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: v.1.5.3
Version ID: 42177ba7

Versions

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

Description

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

References

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

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

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

code	term
10007009	Coffin-Siris syndrome
1003374009	Microlissencephaly
1003375005	Metachromatic leukodystrophy due to sphingolipid activator protein I deficiency
1003444000	Type 3 lissencephaly
1003445004	Lumbosacral spina bifida aperta with hydrocephalus
1003447007	Pelizaeus-Merzbacher disease null syndrome
1003448002	Lumbosacral spina bifida aperta
1003465006	Familial spinal neurofibromatosis
1003881009	Pelizaeus-Merzbacher disease in female carrier
100721000119109	High grade astrocytoma of brain
100731000119107	Low grade astrocytoma of brain
100941000119100	Epilepsy in mother complicating pregnancy
1010464002	Agenesis of right hemisphere of cerebellum
1010465001	Agenesis of left hemisphere of cerebellum
1010630006	X-linked complicated corpus callosum dysgenesis
1010642001	Sporadic infantile bilateral striatal necrosis
1010643006	Thoracolumbosacral spina bifida aperta
1010644000	Spina bifida aperta of upper thoracic spine
1010653007	Segmental neurofibromatosis type 1
1010712009	Autosomal dominant Emery-Dreifuss muscular dystrophy
101421000119107	Dementia due to Parkinson's disease
102831000119104	Paralytic syndrome of both lower limbs as sequela of stroke
1032761000000105	Intraventricular (nontraumatic) haemorrhage, grade 4, of fetus and newborn
10349009	Multi-infarct dementia with delirium
103761000119107	Paralytic syndrome of all four limbs as sequela of stroke
103931000119102	Hepatic coma due to hepatitis
10394003	Friedreich's ataxia
104981000119104	Oligodendroglioma of cerebrum
1052237009	Paralysis of left side of tongue
1052238004	Paralysis of right side of tongue
1052243006	Hemiparesis of left side of face
1052244000	Hemiparesis of right side of face
1052326006	Rachischisis partialis
10532003	Primary degenerative dementia of the Alzheimer type, presenile onset, with depression
105421000119105	Early onset Alzheimer's disease with behavioral disturbance
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
107581000119103	Astrocytoma of brain stem
1078001000000105	Haemorrhagic stroke
1078223005	Thrombosis of cerebral venous sinus due to and following surgical procedure
1082511000119102	Hepatic coma due to acute hepatic failure
1082621000119108	Hepatic coma due to alcoholic liver failure
1085091000119108	Hepatic coma due to chronic hepatic failure
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
1092691000119109	Hepatic coma due to subacute liver failure
109478007	Kohlschutter's syndrome
109561000	Cerebrofacial dysplasia
109911004	Overlapping malignant neoplasm of brain and other parts of the central nervous system
109912006	Overlapping malignant neoplasm of brain
109915008	Primary malignant neoplasm of meninges
11045000	Supranuclear facial nerve paralysis
1105051000000102	Subacute combined degeneration of spinal cord due to use of nitrous oxide
110997000	Fahr's syndrome
111028009	Arteriopathic granular atrophy of cerebral cortex
111033008	Circumscribed atrophy of brain
111296006	Basilar artery embolism
111297002	Nonparalytic stroke
111298007	Chronic cerebral ischemia
111299004	Atheroma of cerebral arteries
111337001	Dyke-Davidoff-Masson syndrome
111383007	Dysmorphic sialidosis, juvenile form
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
111504002	Walker-Warburg congenital muscular dystrophy
111505001	Muscle-eye-brain disease, congenital muscular dystrophy
111506000	Distal muscular dystrophy, Miyoshi type
111508004	Emery-Dreifuss muscular dystrophy
111936002	Cerebral sarcoidosis
1131000119105	Sequela of cerebrovascular accident
11442006	Hereditary sensory neuropathy
11471000224106	Diffuse intrinsic pontine glioma
11538006	Quadriplegia
116288000	Paralytic stroke
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
12237911000119109	Amaurosis fugax of left eye
12237951000119105	Amaurosis fugax of right eye
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
12367511000119101	Paraplegia due to and following cerebrovascular accident
1239331000000100	Significant intellectual disability
123950001	Rheumatic chorea without heart involvement
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
125921000119106	Hepatic coma due to acute hepatitis C
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
128188000	Cerebral palsy
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
129609000	Spinocerebellar ataxia
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
133301000119102	Degenerative brain disorder caused by alcohol
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
134811000119108	Severe hypoxic ischemic encephalopathy of newborn
134821000119101	Moderate hypoxic ischemic encephalopathy of newborn
134831000119103	Mild hypoxic ischemic encephalopathy of newborn
135491000119100	Myelopathy due to benign neoplastic disease
135511000119105	Myelopathy due to malignant neoplastic disease
135761000119101	Cerebral degeneration due to alcoholism
135781000119105	Cerebral degeneration due to hypothyroidism
135811000119107	Lewy body dementia with behavioral disturbance
137592291000119101	Acute cerebrovascular accident due to occlusion of right posterior cerebral artery
137991000119103	Seizure disorder as sequela of stroke
13920009	Hepatic encephalopathy
13973009	Grand mal status
140281000119108	Hemiparesis as late effect of cerebrovascular disease
14055002	Hydrocephalus ex vacuo
14070001	Multi-infarct dementia with depression
140881000119109	Compression of brain co-occurrent and due to spontaneous cerebral hemorrhage
140911000119109	Ischemic stroke with coma
140921000119102	Ischemic stroke without coma
141991000119109	Delusions in Alzheimer's disease
142001000119106	Depressed mood in Alzheimer's disease
142011000119109	Alzheimer's disease co-occurrent with delirium
142031000119104	Visual field defect due to and following cerebrovascular accident
14210003	Lipofuscinosis
14246007	Embolism of intracranial venous sinus
142851000119103	Spontaneous cerebellar hemorrhage
14309005	Anterior choroidal artery syndrome
143521000119103	Nontraumatic intraparenchymal cerebral hemorrhage
14401000119109	Partial frontal lobe epilepsy
14447001	Dandy-Walker syndrome
145741000119101	Apraxia as late effect of cerebrovascular disease
14637005	Late-infantile neuronal ceroid lipofuscinosis
146371000119104	Hepatic coma due to chronic hepatitis C
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
15139001	Chronic brain-hydrocephalus syndrome
15182000	Coffin-Lowry syndrome
153091000119109	Hepatic coma due to chronic hepatitis B with delta agent
15523002	Benign focal epilepsy of childhood
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
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
15742000	Thrombosis of inferior sagittal sinus
1581000119101	Dementia of the Alzheimer type with behavioral disturbance
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
16000351000119109	Cerebrovascular accident due to occlusion of left posterior cerebral artery
16000391000119104	Cerebrovascular accident due to occlusion of right posterior cerebral artery
16000431000119109	Cerebrovascular accident due to occlusion of right middle cerebral artery
16000511000119103	Cerebrovascular accident due to occlusion of left middle cerebral artery
16002031000119102	Cerebrovascular accident due to thrombus of right middle cerebral artery
16002111000119106	Cerebrovascular accident due to thrombus of left middle cerebral artery
16023911000119108	Cerebrovascular accident due to occlusion of right carotid artery
16023991000119104	Cerebrovascular accident due to occlusion of left pontine artery
16024031000119100	Cerebrovascular accident due to occlusion of right pontine artery
16024111000119109	Cerebrovascular accident due to occlusion of left carotid artery
16024151000119105	Cerebrovascular accident due to occlusion of left cerebellar artery
16024271000119107	Cerebrovascular accident due to occlusion of right cerebellar artery
16026951000119102	Cerebrovascular accident due to stenosis of right carotid artery
16026991000119107	Cerebrovascular accident due to stenosis of left carotid artery
16058431000119104	White matter disease
16060001	Hepatic coma due to viral hepatitis A
16061002	Endophlebitis of lateral venous sinus
16171003	Double athetosis
16218291000119100	Acute cerebral ischemia
16219201000119101	Behavioral disturbance co-occurrent and due to late onset Alzheimer dementia
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
163601006	On examination - hemiplegia
163604003	On examination - paraplegia
163605002	On examination - quadriplegia
163606001	On examination - diplegia
16371781000119100	Cerebellar stroke
16415361000119105	Radiologically isolated syndrome
16418006	Embolism of basilar sinus
16476641000119100	Acquired arteriovenous fistula of dura of cerebrum
16517004	Cerebral lipidosis
16520041000119104	Congenital fenestration of basilar artery
166071000000101	Congenital dilated lateral ventricles of brain
16644681000119102	Cerebrovascular accident due to occlusion of bilateral pontine arteries
16661931000119102	Cerebrovascular accident due to stenosis of bilateral vertebral arteries
16661971000119104	Cerebrovascular accident due to stenosis of bilateral carotid arteries
16662331000119106	Aneurysm of right vertebral artery
16662371000119109	Aneurysm of left vertebral artery
1670004	Cerebral hemiparesis
16703491000119101	Memory deficit due to and following spontaneous intracerebral hemorrhage
16703551000119107	Memory deficit due to and following cerebrovascular disease
16703661000119105	Memory deficit due to and following cerebrovascular accident
16703711000119100	Memory deficit due to and following embolic 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
16818591000119108	Calcification of basal ganglia
16851005	Mitochondrial myopathy
16891111000119104	Cryptogenic stroke
171822009	Acute atrophic spinal paralysis
17258002	Chronic anoxic encephalopathy
17409003	Facial hemiparesis
17761000119109	High lumbar myelomeningocele
17771000119103	Low lumbar myelomeningocele
17944005	Cerebral calcification
18058007	Phlebitis of intracranial venous sinus
182961000119101	Acute disseminated encephalomyelitis following infectious disease
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
186624004	Hepatic coma due to acute hepatitis B with delta agent
186628001	Hepatic coma due to viral hepatitis C
186831000119104	Apraxia due to and following cerebrovascular accident
186893003	Rupture of syphilitic cerebral aneurysm
18756002	Juvenile GM1 gangliosidosis
187931000119106	Atypical absence epilepsy
188280007	Malignant neoplasm of cerebrum (excluding lobes and ventricles)
188281006	Malignant neoplasm of basal ganglia
188282004	Malignant neoplasm of cerebral cortex
188283009	Malignant neoplasm of corpus striatum
188285002	Malignant neoplasm of globus pallidus
188286001	Malignant tumor of hypothalamus
188287005	Malignant neoplasm of thalamus
188289008	Malignant neoplasm of hippocampus
188290004	Malignant neoplasm of uncus
188292007	Malignant tumor of choroid plexus
188293002	Malignant neoplasm of floor of cerebral ventricle
188295009	Malignant neoplasm of cerebral peduncle
188296005	Malignant neoplasm of medulla oblongata
188297001	Malignant neoplasm of midbrain
188298006	Malignant neoplasm of pons
188301005	Malignant neoplasm of corpus callosum
188302003	Malignant neoplasm of tapetum
188308004	Malignant neoplasm of olfactory bulb
188312005	Malignant neoplasm of cerebral dura mater
188313000	Malignant neoplasm of cerebral arachnoid mater
188315007	Malignant neoplasm of cerebral pia mater
188317004	Malignant neoplasm of spinal dura mater
188318009	Malignant neoplasm of spinal arachnoid mater
188319001	Malignant neoplasm of spinal pia mater
188339002	Malignant neoplasm of pituitary gland and craniopharyngeal duct
188340000	Malignant tumor of craniopharyngeal duct
18842008	Corticobasal degeneration
188462001	Secondary malignant neoplasm of brain and spinal cord
18927009	Niemann-Pick disease, type D
19091006	Pallidoluysian degeneration
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
191471000	Korsakov's alcoholic psychosis with peripheral neuritis
191475009	Chronic alcoholic brain syndrome
191493005	Drug-induced dementia
191519005	Dementia associated with another disease
192673008	Sarcoid meningitis
192685000	Subacute sclerosing panencephalitis
192730008	Toxic encephalitis
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
192761004	Thrombosis transverse 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
192772009	Thrombophlebitis lateral venous sinus
192781003	Leukodystrophy
192782005	Galactosylceramide beta-galactosidase deficiency
192787004	B variant hexosaminidase A deficiency
192788009	Retinal dystrophy in cerebroretinal lipidosis
192791009	Cerebral degeneration in Gaucher's disease
192792002	Cerebral degeneration in Niemann-Pick disease
192794001	Cerebral degeneration associated with another disorder
192795000	Cerebral degeneration in Hunter's disease
192796004	Cerebral degeneration in mucopolysaccharidosis
192805000	Acquired communicating hydrocephalus
192811002	Alcoholic encephalopathy
192812009	Cerebral degeneration due to beriberi
192813004	Cerebral degeneration due to cerebrovascular disease
192814005	Cerebral degeneration due to congenital hydrocephalus
192815006	Cerebral degeneration due to neoplastic disease
192816007	Myxedema encephalopathy
192817003	Cerebral degeneration due to vitamin B12 deficiency
192818008	Cerebral degeneration due to Creutzfeldt-Jakob disease
192819000	Cerebral degeneration due to progressive multifocal leukoencephalopathy
192845009	Myoclonic encephalopathy
192871008	Early onset cerebellar ataxia with myoclonus
192874000	Cerebellar ataxia associated with another disorder
192876003	Myxedema cerebellar degeneration
192877007	Paraneoplastic cerebellar degeneration
192894009	Syringomyelia and syringobulbia
192897002	Myelopathy due to acute infarction of spinal cord
192898007	Myelopathy due to arterial thrombosis of spinal cord
192900009	Myelopathy due to hematomyelia
192904000	Myelopathy due to another disorder
192906003	Myelopathy due to neoplastic disease
192926004	Multiple sclerosis of the brainstem
192927008	Multiple sclerosis of the spinal cord
192928003	Generalized multiple sclerosis
192929006	Exacerbation of multiple sclerosis
192949002	Congenital paraplegia
192958009	Hypotonic cerebral palsy
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
193003000	Mesiobasal limbic 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
