Chronic Neurological Disease including Significant Learning Disorder
Codelist metadata
-
Coding system
- SNOMED CT
-
Coding system release
- unknown
-
Organisation
- PRIMIS Covid Vaccination Uptake Reporting (old)
-
Codelist ID
- primis-covid19-vacc-uptake-old/cns_cov_cod
-
Version Tag
- v1
-
Version ID
- 47436ed7
Versions
About
Description
Taken from the CNS_COV_COD
field in SARS-CoV2 COVID19 Vaccination Uptake Reporting Codes 20_21 v1, published by PRIMIS.
© PRIMIS - the University of Nottingham 2021
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 |
100491000119103 | Myelopathy co-occurrent and due to spinal stenosis of lumbar region |
100511000119108 | Myelopathy co-occurrent and due to spinal stenosis of thoracic region |
10068001 | Sensory somatic cortical disorder |
100721000119109 | High grade astrocytoma of brain |
100731000119107 | Low grade astrocytoma of brain |
10082001 | Progressive rubella panencephalitis |
100941000119100 | Epilepsy in mother complicating pregnancy |
101421000119107 | Dementia due to Parkinson's disease |
102448004 | Drug-induced dyskinesia |
102449007 | Tardive dyskinesia |
10256000 | Brain stem laceration without open intracranial wound AND with loss of consciousness |
10277002 | Cerebellopontine angle syndrome |
102831000119104 | Paralytic syndrome of both lower limbs as sequela of stroke |
10310006 | Open fracture of C1-C4 level with incomplete spinal cord lesion |
10327003 | Cocaine-induced mood disorder |
1032761000000105 | Intraventricular (nontraumatic) haemorrhage, grade 4, of fetus and newborn |
10340008 | Isolated gonadotropin deficiency |
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 |
104431000119107 | Lipomyelomeningocele |
10481000119108 | Colloid brain cyst |
104981000119104 | Oligodendroglioma of cerebrum |
10532003 | Primary degenerative dementia of the Alzheimer type, presenile onset, with depression |
105421000119105 | Early onset Alzheimer's disease with behavioral disturbance |
105451000119102 | Amnestic disorder associated with general medical condition |
1055001 | Stenosis of precerebral artery |
10575009 | Open fracture of vertebral column with spinal cord injury |
106014008 | Organic mental disorder of unknown etiology |
106018006 | Hereditary degenerative disease of central nervous system |
106021000119105 | Multi-infarct dementia due to atherosclerosis |
106071000119106 | Secondary hypothalamic insufficiency |
10649000 | Hyperpituitarism |
10651001 | Temporal lobectomy behavior syndrome |
10677711000119101 | Encephalopathy caused by Influenza A virus |
10701000119109 | Refractory complex partial seizure with impairment of consciousness |
10736002 | Isolated thyroliberin deficiency |
10750951000119106 | Epilepsy in mother complicating childbirth |
10752641000119102 | Eclampsia with pre-existing hypertension in childbirth |
107581000119103 | Astrocytoma of brain stem |
1078001000000105 | Haemorrhagic stroke |
1082451000119102 | Encephalitis caused by Actinomyces |
1082511000119102 | Hepatic coma due to acute hepatic failure |
1082621000119108 | Hepatic coma due to alcoholic liver failure |
1084741000119103 | Meningoencephalitis due to Blastomyces dermatitidis |
1085091000119108 | Hepatic coma due to chronic hepatic failure |
1086061000119109 | Diphtheria radiculomyelitis |
108691000119102 | Spasticity as sequela of stroke |
1086991000119103 | Gonococcal abscess of brain |
1087451000000109 | Late onset alcohol-induced psychosis |
1087461000000107 | Late onset substance-induced psychosis |
1087481000000103 | Late onset cocaine-induced psychosis |
1087491000000101 | Late onset lysergic acid diethylamide-induced psychosis |
1087501000000107 | Late onset cannabinoid-induced psychosis |
1087511000000109 | Late onset amphetamine-induced psychosis |
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 |
1089811000119106 | Meningoencephalitis caused by Acanthamoeba |
1089821000119104 | Meningoencephalitis due to Chagas disease |
1092691000119109 | Hepatic coma due to subacute liver failure |
10943311000119108 | Contusion of right cerebrum |
10943471000119107 | Contusion of left cerebrum |
109478007 | Kohlschutter's syndrome |
10948005 | Thoracic spondylosis with myelopathy |
109561000 | Cerebrofacial dysplasia |
109905002 | Acquired myelocele |
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 |
110030002 | Concussion injury of brain |
110150000 | Spinal cord concussion |
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 |
111395007 | Nephrogenic diabetes insipidus |
111479008 | Organic mental disorder |
111480006 | Psychoactive substance-induced organic dementia |
111487009 | Dream anxiety disorder |
111488004 | Kleine-Levin syndrome |
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 |
111548007 | Syndrome of diencephalo-hypophyseal origin |
111558006 | Insulin coma |
111568001 | Hypothalamic syndrome |
111633007 | Open fracture of sacrum AND/OR coccyx with complete cauda equina lesion |
111641000119102 | Congenital choroid plexus cyst |
111681000 | Extradural hemorrhage following injury with open intracranial wound AND loss of consciousness |
111851005 | Subacute adenoviral encephalitis |
111872008 | Post measles encephalitis |
111897007 | Acute necrotizing encephalitis |
111936002 | Cerebral sarcoidosis |
11197005 | Hydromyelia |
11265003 | Hemichorea |
1131000119105 | Sequela of cerebrovascular accident |
11387009 | Psychoactive substance-induced organic mental disorder |
11413003 | Incomplete spinal cord lesion at T1-T6 level without bone injury |
11442006 | Hereditary sensory neuropathy |
11471000224106 | Diffuse intrinsic pontine glioma |
11538006 | Quadriplegia |
116288000 | Paralytic stroke |
116401000119105 | Recurrent complex partial epilepsy |
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 |
117891000119100 | Simple partial seizure |
11807002 | Injury at C5-C7 level with spinal cord injury AND without bone injury |
11862006 | Drug-induced myelopathy |
118951003 | Drug-induced nephrogenic diabetes insipidus |
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 |
12275031000119106 | Congenital cerebral ventriculomegaly |
12331003 | Gigantism due to somatostatin deficiency |
12348006 | Presenile dementia |
12367511000119101 | Paraplegia due to and following cerebrovascular accident |
123758004 | Complex pituitary endocrine disorder |
123759007 | Prepuberal hyperpituitarism |
123760002 | Prepuberal panhypopituitarism |
123763000 | Houssay's syndrome |
1239331000000100 | Significant intellectual disability |
12394009 | Miscarriage with cerebral anoxia |
123950001 | Rheumatic chorea without heart involvement |
123953004 | Idiopathic hypogonadotropic hypogonadism |
12398201000119102 | Anxiety disorder caused by methamphetamine |
12398281000119105 | Methamphetamine withdrawal |
124001000119104 | Status migrainosus co-occurrent and due to migraine without aura |
1240561000000108 | Encephalopathy due to disease caused by Severe acute respiratory syndrome coronavirus 2 |
124081000119107 | Menstrual status migrainosus |
124171000119105 | Chronic intractable migraine without aura |
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 |
125609005 | Open fracture of cervical region with spinal cord injury |
12589008 | Brain stem laceration with open intracranial wound |
125921000119106 | Hepatic coma due to acute hepatitis C |
126011000119107 | Acquired caroticocavernous sinus fistula |
12677003 | Tuberculosis of brain |
126944002 | Brain disorder resulting from a period of impaired oxygen delivery to the brain |
126945001 | Perinatal anoxic-ischemic brain injury |
126947009 | Cerebellopontine angle tumor |
126948004 | Cerebellopontine angle meningioma |
126952004 | Neoplasm of brain |
126953009 | Neoplasm of cerebrum |
126954003 | Neoplasm of frontal lobe |
126955002 | Neoplasm of temporal lobe |
126956001 | Neoplasm of parietal lobe |
126957005 | Neoplasm of occipital lobe |
126958000 | Neoplasm of cerebral ventricle |
126960003 | Neoplasm of cerebellum |
126961004 | Neoplasm of brain stem |
126962006 | Neoplasm of spinal cord |
126964007 | Neoplasm of spinal meninges |
127024001 | Neoplasm of pituitary gland |
127025000 | Neoplasm of craniopharyngeal duct |
127026004 | Neoplasm of pineal gland |
127294003 | Traumatic AND/OR non-traumatic brain injury |
127295002 | Traumatic brain injury |
127298000 | Traumatic brain injury with loss of consciousness |
127299008 | Traumatic brain injury with brief loss of consciousness |
127300000 | Traumatic brain injury with moderate loss of consciousness |
