2O |
| 725047007 | Autosomal recessive Charcot-Marie-Tooth disease with hoarseness |
| 725048002 | Charcot-Marie-Tooth disease type 2B1 |
| 725097006 | Crisponi syndrome |
| 725139005 | Spastic paraplegia, optic atrophy, neuropathy syndrome |
| 725146001 | Atypical juvenile parkinsonism |
| 725163002 | X-linked spasticity, intellectual disability, epilepsy syndrome |
| 725296006 | Mucolipidosis type IV |
| 725420009 | Congenital muscular dystrophy Paradas type |
| 725464001 | Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy |
| 725898002 | Delirium co-occurrent with dementia |
| 725907002 | Autosomal recessive limb girdle muscular dystrophy type 2Y |
| 726031001 | Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome |
| 726051002 | Myotonia congenita |
| 726107008 | Distal myopathy Welander type |
| 72655000 | Alternating hypoglossal hemiplegia |
| 726614009 | Autosomal recessive limb girdle muscular dystrophy type 2P |
| 726615005 | Autosomal recessive limb girdle muscular dystrophy type 2Q |
| 726616006 | Autosomal recessive limb girdle muscular dystrophy type 2L |
| 726617002 | Autosomal recessive limb girdle muscular dystrophy type 2N |
| 726618007 | Autosomal recessive limb girdle muscular dystrophy type 2M |
| 726669007 | Central nervous system calcification, deafness, tubular acidosis, anemia syndrome |
| 726704006 | Cataract, congenital heart disease, neural tube defect syndrome |
| 73173006 | Spasm of cerebral arteries |
| 73192008 | Multiple AND bilateral precerebral artery stenosis |
| 732245008 | Pure mitochondrial myopathy |
| 732261005 | Cyprus facial neuromusculoskeletal syndrome |
| 732264002 | Coenzyme A synthase protein associated neurodegeneration |
| 732929002 | Autosomal recessive limb girdle muscular dystrophy type 2S |
| 732930007 | Autosomal recessive limb girdle muscular dystrophy type 2T |
| 732931006 | Autosomal recessive limb girdle muscular dystrophy type 2R |
| 732951005 | Mitochondrial myopathy, lactic acidosis, deafness syndrome |
| 732959007 | Beta-propeller protein-associated neurodegeneration |
| 73297009 | Muscular dystrophy |
| 733028000 | Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome |
| 733032006 | Epilepsy telangiectasia syndrome |
| 733044009 | Dermatoleukodystrophy |
| 733068001 | Absent tibia, polydactyly, arachnoid cyst syndrome |
| 733071009 | Deafness, small bowel diverticulosis, neuropathy syndrome |
| 733082001 | Early-onset Lafora body disease |
| 733091002 | Isolated hereditary congenital facial paralysis |
| 733184002 | Dementia caused by heavy metal exposure |
| 733185001 | Dementia following injury caused by exposure to ionizing radiation |
| 733190003 | Dementia due to primary malignant neoplasm of brain |
| 733191004 | Dementia due to chronic subdural hematoma |
| 733192006 | Dementia due to herpes encephalitis |
| 733194007 | Dementia co-occurrent and due to Down syndrome |
| 733195008 | Epilepsy of infancy with migrating focal seizures |
| 733199002 | Multifocal cerebral infarction due to and following procedure on cardiovascular system |
| 733469003 | Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome |
| 733489002 | Distal myopathy with posterior leg and anterior hand involvement |
| 733599009 | Adult-onset multiple mitochondrial deoxyribonucleic acid deletion syndrome due to deoxyguanosine kinase deficiency |
| 733623005 | Autism spectrum disorder, epilepsy, arthrogryposis syndrome |
| 733630004 | Deficiency of alpha-ketoglutarate dehydrogenase |
| 733636005 | 3-phosphoglycerate dehydrogenase deficiency juvenile form |
| 733650000 | Adult familial nephronophthisis with spastic quadriparesia syndrome |
| 73390009 | Endophlebitis of cavernous venous sinus |
| 733926004 | Ganglioneuroblastoma of central nervous system |
| 734017008 | Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome |
| 734022008 | Wolfram-like syndrome |
| 734066005 | Diffuse large B-cell lymphoma of central nervous system |
| 734099007 | Neuroblastoma of central nervous system |
| 734326000 | Stenosis of left vertebral artery |