193069004	Intracranial hypotension following ventricular shunting
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
195154000	Ruptured berry aneurysm
195160000	Intracranial subarachnoid hemorrhage from vertebral artery
195165005	Basal ganglia hemorrhage
195167002	External capsule hemorrhage
195168007	Intracerebral hemorrhage with intraventricular hemorrhage
195169004	Intracerebral hemorrhage, multiple localized
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
195200006	Carotid artery syndrome hemispheric
195205001	Impending cerebral ischemia
195206000	Intermittent cerebral ischemia
195209007	Middle cerebral artery syndrome
195210002	Anterior cerebral artery syndrome
195211003	Posterior cerebral artery syndrome
195212005	Brainstem stroke syndrome
195213000	Cerebellar stroke syndrome
195216008	Left sided cerebral hemisphere cerebrovascular accident
195217004	Right sided cerebral hemisphere cerebrovascular accident
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
203934001	Cervical spina bifida with hydrocephalus
203935000	Thoracic spina bifida with hydrocephalus
203936004	Lumbar spina bifida with hydrocephalus
203941007	Cervical spina bifida with hydrocephalus - open
203942000	Thoracic spina bifida with hydrocephalus - open
203943005	Lumbar spina bifida with hydrocephalus - open
203944004	Sacral spina bifida with hydrocephalus - open
203946002	Spina bifida with hydrocephalus - closed
203948001	Cervical spina bifida with hydrocephalus - closed
203949009	Thoracic spina bifida with hydrocephalus - closed
203950009	Lumbar spina bifida with hydrocephalus - closed
203951008	Sacral spina bifida with hydrocephalus - closed
203954000	Spina bifida with hydrocephalus of late onset
203957007	Dandy-Walker syndrome with spina bifida
203974007	Cervical hydromyelocele
203975008	Thoracic hydromyelocele
203976009	Lumbar hydromyelocele
203985009	Cervical meningomyelocele
203986005	Thoracic meningomyelocele
203987001	Lumbar meningomyelocele
203990007	Cervical myelocele
203991006	Thoracic myelocele
203992004	Lumbar myelocele
204003007	Cervical spina bifida without hydrocephalus - open
204004001	Thoracic spina bifida without hydrocephalus - open
204005000	Lumbar spina bifida without hydrocephalus - open
204006004	Sacral spina bifida without hydrocephalus - open
204036008	Lissencephaly
204040004	Agenesis of cerebrum
204042007	Congenital malformation of corpus callosum
204043002	Hypoplasia of corpus callosum
204044008	Aplasia of corpus callosum
204049003	Aplasia of cerebellum
204052006	Cebocephaly
20415001	Progressive sclerosing poliodystrophy
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
20484008	Prion disease
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
205749001	Congenital absence of pituitary gland
20725005	Familial visceral neuropathy
20908003	Subcortical cerebral hemorrhage
21007002	Wernicke's disease
21086008	Cockayne syndrome
21111006	Complete trisomy 13 syndrome
21201006	Sporadic cerebellar degeneration
21258007	Thrombosis of lateral venous sinus
21263006	Myxedema coma
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
21601000119103	Hypoxic ischemic encephalopathy due to birth trauma
21634003	Borjeson-Forssman-Lehmann syndrome
21921000119103	Dementia co-occurrent and due to Pick's disease
2198002	Visceral epilepsy
22126005	Hereditary neuraxial edema
22255007	Progressive multifocal leukoencephalopathy
223176004	Cerebellar disorder
22381000119105	Primary degenerative dementia
22386003	Syphilitic optic atrophy
224186005	Cerebellar deficiency syndrome
22443004	Vestibulocerebellar ataxia
22471005	Hemispheric cerebellar agenesis
22811006	Leukoencephalopathy
22881000119100	Quadriplegia with quadriparesis
230156002	Malignant meningitis
230180003	Human immunodeficiency virus leukoencephalopathy
230191005	Rasmussen syndrome
230193008	Neurosarcoidosis
230202002	Vacuolar myelopathy
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
230225001	Septic thrombophlebitis of great cerebral vein
230226000	System disorder of the nervous system
230227009	Early onset cerebellar ataxia
230228004	Early onset cerebellar ataxia with retained tendon reflexes
230229007	Early onset cerebellar ataxia with hypogonadism
230230002	Early onset cerebellar ataxia with retinitis pigmentosa and optic atrophy
230231003	Early onset cerebellar ataxia with essential tremor
230232005	Late onset cerebellar ataxia
230233000	Progressive cerebellar ataxia
230234006	Periodic ataxia
230235007	Olivopontocerebellar atrophy with slow eye movement
230236008	Olivopontocerebellar atrophy with blindness
230237004	Progressive spinocerebellar ataxia with decreased tendon reflexes
230238009	Progressive spinocerebellar ataxia with retained tendon reflexes
230239001	Progressive cerebellar ataxia with palatal myoclonus
230240004	Progressive cerebellar ataxia with hypogonadism
230241000	Secondary cerebellar degeneration
230242007	Drug-induced cerebellar ataxia
230243002	Cerebellar ataxia caused by toxin
230244008	Disorder primarily affecting the motor pathways
230246005	Progressive bulbar palsy of childhood
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
230260007	Pure hereditary spastic paraplegia
230261006	Complicated hereditary spastic paraplegia
230263009	Autosomal dominant spastic paraplegia type 17
230264003	Troyer syndrome
230265002	Familial Alzheimer's disease of early onset
230266001	Non-familial Alzheimer's disease of early onset
230267005	Familial Alzheimer's disease of late onset
230268000	Non-familial Alzheimer's disease of late onset
230269008	Focal Alzheimer's disease
230270009	Frontotemporal dementia
230271008	Pick's disease with Pick bodies
230272001	Pick's disease with Pick cells and no Pick bodies
230273006	Frontotemporal degeneration
230274000	Frontal lobe degeneration with motor neurone disease
230278002	Progressive aphasia
230279005	Non-Alzheimer's progressive dysphasia
230280008	Progressive aphasia in Alzheimer's disease
230281007	Argyrophilic grain disease
230282000	Post-traumatic dementia
230283005	Punch drunk syndrome
230284004	Spongiform encephalopathy
230285003	Vascular dementia of acute onset
230286002	Subcortical vascular dementia
230287006	Mixed cortical and subcortical vascular dementia
230288001	Semantic dementia
230289009	Patchy dementia
230291001	Juvenile Parkinson's disease
230296006	Vascular parkinsonism
230297002	Multiple system atrophy
230298007	Disorder presenting primarily with chorea
230299004	Juvenile onset Huntington's disease
230300007	Late onset Huntington's disease
230301006	Akinetic-rigid form of Huntington's disease
230302004	Pallidal degeneration
230305002	Chronic hepatocerebral degeneration
230307005	Chorea in systemic lupus erythematosus
230309008	Kinesiogenic choreoathetosis
230311004	Basal ganglia degeneration with calcification
230312006	Aicardi Goutieres syndrome
230313001	Autosomal dominant late onset basal ganglia degeneration
230319002	Autosomal dominant idiopathic familial dystonia
230320008	Autosomal recessive idiopathic familial dystonia
230329009	Posthemiplegic dystonia
230352008	Encephalopathy due to vitamin deficiency
230353003	Morel laminar sclerosis
230354009	Drug-induced encephalopathy
230355005	Encephalopathy caused by heavy metal
230357002	Urate encephalopathy
230359004	Secondary amyloid encephalopathy
230360009	Encephalopathy caused by radiation damage
230361008	Sepsis-associated encephalopathy
230363006	Progressive neuronal degeneration of childhood
230364000	Progressive neuronal degeneration without liver cirrhosis
230365004	Neuroaxonal dystrophy
230366003	Late infantile and juvenile neuroaxonal dystrophy
230367007	Neuroaxonal leukodystrophy
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
230377009	Extrapontine myelinolysis
230379007	Subacute necrotizing myelitis
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
230391003	Amygdalo-hippocampal epilepsy
230392005	Rhinencephalic epilepsy
230393000	Lateral temporal epilepsy
230394006	Frontal lobe epilepsy
230395007	Supplementary motor epilepsy
230396008	Cingulate 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
230405003	Chronic progressive epilepsia partialis continua of childhood
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
230421008	Myoclonic astatic epilepsy
230422001	Myoclonic absence epilepsy
230423006	Unverricht-Lundborg syndrome
230425004	Lafora disease
230426003	Myoclonic epilepsy with ragged red fibers
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
230521006	Optic radiation disorder
230522004	Inflammatory disorder of optic radiation
230523009	Infarction of optic radiation
230525002	Compression of optic radiation
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
230690007	Cerebrovascular accident
230691006	Cerebrovascular accident due to occlusion of cerebral artery
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
230709005	Massive supratentorial cerebral hemorrhage
230710000	Lobar cerebral hemorrhage
230711001	Thalamic hemorrhage
230712008	Lacunar hemorrhage
230713003	Stroke of uncertain pathology
230714009	Anterior circulation stroke of uncertain pathology
230715005	Posterior circulation stroke of uncertain pathology
230716006	Carotid territory transient ischemic attack
230717002	Vertebrobasilar territory transient ischemic attack
230720005	Cerebral venous thrombosis of straight sinus
230721009	Cerebral venous thrombosis of sigmoid sinus
230722002	Cerebral venous thrombosis of cortical vein
230723007	Cerebral venous thrombosis of great cerebral 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
230741004	Venous infarction of spinal cord
230745008	Hydrocephalus
230746009	Obstructive hydrocephalus
230747000	Isolated fourth ventricle hydrocephalus
230748005	Intermittently raised pressure hydrocephalus
230749002	Postmeningitic hydrocephalus
230751003	Post-traumatic hydrocephalus
230752005	Hydrocephalus due to cerebrospinal fluid absorption defect
230753000	Hydrocephalus due to cerebrospinal fluid overproduction
230769007	Periventricular leukomalacia
230773005	Spastic cerebral palsy
230780007	Dyskinetic cerebral palsy
230781006	Dystonic/rigid cerebral palsy
230784003	Congenital pseudobulbar palsy
230806005	Brain ventricular shunt infection
230807001	Brain ventricular shunt displacement
230808006	Brain ventricular shunt obstruction
23150001	Proteus syndrome
232036006	Cilioretinal artery occlusion
232059000	Laurence-Moon syndrome
23276006	Ventricular hemorrhage
233718008	Pulmonary tuberous sclerosis
233964008	Internal carotid artery stenosis
233983001	Ruptured cerebral aneurysm
233988005	Carotid artery aneurysm
234142008	Cerebral arteriovenous malformation
234149004	Congenital arteriovenous fistula of brain
23501004	Arginase deficiency
2355008	Rud's syndrome
236529001	Prune belly syndrome with pulmonic stenosis, mental retardation and deafness
23671000119107	Sequela of ischemic cerebral infarction
23728006	Partial bilateral paralysis
23732000	Primary cerebellar degeneration
23740006	Bilateral paralysis of tongue
237612000	Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction
237701005	Pituitary apoplexy
237702003	Pituitary hemorrhage
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
23931000119104	Hydrocephalus due to Arnold Chiari malformation type 2
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
24059009	Acute cerebellar ataxia caused by varicella
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
24654003	Weber-Gubler syndrome
24700007	Multiple sclerosis
2495006	Congenital cerebral arteriovenous aneurysm
249892007	Progressive pseudobulbar palsy
25044007	Neuromyelitis optica
25133001	Completed stroke
253098009	Neural tube defect
253113003	Rachischisis with hydrocephalus
253114009	Myelocele with hydrocephalus
253115005	Hydromyelocele with hydrocephalus
253116006	Fissured spine with hydrocephalus
253118007	Thoracolumbar spina bifida with hydrocephalus - closed
253119004	Hemimyelocele
253120005	Lipomeningocele
253131002	Hydrocephalus associated with late onset aqueduct stenosis
253132009	External hydrocephalus
253133004	Hydrocephalus with anomaly of aqueduct of Sylvius
253136007	Lobar holoprosencephaly
253137003	Alobar holoprosencephaly
253138008	Semi-lobar holoprosencephaly
253139000	Agenesis of corpus callosum with lipoma
253140003	Partial agenesis of corpus callosum
253142006	Atrophy of corpus callosum
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
253172000	Agenesis of cerebellum
253174004	Aplasia of the vermis
253175003	Familial aplasia of the vermis
253176002	Gillespie syndrome
253186001	Chiari malformation type III
253194008	Aneurysm of the vein of Galen
25362006	Phytanic acid storage disease
253699002	Isolation of common carotid artery
254092004	Saldino-Mainzer dysplasia
254243001	Ash leaf spot, tuberous sclerosis
254775002	Bregeat's syndrome
254938000	Astrocytoma of brain
254940005	Oligodendroglioma of brain
254948003	Astrocytoma of spinal cord
254950006	Oligodendroglioma of spinal cord
254955001	Pituitary carcinoma
254969001	Malignant tumor of olfactory tract
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
255112006	Malignant tumor of pituitary and hypothalamus
256321009	Disorder of neuromuscular transmission
257277002	Combined disorder of muscle AND peripheral nerve
25772007	Multi-infarct dementia with delusions
2584003	Cerebral degeneration in childhood
2593002	Dubowitz's syndrome
26015003	Maroteaux-Lamy syndrome, intermediate form
26021000119107	Vertigo as sequela of cerebrovascular disease
26206000	Hepatic coma due to viral hepatitis B
262692002	Burst lobe of brain
262711004	Transection of cervical cord
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
268143001	Spina bifida with hydrocephalus - open
268146009	Spina bifida without hydrocephalus - open
26852004	Primary degenerative dementia of the Alzheimer type, senile onset, with depression
268612007	Senile and presenile organic psychotic conditions
26929004	Alzheimer's disease
26954004	Thrombophlebitis of superior sagittal sinus
27148008	Hereditary motor end-plate disease
271569006	Communicating hydrocephalus
271986005	Disorder of brain ventricular shunt
272202251000119109	Acute cerebrovascular accident due to occlusion of right middle cerebral artery
274100004	Cerebral hemorrhage
275363001	Rupture of superficial cerebral vein
275434003	Stroke in the puerperium
275468009	Congenital quadriplegia
276219001	Occipital cerebral infarction
276220007	Foville syndrome
276221006	Millard-Gubler syndrome
276222004	Top of basilar syndrome
27642008	Dysmorphic sialidosis, congenital form
276594006	Perinatal rupture of superficial cerebral vein
276599001	Cerebral leukomalacia
276706004	Perinatal cerebral ischemia
276722003	Intracerebellar and posterior fossa hemorrhage
276826005	Malignant glioma of brain
276827001	Malignant glioma of spinal cord
276828006	Glioblastoma multiforme of brain
276829003	Glioblastoma multiforme of spinal cord