127301001 | Traumatic brain injury with prolonged loss of consciousness |
127302008 | Traumatic brain injury with no loss of consciousness |
127303003 | Cortex laceration |
127304009 | Cerebellar contusion |
127305005 | Brain stem contusion |
127306006 | Cerebellar laceration |
127307002 | Brain stem laceration |
127308007 | Intracranial hemorrhage following injury with loss of consciousness |
127309004 | Intracranial hemorrhage following injury with brief loss of consciousness |
127310009 | Intracranial hemorrhage following injury with moderate loss of consciousness |
127311008 | Intracranial hemorrhage following injury with prolonged loss of consciousness AND return to pre-existing conscious level |
127312001 | Intracranial hemorrhage following injury with prolonged loss of consciousness without return to pre-existing conscious level |
127324008 | Myoclonic disorder |
127551000119100 | Congenital hypoplasia of brain |
128128003 | Disorder of cerebral cortex |
128171000119104 | Spontaneous caroticocavernous sinus fistula |
128188000 | Cerebral palsy |
128190004 | Inherited metabolic disorder of nervous system |
128191000 | Encephalomyelitis co-occurrent and due to rubella |
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 |
128211000119102 | Meningoencephalitis due to free-living ameba |
128212001 | Spinal muscular atrophy, type II |
128213006 | Neuromuscular junction disorder |
128218002 | Disorder of intracranial venous sinus |
128328009 | Suprasellar syndrome |
128329001 | Disorder of visual cortex |
128431009 | Internal hydrocephalus |
128470003 | Pineal gland disorder |
12853006 | Embolism of torcular Herophili |
128608001 | Cerebral arterial aneurysm |
128609009 | Intracranial aneurysm |
128612007 | Focal motor seizure |
128613002 | Seizure disorder |
128614008 | Infectious disease of brain |
12912004 | Brain injury with open intracranial wound AND no loss of consciousness |
129132000 | Bacterial infectious disease of brain |
129583005 | Paralysis of palate |
129596006 | Menopausal muscular dystrophy syndrome |
129606007 | Frontal lobe syndrome |
129608008 | Progressive pyramidopallidal degeneration |
129609000 | Spinocerebellar ataxia |
129614001 | Paralysis of vagus, spinal accessory and hypoglossal nerves |
129615000 | Nucleus ambiguus-hypoglossal nerve syndrome |
129620000 | Scapuloperoneal muscular dystrophy |
129621001 | Nemaline myopathy, early onset type |
129622008 | Nemaline myopathy, late onset type |
129633006 | Induced female hypogonadism syndrome |
130121000119104 | Dementia due to Rett's syndrome |
13194006 | Anterior cord syndrome co-occurrent and due to closed fracture of T7-T12 level |
13196008 | Secondary diabetes insipidus |
13225007 | Rubella meningoencephalitis |
13289004 | Intracranial hemorrhage following injury with open intracranial wound AND loss of consciousness |
133301000119102 | Degenerative brain disorder caused by alcohol |
13386009 | Intraspinal embolic abscess |
133951000119104 | Temporal lobe sclerosis |
133981000119106 | Dysarthria as late effects of cerebrovascular disease |
133991000119109 | Fluency disorder as sequela of cerebrovascular disease |
134209002 | Prolactinoma |
13456001 | Closed fracture of T1-T6 level with incomplete spinal cord lesion |
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 |
135801000119109 | Compression of brain due to focal lesion |
135811000119107 | Lewy body dementia with behavioral disturbance |
135884009 | Benign neoplasm of pons |
13752003 | Brain injury with open intracranial wound AND loss of consciousness |
137991000119103 | Seizure disorder as sequela of stroke |
1383008 | Hallucinogen mood disorder |
13847000 | Partial seizure with impaired consciousness |
13920009 | Hepatic encephalopathy |
13973009 | Grand mal status |
140281000119108 | Hemiparesis as late effect of cerebrovascular disease |
14055002 | Hydrocephalus ex vacuo |
140621000119106 | Memory disorder co-occurrent and due to organic brain damage |
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 |
141091000119105 | Compression of brain co-occurrent and due to nontraumatic subarachnoid hemorrhage |
141151000119101 | Nontraumatic subdural hematoma with brain compression |
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 |
14289006 | Myopathy in hypopituitarism |
142971000119102 | Encephalopathy caused by H1N1 influenza |
14309005 | Anterior choroidal artery syndrome |
143521000119103 | Nontraumatic intraparenchymal cerebral hemorrhage |
14401000119109 | Partial frontal lobe epilepsy |
14405000 | Spinal subdural abscess |
14415006 | Pneumocephalus |
14434006 | Cerebellar laceration with open intracranial wound AND no loss of consciousness |
14447001 | Dandy-Walker syndrome |
144581000000105 | Fetal open spina bifida |
14493003 | Anterior cord syndrome co-occurrent and due to closed fracture of T1-T6 level |
14521008 | Visual seizure |
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 |
14784000 | Opioid-induced organic mental disorder |
148871000119109 | Weakness as a late effect of cerebrovascular accident |
14900002 | Radiotherapy-induced hypopituitarism |
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 |
15244003 | Neuroleptic malignant syndrome |
15277004 | Hallucinogen-induced anxiety disorder |
153091000119109 | Hepatic coma due to chronic hepatitis B with delta agent |
15316002 | Simian B encephalomyelitis |
15523002 | Benign focal epilepsy of childhood |
15552004 | Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts |
15631251000119109 | Blepharospasm of right eyelid |
15631291000119104 | Blepharospasm of left eyelid |
15631331000119105 | Blepharospasm of bilateral eyelids |
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 |
15671007 | Encephalocele of orbit |
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 |
15771004 | Diabetes insipidus |
15782007 | 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced parkinsonism |
15802004 | Dystonia |
1581000119101 | Dementia of the Alzheimer type with behavioral disturbance |
15863451000119107 | Lipoma of brain |
1591000119103 | Dementia with behavioral disturbance |
15913031000119100 | Cortical blindness of bilateral sides of brain |
1593000 | Infantile hemiplegia |
15938005 | Eclampsia |
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 |
15985791000119101 | Dystonia of right hand |
15985831000119107 | Dystonia of left hand |
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 |
16026008 | Congenital cerebellar hypoplasia |
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 |
16219341000119105 | Myelopathy due to spinal cord compression |
16236661000119100 | Delirium due to methamphetamine intoxication |
16236701000119107 | Delirium due to drug withdrawal |
16260551000119106 | Dysphasia due to and following cerebrovascular accident |
162702000 | On examination - mentally confused |
16270221000119108 | Acute akathisia caused by drug |
16276361000119109 | Vascular dementia without behavioral disturbance |
16279021000119106 | Delirium due to opioid withdrawal |
16279401000119108 | Occlusion of right cilioretinal artery |
16279441000119105 | Occlusion of left cilioretinal artery |
16300007 | Spinal cord abscess |
16319002 | Cortex contusion without open intracranial wound AND with concussion |
163591007 | On examination - petit mal fit |
163593005 | On examination - psychomotor fit |
163594004 | On examination - salaam attack |
163601006 | On examination - hemiplegia |
163604003 | On examination - paraplegia |
163605002 | On examination - quadriplegia |
163606001 | On examination - diplegia |
163665004 | On examination - athetosis |
16371781000119100 | Cerebellar stroke |
164110008 | On examination - cranial 7 -paralysis-upper motor neuron |
16415361000119105 | Radiologically isolated syndrome |
16418006 | Embolism of basilar sinus |
16476641000119100 | Acquired arteriovenous fistula of dura of cerebrum |
16517004 | Cerebral lipidosis |
16576004 | Shy-Drager syndrome |
166071000000101 | Congenital dilated lateral ventricles of brain |
16631009 | Transverse myelopathy syndrome |
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 |
16695002 | Open fracture of T1-T6 level with spinal cord injury |
1670004 | Cerebral hemiparesis |
16703551000119107 | Memory deficit due to and following cerebrovascular disease |
16703661000119105 | Memory deficit due to and following cerebrovascular accident |
16703761000119102 | Memory deficit due to and following ischemic cerebrovascular accident |