| 734327009 | Stenosis of right vertebral artery |
| 734374000 | Thrombosis of left carotid artery |
| 734382000 | Thrombosis of right carotid artery |
| 734383005 | Thrombosis of left middle cerebral artery |
| 734384004 | Thrombosis of right middle cerebral artery |
| 734396006 | Spontaneous rupture of left posterior communicating artery |
| 734397002 | Spontaneous rupture of right posterior communicating artery |
| 734434007 | Pyridoxine-dependent epilepsy |
| 734879002 | Ruptured aneurysm of right posterior communicating artery |
| 734880004 | Ruptured aneurysm of left posterior communicating artery |
| 734959006 | Embolus of left cerebellar artery |
| 734960001 | Embolus of right cerebellar artery |
| 734961002 | Embolus of left posterior cerebral artery |
| 734963004 | Embolus of right posterior cerebral artery |
| 734964005 | Embolus of left middle cerebral artery |
| 734965006 | Embolus of right middle cerebral artery |
| 735114006 | Occlusion of right pontine artery |
| 735115007 | Occlusion of left pontine artery |
| 735131004 | Occlusion of left cerebellar artery |
| 735132006 | Occlusion of right cerebellar artery |
| 73663008 | Neurologic xeroderma pigmentosum |
| 737159004 | Aneurysm of basilar artery |
| 737160009 | Dissection of basilar artery |
| 7379000 | Pseudobulbar palsy |
| 74073002 | Cerebellar hemangioblastomatosis |
| 75023009 | Post-traumatic epilepsy |
| 75046006 | Combined pyramidal-extrapyramidal syndrome |
| 75072002 | Nemaline myopathy |
| 75111000 | Painful ophthalmoplegia |
| 751371000000107 | Personal history of transient ischaemic attack |
| 75138007 | Endophlebitis of superior sagittal sinus |
| 75299005 | Spastic spinal syphilitic paralysis |
| 75491005 | Amyotrophia congenita |
| 75543006 | Cerebral embolism |
| 76043009 | Hereditary sensory-motor neuropathy, type V |
| 762350007 | Dementia due to prion disease |
| 762351006 | Dementia due to and following injury of head |
| 762352004 | Demyelination due to systemic vasculitis |
| 762629007 | Occlusion of right middle cerebral artery by embolus |
| 762630002 | Occlusion of left middle cerebral artery by embolus |
| 762632005 | Occlusion of left cerebellar artery by embolus |
| 762633000 | Occlusion of right cerebellar artery by embolus |
| 762648006 | Stenosis of right cerebellar artery |
| 762649003 | Stenosis of left cerebellar artery |
| 762651004 | Occlusion of right posterior cerebral artery by embolus |
| 762652006 | Occlusion of left posterior cerebral artery by embolus |
| 762707000 | Subcortical dementia |
| 763067000 | Autosomal dominant congenital benign spinal muscular atrophy |
| 763135001 | Charcot-Marie-Tooth disease type 4E |
| 763136000 | Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome |
| 763314009 | Congenital muscular dystrophy with hyperlaxity |
| 763315005 | Congenital myopathy with myasthenic-like onset |
| 763345008 | Charcot-Marie-Tooth disease type 4B3 |
| 763347000 | X-linked Charcot-Marie-Tooth disease type 6 |
| 763400005 | X-linked Charcot-Marie-Tooth disease type 4 |
| 763455008 | X-linked Charcot-Marie-Tooth disease type 1 |
| 763457000 | X-linked Charcot-Marie-Tooth disease type 2 |
| 763458005 | X-linked Charcot-Marie-Tooth disease type 3 |
| 763460007 | X-linked Charcot-Marie-Tooth disease type 5 |
| 763533003 | Distal hereditary motor neuropathy Jerash type |
| 763534009 | Hot water reflex epilepsy |
| 763622006 | Thinking epilepsy |
| 763632004 | Startle epilepsy |
| 763669001 | Spastic ataxia with congenital miosis |
| 763718009 | Finnish upper limb onset distal myopathy |
| 763743003 | Intellectual disability, spasticity, ectrodactyly syndrome |
| 763776004 | Kelch like family member 9 related early-onset distal myopathy |
| 763802009 | Micturition induced epilepsy |
| 763827002 | Orgasm induced epilepsy |
| 763829004 | Oculopharyngodistal myopathy |
| 763895001 | Myosclerosis |
| 76402003 | Carotid artery insufficiency syndrome |
| 764453009 | Action myoclonus renal failure syndrome |
| 764522009 | Familial focal epilepsy with variable foci |