276836002	Primary cerebral lymphoma
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
277373000	Severe childhood autosomal recessive muscular dystrophy
277461004	Anaplastic astrocytoma of brain
277505007	Medulloblastoma of cerebellum
277526007	Diffuse melanosis of meninges
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
278512001	Ataxic cerebral palsy
278849000	Cerebral atrophy
278855005	Frontal lobe degeneration
278857002	Dementia of frontal lobe type
279982005	Cerebral degeneration presenting primarily with dementia
28055006	West syndrome
281004	Dementia associated with alcoholism
281240008	Extension of cerebrovascular accident
281411007	Spastic diplegia
281560004	Neuroblastoma of brain
281899002	Congenital hydrocephalus caused by toxoplasmosis
28318001	Basilar hemorrhage
28366008	Cerebral arteritis
28394000	Toxic encephalopathy
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
28534004	Spastic paralysis due to intracranial birth injury
285641009	Metastasis to brain of unknown primary
28634005	Cerebral ataxia
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
290621000119101	Cognitive deficit due to and following cerebrovascular disease
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
291511000119103	Spontaneous hemorrhage of deep cerebral hemisphere
291521000119105	Spontaneous hemorrhage of cortical intracerebral hemisphere
291531000119108	Spontaneous hemorrhage of cerebral hemisphere
291541000119104	Spontaneous hemorrhage of brain stem
291571000119106	Spontaneous cerebral hemorrhage
29159009	Familial dysautonomia
291621000119109	Cognitive deficit due to and following nontraumatic subarachnoid hemorrhage
291631000119107	Aphasia due to and following non-traumatic subarachnoid hemorrhage
291665000	Postpartum intrapituitary hemorrhage
291681000119108	Dysphagia due to and following non-traumatic subarachnoid hemorrhage
291711000119109	Cognitive deficit due to and following nontraumatic intracerebral hemorrhage
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
292661000119105	Cerebrovascular accident due to stenosis of right vertebral artery
292671000119104	Cerebrovascular accident due to stenosis of left vertebral artery
292681000119101	Cerebrovascular accident due to occlusion of right vertebral artery
292691000119103	Cerebrovascular accident due to 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
29570005	Leigh's disease
29618004	Striatonigral degeneration
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
2992000	Pigmentary pallidal degeneration
29941000119105	Ataxia as sequela of cerebrovascular disease
29951000119107	Ataxic hemiparesis
30023002	Hydranencephaly
300920004	Carotid atherosclerosis
300992002	Alcohol-induced cerebellar ataxia
301764006	Hematoma of brain
301765007	Cerebellar hematoma
302213007	Caroticocavernous sinus fistula
30278004	Kundrat's syndrome
302878004	Intracranial septic thrombophlebitis
302879007	Septic thrombophlebitis of cavernous sinus
302880005	Septic thrombophlebitis of sagittal sinus
302881009	Septic thrombophlebitis of lateral sinus
302882002	Hydrocephalus associated with congenital aqueduct stenosis
302887008	Neuropathy in secondary amyloidosis
302904002	Infarction of visual cortex
302909007	Diffuse cerebrovascular disease
30400005	Middle meningeal hemorrhage following injury
304603007	Variant Creutzfeldt-Jakob disease
305719002	Neuromyotonia
307212006	Brain ventricular shunt malfunction
307356008	Motor epilepsy
307357004	Jacksonian, focal or motor epilepsy
307359001	Congenital agenesis of brainstem nuclei
307360006	Leucodystrophy without a known biochemical basis
307362003	Intracranial venous septic embolism
307363008	Multiple lacunar infarcts
30753002	Normal pressure hydrocephalus
307649006	Microglioma
307756005	Cerebral palsy, not congenital or infantile, acute
307766002	Left sided cerebral infarction
307767006	Right sided cerebral infarction
308634000	Spinal demyelination
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
312991009	Senile dementia of the Lewy body type
313434001	Residual hemiplegia
315608004	Cardiomyopathy in Duchenne muscular dystrophy
31839002	Myasthenia gravis, adult form
32112006	Phlebitis of inferior sagittal sinus
32162001	Facial hemiplegia
322112361000132104	Epilepsy due to scarring of brain
32680009	Nothnagel's syndrome
32728005	Hemorrhage due to ruptured congenital cerebral aneurysm
32875003	Inhalant-induced persisting dementia
329361000119107	Cerebrovascular accident due to occlusion of right middle cerebral artery by embolus
329371000119101	Cerebrovascular accident due to occlusion of left middle cerebral artery by embolus
329421000119107	Cerebrovascular accident due to occlusion of right posterior cerebral artery by embolus
329431000119105	Cerebrovascular accident due to occlusion of left posterior cerebral artery by embolus
329451000119104	Cerebrovascular accident due to occlusion of right cerebellar artery by embolus
329461000119102	Cerebrovascular accident due to occlusion of left cerebellar artery by embolus
329481000119106	Occlusion of right middle cerebral artery
329491000119109	Occlusion of left middle cerebral artery
329501000119102	Occlusion of bilateral middle cerebral arteries
329541000119100	Occlusion of bilateral anterior cerebral arteries
329561000119101	Occlusion of right posterior cerebral artery
329571000119107	Occlusion of left posterior cerebral artery
329641000119104	Cerebrovascular accident due to thrombus of basilar artery
329651000119102	Cerebrovascular accident due to thrombus of right carotid artery
329671000119106	Traumatic subarachnoid hemorrhage with loss of consciousness
330411000119109	Lacunar ataxic hemiparesis of left nondominant side
330421000119102	Lacunar ataxic hemiparesis of right nondominant side
330791000119108	Cerebrovascular accident due to thrombus of left carotid artery
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
341551000000108	Cerebral degeneration in Parkinson's disease
341801000119101	Occlusion of left central retinal artery
34181000119102	Cerebral infarction due to occlusion of basilar artery
34184002	Corpus callosum syndrome
34191000119104	Cerebral infarction due to vertebral artery occlusion
34209003	Cerebral hemiplegia
3456001	Chronic progressive non-hereditary chorea
346410121000119101	Acute cerebrovascular accident due to thrombosis of left middle cerebral artery
347011000119102	Occlusion of bilateral central retinal arteries
34781003	Vertebral artery syndrome
35145002	Uremic encephalopathy
352818000	Tonic-clonic epilepsy
35386004	Cavernous sinus syndrome
35691006	Combined deficiency of sialidase AND beta galactosidase
359629000	Progressive post hemorrhagic ventricular dilatation
359634001	Infantile posthemorrhagic hydrocephalus
359686005	Van Bogaert's sclerosing leukoencephalitis
36025004	Fibrous skin tumor of tuberous sclerosis
360353005	Thyrotoxicosis due to pituitary thyroid hormone resistance
361000119103	Paralytic syndrome on one side of the body as late effect of cerebrovascular accident
361123003	Psychomotor epilepsy
361272001	Cerebellar ataxia due to alcoholism
361273006	Alcoholic cerebellar degeneration
36179005	Reversible ischemic neurologic deficit syndrome
363235000	Hereditary disorder of nervous system
363467004	Malignant neoplasm of frontal lobe
363468009	Malignant neoplasm of temporal lobe
363469001	Malignant neoplasm of parietal lobe
363470000	Malignant neoplasm of occipital lobe
363471001	Malignant neoplasm of cerebral ventricles
363473003	Malignant neoplasm of brainstem
363474009	Malignant neoplasm of cerebral meninges
363475005	Malignant tumor of spinal cord
363476006	Malignant neoplasm of spinal meninges
363482009	Malignant tumor of pituitary gland
363483004	Malignant tumor of pineal gland
363497007	Malignant tumor of meninges
363498002	Malignant tumor of optic nerve
36803009	Idiopathic generalized epilepsy
3681008	Thrombophlebitis of torcular Herophili
370987005	Anaplastic astrocytoma of spinal cord
371024007	Senile dementia with delusion
371026009	Senile dementia with psychosis
371029002	Ischemic disorder of spinal cord
371040005	Thrombotic stroke
371041009	Embolic stroke
371076006	Congenital syringomyelia
371077002	Ventriculoperitoneal shunt malfunction
371079004	Paraplegic cerebral palsy
371116000	Posthemorrhagic hydrocephalus
371120001	Quadriplegic spinal paralysis
371121002	Neonatal stroke
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
372477008	Post-traumatic syrinx
37340000	Motor neuron disease
37356005	Myoclonic seizure
373587001	Chiari malformation type II
373606000	Occlusive stroke
37650008	Hereditary cerebellar degeneration
37934003	Mitochondrial-lipid-glycogen storage myopathy
37943007	Multiple AND bilateral precerebral artery embolism
37960002	Sanger-Brown cerebellar ataxia
38023001	Locked in syndrome
380941000000104	Progressive encephalopathy with oedema, hypsarrhythmia and optic atrophy syndrome
38116000	Hydromyelocele
38228000	Paralysis of tongue
384993003	Periventricular hemorrhagic venous infarct
38523005	Syphilitic parkinsonism
386766007	Marchiafava-Bignami disease
38742007	Central retinal artery occlusion
387732009	Becker muscular dystrophy
38795005	Sialidosis
389098007	Anoxic encephalopathy
389100007	Ischemic encephalopathy
389101006	Anoxic-ischemic encephalopathy
389271000	Spondyloenchondromatosis with basal ganglia calcification
390936003	Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
39194005	Visual epilepsy
39390005	Niemann-Pick disease, type B
396338004	Metachromatic leucodystrophy
39745004	Chronic progressive epilepsia partialis continua
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
39912006	Hereditary spastic paraplegia
39925003	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
40076141000119107	Acute cerebrovascular accident due to occlusion of left posterior cerebral artery
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
403856000	Port-wine stain in proteus syndrome
40425004	Postconcussion syndrome
40450001	Embolism of superior sagittal sinus
404664002	Malignant optic glioma
404689008	Alternating hemiplegia
4061000119104	Myelomeningocele without hydrocephalus
40632002	Charcot-Marie-Tooth disease, type IA
4069002	Anoxic brain damage during AND/OR resulting from a procedure
40700009	Severe intellectual disability
407573811000119100	Acute cerebrovascular accident due to occlusion of right carotid artery
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
4088009	Acquired hydrocephalus
40946000	Hepatic coma due to viral hepatitis
40980002	Spastic paralysis due to birth injury
410014007	Post-traumatic communicating hydrocephalus
410015008	Post-traumatic non-communicating hydrocephalus
410057002	Hereditary AND/OR degenerative disease of central nervous system
41040004	Complete trisomy 21 syndrome
4113009	Arrested hydrocephalus
41142009	Globoid cell leukodystrophy, late-onset
41283003	Cerebro-oculo-facio-skeletal syndrome
413101007	Stress-induced epilepsy
413102000	Infarction of basal ganglia
413758000	Cardioembolic stroke
414667000	Meningomyelocele
414927004	Ocular myasthenia with strabismus
41574007	Paramyotonia congenita
41590007	Familial amyloid polyneuropathy, Jewish type
416780008	Primary degenerative dementia of the Alzheimer type, presenile onset
416792008	Vein of Galen malformation
416975007	Primary degenerative dementia of the Alzheimer type, senile onset
417017003	Acute cerebellar syndrome
41713005	Benedikt's syndrome
418143002	Cerebral degeneration
4183003	Charcot-Marie-Tooth disease, type IC
42012007	Neuronal ceroid lipofuscinosis
420146005	Cerebral degeneration associated with generalized lipidosis
420244003	Encephalitis associated with acquired immunodeficiency syndrome
420452002	Myelopathy associated with acquired immunodeficiency syndrome
420554003	Progressive multifocal leukoencephalopathy associated with acquired immunodeficiency syndrome
420614009	Organic dementia associated with acquired immunodeficiency syndrome
420675003	Supranuclear gaze palsy
420718004	Central nervous system demyelinating disease associated with acquired immunodeficiency syndrome
420774007	Organic brain syndrome associated with acquired immunodeficiency syndrome
420788006	Intraocular non-Hodgkin malignant lymphoma
421023003	Presenile dementia associated with acquired immunodeficiency syndrome
421283008	Primary lymphoma of brain associated with acquired immunodeficiency syndrome
421315006	Myelitis associated with acquired immunodeficiency syndrome
421415007	Subacute adenoviral encephalitis associated with acquired immunodeficiency syndrome
421529006	Dementia associated with acquired immunodeficiency syndrome
421827003	Encephalopathy associated with acquired immunodeficiency syndrome
421998001	Central nervous disorder associated with acquired immunodeficiency syndrome
422089004	Encephalomyelitis associated with acquired immunodeficiency syndrome
422474003	Partial absence of septum pellucidum
422504002	Ischemic stroke
422513000	Epilepsy, not refractory
422724001	Refractory localization-related epilepsy
422873003	Refractory epilepsia partialis continua
42295001	Familial amyloid polyneuropathy
423144007	Multifactorial encephalopathy
42369001	Pallidopontonigral degeneration
423771003	Acquired neuromuscular ptosis
424099008	Hepatic coma due to acute hepatitis B
424151006	Anaplastic glioma of brain
424276002	Malignant glioma of brainstem
42429001	Cerebromeningeal hemorrhage
424334007	Malignant tumor of spinal cord, intramedullary
424340000	Hepatic coma due to chronic hepatitis B
424549003	Malignant tumor of spinal cord, extramedullary
424761009	Paraneoplastic encephalomyelitis
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
425522009	Hyperammonemic encephalopathy
425687007	Spina bifida aperta of cervical spine
425882004	Paralytic syndrome as late effect of stroke
425932008	Thrombosis of posterior communicating artery
425957003	Non-traumatic intracerebral ventricular hemorrhage
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
426983002	Infarction of medulla oblongata
427020007	Cerebral vasculitis
427216002	Spina bifida aperta of thoracic spine
427296003	Thalamic infarction
427432001	Paralytic syndrome as late effect of thalamic stroke
42769004	Diffuse Lewy body disease with spongiform cortical change
427943001	Ophthalmoplegia due to diabetes mellitus
428061005	Malignant neoplasm of brain
428700003	Primary progressive multiple sclerosis
429033009	Malignant neoplasm of cerebrum
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
431266005	Intraparenchymal hematoma of brain
431421000124103	Arteriosclerosis of carotid artery
432249006	Infarction of spinal cord
432504007	Cerebral infarction
432616009	Infection of ventriculoperitoneal shunt
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
43486001	Hemiplegic cerebral palsy
43532007	Hereditary oculoleptomeningeal amyloid angiopathy