16703821000119101 | Memory deficit due to and following hemorrhagic cerebrovascular accident |
16709811000119106 | Spontaneous hemorrhage of subarachnoid space from anterior communicating artery |
16818591000119108 | Calcification of basal ganglia |
16851005 | Mitochondrial myopathy |
1686006 | Sedative, hypnotic AND/OR anxiolytic-induced anxiety disorder |
16901001 | Central European encephalitis |
17151000119108 | Partial growth hormone deficiency |
17169009 | Cerebellar contusion without open intracranial wound AND with loss of consciousness |
171822009 | Acute atrophic spinal paralysis |
17258002 | Chronic anoxic encephalopathy |
17262008 | Non-alcoholic Korsakoff's psychosis |
1734006 | Fracture of vertebral column with spinal cord injury |
17409003 | Facial hemiparesis |
17496003 | Organic anxiety disorder |
17498002 | Cortex contusion without open intracranial wound AND with loss of consciousness |
1767005 | Fisher's syndrome |
17761000119109 | High lumbar myelomeningocele |
17771000119103 | Low lumbar myelomeningocele |
17819003 | Brain stem laceration without open intracranial wound AND with concussion |
17944005 | Cerebral calcification |
17949000 | Meningoencephalitis due to acquired toxoplasmosis |
18058007 | Phlebitis of intracranial venous sinus |
18071005 | Meningococcal encephalitis |
18200000 | Autosomal recessive isolated somatotropin deficiency |
1829003 | Microcephalus |
182961000119101 | Acute disseminated encephalomyelitis following infectious disease |
18322005 | Thrombosis of torcular Herophili |
1845001 | Paraparesis |
18541000119100 | Borderline cognitive developmental delay |
186217006 | Tuberculous abscess of brain |
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 |
186498004 | Epidemic encephalitis |
186499007 | Encephalitis lethargica |
186509002 | Postvaricella encephalitis |
18653004 | Alcohol intoxication delirium |
186591007 | Russian spring-summer encephalitis |
186624004 | Hepatic coma due to acute hepatitis B with delta agent |
186628001 | Hepatic coma due to viral hepatitis C |
186791009 | Plasmodium falciparum malaria with cerebral complications |
186831000119104 | Apraxia due to and following cerebrovascular accident |
18689007 | Inhalant intoxication delirium |
186893003 | Rupture of syphilitic cerebral aneurysm |
187080002 | Pheohyphomycotic brain abscess |
187094001 | Cerebral cryptococcosis |
187100003 | Rhinocerebral mucormycosis |
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 |
18871009 | Cerebellar vertigo |
18894005 | Legal abortion with cerebral anoxia |
189016009 | Lipoma of spinal canal - intradural |
189017000 | Lipoma of spinal cord |
189162003 | Benign neoplasm of brain, supratentorial |
189167009 | Spinal meningioma |
189179009 | Craniopharyngioma |
189198006 | Epileptic drop attack |
18927009 | Niemann-Pick disease, type D |
189487001 | Neoplasm of uncertain or unknown behavior of brain, supratentorial |
189488006 | Neoplasm of uncertain or unknown behavior of brain, infratentorial |
18960007 | Closed fracture of T7-T12 level with incomplete spinal cord lesion |
190330002 | Hyperosmolar coma due to type 1 diabetes mellitus |
190331003 | Hyperosmolar coma due to type 2 diabetes mellitus |
190470005 | Idiopathic panhypopituitarism |
190471009 | Post-birth injury panhypopituitarism |
190472002 | Post-infarction panhypopituitarism |
190480009 | Follicle stimulating hormone deficiency |
190481008 | Luteinizing hormone deficiency |
190492009 | Diencephalic syndrome secondary to tumor |
190502001 | Pituitary-dependent Cushing's disease |
19091006 | Pallidoluysian degeneration |
19109004 | Syringomyelobulbia |
191447007 | Organic psychotic condition |
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 |
191476005 | Alcohol withdrawal hallucinosis |
191478006 | Alcoholic paranoia |
191480000 | Alcohol withdrawal syndrome |
191492000 | Drug-induced delirium |
191493005 | Drug-induced dementia |
191494004 | Drug-induced amnestic syndrome |
191499009 | Transient organic psychoses |
191501001 | Acute confusional state, post-traumatic |
191502008 | Acute confusional state, of infective origin |
191503003 | Acute confusional state, of endocrine origin |
191504009 | Acute confusional state, of metabolic origin |
191505005 | Acute confusional state, of cerebrovascular origin |
191507002 | Subacute delirium |
191508007 | Subacute confusional state, post-traumatic |
191509004 | Subacute confusional state, of infective origin |
191510009 | Subacute confusional state, of endocrine origin |
191511008 | Subacute confusional state, of metabolic origin |
191512001 | Subacute confusional state, of cerebrovascular origin |
191519005 | Dementia associated with another disease |
191990001 | Transient childhood tic |
192003008 | Sleep drunkenness |
192072002 | Organic memory impairment |
19210000 | Brain stem laceration with open intracranial wound AND no loss of consciousness |
19233004 | Cerebellar contusion with open intracranial wound AND loss of consciousness |
192454004 | Nonorganic insomnia |
192673008 | Sarcoid meningitis |
192685000 | Subacute sclerosing panencephalitis |
192686004 | Polioencephalitis |
192687008 | Arbovirus encephalitis |
192689006 | Rubella encephalitis |
192701001 | Toxoplasma encephalitis |
192704009 | Post-immunization encephalitis |
192705005 | Post-bacillus Calmette-Guerin vaccination encephalitis |
192706006 | Post typhoid vaccination encephalitis |
192707002 | Post paratyphoid vaccination encephalitis |
192708007 | Post cholera vaccination encephalitis |
192709004 | Post plague vaccination encephalitis |
192710009 | Post tetanus vaccination encephalitis |
192711008 | Post diphtheria vaccination encephalitis |
192712001 | Post pertussis vaccination encephalitis |
192713006 | Post smallpox vaccination encephalitis |
192714000 | Post rabies vaccination encephalitis |
192715004 | Post typhus vaccination encephalitis |
192716003 | Post yellow fever vaccination encephalitis |
192717007 | Post measles vaccination encephalitis |
192718002 | Post polio vaccination encephalitis |
192719005 | Post mumps vaccination encephalitis |
192720004 | Post rubella vaccination encephalitis |
192721000 | Post influenza vaccination encephalitis |
192722007 | Post hepatitis A vaccination encephalitis |
192723002 | Post hepatitis B vaccination encephalitis |
192724008 | Post mixed vaccination encephalitis |
192727001 | Post-infectious encephalitis |
192730008 | Toxic encephalitis |
192737006 | Intracranial and intraspinal abscesses |
192753009 | Phlebitis and thrombophlebitis of intracranial sinuses |
192755002 | Embolism superior longitudinal sinus |
192759008 | Cerebral venous sinus thrombosis |
192760003 | Thrombosis of superior longitudinal sinus |
19276002 | Congenital cerebral cyst |
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 |
192859002 | Fragments of torsion dystonia |
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 |
192899004 | Myelopathy due to edema of spinal cord |
192900009 | Myelopathy due to hematomyelia |
192904000 | Myelopathy due to another disorder |
192905004 | Myelopathy due to intervertebral disc disease |
192906003 | Myelopathy due to neoplastic disease |
192907007 | Myelopathy due to spondylosis |
192926004 | Multiple sclerosis of the brainstem |
192927008 | Multiple sclerosis of the spinal cord |
192929006 | Exacerbation of multiple sclerosis |
192949002 | Congenital paraplegia |
192958009 | Hypotonic cerebral palsy |
192964002 | Flaccid tetraplegia |
192965001 | Spastic tetraplegia |
192966000 | Flaccid paraplegia |
192967009 | Spastic paraplegia |
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 |
193004006 | Epileptic automatism |
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 |
193028008 | Sick headache |
193030005 | Migraine variants |
193031009 | Cluster headache syndrome |
193039006 | Complicated migraine |
193069004 | Intracranial hypotension following ventricular shunting |
193072006 | Adhesions - spinal meninges |
193073001 | Cyst of spinal meninges |
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 |
193225000 | Hereditary progressive muscular dystrophy |
193227008 | Pelvic muscular dystrophy |
193230001 | Distal muscular dystrophy with juvenile onset |
193237003 | Myotonic disorder |
193238008 | Infantile myotonia |
19350004 | Athetosis with rigidity |
193756007 | Charles Bonnet syndrome |
194068002 | Visual cortex disorder due to neoplasm |
194069005 | Visual cortex disorder due to vascular disorder |