| 764525006 | Cylindrical spirals myopathy |
| 764730007 | Autosomal dominant Charcot-Marie-Tooth disease type 2 due to kinesin family member 5A mutation |
| 764733009 | Progressive external ophthalmoplegia, myopathy, emaciation syndrome |
| 764812008 | Autosomal recessive myogenic arthrogryposis multiplex congenita |
| 764850002 | Autosomal dominant Charcot-Marie-Tooth disease type 2A2 |
| 764854006 | Autosomal dominant slowed nerve conduction velocity |
| 764859001 | Laing early-onset distal myopathy |
| 764944006 | Congenital muscular dystrophy type 1B |
| 764945007 | Congenital myopathy with internal nuclei and atypical cores |
| 765046002 | Autosomal dominant Charcot-Marie-Tooth disease type 2U |
| 765047006 | SURF1, cytochrome c oxidase assembly factor related Charcot-Marie-Tooth disease type 4 |
| 765093009 | Rolandic epilepsy, speech dyspraxia syndrome |
| 765170001 | Sodium voltage-gated channel alpha subunit 8-related epilepsy with encephalopathy |
| 765197008 | Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier |
| 765202001 | Familial multiple benign meningioma |
| 765216006 | Audiogenic epilepsy |
| 765325002 | Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease |
| 765331004 | Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis |
| 765434008 | Human immunodeficiency virus type I enhancer binding protein 2 related intellectual disability |
| 765744006 | Autosomal dominant intermediate Charcot-Marie-Tooth disease type A |
| 765745007 | Autosomal dominant intermediate Charcot-Marie-Tooth disease type B |
| 765746008 | Autosomal dominant intermediate Charcot-Marie-Tooth disease type C |
| 765747004 | Autosomal dominant intermediate Charcot-Marie-Tooth disease type D |
| 765758008 | Microcephalic primordial dwarfism Montreal type |
| 766032007 | Holoprosencephaly, ectrodactyly, cleft lip, cleft palate syndrome |
| 766044005 | Acute encephalopathy with biphasic seizures and late reduced diffusion |
| 766251006 | Lethal infantile mitochondrial myopathy |
| 76670001 | Duchenne muscular dystrophy |
| 766752000 | Neurolymphomatosis |
| 766753005 | Nijmegen breakage syndrome-like disorder |
| 766764008 | X-linked distal spinal muscular atrophy type 3 |
| 766815007 | Perioral myoclonia with absences |
| 766931003 | Hypomyelination neuropathy arthrogryposis syndrome |
| 766977007 | Severe early-onset axonal neuropathy due to mitofusin 2 deficiency |
| 766987006 | Moebius syndrome |
| 768473009 | Purine rich element binding protein A syndrome |
| 768555009 | 5q31.3 microdeletion syndrome |
| 768666006 | Syntaxin binding protein 1 encephalopathy with epilepsy |
| 76880004 | Angelman syndrome |
| 769065000 | Tubulin beta 4A class IVa related leukodystrophy |
| 77015008 | Crossed hemiplegia |
| 770430000 | Autosomal recessive distal spinal muscular atrophy type 3 |
| 770431001 | Early-onset epileptic encephalopathy and intellectual disability due to glutamate receptor, ionotropic, N-methyl-D-aspartate, subunit 2A mutation |
| 770438007 | Infantile spasm and broad thumb syndrome |
| 770560008 | Lissencephaly due to LIS1 mutation |
| 770596007 | Rippling muscle disease with myasthenia gravis |
| 770623004 | Benign occipital lobe epilepsy |
| 770624005 | Benign partial epilepsy of infancy with complex partial seizures |
| 770625006 | Combined immunodeficiency with faciooculoskeletal anomalies syndrome |
| 770626007 | Congenital Horner syndrome |
| 770627003 | Desmin-related myofibrillar myopathy |
| 770630005 | Distal hereditary motor neuropathy type 1 |
| 770655004 | Microcephalus, brain defect, spasticity, hypernatremia syndrome |
| 770723007 | Optic atrophy, intellectual disability syndrome |
| 770727008 | Spinal muscular atrophy with respiratory distress type 2 |
| 770758009 | New-onset refractory status epilepticus |
| 770759001 | Autosomal dominant intermediate Charcot-Marie-Tooth disease type F |
| 770786001 | Hereditary inclusion body myopathy type 4 |
| 770792007 | Adult-onset distal myopathy due to valosin containing protein mutation |