43647007	Juvenile paralysis agitans of Hunt
43658003	Vertebral artery obstruction
438511000	Benign multiple sclerosis
438513002	Cerebral degeneration due to Parkinson's disease
439567002	Malignant multiple sclerosis
43977004	Corticostriatal-spinal degeneration
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
442212003	Residual cognitive deficit as late effect of cerebrovascular accident
442300000	Rhombencephalosynapsis
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
443153007	Inflammation of brain and spinal cord caused by toxic substance
44359008	Metachromatic leukodystrophy, juvenile type
443929000	Small vessel cerebrovascular disease
44395000	Spastic tetraplegia with rigidity syndrome
444024002	Multiple system atrophy, cerebellar variant
444172003	Recurrent transient cerebral ischemic attack
444197004	Multiple system atrophy, Parkinson variant
444657001	Superior cerebellar artery syndrome
444860006	Meningomyelocele of lumbosacral spine
444980006	Sporadic olivopontocerebellar atrophy
445109004	Isolation of left common carotid artery
445166009	Cystic degeneration of brain
445252005	Glucose transporter protein type 1 deficiency syndrome
445349004	Isolation of right common carotid artery
445355009	Refractory epilepsy
445423005	Paraneoplastic subacute necrotic myelopathy
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
447292006	Mitochondrial encephalomyopathy
447351004	Vanishing white matter disease
447378002	Acute paralytic poliomyelitis caused by Human poliovirus 3
4477007	Juvenile myopathy AND lactate acidosis
448045004	Fragile X associated tremor ataxia syndrome
448054001	Adult onset autosomal dominant leukodystrophy
448218008	Malignant neoplasm of cerebellopontine angle
448227009	X-linked periventricular heterotopia
448248006	Malignant neoplasm of axial suprasellar region of brain
448250003	Malignant teratoma of pineal region
448254007	Non-Hodgkin's lymphoma of central nervous system
448314007	Malignant epithelial neoplasm of spinal cord
448863000	Malignant epithelial neoplasm of pineal gland
448989001	Malignant epithelial neoplasm of brain
448995000	Follicular non-Hodgkin's lymphoma of central nervous system
449020009	Intraparenchymal hemorrhage of brain
449221001	Diffuse non-Hodgkin's lymphoma of central nervous system
449253005	Malignant epithelial neoplasm of hypothalamus
449305009	Paraneoplastic sensory neuropathy
449420002	Malignant neoplasm of cerebellum
449901005	Hepatic encephalopathy in fulminant hepatic failure
449902003	Portal systemic encephalopathy
449903008	Dural arteriovenous fistula of spinal cord
450886002	Posterior reversible encephalopathy syndrome
451037005	Hemorrhage in globus pallidus
451038000	Hemorrhage in caudate nucleus
451039008	Hemorrhage in putamen
45502001	Cerebrovascular amyloidosis
45639009	Hereditary cerebral amyloid angiopathy, Icelandic type
45814002	Birnbaum's syndrome
45853006	Roussy-Lévy syndrome
45864009	Senile degeneration of brain
45897005	Jervis' syndrome
460307002	Systemic to pulmonary collateral artery from right carotid artery
460312001	Systemic to pulmonary collateral artery from left carotid artery
460880006	Arteriovenous fistula of great cerebral vein of Galen
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
46421000119102	Behavior disorder as sequela of cerebral infarction
4645000	Senile brain amyloidosis
46583221000119102	Acute cerebrovascular accident due to stenosis of left carotid artery
46659004	Von Hippel-Lindau syndrome
46804001	Severe x-linked myotubular myopathy
46826000	Rheumatic chorea
47032000	Congenital hydrocephalus
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
4817008	Primary degenerative dementia of the Alzheimer type, senile onset, with delirium
48248005	Thrombophlebitis of inferior sagittal sinus
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
48721008	Quadriplegic cerebral palsy
49049000	Parkinson's disease
49422009	Cortical hemorrhage
49562005	Adult chronic GM 2 gangliosidosis
49692006	Schilder's disease
49776008	Centrencephalic epilepsy
49793008	Hereditary motor neuron disease
50122000	Metabolic encephalopathy
502836591000119106	Acute cerebrovascular accident due to occlusion of left carotid artery
50582007	Hemiplegia
508171000000105	Severe learning disability
50866000	Childhood absence epilepsy
509341000000107	Petit-mal epilepsy
50967008	Gangliosidosis
5102002	Agenesis of corpus callosum
5134006	Familial amyloid polyneuropathy, type VI
51399001	Toxic encephalopathy caused by lead
51500006	Complete trisomy 18 syndrome
51928006	General paresis - neurosyphilis
51984006	Dysmorphic sialidosis, infantile form
52165006	Niemann-Pick disease, type A
52186006	Dysmorphic sialidosis
52201006	Internal capsule hemorrhage
52448006	Dementia
52522001	Degenerative brain disorder
5262007	Spinal muscular atrophy
52677002	Deficiency of N-acetylgalactosamine-4-sulfatase
52713000	Infantile neuroaxonal dystrophy
53318002	Spina bifida with hydrocephalus
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
54304004	Progressive bulbar palsy
54364001	Lethal neonatal spasticity
54411001	Peutz-Jeghers syndrome
54502004	Primary degenerative dementia of the Alzheimer type, presenile onset, with delusions
54519002	Basilar artery stenosis
54794009	Ectopic gray matter in centrum ovale
55009008	Primary degenerative dementia of the Alzheimer type, senile onset, with delusions
55016009	Congenital muscular hypertrophy-cerebral syndrome
55051001	Myasthenia gravis, juvenile form
55382008	Cerebral atherosclerosis
55623006	Toxic encephalopathy caused by mercury
55637002	Spinal hemiplegia
55709000	Ethmocephalus
55734000	Endophlebitis of basilar sinus
56155002	Hemispheric cerebral agenesis
56267009	Multi-infarct dementia
56384000	Embolism of inferior sagittal sinus
56453003	Hereditary cerebral amyloid angiopathy, Dutch type
56989000	Eaton-Lambert syndrome
57803009	Rheumatic chorea with heart involvement
57917004	Seckel syndrome
57938005	Congenital myotonia, autosomal dominant form
57981008	Progressing stroke
58193001	Diplegic cerebral palsy
5822000	Athetosis with spastic paraplegia
58258004	Infantile neuronal ceroid lipofuscinosis
58263000	Maroteaux-Lamy syndrome, severe form
58459009	Sphingomyelin/cholesterol lipidosis
58557008	Spina bifida aperta
58756001	Huntington's chorea
58795000	Distal muscular dystrophy
590005	Congenital aneurysm of anterior communicating artery
59103002	Cerebral paralysis with homolateral ataxia
59178007	Menkes kinky-hair syndrome
595899961000119100	Acute cerebrovascular accident of basal ganglia
5963005	Subacute neuronopathic Gaucher's disease
59636002	Pelizaeus-Merzbacher disease, connatal variant
59651006	Sedative, hypnotic AND/OR anxiolytic-induced persisting dementia
60146005	Bailey-Cushing syndrome
60192008	Lethal multiple pterygium syndrome
60389000	Paraplegia
60576007	Subacute combined degeneration of spinal cord
60706008	Phlebitis of torcular Herophili
608874000	Eaton Lambert syndrome with underlying malignancy
60935008	Paramyoclonus multiplex
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
61165007	Hereditary nephrogenic diabetes insipidus
6118003	Demyelinating disease of central nervous system
61200008	Pallidonigroluysian degeneration
61663001	Juvenile neuronal ceroid lipofuscinosis
61687004	Endophlebitis of inferior sagittal sinus
61819007	Rachischisis
62009002	Adult neuronal ceroid lipofuscinosis
6204001	Juvenile myoclonic epilepsy
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
63230211000119103	Acute cerebrovascular accident due to occlusion of left middle cerebral artery
63795001	Thrombosis of intracranial venous sinus of pregnancy AND/OR puerperium
64009001	Basilar artery syndrome
64228003	Paralysis of diaphragm
64383006	Werdnig-Hoffmann disease
64586002	Carotid artery stenosis
64624009	Hypoglycemic encephalopathy
6475002	Primary degenerative dementia of the Alzheimer type, presenile onset, uncomplicated
64764001	Acute paralytic poliomyelitis, bulbar
64775002	Vertebral artery thrombosis
6481005	Diplegia
64855000	Pelizaeus-Merzbacher disease
65017003	Hereditary peripheral neuropathy
65084004	Vertebral artery embolism
65096006	Primary degenerative dementia of the Alzheimer type, presenile onset, with delirium
65120008	Generalized convulsive epilepsy
652287331000119104	Acute cerebrovascular accident of brainstem
65312002	Cerebral arteriosclerosis
65433005	Mechanical complication of ventricular communicating shunt
65587001	Congenital anomaly of cerebrovascular system
65764006	Pseudo-Hurler polydystrophy
6594005	Cerebrovascular disorder in the puerperium
66010009	Supranuclear paralysis
66108005	Primary degenerative dementia of the Alzheimer type, senile onset, uncomplicated
66521008	Deficiency of cerebroside-sulfatase
66751000	Niemann-Pick disease, type C
66881004	Choreoacanthocytosis
67155006	Gerstmann-Straussler-Scheinker syndrome
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
672561000119103	Cognitive deficit due to and following ischemic cerebrovascular accident
672571000119109	Cognitive deficit 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
67761004	Olivopontocerebellar degeneration
67771000119102	Grade 2 astrocytoma of brain
67854007	Maroteaux-Lamy syndrome, mild form
67855008	Niemann-Pick disease, type C, subacute form
67992007	Multiple AND bilateral precerebral artery obstruction
6807001	Central pontine myelinolysis
68107009	Cerebral paresis with homolateral ataxia
68116008	Dentatorubropallidoluysian degeneration
68186003	Congenital myopathy with abnormal subcellular organelles
68390005	Sphingolipid activator protein 1 deficiency
684911000119105	Primary glioblastoma multiforme of frontal lobe
68504005	Ataxia-telangiectasia syndrome
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
690341000119100	Cognitive deficit due to and following embolic cerebrovascular accident
690351000119103	Dysphasia due to and following embolic cerebrovascular accident
69116000	Moyamoya disease
69131009	Spinal ataxia
691461000119103	Acquired cerebral atrophy
693158221000119105	Acute cerebrovascular accident due to stenosis of right carotid artery
69463008	Maroteaux-Lamy syndrome
69482004	Korsakoff's psychosis
69798007	Carotid artery obstruction
697991001	Paralysis of uvula
698021005	Autosomal dominant nocturnal frontal lobe epilepsy
698279003	X-linked dystonia parkinsonism
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
698687007	Post-traumatic dementia with behavioral change
698725008	Dementia associated with neurosyphilis
698726009	Dementia associated with viral encephalitis
698736001	Postoperative communicating hydrocephalus
698737005	Postmeningitic obstructive hydrocephalus
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
698761003	Refractory juvenile myoclonic 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
698954005	Primary degenerative dementia of the Alzheimer type, senile onset in remission
698955006	Primary degenerative dementia of the Alzheimer type, presenile onset in remission
699184009	Perry syndrome
699190008	Paroxysmal extreme pain disorder
699299001	Neuroferritinopathy
699318007	Supratentorial primitive neuroectodermal tumor
699328003	Myoclonic epilepsy myopathy sensory ataxia
699688008	Generalized epilepsy with febrile seizures plus
699706000	Embolism of middle cerebral artery
699866005	Progressive bulbar palsy with sensorineural deafness
700063005	Megalencephaly capillary malformation
700467001	Reversible cerebral vasoconstriction syndrome
70199000	I-cell disease
702314005	Non-spastic cerebral palsy
702315006	Dystonic cerebral palsy
702316007	Choreic cerebral palsy
702317003	Chorea-athetoid cerebral palsy
702318008	Mixed cerebral palsy
702319000	Bilateral cerebral palsy
702320006	Triplegic cerebral palsy
702321005	Pentaplegic cerebral palsy
702323008	Rapid onset dystonia parkinsonism
702326000	Progressive myoclonus epilepsy with ataxia
702327009	Monocarboxylate transporter 8 deficiency
702343002	Early onset myopathy with fatal cardiomyopathy
702344008	Pitt-Hopkins syndrome
702347001	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
702356009	X-linked intellectual disability-psychosis-macroorchidism syndrome
702363009	Cold-induced sweating syndrome
702375004	Familial isolated pituitary adenoma
702376003	Huntington disease-like syndrome
702377007	Hypermanganesemia with dystonia, polycythemia, and cirrhosis
702379005	Hypomyelination and congenital cataract
702382000	Inclusion body myopathy 2
702383005	Distal myopathy 2
702393003	Frontotemporal dementia with gene located on 3p11
702419001	Fatty acid hydroxylase associated neurodegeneration
702421006	Familial encephalopathy with neuroserpin inclusion bodies
702423009	Deafness-dystonia-optic neuronopathy syndrome
702426001	GRN-related frontotemporal dementia
702427005	Hereditary diffuse leukoencephalopathy with spheroids
702429008	Frontotemporal dementia with parkinsonism-17
702433001	Congenital cataracts, facial dysmorphism and neuropathy
702437000	Amish lethal microcephaly
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
702448007	Dystonia 6
702450004	FOXG1 syndrome
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
703156006	Deep hemispheric cerebral hemorrhage
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
703369003	Microcephaly-capillary malformation syndrome
703429003	Malignant optic glioma of adulthood
70350007	Degenerative myelopathy
703522009	Biotin-thiamine-responsive basal ganglia disease
703524005	Spinal muscular atrophy with progressive myoclonic epilepsy
703526007	Progressive epilepsy-intellectual disability syndrome Finnish type
703535000	Mowat-Wilson syndrome
703536004	Megalencephalic leukoencephalopathy with subcortical cysts
703537008	Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation
703542000	Retinal detachment and occipital encephalocele
703543005	Infantile ascending hereditary spastic paralysis
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
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
711158005	Spinocerebellar ataxia type 36
711403001	Cerebral folate transport deficiency
711406009	Autosomal recessive axonal neuropathy with neuromyotonia
711409002	3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome
711482008	Cerebroretinal microangiopathy with calcifications and cysts
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
713060000	Sporadic Creutzfeldt-Jakob disease
713081000	Dissection of cerebral artery
713265001	Nontraumatic ruptured cerebral aneurysm
713325002	Primary cerebral lymphoma co-occurrent with human immunodeficiency virus infection
713327005	Malignant meningioma of meninges of brain
713401006	Combined D-2-hydroxyglutaric aciduria and L-2-hydroxyglutaric aciduria
713425003	Spinal cord compression due to metastasis to spine
713487008	Progressive multifocal leukoencephalopathy co-occurrent with human immunodeficiency virus infection