194070006 | Inflammatory disorder of visual cortex |
19445006 | Opioid-induced psychotic disorder with hallucinations |
195154000 | Ruptured berry aneurysm |
195155004 | Subarachnoid hemorrhage from carotid siphon and bifurcation |
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 |
1973000 | Sedative, hypnotic AND/OR anxiolytic-induced psychotic disorder with delusions |
198438009 | Menopausal headache |
198990007 | Eclampsia - delivered |
198991006 | Eclampsia - delivered with postnatal complication |
198992004 | Eclampsia in pregnancy |
198993009 | Eclampsia with postnatal complication |
19903002 | Adductor spastic dysphonia |
199451000000106 | Simple partial epileptic seizure |
19972008 | Postencephalitic parkinsonism |
200071001 | Obstetric spinal and epidural anesthesia-induced headache |
200072008 | Spinal and epidural anesthesia-induced headache during pregnancy |
200073003 | Spinal and epidural anesthesia-induced headache during the puerperium |
200076006 | Spinal and epidural anesthesia-induced headache during labor and delivery |
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 |
202661006 | Single-level cervical spondylosis with myelopathy |
202662004 | Two-level cervical spondylosis with myelopathy |
202663009 | Multiple-level cervical spondylosis with myelopathy |
202664003 | Cervical myelopathy |
202670009 | Single-level thoracic spondylosis with myelopathy |
202671008 | Two-level thoracic spondylosis with myelopathy |
202672001 | Multiple-level thoracic spondylosis with myelopathy |
202683005 | Cervical spondylosis with radiculopathy |
202684004 | Single-level cervical spondylosis with radiculopathy |
202685003 | Two-level cervical spondylosis with radiculopathy |
202686002 | Multiple-level cervical spondylosis with radiculopathy |
202688001 | Thoracic spondylosis with radiculopathy |
202689009 | Single-level thoracic spondylosis with radiculopathy |
202690000 | Two-level thoracic spondylosis with radiculopathy |
202692008 | Multiple-level thoracic spondylosis with radiculopathy |
202729001 | Cervical disc prolapse with myelopathy |
202730006 | Thoracic disc prolapse with myelopathy |
202830000 | Recurrent atlantoaxial subluxation with myelopathy |
20305008 | Congenital myotonia, autosomal recessive form |
2032001 | Cerebral edema |
20377001 | Open fracture of C5-C7 level with incomplete spinal cord lesion |
20385005 | Opioid-induced psychotic disorder with delusions |
203927003 | Iniencephaly - closed |
203928008 | Iniencephaly - open |
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 |
203955004 | Spina bifida with stenosis of aqueduct of Sylvius |
203957007 | Dandy-Walker syndrome with spina bifida |
203967002 | Spinal hydromeningocele |
203969004 | Cervical spinal hydromeningocele |
203974007 | Cervical hydromyelocele |
203975008 | Thoracic hydromyelocele |
203976009 | Lumbar hydromyelocele |
203980004 | Cervical spinal meningocele |
203981000 | Thoracic spinal meningocele |
203982007 | Lumbar spinal meningocele |
203985009 | Cervical meningomyelocele |
203986005 | Thoracic meningomyelocele |
203987001 | Lumbar meningomyelocele |
203990007 | Cervical myelocele |
203991006 | Thoracic myelocele |
203992004 | Lumbar myelocele |
203994003 | Myelocystocele |
203996001 | Cervical myelocystocele |
203997005 | Thoracic myelocystocele |
203998000 | Lumbar myelocystocele |
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 |
204008003 | Spina bifida without hydrocephalus - closed |
204010001 | Cervical spina bifida without hydrocephalus - closed |
204011002 | Thoracic spina bifida without hydrocephalus - closed |
204012009 | Lumbar spina bifida without hydrocephalus - closed |
204013004 | Sacral spina bifida without hydrocephalus - closed |
204021005 | Encephalomyelocele |
204036008 | Lissencephaly |
204040004 | Agenesis of cerebrum |
204042007 | Congenital malformation of corpus callosum |
204043002 | Hypoplasia of corpus callosum |
204044008 | Aplasia of corpus callosum |
204046005 | Anomalies of hypothalamus |
204047001 | Anomalies of cerebellum |
204049003 | Aplasia of cerebellum |
204052006 | Cebocephaly |
204061006 | Foramen of Magendie atresia |
204062004 | Foramen of Luschka atresia |
204067005 | Single congenital cerebral cyst |
204068000 | Multiple congenital cerebral cysts |
204074000 | Multiple brain anomalies |
204081007 | Spinal cord hypoplasia |
2041006 | Eunuchoid gigantism |
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 |
205425003 | Sacral agenesis |
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 |
205750001 | Accessory pituitary gland |
206223002 | Spinal cord laceration due to birth trauma |
206224008 | Spinal cord rupture due to birth trauma |
206238001 | Cerebral edema due to birth injury |
206578007 | Neonatal cerebral leukomalacia |
20725005 | Familial visceral neuropathy |
207998001 | Closed fracture of cervical spine with cord lesion |
208000003 | Closed spinal fracture with complete cervical cord lesion, C1-4 |
208001004 | Closed spinal fracture with anterior cervical cord lesion, C1-4 |
208003001 | Closed spinal fracture with posterior cervical cord lesion, C1-4 |
208006009 | Closed spinal fracture with complete cervical cord lesion, C5-7 |
208007000 | Closed spinal fracture with anterior cervical cord lesion, C5-7 |
208009002 | Closed spinal fracture with posterior cervical cord lesion, C5-7 |
208012004 | Open fracture of cervical spine with spinal cord lesion |
208014003 | Open spinal fracture with complete cervical cord lesion, C1-4 |
208017005 | Open spinal fracture with posterior cervical cord lesion, C1-4 |
208020002 | Open spinal fracture with complete cervical cord lesion, C5-7 |
208022005 | Open spinal fracture with central cervical cord lesion, C5-7 |
208023000 | Open spinal fracture with posterior cervical cord lesion, C5-7 |
208028009 | Closed spinal fracture with complete thoracic cord lesion, T1-6 |
208029001 | Closed spinal fracture with anterior thoracic cord lesion, T1-6 |
208031005 | Closed spinal fracture with posterior thoracic cord lesion, T1-6 |
208034002 | Closed spinal fracture with complete thoracic cord lesion,T7-12 |
208035001 | Closed spinal fracture with anterior thoracic cord lesion,T7-12 |
208037009 | Closed spinal fracture with posterior thoracic cord lesion, T7-12 |
208042001 | Open spinal fracture with complete thoracic cord lesion, T1-6 |
208043006 | Open spinal fracture with anterior thoracic cord lesion, T1-6 |
208045004 | Open spinal fracture with posterior thoracic cord lesion, T1-6 |
208048002 | Open spinal fracture with complete thoracic cord lesion, T7-12 |
208049005 | Open spinal fracture with anterior thoracic cord lesion, T7-12 |
208051009 | Open spinal fracture with posterior thoracic cord lesion, T7-12 |
208056004 | Closed spinal fracture with complete lumbar cord lesion |
208057008 | Closed spinal fracture with anterior lumbar cord lesion |
208058003 | Closed spinal fracture with central lumbar cord lesion |
208059006 | Closed spinal fracture with posterior lumbar cord lesion |
208063004 | Open spinal fracture with complete lumbar cord lesion |
208064005 | Open spinal fracture with anterior lumbar cord lesion |
208065006 | Open spinal fracture with central lumbar cord lesion |
208066007 | Open spinal fracture with posterior lumbar cord lesion |
20876004 | Inhalant-induced anxiety disorder |
20899000 | Brain stem laceration without open intracranial wound |
20900005 | Nonfamilial asexual dwarfism |
209048009 | Closed spinal dislocation with complete cervical cord lesion |
209049001 | Closed spinal dislocation with anterior cervical cord lesion |
209050001 | Closed spinal dislocation with central cervical cord lesion |
209051002 | Closed spinal dislocation with posterior cervical cord lesion |
209066004 | Open spinal dislocation with complete cervical cord lesion |
209067008 | Open spinal dislocation with anterior cervical cord lesion |
209068003 | Open spinal dislocation with central cervical cord lesion |
209069006 | Open spinal dislocation with posterior cervical cord lesion |
209077005 | Closed spinal dislocation with complete thoracic cord lesion |
209078000 | Closed spinal dislocation with anterior thoracic cord lesion |
209079008 | Closed spinal dislocation with central thoracic cord lesion |
209080006 | Closed spinal dislocation with posterior thoracic cord lesion |
20908003 | Subcortical cerebral hemorrhage |
209082003 | Closed spinal dislocation with complete lumbar cord lesion |
209083008 | Closed spinal dislocation with anterior lumbar cord lesion |