| 77097004 | Oculopharyngeal muscular dystrophy |
| 771081007 | Distal hereditary motor neuropathy type 7 |
| 771141002 | Benign partial epilepsy with secondarily generalized seizures in infancy |
| 771143004 | Hereditary motor and sensory neuropathy type 5 |
| 771144005 | Hereditary motor and sensory neuropathy with acrodystrophy |
| 771147003 | Isolated arhinencephaly |
| 771238004 | Spinal atrophy, ophthalmoplegia, pyramidal syndrome |
| 771261002 | Digital extensor muscle aplasia with polyneuropathy |
| 771263004 | Ptosis and vocal cord paralysis syndrome |
| 771267003 | Congenital muscular dystrophy with integrin alpha-7 deficiency |
| 771272007 | Congenital muscular dystrophy due to lamin A/C mutation |
| 771302009 | Autosomal recessive lower motor neuron disease with childhood onset |
| 771304005 | Benign nocturnal alternating hemiplegia of childhood |
| 771307003 | Charcot-Marie-Tooth disease type 2B5 |
| 771334000 | Autosomal dominant limb-girdle muscular dystrophy type 1H |
| 771336003 | Polymicrogyria with optic nerve hypoplasia |
| 771448004 | Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency |
| 771471002 | Optic nerve edema, splenomegaly syndrome |
| 771475006 | Young adult-onset distal hereditary motor neuropathy |
| 771509001 | Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial deoxyribonucleic acid mutation |
| 771514002 | Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome |
| 772129007 | Autosomal dominant childhood-onset proximal spinal muscular atrophy |
| 773230003 | Cyclin-dependent kinase-like 5 deficiency |
| 773306002 | Congenital lethal myopathy Compton North type |
| 773308001 | Autosomal recessive intermediate Charcot-Marie-Tooth disease type A |
| 773330000 | Autosomal recessive intermediate Charcot-Marie-Tooth disease type B |
| 773393001 | Autosomal dominant Charcot-Marie-Tooth disease type 2Q |
| 773398005 | Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome |
| 773414009 | Autosomal recessive intermediate Charcot-Marie-Tooth disease type C |
| 773415005 | Contiguous ABCD1 DXS1357E deletion syndrome |
| 773421009 | Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression |
| 773492007 | Childhood-onset spasticity with hyperglycinemia |
| 773555005 | Severe neurodegenerative syndrome with lipodystrophy |
| 773643006 | Multiple congenital anomalies, hypotonia, seizures syndrome type 2 |
| 773648002 | Congenital cataract, hearing loss, severe developmental delay syndrome |
| 773737004 | Nephrocystin 3-related Meckel-like syndrome |
| 774069007 | Protein kinase cAMP-dependent type I regulatory subunit beta-related neurodegenerative dementia with intermediate filaments |
| 774070008 | Fibulin 1-related developmental delay, central nervous system anomaly, syndactyly syndrome |
| 774147002 | Charcot-Marie-Tooth disease type 2R |
| 774149004 | Severe intellectual disability, progressive postnatal microcephaly, midline stereotypic hand movements syndrome |
| 774150004 | Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome |
| 774205007 | Growth and developmental delay, hypotonia, vision impairment, lactic acidosis syndrome |
| 77461000119109 | Myasthenia gravis with exacerbation |
| 77471000119103 | Myasthenia gravis without exacerbation |
| 77659000 | Paraneoplastic neuropathy |
| 777999008 | Hypomyelination with brain stem and spinal cord involvement and leg spasticity |
| 778001003 | Potassium voltage-gated channel subfamily Q member 2 related epileptic encephalopathy |
| 778003000 | Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain |
| 778021002 | Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome |
| 778027003 | Primary CD59 deficiency |
| 778047006 | Myoclonic epilepsy in non-progressive encephalopathy |
| 778063003 | Cryptogenic late-onset epileptic spasms |
| 77835008 | Ophthalmoplegia plus syndrome |
| 77956009 | Steinert myotonic dystrophy syndrome |
| 780827006 | Synaptic Ras GTPase activating protein 1- related intellectual disability |
| 78097002 | Total ophthalmoplegia |