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
715338007	Fatal infantile lactic acidosis co-occurrent with methylmalonic aciduria
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
715366004	Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1
715369006	Autosomal recessive cerebelloparenchymal disorder type 3
715371006	Cerebellar ataxia co-occurrent with ectodermal dysplasia
715406003	Isolated lissencephaly type 1 without known genetic defect
715415005	Richards-Rundle syndrome
715419004	Lethal congenital contracture syndrome type 2
715422002	Craniotelencephalic dysplasia
715429006	Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome
715434005	Holoprosencephaly craniosynostosis syndrome
715436007	Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration
715462003	Microcephalus co-occurrent with cervical spine fusion anomaly
715463008	Congenital pontocerebellar hypoplasia type 2
715464002	Microcephalus microcornea syndrome of Seemanova type
715465001	Spinocerebellar degeneration co-occurrent with macular corneal dystrophy
715482004	Microcephalic primordial dwarfism of Toriello type
715483009	Olivopontocerebellar atrophy co-occurrent with sensorineural hearing loss
715491000	Autosomal recessive spastic paraplegia type 11
715504003	Spastic paraparesis co-occurrent with deafness
715564000	Paroxysmal dystonic choreoathetosis with episodic ataxia and spasticity
715565004	Lethal arthrogryposis co-occurrent with anterior horn cell disease
715574002	Posterior cortical atrophy syndrome
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
715662009	Iatrogenic Jakob-Creutzfeldt disease
715665006	Hereditary motor and sensory neuropathy Okinawa type
715666007	Charcot-Marie-Tooth disease type IE
715726000	Spinocerebellar ataxia type 7
715737004	Parkinsonism co-occurrent with dementia of Guadeloupe
715748006	Spinocerebellar ataxia type 1
715751004	Spinocerebellar ataxia type 2
715752006	Spinocerebellar ataxia type 6
715753001	Spinocerebellar ataxia type 8
715754007	Spinocerebellar ataxia type 10
715755008	Spinocerebellar ataxia type 4
715768000	Autosomal dominant dopa responsive dystonia
715776003	Spastic paraplegia type 7
715777007	Primary dystonia type 2
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
715807002	Familial Creutzfeldt-Jakob
715817007	Lissencephaly co-occurrent with congenital cerebellar hypoplasia
715819005	Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B
715820004	Lissencephaly co-occurrent with congenital cerebellar hypoplasia type C
715821000	Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D
715822007	Lissencephaly co-occurrent with congenital cerebellar hypoplasia type F
715824008	Spinocerebellar ataxia type 28
715825009	Spinocerebellar ataxia type 29
715826005	Spinocerebellar ataxia type 31
715827001	Autosomal recessive dopa responsive dystonia
715904005	Pineal parenchymal tumor of intermediate differentiation
715951007	Acrocallosal syndrome
715952000	Waardenburg syndrome co-occurrent with Hirschsprung disease
715980003	Encephalopathy due to sulfite oxidase deficiency
715981004	Autosomal recessive primary microcephaly
715984007	Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome
715990006	Agenesis of cerebellum and hydrocephalus syndrome
716023007	Prominent glabella with microcephaly and hypogenitalism syndrome
716051003	Cerebrovascular accident during surgery
716091000	Holoprosencephaly and postaxial polydactyly syndrome
716107009	Early onset parkinsonism and intellectual disability syndrome
716108004	Macrocephaly with spastic paraplegia and dysmorphism syndrome
716112005	Microcephaly with deafness and intellectual disability syndrome
716169009	Holoprosencephaly sequence with hypokinesia and congenital joint contracture syndrome
716198008	Growth delay with hydrocephalus and lung hypoplasia syndrome
716200002	Nephrogenic diabetes insipidus and intracranial calcification syndrome
716233007	Steinfeld syndrome
716243005	Deafness with malformation of ear and facial palsy syndrome
716278005	Jeavons syndrome
716281000	Primary progressive non fluent aphasia
716335003	Congenital suprabulbar paresis
716380002	Logopenic progressive aphasia
716662004	Autosomal dominant late onset Parkinson disease
716664003	Primary dystonia 21
716667005	Right temporal atrophy variant frontotemporal dementia
716696006	Autosomal dominant centronuclear myopathy
716706009	Female restricted epilepsy with intellectual disability syndrome
716724006	Spinocerebellar ataxia type 15/16
716745004	Livedo reticularis and cerebrovascular accident syndrome
716994006	Behavioral variant of frontotemporal dementia
716996008	Hypoplasia of corpus callosum and mental retardation with adducted thumbs and spasticity and hydrocephalus syndrome
716997004	Joubert syndrome
716998009	Joubert syndrome with ocular defect
716999001	Joubert syndrome with renal defect
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
717052002	Maternally inherited Leigh syndrome
717054001	Maternally inherited mitochondrial dystonia
717185008	Deficiency of leukotriene C4 synthase
717223008	X-linked epilepsy with learning disability and behavior disorder syndrome
717225001	Benign adult familial myoclonic epilepsy
717266001	Sensory ataxic neuropathy with dysarthria and ophthalmoparesis syndrome
717276003	Folinic acid responsive seizure syndrome
717332007	Cerebellar ataxia Cayman type
717632002	X-linked lissencephaly with agenesis of corpus callosum and genital anomaly syndrome
71779008	X-linked hydrocephalus syndrome
717812000	Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome
717822006	Goldberg Shprintzen megacolon syndrome
717825008	Hereditary sensory and autonomic neuropathy type 1B
717826009	Hereditary sensory and autonomic neuropathy with deafness and global delay
717827000	Hereditary sensory and autonomic neuropathy with spastic paraplegia
717859007	Hydrocephalus, cardiac malformation, dense bone syndrome
717942003	Brain dopamine-serotonin vesicular transport disease
717943008	Brain malformation, congenital heart disease, postaxial polydactyly syndrome
717964007	Juvenile primary lateral sclerosis
717968005	Melanoma and neural system tumor syndrome
717977003	Lissencephaly syndrome Norman Roberts type
718103001	Hereditary geniospasm
718174008	Infantile striatonigral degeneration
718176005	Autosomal recessive limb girdle muscular dystrophy type 2C
718177001	Autosomal recessive limb girdle muscular dystrophy type 2F
718179003	Autosomal recessive limb girdle muscular dystrophy type 2B
718180000	Autosomal recessive limb girdle muscular dystrophy type 2I
718182008	Combined pituitary hormone deficiency genetic form
718210003	Deficiency of monoamine oxidase A
718212006	Mitochondrial encephalocardiomyopathy due to transmembrane protein 70 mutation
718214007	Mitochondrial neurogastrointestinal encephalomyopathy syndrome
718219002	Congenital lactic acidosis Saguenay-Lac-Saint-Jean type
718221007	Behr syndrome
71831005	Symptomatic generalized epilepsy
718551002	Moyamoya disease with early onset achalasia
718555006	Juvenile amyotrophic lateral sclerosis
718556007	Cranio-cerebello-cardiac dysplasia syndrome
718572004	Bethlem myopathy
718573009	Achalasia microcephaly syndrome
718576001	Hydrocephalus with cleft palate and joint contracture syndrome
718605009	Congenital pontocerebellar hypoplasia type 7
718606005	Congenital pontocerebellar hypoplasia type 6
718607001	Congenital pontocerebellar hypoplasia type 5
718608006	Congenital pontocerebellar hypoplasia type 4
718609003	Congenital pontocerebellar hypoplasia type 3
718610008	Congenital pontocerebellar hypoplasia type 1
718611007	Congenital pontocerebellar hypoplasia type 8
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
718752007	Episodic ataxia type 7
718753002	Episodic ataxia type 6
718754008	Episodic ataxia type 4
718755009	Episodic ataxia type 3
718756005	Episodic ataxia type 5
718759003	Lissencephaly due to tubulin alpha 1A mutation
718769009	Spinocerebellar ataxia type 26
718770005	Spinocerebellar ataxia type 25
718771009	Spinocerebellar ataxia type 20
718772002	Spinocerebellar ataxia type 23
718774001	Spinocerebellar ataxia type 21
718847005	X-linked neurodegenerative syndrome Hamel type
718849008	X-linked neurodegenerative syndrome Bertini type
718850008	Autosomal recessive limb girdle muscular dystrophy type 2E
719021005	DK phocomelia syndrome
719043002	Vertebral abnormality, anal atresia, cardiac abnormality, tracheo-esophageal fistula, renal anomaly, limb defect syndrome with hydrocephalus
719069008	Shprintzen Goldberg craniosynostosis syndrome
719103009	Autosomal recessive spastic paraplegia type 39
719136005	X-linked intellectual disability with cerebellar hypoplasia syndrome
719139003	X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizure syndrome
719140001	X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome
719164000	Symmetrical thalamic calcification
719205008	Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome
719207000	Spinocerebellar ataxia type 11
719208005	Spinocerebellar ataxia type 12
719209002	Spinocerebellar ataxia type 13
719210007	Spinocerebellar ataxia type 14
719249005	Spinocerebellar ataxia type 17
719250005	Spinocerebellar ataxia type 18
719251009	Spinocerebellar ataxia type 19
719252002	Spinocerebellar ataxia type 27
719253007	Spinocerebellar ataxia type 30
719254001	Spinocerebellar ataxia type 32
719255000	Spinocerebellar ataxia type 34
719267003	Progressive cavitating leukoencephalopathy
719276005	Primary dystonia type 4
719278006	Primary dystonia type 13
719300001	Spinocerebellar ataxia type 35
719301002	Spinocerebellar ataxia type 37
719302009	Spinocerebellar ataxia type 5
719377004	Microcephalus with albinism and digital anomaly syndrome
719378009	Microcephalus with brachydactyly and kyphoscoliosis syndrome
719379001	Microcephalus with cardiac defect and lung malsegmentation syndrome
719380003	Microcephalus cardiomyopathy syndrome
719394002	Microcephalus cleft palate syndrome
719395001	Microcephalus facio-cardio-skeletal syndrome Hadziselimovic type
719403003	Leukoencephalopathy co-occurrent with bilateral anterior temporal lobe cysts
719405005	Leukoencephalopathy with metaphyseal chondrodysplasia syndrome
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
719516000	Autosomal dominant focal dystonia DYT25 type
719717006	Psychosis co-occurrent and due to Parkinson's disease
719810000	X-linked intellectual disability with seizure and psoriasis syndrome
719815005	X-linked myopathy with excessive autophagy
719816006	X-linked sideroblastic anemia with spinocerebellar ataxia
719817002	X-linked spinocerebellar ataxia type 3
719818007	X-linked spinocerebellar ataxia type 4
719819004	Xeroderma pigmentosum and Cockayne syndrome complex
719824001	Vici syndrome
719826004	X-linked intellectual disability with acromegaly and hyperactivity syndrome
719833004	Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome
719836007	X-linked distal arthrogryposis multiplex congenita
719838008	X-linked hereditary sensory and autonomic neuropathy with deafness
7199000	Tuberous sclerosis syndrome
719947004	Craniofacial dysmorphism with coloboma of eye and corpus callosum agenesis 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
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
720010009	Microphthalmia with brain atrophy syndrome
720410001	Acrootoocular syndrome
720466001	Adult-onset dystonia parkinsonism
720494009	Anonychia with microcephaly syndrome
720498007	Aphalangy and syndactyly with microcephaly syndrome
720517001	Ataxia with deafness and intellectual disability syndrome
720518006	Athabaskan brainstem dysgenesis 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
720576001	Brain calcification Rajab type
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
720750004	Spinocerebellar degeneration and corneal dystrophy syndrome
720809000	Dissection of external carotid artery
720813007	Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome
720815000	Capra DeMarco syndrome
720816004	Craniosynostosis and intracranial calcification syndrome
720819006	Curry Jones syndrome
720825005	Cystic leukoencephalopathy without megalencephaly
720830009	Neuronal ceroid lipofuscinosis due to deficiency of cathepsin D
720852000	Cervical hypertrichosis and peripheral neuropathy syndrome
720855003	Cerebrooculonasal syndrome
720864008	Encephalopathy due to prosaposin deficiency
720954000	Filippi syndrome
721008000	Hall Riggs syndrome
721015008	Hydrocephalus with endocardial fibroelastosis and cataract syndrome
721072003	Short stature, pituitary and cerebellar defect and small sella turcica syndrome
721088003	Developmental delay, epilepsy, neonatal diabetes syndrome
721092005	Developmental malformation, deafness, dystonia syndrome
721165001	Variably protease sensitive prionopathy
721207002	Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome
721219005	Familial Alzheimer-like prion disease
721221000	Hirschsprung disease with deafness and polydactyly syndrome
721222007	Hirschsprung disease with type D brachydactyly syndrome
721223002	Hirschsprung disease with nail hypoplasia and dysmorphism
721228006	Huntington disease-like 2
721229003	Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome
721231007	Hydrocephalus with obesity and hypogonadism syndrome
721255002	Acquired prion disease
721297008	Galloway Mowat syndrome
721842008	Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome
721843003	Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome
721846006	Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome
721847002	Joubert syndrome with congenital hepatic fibrosis
721862000	Joubert syndrome with oculorenal defect
721873007	Joubert syndrome with orofaciodigital defect
721903007	Microcephaly, hypogammaglobulinemia, abnormal immunity syndrome
721974000	Lowry MacLean syndrome
721975004	Epiphyseal dysplasia, microcephalus, nystagmus syndrome
721979005	Lymphedema and cerebral arteriovenous anomaly syndrome
722004001	Agenesis of internal carotid artery
722006004	Isotretinoin embryopathy-like syndrome
722033000	Macrocephaly, short stature, paraplegia syndrome
722036008	Megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome
722055008	Oculopalatocerebral syndrome
722056009	Oculocerebrofacial syndrome Kaufman type
722064003	Odontoleukodystrophy
722110003	Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome
722201004	Median cleft of upper lip, corpus callosum lipoma, cutaneous polyp syndrome
722209002	Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome
722212004	Severe X-linked mitochondrial encephalomyopathy
722213009	Severe X-linked intellectual disability Gustavson type
722281001	Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome
722282008	Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome
722283003	Agnathia, holoprosencephaly, situs inversus syndrome