209084002 | Closed spinal dislocation with central lumbar cord lesion |
209085001 | Closed spinal dislocation with posterior lumbar cord lesion |
209092006 | Open spinal dislocation with complete thoracic cord lesion |
209093001 | Open spinal dislocation with anterior thoracic cord lesion |
209094007 | Open spinal dislocation with central thoracic cord lesion |
209095008 | Open spinal dislocation with posterior thoracic cord lesion |
209097000 | Open spinal dislocation with complete lumbar cord lesion |
209098005 | Open spinal dislocation with anterior lumbar cord lesion |
209100005 | Open spinal dislocation with central lumbar cord lesion |
209101009 | Open spinal dislocation with posterior lumbar cord lesion |
209145009 | Closed spinal subluxation with complete cervical cord lesion |
209146005 | Closed spinal subluxation with anterior cervical cord lesion |
209147001 | Closed spinal subluxation with central cervical cord lesion |
209148006 | Closed spinal subluxation with posterior cervical cord lesion |
209162004 | Open spinal subluxation with complete cervical cord lesion |
209163009 | Open spinal subluxation with anterior cervical cord lesion |
209164003 | Open spinal subluxation with central cervical cord lesion |
209165002 | Open spinal subluxation with posterior cervical cord lesion |
209173006 | Closed spinal subluxation with complete thoracic cord lesion |
209174000 | Closed spinal subluxation with anterior thoracic cord lesion |
209175004 | Closed spinal subluxation with central thoracic cord lesion |
209176003 | Closed spinal subluxation with posterior thoracic cord lesion |
209178002 | Closed spinal subluxation with complete lumbar cord lesion |
209179005 | Closed spinal subluxation with anterior lumbar cord lesion |
209180008 | Closed spinal subluxation with central lumbar cord lesion |
209181007 | Closed spinal subluxation with posterior lumbar cord lesion |
209188001 | Open spinal subluxation with complete thoracic cord lesion |
209189009 | Open spinal subluxation with anterior thoracic cord lesion |
209190000 | Open spinal subluxation with central thoracic cord lesion |
209191001 | Open spinal subluxation with posterior thoracic cord lesion |
209193003 | Open spinal subluxation with complete lumbar cord lesion |
209194009 | Open spinal subluxation with anterior lumbar cord lesion |
209195005 | Open spinal subluxation with central lumbar cord lesion |
209196006 | Open spinal subluxation with posterior lumbar cord lesion |
209827006 | Concussion with less than 1 hour loss of consciousness |
209845006 | Cortex contusion with open intracranial wound, with no loss of consciousness |
209864000 | Cortex laceration with open intracranial wound, with no loss of consciousness |
209883007 | Hind brain contusion with open intracranial wound, with no loss of consciousness |
209900006 | Hind brain laceration with open intracranial wound |
209902003 | Hind brain laceration with open intracranial wound, with no loss of consciousness |
209903008 | Hind brain laceration with open intracranial wound, with less than 1 hour loss of consciousness |
209920007 | Brain contusion with open intracranial wound, with no loss of consciousness |
209921006 | Brain contusion with open intracranial wound, with more than 1 hour loss of consciousness |
209940000 | Subarachnoid hemorrhage following injury with open intracranial wound, with no loss of consciousness |
209958006 | Subdural hemorrhage following injury with open intracranial wound, with no loss of consciousness |
209978003 | Extradural hemorrhage following injury with open intracranial wound, with no loss of consciousness |
210038008 | Focal brain injury |
21007002 | Wernicke's disease |
21086008 | Cockayne syndrome |
2109003 | Isolated somatotropin deficiency |
21095000 | Secondary hyperprolactinemia |
21111006 | Complete trisomy 13 syndrome |
21201006 | Sporadic cerebellar degeneration |
212142000 | Visual cortex injury |
212169004 | Thoracic cord injury without spinal bone injury |
212171004 | Complete thoracic cord injury, without bony injury, T1-6 |
212172006 | Anterior thoracic cord injury, without bony injury, T1-6 |
212173001 | Central thoracic cord injury, without bony injury, T1-6 |
212174007 | Posterior thoracic cord injury without bony injury, T1-6 |
212177000 | Complete thoracic cord injury, without bony injury, T7-12 |
212178005 | Anterior thoracic cord injury, without bony injury, T7-12 |
212179002 | Central thoracic cord injury, without bony injury, T7-12 |
212180004 | Posterior thoracic cord injury without bony injury, T7-12 |
212183002 | Lumbar cord injury without spinal bone injury |
212185009 | Complete lumbar cord injury without bony injury |
212186005 | Anterior lumbar cord injury without bony injury |
212187001 | Central lumbar cord injury without bony injury |
212188006 | Posterior lumbar cord injury without bony injury |
212194003 | Spinal cord injury of multiple sites without spinal bone injury |
212356007 | Concussion and edema of cervical spinal cord |
212358008 | Concussion and edema of thoracic spinal cord |
212360005 | Concussion and edema of lumbar spinal cord |
21244005 | Borries' syndrome |
21258007 | Thrombosis of lateral venous sinus |
21263006 | Myxedema coma |
213044006 | Mechanical complication of carotid artery bypass |
213054005 | Mechanical complication of dorsal column stimulator |
213208008 | Anoxic brain damage complication |
213209000 | Cerebral anoxia complication |
21350002 | Colloid cyst of third ventricle |
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 |
21831000119109 | Phencyclidine psychosis |
21921000119103 | Dementia co-occurrent and due to Pick's disease |
21978005 | Anterior cord syndrome co-occurrent and due to open fracture of C1-C4 level |
2198002 | Visceral epilepsy |
22126005 | Hereditary neuraxial edema |
22255007 | Progressive multifocal leukoencephalopathy |
22306000 | Transient somatotropin deficiency |
223176004 | Cerebellar disorder |
22381000119105 | Primary degenerative dementia |
22383006 | Closed fracture of vault of skull with cerebral laceration AND/OR contusion |
224186005 | Cerebellar deficiency syndrome |
22419002 | Mood disorder with mixed features due to general medical condition |
22443004 | Vestibulocerebellar ataxia |
22451001 | Idiopathic torsion dystonia |
22471005 | Hemispheric cerebellar agenesis |
22719003 | Neuroleptic-induced acute akathisia |
22811006 | Leukoencephalopathy |
22819008 | Laceration of brain with open intracranial wound |
22881000119100 | Quadriplegia with quadriparesis |
229247004 | Mirror movements |
229676007 | Language-related cognitive disorder |
229692002 | Oral dystonia |
229694001 | Oral dyskinesia |
22973003 | Closed fracture of vertebral column with spinal cord injury |
230144003 | Chronic echovirus meningoencephalitis |
230156002 | Malignant meningitis |
230157006 | Viral ventriculitis, brain |
230158001 | Bacterial ventriculitis, brain |
230159009 | Fungal ventriculitis, brain |
230160004 | Malignant ventriculitis, brain |
230161000 | Acute viral encephalitis |
230162007 | Enteroviral encephalitis |
230166005 | Rocio virus encephalitis |
230168006 | Tensaw encephalitis |
230170002 | Kumlinge virus encephalitis |
230174006 | Rhabdovirus encephalitis |
230175007 | Infectious mononucleosis encephalitis |
230176008 | Herpes zoster encephalitis |
230177004 | Herpes simiae encephalitis |
230179001 | Chronic viral encephalitis |
230180003 | Human immunodeficiency virus leukoencephalopathy |
230181004 | Bacterial encephalitis |
230182006 | Late syphilitic encephalitis |
230183001 | Fungal encephalitis |
230185008 | Amebic encephalitis |
230186009 | Primary amebic encephalitis |
230187000 | Granulomatous amebic encephalitis |
230188005 | Post-influenza encephalitis |
230189002 | Focal encephalitis |
230190006 | Brainstem encephalitis |
230191005 | Rasmussen syndrome |
230192003 | Limbic encephalitis |
230193008 | Neurosarcoidosis |
230194002 | Neuro - Whipple's disease |
230197009 | Acute viral transverse myelitis |
230198004 | Varicella transverse myelitis |
230199007 | Post-infectious encephalomyelitis |
230202002 | Vacuolar myelopathy |
230208003 | Cerebral pyogenic abscess |
230209006 | Actinomycotic brain abscess |
230210001 | Brainstem pyogenic abscess |
230211002 | Multiple intracranial pyogenic abscesses |
230213004 | Candidal brain abscess |
230214005 | Cerebral hydatid cyst |
230215006 | Cerebral cysticercosis |
230216007 | Intraspinal pyogenic abscess |