| 782675008 | Distal myopathy with anterior tibial onset |
| 782723007 | Severe intellectual disability, progressive spastic diplegia syndrome |
| 782739000 | Male emopamil-binding protein disorder with neurological defect |
| 782742006 | Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons |
| 782744007 | Lipoic acid synthetase deficiency |
| 782752005 | Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome |
| 782754006 | Foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis syndrome |
| 782822006 | Infantile cerebellar and retinal degeneration |
| 782824007 | Sodium channelopathy-related small fiber neuropathy |
| 782826009 | Charcot-Marie-Tooth disease type 2P |
| 782829002 | Autosomal dominant Charcot-Marie-Tooth disease type 2O |
| 782881002 | Hereditary sensorimotor neuropathy with hyperelastic skin |
| 782886007 | Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome |
| 782887003 | Inherited congenital spastic tetraplegia |
| 782941005 | Richieri Costa-da Silva syndrome |
| 782945001 | Ophthalmoplegia, intellectual disability, lingua scrotalis syndrome |
| 783057002 | DNA replication helicase/nuclease 2-related mitochondrial deoxyribonucleic acid deletion syndrome |
| 78306007 | Epidural ascending spinal paralysis |
| 783065004 | Autosomal recessive optic atrophy type 7 |
| 783091003 | 46,XY gonadal dysgenesis, motor and sensory neuropathy syndrome |
| 783148005 | Distal nebulin myopathy |
| 783160006 | Hereditary gelsolin amyloidosis |
| 783166000 | Distal anoctaminopathy |
| 783175003 | Congenital muscular dystrophy without intellectual disability |
| 783413008 | Multiple aneurysms of cerebral artery |
| 783415001 | Aneurysm of internal carotid bifurcation |
| 783416000 | Aneurysm of anterior cerebral artery |
| 783417009 | Aneurysm of posterior inferior cerebellar artery |
| 783418004 | Aneurysm of anterior communicating artery |
| 783419007 | Aneurysm of posterior cerebral artery |
| 783420001 | Aneurysm of middle cerebral artery |
| 783421002 | Aneurysm of posterior communicating artery |
| 783422009 | Aneurysm of internal carotid-anterior communicating artery zone |
| 783423004 | Aneurysm of internal carotid-posterior communicating artery zone |
| 783550006 | Hereditary sensory and autonomic neuropathy type 7 |
| 783554002 | Autosomal recessive limb girdle muscular dystrophy type 2U |
| 783558004 | Combined oxidative phosphorylation defect type 11 |
| 783618006 | Lower motor neuron syndrome with late-adult onset |
| 783629005 | Congenital aneurysm of cerebral artery |
| 783630000 | Congenital aneurysm of precerebral artery |
| 783707003 | Cerebral aneurysm due to dissection of cerebral artery |
| 783716004 | Acquired aneurysm of cerebral artery |
| 783722008 | Myopathy and diabetes mellitus |
| 783731008 | Fibromuscular dysplasia of wall of carotid artery |
| 783733006 | Fibromuscular dysplasia of wall of bilateral carotid arteries |
| 783739005 | Familial temporal lobe epilepsy |
| 784341001 | Amyotrophic lateral sclerosis type 4 |
| 784346006 | Navajo neurohepatopathy |
| 784347002 | Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome |
| 784352007 | X-linked scapuloperoneal muscular dystrophy |
| 784370005 | Mitochondrial myopathy with reversible cytochrome C oxidase deficiency |
| 784372002 | Familial mesial temporal lobe epilepsy with febrile seizures |
| 784377008 | Autosomal dominant epilepsy with auditory features |
| 784391002 | Autosomal dominant adult-onset proximal spinal muscular atrophy |
| 78468005 | Erb's muscular dystrophy |
| 785299009 | Cobblestone lissencephaly without muscular or ocular involvement |
| 785809005 | Mills syndrome |
| 785810000 | Synucleinopathy |
| 78689005 | Chronic brain syndrome |
| 787037000 | Congenital muscular dystrophy type 1A |
| 787044009 | Stenosis of bilateral carotid arteries |
| 787172004 | Childhood-onset autosomal recessive myopathy with external ophthalmoplegia |
| 788417006 | Alopecia, epilepsy, intellectual disability syndrome Moynahan type |
| 788454002 | Stenosis of bilateral vertebral arteries |