722293005	Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome
722294004	Autosomal dominant intermediate Charcot-Marie-Tooth disease type E
722377004	Paraganglioma and gastric stromal sarcoma syndrome
722380003	Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome
722381004	Congenital cataract, nephropathy, encephalopathy syndrome
722385008	Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma syndrome
722386009	Celiac disease with epilepsy and cerebral calcification syndrome
722389002	Congenital hereditary facial paralysis with variable hearing loss syndrome
722390006	Congenital intrauterine infection-like syndrome
722432000	Duane anomaly, myopathy, scoliosis syndrome
722435003	Dystonia 16
722451006	Gomez Lopez Hernandez syndrome
722453009	Cutaneous mastocytosis, short stature, hearing loss syndrome
722455002	Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome
722456001	Intellectual disability, developmental delay, contracture syndrome
722488009	Neurodegeneration due to 3-hydroxyisobutyryl coenzyme A hydrolase deficiency
722493007	Familial caudal dysgenesis
722599008	Parkinsonism due to hereditary spastic paraplegia
722600006	Non-amnestic Alzheimer disease
722601005	White matter disorder caused by infection
722602003	White matter disorder caused by toxin
722615007	Focal hemorrhagic contusion of cerebrum
722633001	Multiple traumatic hemorrhages of brain tissue
722671009	Metastatic malignant neoplasm of meninges
722718001	Primary malignant meningioma
722762005	Ganglioside GM3 synthase deficiency
722763000	Infantile dystonia parkinsonism
722929005	Perinatal arterial ischemic stroke
722966004	Chorea due to heredodegenerative disorder
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
722985001	Acute venous infarction of spinal cord
722986000	Chronic venous infarction of spinal cord
722987009	Amyotrophic lateral sclerosis plus syndrome
722992006	Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi
722997000	Inherited autonomic nervous system disorder
723082006	Silent cerebral infarct
723083001	Late effects of cerebral ischemic stroke
723084007	Sequela of non-traumatic intracerebral hemorrhage
723123001	Ischemic vascular dementia
723124007	Primary progressive apraxia of speech
723125008	Epileptic encephalopathy
723151005	Permanent vegetative state
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
723307008	Ethylmalonic encephalopathy
723308003	Epidermolysis bullosa simplex with muscular dystrophy
723309006	Endocrine-cerebro-osteodysplasia syndrome
723359002	Familial acute necrotizing encephalopathy
723366001	Macrostomia, preauricular tag, external ophthalmoplegia syndrome
723390000	Rapidly progressive dementia
723404002	Microcephalic osteodysplastic dysplasia Saul Wilson type
723405001	Microlissencephaly micromelia syndrome
723441001	Non-progressive cerebellar ataxia with intellectual disability
723452007	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome
723497003	Peripheral neuropathy with sensorineural hearing impairment syndrome
723501008	Renier Gabreels Jasper syndrome
723557004	Thiamine-responsive encephalopathy
723612001	Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome
723621000	Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome
723622007	X-linked spastic paraplegia type 2
723675006	Sialidosis type 1
723676007	Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome
723819007	Autosomal dominant spastic paraplegia type 36
723820001	Autosomal dominant spastic paraplegia type 4
723821002	Autosomal recessive spastic paraplegia type 44
723822009	Autosomal recessive spastic paraplegia type 46
723823004	Autosomal recessive spastic paraplegia type 53
723824005	Autosomal recessive spastic paraplegia type 54
723825006	Autosomal recessive spastic paraplegia type 55
723826007	Autosomal recessive spastic paraplegia type 57
723830005	Keratosis follicularis, dwarfism, cerebral atrophy syndrome
723857007	Silent micro-hemorrhage of brain
723992000	Kufor Rakeb syndrome
723999009	Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome
724002003	Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome
724065003	Autosomal recessive posterior column ataxia and retinitis pigmentosa
724067006	Permanent neonatal diabetes mellitus with cerebellar agenesis syndrome
724091002	Neuroectodermal melanolysosomal disease
724097003	Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome
724138007	Mitochondrial myopathy with sideroblastic anemia syndrome
724141003	Microcephalic primordial dwarfism due to zinc finger protein 335 deficiency
724146008	Metaphyseal chondromatosis co-occurrent with D-2 hydroxyglutaric aciduria
724172004	McLeod neuroacanthocytosis syndrome
724207001	Kleefstra syndrome
724226009	Infantile osteopetrosis with neuroaxonal dysplasia syndrome
724227000	Infantile onset spinocerebellar ataxia
724228005	Infantile choroidocerebral calcification syndrome
724283004	Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum
724349009	Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome
724351008	Hereditary hyperekplexia
724357007	Hereditary cerebral hemorrhage with amyloidosis
724385009	Growth delay due to insulin-like growth factor type 1 deficiency
724424009	Cerebral ischemic stroke due to small artery occlusion
724425005	Cerebral ischemic stroke due to intracranial large artery atherosclerosis
724426006	Cerebral ischemic stroke due to extracranial large artery atherosclerosis
724427002	Asymptomatic stenosis of intracranial artery
724428007	Asymptomatic stenosis of extracranial artery
724429004	Stroke co-occurrent with migraine
724549005	Epilepsy due to infectious disease of central nervous system
724565006	White matter disorder due to nutritional deficiency
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
724764007	Chorea co-occurrent and due to Huntington disease-like condition
724765008	Chorea co-occurrent and due to dentatorubropallidoluysian degeneration
724766009	Chorea co-occurrent and due to Wilson disease
724769002	Ataxia co-occurrent and due to phytanic acid storage disease
724775006	X-linked hereditary spastic paraplegia
724776007	Dementia due to disorder of central nervous system
724777003	Dementia due to infectious disease
724778008	Progressive relapsing multiple sclerosis
724779000	White matter disorder co-occurrent and due to cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
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
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
724988000	Epilepsy co-occurrent and due to degenerative brain disorder
724989008	Epilepsy co-occurrent and due to mesial temporal sclerosis
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
725001004	Idiopathic syringomyelia
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
725132001	Ischemic stroke without residual deficits
725139005	Spastic paraplegia, optic atrophy, neuropathy syndrome
725146001	Atypical juvenile parkinsonism
725163002	X-linked spasticity, intellectual disability, epilepsy syndrome
725296006	Mucolipidosis type IV
725392005	Autosomal dominant striatal neurodegeneration
725394006	Autosomal recessive ataxia due to ubiquinone deficiency
725408001	Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2
725413002	Febrile infection related epilepsy syndrome
725420009	Congenital muscular dystrophy Paradas type
725433003	Autosomal recessive cerebellar ataxia Beauce type
725461009	Microcephalic osteodysplastic primordial dwarfism types I and III
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
726606003	Autosomal recessive spastic paraplegia type 32
726607007	Autosomal recessive spastic paraplegia type 26
726608002	Autosomal recessive spastic paraplegia type 23
726609005	Autosomal recessive spastic paraplegia type 64
726610000	Autosomal recessive spastic paraplegia type 63
726611001	Autosomal recessive spastic paraplegia type 61
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
726622002	Spastic paraplegia with Paget disease of bone syndrome
726669007	Central nervous system calcification, deafness, tubular acidosis, anemia syndrome
726702005	Epileptic encephalopathy with global cerebral demyelination
726704006	Cataract, congenital heart disease, neural tube defect syndrome
72836002	Hepatic coma
73020009	Cerebral hemisphere hemorrhage
73173006	Spasm of cerebral arteries
73192008	Multiple AND bilateral precerebral artery stenosis
732245008	Pure mitochondrial myopathy
732246009	X-linked intellectual disability, limb spasticity, retinal dystrophy, diabetes insipidus syndrome
732251003	Cortical blindness, intellectual disability, polydactyly syndrome
732261005	Cyprus facial neuromusculoskeletal syndrome
732264002	Coenzyme A synthase protein associated neurodegeneration
732923001	Hemorrhage of medulla oblongata
732926009	Hydrocephalus, tall stature, joint laxity syndrome
732927000	Split hand, obstructive uropathy, spina bifida, diaphragmatic defect syndrome
732929002	Autosomal recessive limb girdle muscular dystrophy type 2S
732930007	Autosomal recessive limb girdle muscular dystrophy type 2T
732932004	Autosomal recessive spastic paraplegia type 18
732933009	Autosomal recessive spastic paraplegia type 25
732948003	Autosomal dominant spastic paraplegia type 10
732949006	Autosomal dominant spastic paraplegia type 6
732951005	Mitochondrial myopathy, lactic acidosis, deafness syndrome
732958004	Spastic paraplegia with precocious puberty syndrome
732959007	Beta-propeller protein-associated neurodegeneration
73297009	Muscular dystrophy
733028000	Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome
733029008	Autosomal dominant spastic paraplegia type 29
733031004	Epilepsy, microcephaly, skeletal dysplasia syndrome
733032006	Epilepsy telangiectasia syndrome
733033001	Spinocerebellar ataxia dysmorphism syndrome
733044009	Dermatoleukodystrophy
733049004	Encephalopathy, intracerebral calcification, retinal degeneration syndrome
733065003	Myoclonus, cerebellar ataxia, deafness syndrome
733068001	Absent tibia, polydactyly, arachnoid cyst syndrome
733071009	Deafness, small bowel diverticulosis, neuropathy syndrome
733072002	Alaninuria, microcephaly, dwarfism, enamel hypoplasia, diabetes mellitus syndrome
733082001	Early-onset Lafora body disease
733086003	Pseudoprogeria syndrome
733089005	Spastic paraplegia, nephritis, deafness syndrome
733091002	Isolated hereditary congenital facial paralysis
733092009	Microcephalus, hypergonadotropic hypogonadism, short stature syndrome
733094005	Dandy-Walker malformation with postaxial polydactyly syndrome
733096007	Thyrocerebrorenal syndrome
733113002	Hypogonadotropic hypogonadism retinitis pigmentosa syndrome
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
733193001	Dementia co-occurrent and due to progressive multifocal leukoencephalopathy
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
733417008	Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome
733418003	Joubert syndrome with Jeune asphyxiating thoracic dystrophy
733422008	Prion protein systemic amyloidosis
733452000	Leukoencephalopathy, dystonia, motor neuropathy syndrome
733455003	Spastic paraplegia, glaucoma, intellectual disability syndrome
733469003	Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome
733472005	Microcephalus, glomerulonephritis, marfanoid habitus 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
733604003	Microcephalus, lymphedema, chorioretinopathy syndrome
733623005	Autism spectrum disorder, epilepsy, arthrogryposis syndrome
733630004	Deficiency of alpha-ketoglutarate dehydrogenase
733636005	3-phosphoglycerate dehydrogenase deficiency juvenile form
733637001	3-phosphoglycerate dehydrogenase deficiency infantile 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
734020000	Spinocerebellar ataxia type 40
734021001	Spinocerebellar ataxia type 38
734023003	Sporadic adult-onset ataxia of unknown etiology
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
73495003	Dyssynergia cerebellaris myoclonica
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
735206008	Communicating hydrocephalus due to and following traumatic hemorrhage
735421004	Leukoencephalopathy with brain stem and spinal cord involvement and high lactate syndrome
735556002	Abscess of corpus callosum
735749005	Myelomeningocele co-occurrent with hydrocephalus
735757008	Primary ganglioneuroblastoma of brain
73663008	Neurologic xeroderma pigmentosum
737159004	Aneurysm of basilar artery
737160009	Dissection of basilar artery
737227004	Autosomal dominant hereditary spastic paraplegia
737228009	Progressive focal cortical atrophy
737229001	White matter disorder due to vascular abnormality
737230006	White matter disorder due to ischemia
737231005	Traumatic hemorrhage of thalamus
737232003	Traumatic hemorrhage of basal ganglia
7379000	Pseudobulbar palsy
738211801000119107	Acute cerebrovascular accident due to thrombosis of right middle cerebral artery
738478141000119101	Acute cerebrovascular accident due to occlusion of right cerebellar artery
73935008	Toxic encephalopathy caused by hydroxyquinoline
74073002	Cerebellar hemangioblastomatosis
74267005	Toxic encephalopathy caused by carbon tetrachloride
74351001	Reye's syndrome
75019001	Athetoid cerebral palsy
75023009	Post-traumatic epilepsy
75038005	Cerebellar hemorrhage
75046006	Combined pyramidal-extrapyramidal syndrome
75072002	Nemaline myopathy
751371000000107	Personal history of transient ischaemic attack
75138007	Endophlebitis of superior sagittal sinus
75143000	Toxic encephalitis caused by thallium
75299005	Spastic spinal syphilitic paralysis
75491005	Amyotrophia congenita
75543006	Cerebral embolism
758664007	Isolated follicle stimulating hormone deficiency
75968004	Sotos' syndrome
76043009	Hereditary sensory-motor neuropathy, type V
76156000	Juvenile cerebellar degeneration AND myoclonus
762005171000119101	Acute cerebrovascular accident due to ischemia
762295002	Congenital obstructive hydrocephalus
762297005	White matter disorder due to vitamin B12 deficiency
762350007	Dementia due to prion disease
762351006	Dementia due to and following injury of head
762352004	Demyelination due to systemic vasculitis
762457009	Astroblastoma of brain
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
763068005	Autosomal dominant spastic paraplegia type 31
763069002	Autosomal dominant spastic paraplegia type 41
763070001	Autosomal dominant spastic paraplegia type 42
763130006	Cleft palate, large ears, small head syndrome
763135001	Charcot-Marie-Tooth disease type 4E
763136000	Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome
763312008	Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome
763314009	Congenital muscular dystrophy with hyperlaxity
763315005	Congenital myopathy with myasthenic-like onset
763344007	Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome
763345008	Charcot-Marie-Tooth disease type 4B3
763347000	X-linked Charcot-Marie-Tooth disease type 6