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 |
23024003 | Macrogyria |
230241000 | Secondary cerebellar degeneration |
230242007 | Drug-induced cerebellar ataxia |
230243002 | Cerebellar ataxia caused by toxin |
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 |
230292008 | Secondary parkinsonism |
230293003 | Carbon monoxide-induced parkinsonism |
230294009 | Manganese-induced parkinsonism |
230295005 | Parkinsonism with calcification of basal ganglia |
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 |
230310003 | Paroxysmal dystonia |
230311004 | Basal ganglia degeneration with calcification |
230312006 | Aicardi Goutieres syndrome |
230313001 | Autosomal dominant late onset basal ganglia degeneration |
230314007 | Sandifer syndrome |
230315008 | Drug-induced dystonia |
230316009 | Drug-induced acute dystonia |
230317000 | Drug-induced tardive dystonia |
230318005 | Idiopathic familial dystonia |
230319002 | Autosomal dominant idiopathic familial dystonia |
230320008 | Autosomal recessive idiopathic familial dystonia |
230321007 | Idiopathic non-familial dystonia |
230322000 | Isolated cervical dystonia |
230323005 | Spasmodic retrocollis |
230324004 | Isolated blepharospasm |
230325003 | Meige syndrome |
230326002 | Idiopathic orofacial dystonia |
230327006 | Edentulous orofacial dystonia |
230328001 | Isolated oromandibular dystonia |
230329009 | Posthemiplegic dystonia |
230330004 | Occupational dystonia |
230332007 | Diurnal dystonia |
230333002 | Drug-induced akathisia |
230334008 | Drug-induced tic |
230335009 | Facial tic disorder |
230336005 | Vocal tic disorder |
230337001 | Motor tic disorder |
230338006 | Gestural tic disorder |
230343004 | Symptomatic myoclonus |
230344005 | Post-anoxic myoclonus |
230345006 | Postencephalitic myoclonus |
230346007 | Drug-induced myoclonus |
230347003 | Segmental cord myoclonus |
230348008 | Palatal-tympanic myoclonus |
230349000 | Hyoid myoclonus |
230350000 | Opsoclonus-myoclonus syndrome |
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 |
230377009 | Extrapontine myelinolysis |
230378004 | Acute non-infective transverse myelitis |
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 |
230431001 | Situation-related seizures |
230432008 | Familial febrile convulsions |
230433003 | Isolated seizures |
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 |
230455006 | Self-induced non-photosensitive 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 |
230462002 | Migraine with typical aura |
230464001 | Non-familial hemiplegic migraine |
230465000 | Migraine aura without headache |
230466004 | Alternating hemiplegia of childhood |
230467008 | Status migrainosus |
230468003 | Migraine with ischemic complication |
230470007 | Episodic tension-type headache |
230471006 | Chronic tension-type headache |
230472004 | Episodic cluster headache |
230473009 | Chronic cluster headache |
230474003 | Chronic cluster headache unremitting from onset |
230475002 | Chronic cluster headache evolved from episodic cluster headache |
230476001 | Atypical cluster headache |
230488004 | Hypersomnia of non-organic origin |
230500006 | Sleep-related dystonia |
230521006 | Optic radiation disorder |
230522004 | Inflammatory disorder of optic radiation |
230523009 | Infarction of optic radiation |
230525002 | Compression of optic radiation |
230526001 | Compression of visual cortex |
230539002 | Cluster tic syndrome |
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 |
230651008 | Disorders of spinal neurones manifest by hyperactivity |
230652001 | Benign fasciculation-cramp syndrome |
230654000 | Painful legs and moving toes |
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 |
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 |
230754006 | Uncinate herniation |
230755007 | Upwards herniation of cerebellum |
230756008 | Transtentorial herniation |
230757004 | Transtentorial herniation downwards |
230758009 | Transtentorial herniation upwards |
230759001 | Vasogenic cerebral edema |
230760006 | Cytotoxic cerebral edema |
230761005 | Periventricular cerebrospinal fluid edema |
230762003 | High altitude cerebral edema |
230763008 | Cerebral edema due to trauma |
230766000 | Multicystic encephalomalacia |
230769007 | Periventricular leukomalacia |
230773005 | Spastic cerebral palsy |
230780007 | Dyskinetic cerebral palsy |
230781006 | Dystonic/rigid cerebral palsy |
230782004 | Dysequilibrium syndrome |
230784003 | Congenital pseudobulbar palsy |
230786001 | Congenital dysphasia |
230787005 | Congenital expressive dysphasia |
230788000 | Congenital receptive dysphasia |
230790004 | Choroid plexus cyst |
230791000 | Hypothalamic neuronal hamartoma |
230796005 | Non-diabetic hypoglycemic coma |
230801000 | Post-ictal coma |
230802007 | Brainstem death |
230806005 | Brain ventricular shunt infection |
230807001 | Brain ventricular shunt displacement |
230808006 | Brain ventricular shunt obstruction |
231439009 | Toxic confusional state |
231440006 | Delirium of mixed origin |
231442003 | Organic catatonic disorder |
231443008 | Right hemispheric organic affective disorder |
231444002 | Organic bipolar disorder |
231445001 | Organic dissociative disorder |
231446000 | Organic emotionally labile disorder |
231448004 | Age-associated memory impairment |
231449007 | Epileptic psychosis |
231450007 | Psychosis associated with intensive care |
231451006 | Drug-induced intensive care psychosis |
231452004 | Limbic epilepsy personality syndrome |
231453009 | Lobotomy syndrome |
231454003 | Organic pseudopsychopathic personality |
231455002 | Organic pseudoretarded personality |
231456001 | Postleucotomy syndrome |
23186000 | Menstrual migraine |
232036006 | Cilioretinal artery occlusion |
232059000 | Laurence-Moon syndrome |
23276006 | Ventricular hemorrhage |
23283004 | Open fracture of T1-T6 level with incomplete spinal cord lesion |
233718008 | Pulmonary tuberous sclerosis |
23374007 | Atypical absence seizure |
233964008 | Internal carotid artery stenosis |
233983001 | Ruptured cerebral aneurysm |
233988005 | Carotid artery aneurysm |
234005004 | Vertebral artery rupture |
234006003 | Carotid artery rupture |
234142008 | Cerebral arteriovenous malformation |
234149004 | Congenital arteriovenous fistula of brain |
23501004 | Arginase deficiency |
2355008 | Rud's syndrome |
23645006 | Organic mood disorder |
236529001 | Prune belly syndrome with pulmonic stenosis, mental retardation and deafness |
23671000119107 | Sequela of ischemic cerebral infarction |
237120002 | Hypothalamic amenorrhea |
23713006 | Contusion of cerebral cortex |
23728006 | Partial bilateral paralysis |
237283007 | Eclampsia in labor |
23732000 | Primary cerebellar degeneration |
237349002 | Mild postnatal depression |
237351003 | Mild postnatal psychosis |
23740006 | Bilateral paralysis of tongue |
237512007 | Thyrotoxicosis due to thyrotropin-secreting pituitary adenoma |
237577005 | Abnormality of somatostatin secretion |
237578000 | Excessive somatostatin secretion |
237595008 | Abnormality of neurotensine secretion |
237612000 | Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction |
237662005 | Hyperprolactinemia |
237663000 | Idiopathic hyperprolactinemia |
237664006 | Pituitary stalk compression hyperprolactinemia |
237665007 | Drug-induced hyperprolactinemia |
237666008 | Physiological hyperprolactinemia |
237667004 | Lactation hyperprolactinemia |
237668009 | Pregnancy hyperprolactinemia |
237669001 | Adrenocorticotropic hormone hypersecretion |
237670000 | Adrenocorticotropic hormone hypersecretion not causing Cushing syndrome |
237671001 | Gonadotrophin hypersecretion |
237672008 | Luteinizing hormone hypersecretion |
237673003 | Follicle-stimulating hormone hypersecretion |
237674009 | Anterior pituitary hyperplasia |
237675005 | Somatotroph hyperplasia |
237676006 | Lactotroph hyperplasia |
237677002 | Gonadotroph hyperplasia |
237678007 | Thyrotroph hyperplasia |
237680001 | Corticotroph hyperplasia |
237682009 | Panhypopituitarism - anterior and posterior |
237683004 | Panhypopituitarism - X-linked |
237684005 | Sheehan's syndrome |
237685006 | Partial hypopituitarism |
237687003 | Isolated growth hormone deficiency - autosomal dominant |
237688008 | Idiopathic growth hormone deficiency |
237689000 | Growth hormone neurosecretory dysfunction |
237691008 | Psychosocial growth hormone deficiency |
237692001 | Adrenocorticotropic hormone deficiency |
237693006 | Idiopathic adrenocorticotropic hormone deficiency |