| 788455001 | Occlusion of bilateral pontine arteries |
| 788898005 | Dementia caused by volatile inhalant |
| 789005009 | Paralysis of uvula after diphtheria |
| 789674008 | Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder |
| 791000124107 | 2-methyl-3-hydroxybutyric aciduria |
| 7931000119101 | Anterior choroidal artery thrombosis |
| 79633009 | Spastic hemiplegia |
| 79745005 | Reflex epilepsy |
| 80328002 | Progressive cone-rod dystrophy |
| 80544005 | Spongy degeneration of central nervous system |
| 80606009 | Carotid artery embolism |
| 80690008 | Degenerative disease of the central nervous system |
| 80901002 | Endophlebitis of torcular Herophili |
| 80935004 | Flaccid hemiplegia |
| 80976008 | Myasthenic crisis |
| 81211007 | Primary lateral sclerosis |
| 81308009 | Disorder of brain |
| 8166000 | Thrombophlebitis of basilar sinus |
| 816984002 | Progressive multiple sclerosis |
| 81854007 | Alexander's disease |
| 818967003 | Medulloepithelioma of central nervous system |
| 82077006 | Myotubular myopathy |
| 82361000119107 | Altered behavior in dementia due to Huntington chorea |
| 82371000119101 | Dementia due to multiple sclerosis with altered behavior |
| 82381000119103 | Epileptic dementia with behavioral disturbance |
| 82501000119102 | Anaplastic astrocytoma of central nervous system |
| 8269002 | Cerebrospinal angiopathy |
| 827115000 | Autosomal dominant progressive external ophthalmoplegia |
| 827117008 | Autosomal recessive progressive external ophthalmoplegia |
| 8291000119107 | Atonic epilepsy |
| 838275008 | Stenosis of cerebral artery |
| 838307002 | Childhood-onset autosomal dominant optic atrophy |
| 838308007 | Fibromuscular dysplasia of wall of intracranial artery |
| 838309004 | Cerebrovascular abnormality due to Takayasu disease |
| 83832001 | Metachromatic leukodystrophy without arylsulfatase deficiency |
| 838345001 | Autosomal recessive optic atrophy type 6 |
| 840419005 | Dissection of extracranial carotid artery |
| 840420004 | Dissection of extracranial vertebral artery |
| 840422007 | Dissection of anterior cerebral artery |
| 840434004 | Dissection of posterior cerebral artery |
| 840436002 | Dissection of middle cerebral artery |
| 840437006 | Dissection of multiple cerebral arteries |
| 840438001 | Dissection of intracranial vertebral artery |
| 840439009 | Dissection of intracranial carotid artery |
| 840441005 | Dissection of intracranial artery |
| 840464007 | Dementia due to carbon monoxide poisoning |
| 840505007 | Down syndrome co-occurrent with leukemoid reaction associated transient neonatal pustulosis |
| 84160009 | Laryngeal hemiplegia |
| 84161000119100 | Partial epileptic seizure of parietal lobe with impairment of consciousness |
| 84171000119106 | Partial epileptic seizure of frontal lobe with impairment of consciousness |
| 84181000119109 | Partial epileptic seizure of occipital lobe with impairment of consciousness |
| 84191000119107 | Partial epileptic seizure of temporal lobe with impairment of consciousness |
| 84201000119105 | Intractable partial temporal lobe epilepsy with impairment of consciousness |
| 84211000119108 | Intractable partial parietal lobe epilepsy with impairment of consciousness |
| 84216001 | Cerebral venous thrombosis of pregnancy AND/OR puerperium |
| 84221000119101 | Intractable partial frontal lobe epilepsy with impairment of consciousness |
| 84231000119103 | Intractable partial occipital lobe epilepsy with impairment of consciousness |
| 84455002 | Spinal paraplegia |
| 84590007 | Lower motor neuron disease |
| 84757009 | Epilepsy |
| 85102008 | Cerebellar ataxia |
| 85505000 | Adult spinal muscular atrophy |
| 8563000 | Cholinergic crisis |
| 85641006 | Hemianencephaly |
| 85672005 | Anterior horn cell disease |
| 86003009 | Carotid artery thrombosis |
| 86044005 | Amyotrophic lateral sclerosis |
| 860804005 | Epilepsy due to infectious encephalitis |
| 860806007 | Epilepsy due to infectious meningitis |
| 860807003 | Hereditary autonomic neuropathy |
| 860809000 | Hereditary sensory autonomic neuropathy type IIA |