763348005	Autosomal recessive cerebellar ataxia with late-onset spasticity
763349002	Progressive myoclonic epilepsy with dystonia
763350002	Intellectual disability, obesity, brain malformation, facial dysmorphism syndrome
763351003	Spectrin-associated autosomal recessive cerebellar ataxia
763352005	Familial dyskinesia and facial myokymia
763366000	Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome
763367009	Autosomal recessive spastic paraplegia type 48
763369007	Autosomal dominant spastic paraplegia type 37
763370008	X-linked spastic paraplegia type 34
763373005	Autosomal recessive spastic paraplegia type 5A
763374004	Autosomal dominant spastic paraplegia type 12
763375003	Autosomal dominant spastic paraplegia type 19
763376002	Autosomal recessive spastic paraplegia type 28
763377006	Autosomal spastic paraplegia type 30
763400005	X-linked Charcot-Marie-Tooth disease type 4
763402002	Spastic paraplegia, neuropathy, poikiloderma syndrome
763403007	Spastic paraplegia, facial cutaneous lesion syndrome
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
763688008	Deafness, encephaloneuropathy, obesity, valvulopathy syndrome
763715007	Familial hyperprolactinemia
763718009	Finnish upper limb onset distal myopathy
763721006	Hypermethioninemia encephalopathy due to deficiency of adenosine kinase
763722004	Hypotonia, speech impairment, severe cognitive delay syndrome
763743003	Intellectual disability, spasticity, ectrodactyly syndrome
763770005	Familial myoclonus of cerebral cortex
763776004	Kelch like family member 9 related early-onset distal myopathy
763797003	Agenesis of corpus callosum and abnormal genitalia syndrome
763798008	Microcephalus, complex motor and sensory axonal neuropathy syndrome
763802009	Micturition induced epilepsy
763821001	Porencephaly, cerebellar hypoplasia, internal malformations syndrome
763827002	Orgasm induced epilepsy
763829004	Oculopharyngodistal myopathy
763837007	Oro-facial digital syndrome type 14
763861000	Pachygyria, intellectual disability, epilepsy syndrome
763895001	Myosclerosis
76402003	Carotid artery insufficiency syndrome
764095005	Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome
764453009	Action myoclonus renal failure syndrome
764456001	Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency
764522009	Familial focal epilepsy with variable foci
764525006	Cylindrical spirals myopathy
764686003	Autosomal recessive spastic paraplegia type 15
764688002	Autosomal recessive spastic paraplegia type 35
764730007	Autosomal dominant Charcot-Marie-Tooth disease type 2 due to kinesin family member 5A mutation
764732004	Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome
764733009	Progressive external ophthalmoplegia, myopathy, emaciation syndrome
764734003	Autosomal recessive spastic paraplegia type 21
764736001	Autosomal recessive spastic paraplegia type 43
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
764959000	Intellectual disability, myopathy, short stature, endocrine defect syndrome
764962002	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1
765045003	Autosomal recessive spastic paraplegia type 62
765046002	Autosomal dominant Charcot-Marie-Tooth disease type 2U
765047006	SURF1, cytochrome c oxidase assembly factor related Charcot-Marie-Tooth disease type 4
765089003	Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome
765091006	Spinocerebellar ataxia with axonal neuropathy type 1
765093009	Rolandic epilepsy, speech dyspraxia syndrome
765100000	Ribonucleotide reductase regulatory TP53 inducible subunit M2B-related mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form with renal tubulopathy
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
765401006	Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form
765403009	F-box and leucine rich repeat protein 4 related mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form
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
765753004	Autosomal recessive spastic paraplegia type 45
765758008	Microcephalic primordial dwarfism Montreal type
766032007	Holoprosencephaly, ectrodactyly, cleft lip, cleft palate syndrome
766044005	Acute encephalopathy with biphasic seizures and late reduced diffusion
766246000	Marburg acute multiple sclerosis
766251006	Lethal infantile mitochondrial myopathy
76628006	Post-hemiplegic chorea
76670001	Duchenne muscular dystrophy
766752000	Neurolymphomatosis
766753005	Nijmegen breakage syndrome-like disorder
766764008	X-linked distal spinal muscular atrophy type 3
766767001	Autosomal recessive spastic paraplegia type 67
766814006	Autosomal recessive cerebellar ataxia with saccadic intrusion syndrome
766815007	Perioral myoclonia with absences
766818009	X-linked non progressive cerebellar ataxia
766871009	Diencephalic mesencephalic junction dysplasia
766931003	Hypomyelination neuropathy arthrogryposis syndrome
766977007	Severe early-onset axonal neuropathy due to mitofusin 2 deficiency
766987006	Moebius syndrome
767254005	Recurrent benign focal seizures of childhood
767448007	Pineoblastoma
768473009	Purine rich element binding protein A syndrome
768553002	Hypermanganesemia with dystonia
768554008	Hypermanganesemia with dystonia 2
768555009	5q31.3 microdeletion syndrome
768556005	Ataxia pancytopenia syndrome
768663003	Leukoencephalopathy with mild cerebellar ataxia and white matter edema
768666006	Syntaxin binding protein 1 encephalopathy with epilepsy
76880004	Angelman syndrome
769065000	Tubulin beta 4A class IVa related leukodystrophy
77015008	Crossed hemiplegia
770404004	Autosomal recessive chorioretinopathy and microcephaly syndrome
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
770564004	Microcephalic primordial dwarfism Alazami type
770565003	Microcephalic primordial dwarfism Dauber type
770596007	Rippling muscle disease with myasthenia gravis
770604006	X-linked cerebral, cerebellar, coloboma syndrome
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
770628008	Diffuse leptomeningeal melanocytosis
770630005	Distal hereditary motor neuropathy type 1
770643005	Mesial temporal lobe epilepsy with hippocampal sclerosis
770655004	Microcephalus, brain defect, spasticity, hypernatremia syndrome
770678005	Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome
770683002	Secondary syringomyelia
770720005	Autosomal recessive spastic paraplegia type 58
770721009	Microcephaly, thin corpus callosum, intellectual disability syndrome
770722002	Proximal myopathy with extrapyramidal signs
770723007	Optic atrophy, intellectual disability syndrome
770724001	Autosomal recessive spastic paraplegia type 70
770725000	Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
770727008	Spinal muscular atrophy with respiratory distress type 2
770751003	Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome
770755007	Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome
770757004	X-linked parkinsonism with spasticity syndrome
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
770898002	Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency
770939009	Huntington disease-like 3
770941005	Alopecia, progressive neurological defect, endocrinopathy syndrome
77097004	Oculopharyngeal muscular dystrophy
771074000	Microcephaly, short stature, intellectual disability, facial dysmorphism syndrome
771081007	Distal hereditary motor neuropathy type 7
771141002	Benign partial epilepsy with secondarily generalized seizures in infancy
771142009	Cortical dysplasia with focal epilepsy syndrome
771143004	Hereditary motor and sensory neuropathy type 5
771144005	Hereditary motor and sensory neuropathy with acrodystrophy
771146007	Holoprosencephaly with caudal dysgenesis syndrome
771147003	Isolated arhinencephaly
771148008	X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome
771179007	Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome
771184001	Leukoencephalopathy, palmoplantar keratoderma syndrome
771223000	Infantile epileptic dyskinetic encephalopathy
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
7713009	Intrapontine hemorrhage
771302009	Autosomal recessive lower motor neuron disease with childhood onset
771303004	Severe neonatal onset encephalopathy with microcephaly
771304005	Benign nocturnal alternating hemiplegia of childhood
771305006	Progressive polyneuropathy with bilateral striatal necrosis
771307003	Charcot-Marie-Tooth disease type 2B5
771308008	Non-acquired combined pituitary hormone deficiency, sensorineural hearing loss, spine abnormalities syndrome
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
771469002	Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome
771470001	Jawad syndrome
771471002	Optic nerve edema, splenomegaly syndrome
771475006	Young adult-onset distal hereditary motor neuropathy
771476007	Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome
771509001	Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial deoxyribonucleic acid mutation
771514002	Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome
771516000	Solute carrier family 35 member A2 congenital disorder of glycosylation
772129007	Autosomal dominant childhood-onset proximal spinal muscular atrophy
772224009	Warburg micro syndrome
772225005	RAB18, member RAS oncogene family deficiency
773230003	Cyclin-dependent kinase-like 5 deficiency
773280009	Hydrocephalus, blue sclera, nephropathy syndrome
773305003	Microcephaly, polymicrogyria, corpus callosum agenesis syndrome
773306002	Congenital lethal myopathy Compton North type
773307006	Zechi Ceide syndrome
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
773394007	Autosomal recessive frontotemporal pachygyria
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
773425000	Autosomal recessive spastic paraplegia type 59
773492007	Childhood-onset spasticity with hyperglycinemia
773497001	Partial corpus callosum agenesis, cerebellar vermis hypoplasia with posterior fossa cysts syndrome
773498006	Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency
773548008	Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome
773554009	THO complex 6-related developmental delay, microcephaly, facial dysmorphism syndrome
773555005	Severe neurodegenerative syndrome with lipodystrophy
773610007	Chudley McCullough syndrome
773627004	Porencephaly, microcephaly, bilateral congenital cataract syndrome
773643006	Multiple congenital anomalies, hypotonia, seizures syndrome type 2
773645004	Familial infantile gigantism
773648002	Congenital cataract, hearing loss, severe developmental delay syndrome
773664005	Deficiency in anterior pituitary function, variable immunodeficiency syndrome
773665006	Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome
773668008	Childhood encephalopathy due to thiamine pyrophosphokinase deficiency
773672007	Lethal occipital encephalocele, skeletal dysplasia syndrome
773699009	Pitt Hopkins-like 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
774151000	Ferro-cerebro-cutaneous syndrome
774205007	Growth and developmental delay, hypotonia, vision impairment, lactic acidosis syndrome
774206008	Fatal post-viral neurodegenerative disorder
77461000119109	Myasthenia gravis with exacerbation
77471000119103	Myasthenia gravis without exacerbation
775907000	Congenital pontocerebellar hypoplasia type 9
776087007	Autosomal recessive cerebral atrophy
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
778011005	Severe intellectual disability and progressive spastic paraplegia
778021002	Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome
778027003	Primary CD59 deficiency
778029000	FAST kinase domains 2-related infantile mitochondrial encephalomyopathy
778030005	Autosomal recessive spastic paraplegia type 27
778047006	Myoclonic epilepsy in non-progressive encephalopathy
778048001	Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial spastic paraplegia
778060000	Collagen type IV alpha 1 chain related familial vascular leukoencephalopathy
778063003	Cryptogenic late-onset epileptic spasms
778070003	Autosomal dominant primary microcephaly
77817004	Neu-Laxova syndrome
77956009	Steinert myotonic dystrophy syndrome
780827006	Synaptic Ras GTPase activating protein 1- related intellectual disability
782432008	Acquired hydrocephalus of newborn
782670003	Autosomal dominant spastic paraplegia type 3
782675008	Distal myopathy with anterior tibial onset
782690007	Gemignani syndrome
782695002	Primary dystonia DYT17 type
782696001	Recessive mitochondrial ataxia syndrome
782718007	Dystonia aphonia syndrome
782719004	Autosomal recessive cerebellar ataxia due to STIP1 homology and U-box containing protein 1 deficiency
782720005	Congenital pontocerebellar hypoplasia type 10
782721009	Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUN and cysteine rich domain containing beclin 1 interacting protein deficiency
782723007	Severe intellectual disability, progressive spastic diplegia syndrome
782725000	Autosomal recessive spastic paraplegia type 69
782726004	Autosomal recessive spastic paraplegia type 71
782727008	Autosomal spastic paraplegia type 72
782737003	Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome
782739000	Male emopamil-binding protein disorder with neurological defect
782742006	Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons
782743001	Huntington disease-like syndrome due to chromosome 9 open reading frame 72 expansions
782744007	Lipoic acid synthetase deficiency
782746009	Autosomal recessive spastic paraplegia type 60
782747000	Autosomal recessive spastic paraplegia type 66
782752005	Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome
782753000	Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome
782754006	Foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis syndrome
782755007	Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome
782757004	Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome
782771007	Mitochondrial deoxyribonucleic acid depletion syndrome hepatocerebrorenal form
782772000	Congenital muscular dystrophy with intellectual disability and severe epilepsy
782822006	Infantile cerebellar and retinal degeneration
782824007	Sodium channelopathy-related small fiber neuropathy
782825008	Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome
782826009	Charcot-Marie-Tooth disease type 2P
782829002	Autosomal dominant Charcot-Marie-Tooth disease type 2O
782879004	Occipital pachygyria and polymicrogyria
782881002	Hereditary sensorimotor neuropathy with hyperelastic skin
782886007	Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome
782887003	Inherited congenital spastic tetraplegia
782917007	Familial adrenal hypoplasia with absent pituitary luteinizing hormone
782941005	Richieri Costa-da Silva syndrome
782945001	Ophthalmoplegia, intellectual disability, lingua scrotalis syndrome
782951006	Thoracic dysplasia and hydrocephalus syndrome
783005002	Severe microbrachycephaly, intellectual disability, athetoid cerebral palsy syndrome