237694000 | Steroid suppression of adrenocorticotropic hormone secretion |
237695004 | Idiopathic thyroid stimulating hormone deficiency |
237696003 | Familial central diabetes insipidus |
237697007 | Oxytocin deficiency |
237698002 | Iatrogenic hypopituitarism |
237699005 | Post-traumatic hypopituitarism |
237700006 | Hypopituitarism due to iron overload |
237701005 | Pituitary apoplexy |
237702003 | Pituitary hemorrhage |
237703008 | Pituitary fibrosis |
237704002 | Pituitary fibrosis with midline fibrosis |
237705001 | Hypophysitis |
237706000 | Autoimmune hypophysitis |
237707009 | Lymphocytic hypophysitis of pregnancy |
237708004 | Granulomatous giant-cell hypophysitis |
237709007 | Granuloma of pituitary and hypothalamus |
237710002 | Pituitary granuloma |
237711003 | Hypothalamic granuloma |
237714006 | Hamartoma of hypothalamus |
237716008 | Pituitary cyst |
237717004 | Arachnoid cyst of pituitary |
237718009 | Pituitary gland enlarged |
237719001 | Pituitary adenoma with extrasellar extension |
237720007 | Hamartoma of pituitary and hypothalamus |
23772009 | Dysphonia of Gilles de la Tourette's syndrome |
237721006 | Tumor of pituitary and suprasellar region |
237723009 | Pituitary stalk compression |
237724003 | Hypothalamic disorder of appetite |
237725002 | Defective osmoregulation |
237726001 | Osmoregulation defect - absent thirst |
237727005 | Osmoregulation defect - excess thirst |
237728000 | Absent osmoregulation |
237729008 | Reset hypothalamic osmostat |
237730003 | Hypothalamic overactivity |
237731004 | Loss of hypothalamic inhibition |
237733001 | Diencephalic syndrome |
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 |
23871000119106 | Somnambulism co-occurrent with sleep terror disorder |
238826008 | de Barsy syndrome |
238972008 | Cutaneous monosymptomatic delusional psychosis |
238973003 | Delusions of parasitosis |
238974009 | Delusions of infestation |
238975005 | Delusion of foul odor |
238977002 | Delusional hyperhidrosis |
238978007 | Hyperschemazia |
238979004 | Hyposchemazia |
239026002 | Hypohidrosis-diabetes insipidus 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 |
240058001 | Reunion-Indiana Amish type 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 |
240312009 | Cerebral injury due to birth trauma |
240393003 | Listeria cerebritis |
240448007 | Legionella encephalopathy |
240460008 | Acute paralytic poliomyelitis |
240464004 | Rabies coma |
24059009 | Acute cerebellar ataxia caused by varicella |
240845003 | Cerebral loiasis |
240875008 | Cerebral gnathostomiasis |
241006 | Epilepsia partialis continua |
241992009 | Spinal cord decompression injury |
241993004 | Cerebral decompression injury |
241994005 | Cerebellar decompression injury |
2421000119107 | Hallucinations co-occurrent and due to late onset dementia |
24326000 | Metachromatic leukodystrophy, adult type |
2438005 | Iniencephaly |
24392008 | Injury at C1-C4 level with spinal cord injury AND without bone injury |
24473007 | Persistent vegetative state |
24624008 | Aneurysm of internal carotid artery |
24630008 | Listeria meningoencephalitis |
246528007 | Simple partial seizure with focal motor signs without march |
246529004 | Simple partial seizure with focal motor signs with march |
246530009 | Versive seizure |
246531008 | Postural seizure |
246532001 | Phonatory seizure |
246533006 | Simple partial seizure with somatosensory or special sensory dysfunction |
246535004 | Dysphasic seizure |
246536003 | Cognitive seizure |
246537007 | Affective seizure |
246538002 | Seizure causing illusions |
246539005 | Seizure with structured hallucinations |
246540007 | Simple partial seizure followed by impaired consciousness |
24654003 | Weber-Gubler syndrome |
246541006 | Simple partial onset of seizure with automatisms |
246542004 | Complex part seizure with impairment of consciousness only |
246544003 | Partial seizure evolving to secondary generalized seizure |
246546001 | Absence seizure with impairment of consciousness only |
246548000 | Absence seizure with mild clonic components |
246549008 | Absence seizure with atonic components |
246550008 | Absence seizure with tonic components |
246551007 | Absence seizure with automatisms |
246552000 | Absence seizure with autonomic components |
24700007 | Multiple sclerosis |
247400008 | Painful arms and moving fingers |
248260009 | Unrefreshed by sleep |
2495006 | Congenital cerebral arteriovenous aneurysm |
249892007 | Progressive pseudobulbar palsy |
24991000119103 | Thoracic myelopathy |
25044007 | Neuromyelitis optica |
25133001 | Completed stroke |
25185004 | Cerebellar contusion with open intracranial wound AND no loss of consciousness |
25297005 | Psychogenic adductor spastic dysphonia |
253010003 | Microprolactinoma |
253011004 | Macroprolactinoma |
253098009 | Neural tube defect |
253101008 | Congenital cerebral hernia |
253103006 | Frontal encephalocele |
253104000 | Frontoethmoidal encephalocele |
253106003 | Nasofrontal encephalocele |
253107007 | Nasopharyngeal encephalocele |
253108002 | Temporal encephalocele |
253109005 | Parietal encephalocele |
253111001 | Thoracolumbar spina bifida without hydrocephalus - closed |
253113003 | Rachischisis with hydrocephalus |
253114009 | Myelocele with hydrocephalus |
253115005 | Hydromyelocele with hydrocephalus |
253117002 | Closed spina bifida with Arnold-Chiari malformation |
253118007 | Thoracolumbar spina bifida with hydrocephalus - closed |
253119004 | Hemimyelocele |
253120005 | Lipomeningocele |
253124001 | Myelodysplasia of spinal cord |
253125000 | Spinal hamartoma |
253130001 | Secondary microcephaly |
253131002 | Hydrocephalus associated with late onset aqueduct stenosis |
253132009 | External hydrocephalus |
253133004 | Hydrocephalus with anomaly of aqueduct of Sylvius |
253135006 | Defect of telencephalic division |
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 |
253144007 | Cyst of septum pellucidum |
253145008 | Reduction anomaly of hypothalamus |
253147000 | Type 1 lissencephaly |
253148005 | Miller Dieker syndrome |
253149002 | Type 2 lissencephaly |
253151003 | Nodular heterotopia |
253152005 | Laminar heterotopia |
253153000 | Cortical dysplasia |
253154006 | Localized cortical dysplasia |
253156008 | Cortical dysplasia with hemimegalencephaly |
253158009 | Hydranencephaly with proliferative vasculopathy |
253159001 | Schizencephaly |
253160006 | Colpocephaly |
253163008 | Spinal arachnoid cyst |
253164002 | Intradural spinal arachnoid cyst |
253165001 | Extradural spinal arachnoid cyst |
253167009 | Microdysgenesis |
253168004 | Familial megalencephaly |
253169007 | Sporadic megalencephaly |
253170008 | Hemimegalencephaly |
253171007 | Dysgenesis of the cerebellum |
253172000 | Agenesis of cerebellum |
253174004 | Aplasia of the vermis |
253175003 | Familial aplasia of the vermis |
253176002 | Gillespie syndrome |
253177006 | Absence of the vermis |
253178001 | Granular cell hypoplasia |
253179009 | Cerebellar cortical dysplasia |
253180007 | Dysgenesis of the brainstem |
253181006 | Olive dysplasia |
253182004 | Dentate dysplasia |
253183009 | Olivary heterotopia |
253184003 | Chiari malformation |
253185002 | Chiari malformation type I |
253186001 | Chiari malformation type III |
253187005 | Chiari malformation type IV |
253188000 | Abnormality of canalization and retrogressive differentiation |
253189008 | Sacral dysgenesis |
253190004 | Lumbosacral agenesis |
253192007 | Fibrolipoma of filum terminale |
253194008 | Aneurysm of the vein of Galen |
253203003 | Hypoplasia of brain gyri |
25331007 | Injury at T7-T12 level with spinal cord injury AND without bone injury |
25362006 | Phytanic acid storage disease |
253699002 | Isolation of common carotid artery |
25397008 | Aqueduct of Sylvius anomaly |
254092004 | Saldino-Mainzer dysplasia |
254243001 | Ash leaf spot, tuberous sclerosis |
254255007 | Congenital malformation of anterior pituitary |
254256008 | Congenital malformation of posterior pituitary |
254775002 | Bregeat's syndrome |
254936001 | Glial tumor of brain |
254938000 | Astrocytoma of brain |
254939008 | Ependymoma of brain |
254940005 | Oligodendroglioma of brain |
254941009 | Mixed glial tumor of brain |
254942002 | Tumor of choroid plexus |
254943007 | Benign tumor of choroid plexus |
254945000 | Embryonal tumor of brain |
254946004 | Glial tumor of spinal cord |
254947008 | Glioma of spinal cord |
254948003 | Astrocytoma of spinal cord |
254949006 | Ependymoma of spinal cord |