| 860810005 | Hereditary sensory autonomic neuropathy type IIB |
| 860811009 | Hereditary sensory autonomic neuropathy type ID |
| 860812002 | Hereditary sensory autonomic neuropathy type IE |
| 860813007 | Hereditary sensory autonomic neuropathy type IA |
| 860814001 | Hereditary sensory autonomic neuropathy type IC |
| 860815000 | Epilepsy due to neonatal central nervous system infection |
| 860881004 | Flaccid diplegia of lower extremities |
| 86444004 | Niemann-Pick disease, type C, acute form |
| 866050001 | Mixed germ cell neoplasm of central nervous system |
| 866051002 | Motor neuron disease due to lead intoxication |
| 870284000 | Pelizaeus Merzbacher like disease due to HSPD1 mutation |
| 870285004 | Pelizaeus Merzbacher like disease due to SLC16A2 mutation |
| 870286003 | Pelizaeus Merzbacher like disease due to AIMP1 mutation |
| 870287007 | Pelizaeus Merzbacher like disease due to GJC2 mutation |
| 870319003 | Optic atrophy due to late syphilis |
| 870544005 | Occlusion of distal basilar artery |
| 870566003 | Occlusion of anterior choroidal artery |
| 870579007 | Occlusion of branch of basilar artery |
| 870637009 | Dissection of cervical artery |
| 87151000119105 | Malignant glioma of central nervous system |
| 871637001 | Thrombosis of multiple cerebral veins |
| 87551000119101 | Visual disturbance as sequela of cerebrovascular disease |
| 87607002 | Pelizaeus-Merzbacher disease, classic form |
| 87842000 | Generalized neuromuscular exhaustion syndrome |
| 87937009 | Endophlebitis of intracranial venous sinus |
| 88174006 | Basilar artery thrombosis |
| 88922007 | Thrombosis of basilar sinus |
| 88923002 | Progressive muscular atrophy |
| 89142007 | Progressive intracranial arterial occlusion |
| 89437009 | Cerebral paraparesis |
| 89980009 | Thrombosis of cavernous venous sinus |
| 903741000000102 | Uhthoff phenomenon |
| 90520006 | Vertebral artery stenosis |
| 91327001 | Quadriparesis |
| 9133005 | Familial amyloid polyneuropathy, Iowa type |
| 91502009 | Spinocerebellar disease |
| 91601000119109 | Sequela of thrombotic stroke |
| 91637004 | Myasthenia gravis |
| 92341000119107 | Weakness of extremities as sequela of stroke |
| 92503002 | Neurofibromatosis type 2 |
| 92824003 | Neurofibromatosis type 1 |
| 92962004 | Congenital absence of carotid artery |
| 92997002 | Congenital anomaly of carotid artery |
| 93054001 | Congenital dilatation of carotid artery |
| 93153005 | Limb-girdle muscular dystrophy |
| 93312006 | Congenital malposition of carotid artery |
| 93396008 | Congenital stenosis of carotid artery |
| 936271000000100 | Congenital anomaly of precerebral vessel |
| 93744007 | Primary malignant neoplasm of central nervous system |
| 93747000 | Primary malignant neoplasm of cerebral meninges |
| 93931007 | Primary malignant neoplasm of optic nerve |
| 94243009 | Secondary malignant neoplasm of central nervous system |
| 94246001 | Secondary malignant neoplasm of cerebral meninges |
| 943181000000103 | Degenerative disease of basal ganglia |
| 94452002 | Secondary malignant neoplasm of optic nerve |
| 95208000 | Photogenic epilepsy |
| 95235009 | Retroesophageal carotid artery |
| 9537004 | Juvenile GM 2 gangliosidosis |
| 95455008 | Thrombosis of cerebral veins |
| 95458005 | Cerebellar artery occlusion |
| 95461006 | Thrombophlebitis of cerebral vein |
| 95477007 | Congenital degeneration of nervous system |
| 95610008 | Congenital brain damage |
| 95647008 | Upper motor neuron disease |
| 95650006 | Transient hemiplegia |
| 95651005 | Chronic progressive paraparesis |
| 95774001 | Atrophy of optic disc |
| 95775000 | Retrobulbar optic nerve atrophy |
| 9611000119107 | Symptomatic carotid artery stenosis |
| 97381000119100 | Neurogenic bladder due to quadriplegia |
| 97391000119102 | Paraplegia with neurogenic bladder |
| 9753004 | Triplegia |
| 984681000000101 | Profound learning disability |
| 99451000119105 | Cerebral infarction due to stenosis of carotid artery |
Codes not in the full codelist are in faint grey.