783012006	Parkinsonian pyramidal syndrome
783055005	Progressive myoclonic epilepsy type 5
783057002	DNA replication helicase/nuclease 2-related mitochondrial deoxyribonucleic acid deletion syndrome
783060009	Autosomal recessive cerebellar ataxia, psychomotor delay syndrome
78306007	Epidural ascending spinal paralysis
783062001	Progressive myoclonic epilepsy type 6
783064000	Progressive myoclonic epilepsy type 3
783091003	46,XY gonadal dysgenesis, motor and sensory neuropathy syndrome
783094006	Autosomal recessive spastic paraplegia type 14
783139000	Progressive myoclonic epilepsy type 8
783148005	Distal nebulin myopathy
783157004	Leigh syndrome with nephrotic syndrome
783160006	Hereditary gelsolin amyloidosis
783161005	Familial dementia British type
783166000	Distal anoctaminopathy
783174004	Congenital muscular dystrophy with intellectual disability
783175003	Congenital muscular dystrophy without intellectual disability
783176002	Congenital muscular dystrophy with cerebellar involvement
783179009	Cranio-cervical dystonia with laryngeal and upper limb involvement
783203003	Ataxia with tapetoretinal degeneration syndrome
783242003	Adult-onset cervical dystonia DYT23 type
783258000	Familial dementia Danish type
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
783622001	Autosomal dominant spastic paraplegia type 38
783629005	Congenital aneurysm of cerebral artery
783630000	Congenital aneurysm of precerebral artery
783697000	X-linked spastic paraplegia type 16
783698005	Autosomal dominant spastic paraplegia type 13
783701002	Port-wine nevi, mega cisterna magna, hydrocephalus syndrome
783703004	White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome
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
783734000	Mitochondrial deoxyribonucleic acid depletion syndrome, hepatocerebral form due to deoxyguanosine kinase deficiency
783739005	Familial temporal lobe epilepsy
783764008	Autosomal recessive spastic paraplegia type 56
783787000	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
784341001	Amyotrophic lateral sclerosis type 4
784342008	Familial infantile myoclonic epilepsy
784343003	Autosomal recessive spastic ataxia with leukoencephalopathy
784344009	Cortical dysgenesis with pontocerebellar hypoplasia due to tubulin beta 3 class III mutation
784345005	Malignant migrating partial seizures of infancy
784346006	Navajo neurohepatopathy
784347002	Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome
784348007	Familial congenital mirror movements
784352007	X-linked scapuloperoneal muscular dystrophy
784370005	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
784371009	Huntington disease-like 1
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
785298001	Muscle eye brain disease with bilateral multicystic leukodystrophy
785299009	Cobblestone lissencephaly without muscular or ocular involvement
785300001	Infantile-onset autosomal recessive non progressive cerebellar ataxia
785301002	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia
785302009	Adult-onset autosomal recessive cerebellar ataxia
785303004	Multiple congenital anomalies, hypotonia, seizures syndrome
785304005	Autosomal recessive spastic paraplegia type 24
785305006	Autosomal dominant spastic paraplegia type 8
785306007	Lissencephaly co-occurrent with congenital cerebellar hypoplasia type E
785307003	Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A
78569004	Posterior inferior cerebellar artery syndrome
785726009	Hyperekplexia epilepsy syndrome
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
787174003	Intellectual disability, hyperkinetic movement, truncal ataxia syndrome
788310011000119109	Acute cerebrovascular accident due to occlusion of left cerebellar artery
788417006	Alopecia, epilepsy, intellectual disability syndrome Moynahan type
788454002	Stenosis of bilateral vertebral arteries
788455001	Occlusion of bilateral pontine arteries
788880006	Cerebral ischemic stroke due to dissection of artery
788881005	Cerebral ischemic stroke due to aortic arch embolism
788882003	Cerebral ischemic stroke due to global hypoperfusion with watershed infarct
788883008	Cerebral ischemic stroke due to hypercoagulable state
788884002	Cerebral ischemic stroke due to subarachnoid hemorrhage
788898005	Dementia caused by volatile inhalant
788899002	Dementia due to pellagra
788916009	Encephalopathy caused by ammonia
789005009	Paralysis of uvula after diphtheria
789063000	Primary hyperaldosteronism, seizures, neurological abnormalities syndrome
789187001	X-linked acrogigantism due to Xq26 microduplication
789657008	ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis
789674008	Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder
791000124107	2-methyl-3-hydroxybutyric aciduria
792004	Jakob-Creutzfeldt disease
7931000119101	Anterior choroidal artery thrombosis
79341000119107	Mixed dementia
79385002	Lowe syndrome
79591004	Spastic paralysis due to spinal birth injury
79633009	Spastic hemiplegia
79745005	Reflex epilepsy
80098002	Diffuse Lewy body disease
80180004	Pallidonigral degeneration
80328002	Progressive cone-rod dystrophy
80544005	Spongy degeneration of central nervous system
80606009	Carotid artery embolism
80651009	Aicardi's syndrome
80690008	Degenerative disease of the central nervous system
80734006	Marinesco-Sjögren syndrome
80758005	Embolism of lateral venous sinus
80901002	Endophlebitis of torcular Herophili
80935004	Flaccid hemiplegia
80976008	Myasthenic crisis
81211007	Primary lateral sclerosis
81308009	Disorder of brain
813921000000104	Spastic hemiplegic cerebral palsy
81526008	Hydromeningomyelocele
816067005	Diabetes, hypogonadism, deafness, intellectual disability syndrome
816068000	Periventricular nodular heterotopia
816205008	Malignant pituitary blastoma
8166000	Thrombophlebitis of basilar sinus
816984002	Progressive multiple sclerosis
81780002	Beckwith-Wiedemann syndrome
81854007	Alexander's disease
81896006	Dysmorphic sialidosis with renal involvement
818967003	Medulloepithelioma of central nervous system
82058009	Myelocele
82077006	Myotubular myopathy
82346000	Acquired obstructive hydrocephalus
82351000119105	Altered behavior co-occurrent and due to Pick's disease
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
827172005	X-linked progressive cerebellar ataxia
8291000119107	Atonic epilepsy
82959004	Dementia paralytica juvenilis
83157008	Fatal familial insomnia
83304000	Dubini's chorea
833326008	Cortical vascular dementia
838275008	Stenosis of cerebral artery
838276009	Amyotrophic lateral sclerosis, parkinsonism, dementia complex
838308007	Fibromuscular dysplasia of wall of intracranial artery
838309004	Cerebrovascular abnormality due to Takayasu disease
83832001	Metachromatic leukodystrophy without arylsulfatase deficiency
838383000	Chorea caused by toxin
838441009	Mental retardation, adducted thumbs, shuffling gait, aphasia syndrome
83942000	Acute disseminated encephalomyelitis
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
840452004	Classical sporadic Creutzfeldt-Jakob disease
840464007	Dementia due to carbon monoxide poisoning
840465008	Dementia due to iron deficiency
840471002	Hydrocephalus due to Dandy-Walker malformation
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
85592008	Primary progressive cerebellar degeneration
8563000	Cholinergic crisis
85641006	Hemianencephaly
85672005	Anterior horn cell disease
86003009	Carotid artery thrombosis
86044005	Amyotrophic lateral sclerosis
860802009	Ex-vacuo hydrocephalus due to infection
860803004	Hydrocephalus due to tuberculosis of brain
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
860826006	Creutzfeldt-Jakob Disease caused by human growth hormone
860881004	Flaccid diplegia of lower extremities
86188000	Kuru
86444004	Niemann-Pick disease, type C, acute form
864471000000106	Anterior opercular syndrome
866050001	Mixed germ cell neoplasm of central nervous system
866051002	Motor neuron disease due to lead intoxication
866053004	Middle interhemispheric variant of holoprosencephaly
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
870345007	Compression of spinal cord due to cavernous hemangioma
870544005	Occlusion of distal basilar artery
870566003	Occlusion of anterior choroidal artery
870579007	Occlusion of branch of basilar artery
870637009	Dissection of cervical artery
87091000119101	Malignant glioma of cerebrum
87111000119109	Malignant glioma of hypothalamus
87121000119102	Malignant glioma of cerebellum
87151000119105	Malignant glioma of central nervous system
871637001	Thrombosis of multiple cerebral veins
87235005	Dialysis disequilibrium syndrome
87551000119101	Visual disturbance as sequela of cerebrovascular disease
87555007	Claude's syndrome
87607002	Pelizaeus-Merzbacher disease, classic form
87842000	Generalized neuromuscular exhaustion syndrome
878808006	Nongerminomatous germ cell tumor of central nervous system
87937009	Endophlebitis of intracranial venous sinus
879937000	Alpha-N-acetylgalactosaminidase deficiency type 1
880065001	Alpha-N-acetylgalactosaminidase deficiency type 2
880066000	Alpha-N-acetylgalactosaminidase deficiency type 3
880093002	17q11 deletion syndrome
88032003	Amaurosis fugax
881694631000119107	Acute cerebrovascular accident of medulla oblongata
88174006	Basilar artery thrombosis
88518009	Wilson's disease
885831000000109	Choreoathetoid cerebral palsy
88755007	Phlebitis of lateral venous sinus
88922007	Thrombosis of basilar sinus
88923002	Progressive muscular atrophy
890118006	Mowat-Wilson syndrome due to monosomy 2q22
890286007	Bilateral frontoparietal polymicrogyria
890346002	Holoprosencephaly co-occurrent with congenital nasal pyriform aperture stenosis
890368007	Congenital muscular dystrophy type 1C due to fukutin related protein gene mutation
890395002	Congenital muscular dystrophy type 1D large gene mutation
890422008	Cervicothoracic spina bifida aperta with hydrocephalus
890430009	Complete agenesis of vermis
890432001	Cockayne syndrome type 3
890433006	Cockayne syndrome type 1
890434000	Cockayne syndrome type 2
89142007	Progressive intracranial arterial occlusion
894125007	Cervicothoracic spina bifida aperta
89437009	Cerebral paraparesis
89576007	Pallidonigrospinal degeneration
89980009	Thrombosis of cavernous venous sinus
90099008	Subcortical leukoencephalopathy
90253000	Progressive subcortical gliosis
903741000000102	Uhthoff phenomenon
904531000000100	Bilateral spastic cerebral palsy
90520006	Vertebral artery stenosis
90791004	Posthemiplegic ataxia
90811000119100	Low grade malignant glioma of brain
90831000119105	Grade 4 malignant glioma of brain
91327001	Quadriparesis
9133005	Familial amyloid polyneuropathy, Iowa type
91502009	Spinocerebellar disease
915141931000119109	Acute cerebrovascular accident due to embolism of basilar artery
91601000119109	Sequela of thrombotic stroke
91637004	Myasthenia gravis
91952008	Azorean disease
91953003	Azorean disease, type I
91954009	Azorean disease, type II
91955005	Azorean disease, type III
91956006	Azorean disease, type IV
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
931164671000119105	Acute cerebrovascular accident due to embolism of right middle cerebral artery
93153005	Limb-girdle muscular dystrophy
93312006	Congenital malposition of carotid artery
93396008	Congenital stenosis of carotid artery
9345005	Dialysis dementia
93557001	Holorachischisis
936271000000100	Congenital anomaly of precerebral vessel
936648941000119105	Acute cerebrovascular accident due to embolism of left middle cerebral artery
93726004	Primary malignant neoplasm of brain stem
93727008	Primary malignant neoplasm of brain
93744007	Primary malignant neoplasm of central nervous system
93746009	Primary malignant neoplasm of cerebellum
93747000	Primary malignant neoplasm of cerebral meninges
93748005	Primary malignant neoplasm of cerebral ventricle
93749002	Primary malignant neoplasm of cerebrum
93768004	Primary malignant neoplasm of craniopharyngeal duct
93807001	Primary malignant neoplasm of frontal lobe
93928006	Primary malignant neoplasm of occipital lobe
93931007	Primary malignant neoplasm of optic nerve
93946000	Primary malignant neoplasm of parietal lobe
93962006	Primary malignant neoplasm of pineal gland
93964007	Primary malignant neoplasm of pituitary gland
94068003	Primary malignant neoplasm of spinal cord
94069006	Primary malignant neoplasm of spinal meninges
94086000	Primary malignant neoplasm of temporal lobe
94224009	Secondary malignant neoplasm of brain stem
94225005	Secondary malignant neoplasm of brain
94243009	Secondary malignant neoplasm of central nervous system
94245002	Secondary malignant neoplasm of cerebellum
94246001	Secondary malignant neoplasm of cerebral meninges
94247005	Secondary malignant neoplasm of cerebral ventricle
94248000	Secondary malignant neoplasm of cerebrum
94267001	Secondary malignant neoplasm of craniopharyngeal duct
94309003	Secondary malignant neoplasm of frontal lobe
943181000000103	Degenerative disease of basal ganglia
94448002	Secondary malignant neoplasm of occipital lobe
94452002	Secondary malignant neoplasm of optic nerve
94471000	Secondary malignant neoplasm of parietal lobe
94489004	Secondary malignant neoplasm of pineal gland
94491007	Secondary malignant neoplasm of pituitary gland
94600009	Secondary malignant neoplasm of spinal cord
94601008	Secondary malignant neoplasm of spinal meninges
94622002	Secondary malignant neoplasm of temporal lobe
95208000	Photogenic epilepsy
95235009	Retroesophageal carotid artery
9537004	Juvenile GM 2 gangliosidosis
95454007	Brain stem hemorrhage
95455008	Thrombosis of cerebral veins
95456009	Brain stem ischemia
95457000	Brain stem infarction
95458005	Cerebellar artery occlusion
95459002	Cerebellar artery thrombosis
95460007	Cerebellar infarction
95461006	Thrombophlebitis of cerebral vein
95477007	Congenital degeneration of nervous system
95569006	Uremic coma
95610008	Congenital brain damage
95644001	Systemic lupus erythematosus encephalitis
95646004	Cerebellar degeneration
95647008	Upper motor neuron disease
95650006	Transient hemiplegia
95651005	Chronic progressive paraparesis
95830009	Pituitary infarction
9611000119107	Symptomatic carotid artery stenosis
96981000119102	Malignant neoplasm of rectosigmoid junction metastatic to brain
97381000119100	Neurogenic bladder due to quadriplegia
97391000119102	Paraplegia with neurogenic bladder
9753004	Triplegia
97751000119108	Altered behavior in Alzheimer's disease
984681000000101	Profound learning disability
9901000119100	Occlusion of cerebral artery with stroke
99131000119108	Astrocytoma of cerebrum
99451000119105	Cerebral infarction due to stenosis of carotid artery

Codes not in the full codelist are in faint grey.

Chronic Neurological Disease including Significant Learning Disorder

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