254950006 | Oligodendroglioma of spinal cord |
254951005 | Mixed glial tumor of spinal cord |
254954002 | Embryonal tumor of spinal cord |
254955001 | Pituitary carcinoma |
254956000 | Pituitary adenoma |
254957009 | Somatotroph adenoma |
254958004 | Corticotroph adenoma |
254959007 | Thyrotroph adenoma |
254960002 | Gonadotroph adenoma |
254961003 | Mixed-functioning pituitary adenoma |
254962005 | Functionless pituitary adenoma |
254963000 | Pituitary microadenoma |
254964006 | Pituitary mesoadenoma |
254965007 | Pituitary macroadenoma |
254966008 | Suprasellar extension of pituitary adenoma |
254968009 | Tumor of hypothalamus |
254969001 | Malignant tumor of olfactory tract |
254970000 | Benign 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 |
255200003 | Benign tumor of hypothalamus |
256321009 | Disorder of neuromuscular transmission |
257277002 | Combined disorder of muscle AND peripheral nerve |
25772007 | Multi-infarct dementia with delusions |
25816005 | Brain stem compression |
2584003 | Cerebral degeneration in childhood |
2593002 | Dubowitz's syndrome |
26015003 | Maroteaux-Lamy syndrome, intermediate form |
26021000119107 | Vertigo as sequela of cerebrovascular disease |
26037005 | Radiation-induced myelopathy |
260912008 | Abnormal involuntary movement |
26135000 | Syphilitic encephalitis |
26206000 | Hepatic coma due to viral hepatitis B |
262687004 | Cerebellar laceration and contusion |
262688009 | Cortex laceration and contusion |
262689001 | Contusion of cerebrum |
262691009 | Laceration of cerebrum |
262692002 | Burst lobe of brain |
262693007 | Diffuse brain injury |
262694001 | Traumatic generalized cerebral edema |
262695000 | Traumatic focal cerebral edema |
262696004 | Contusion of spinal cord |
262697008 | Contusion of cervical cord |
262698003 | Contusion of thoracic cord |
262699006 | Contusion of lumbar cord |
262700007 | Contusion of sacral cord |
262701006 | Edema of cervical cord |
262702004 | Edema of thoracic cord |
262703009 | Edema of lumbar cord |
262704003 | Edema of sacral cord |
262705002 | Laceration of spinal cord |
262706001 | Laceration of cervical cord |
262707005 | Laceration of thoracic spinal cord |
262708000 | Laceration of lumbar cord |
262709008 | Laceration of sacral cord |
262710003 | Transection of spinal cord |
262711004 | Transection of cervical cord |
262712006 | Transection of thoracic cord |
262713001 | Transection of lumbar cord |
262714007 | Transection of sacral cord |
262718005 | Traumatic spinal cord hemorrhage |
262719002 | Traumatic spinal subarachnoid hemorrhage |
262721007 | Traumatic spinal subdural hematoma |
26298008 | Ketoacidotic coma due to diabetes mellitus |
263179007 | Fracture of transverse process of spine with spinal cord lesion |
264534009 | Hypothalamic injury |
264906008 | Pituitary macroadenoma with extrasellar extension |
265377002 | Symptomatic parkinsonism |
26554009 | Nuclear facial nerve paralysis |
26568002 | Faun tail syndrome |
26594006 | Syringobulbia |
26595007 | Congenital absence of part of brain |
266196000 | Rabies - hydrophobia |
266253001 | Precerebral arterial occlusion |
266254007 | Occlusion of carotid artery |
266257000 | Transient ischemic attack |
26714005 | Cannabis-induced psychotic disorder with hallucinations |
26738009 | Spinal cord injury without spinal bone injury |
267384006 | Coma due to hypoglycemia |
267386008 | Gigantism and acromegaly |
267388009 | Idiopathic hypopituitarism |
267389001 | Post-birth injury hypopituitarism |
267390005 | Post-infarction hypopituitarism |
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 |
268722008 | Non-organic disorder of the sleep-wake schedule |
268956009 | On examination - focal (Jacksonian) fit |
269144002 | Cerebral laceration and contusion |
26929004 | Alzheimer's disease |
26954004 | Thrombophlebitis of superior sagittal sinus |
27040004 | Experimental allergic encephalomyelitis |
270487001 | Non-organic sleep disorder |
271386001 | Post-infective hypopituitarism |
271479005 | Benign neoplasm of pituitary gland and craniopharyngeal duct |
27148008 | Hereditary motor end-plate disease |
271569006 | Communicating hydrocephalus |
27195007 | Chronic non-psychotic brain syndrome |
271969004 | Disorder of dorsal column stimulator |
271986005 | Disorder of brain ventricular shunt |
27270004 | Pituitary dwarfism with large sella turcica |
27358001 | Sylvian aqueduct syndrome |
274100004 | Cerebral hemorrhage |
274156000 | Fracture of cervical spine with cord lesion |
274157009 | Fracture of thoracic spine with cord lesion |
274158004 | Fracture of lumbar spine with cord lesion |
274659008 | Semicoma |
275269004 | Benign cerebral tumor |
275362006 | Falx laceration |
275363001 | Rupture of superficial cerebral vein |
275382005 | Cerebral trauma |
275434003 | Stroke in the puerperium |
275468009 | Congenital quadriplegia |
275470000 | Post-cardiorespiratory arrest coma |
276219001 | Occipital cerebral infarction |
276220007 | Foville syndrome |
276221006 | Millard-Gubler syndrome |
276222004 | Top of basilar syndrome |
27642008 | Dysmorphic sialidosis, congenital form |
276592005 | Perinatal occipital diastasis |
276594006 | Perinatal rupture of superficial cerebral vein |
276595007 | Perinatal nonspecific brain dysfunction |
276596008 | Cerebral irritation |
276597004 | Fifth day fits |
276599001 | Cerebral leukomalacia |
276630006 | Transient hypothyrotropinemia |
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 |
276837006 | Epidermoid cyst of brain |
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 |
277326006 | Spinal cord rupture |
277328007 | Ruptured internal carotid-anterior communicating artery zone aneurysm |
277329004 | Ruptured internal carotid-posterior communicating artery zone aneurysm |
277330009 | Ruptured internal carotid bifurcation aneurysm |
277340007 | Tension pneumocephalus |
277369003 | Hamartoma of brain |
277373000 | Severe childhood autosomal recessive muscular dystrophy |
277456001 | Suprasellar germ cell tumor |
277461004 | Anaplastic astrocytoma of brain |
277476007 | Cerebral ventricular distension |
277478008 | Post-asphyxial encephalopathy |
277479000 | Postnatal hypoxic encephalopathy |
277480002 | Neonatal asphyxial encephalopathy |
277505007 | Medulloblastoma of cerebellum |
277507004 | Pilocytic astrocytoma of cerebellum |
277508009 | Pineal germ cell tumor |
277530005 | Malignant melanoma of meninges |
2776000 | Delirium |
277921008 | Atelencephaly |
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 |
27873005 | Spinopontine degeneration |
278849000 | Cerebral atrophy |
278852008 | Paranoid-hallucinatory epileptic psychosis |
278855005 | Frontal lobe degeneration |
278857002 | Dementia of frontal lobe type |
27908001 | Amebic brain abscess |
27937002 | Anterior cord syndrome co-occurrent and due to open fracture of T7-T12 level |
27956007 | Cocaine intoxication |
27982003 | Brown-Séquard syndrome |
279953009 | Familial neonatal seizures |
279982005 | Cerebral degeneration presenting primarily with dementia |
28055006 | West syndrome |
280994000 | Chronic confusional state |
281004 | Dementia associated with alcoholism |
281240008 | Extension of cerebrovascular accident |
281411007 | Spastic diplegia |
281509000 | Hypoxic-ischemic coma |
28155008 | Extradural hemorrhage following injury with open intracranial wound AND concussion |
281560004 | Neuroblastoma of brain |
28188001 | Brain injury with open intracranial wound |
281899002 | Congenital hydrocephalus caused by toxoplasmosis |
28212002 | Intestinal lipofuscinosis |
282785008 | Anterior cord syndrome |
282786009 | Posterior cord syndrome |
282787000 | Central cord syndrome |
28318001 | Basilar hemorrhage |
28366008 | Cerebral arteritis |
28368009 | Psychoactive substance-induced organic hallucinosis |
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 |
2851000119101 | Anterior pituitary hormone deficiency |
285145004 | Akathisia |
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 |
28676002 | Mood disorder with manic features due to general medical condition |
286914008 | Pituitary, parathyroid, thymus disorder |
286933003 | Confusional state |
28721000119108 | Postvaricella myelitis |
287731003 | Cerebral ischemia |
28778005 | Phrenic nerve paralysis as birth trauma |
28790007 | Obstruction of precerebral artery |
288461000119105 | Psychosis caused by inhalant |
288631000119104 | Vascular dementia with behavioral disturbance |
28864000 | Sedative, hypnotic AND/OR anxiolytic-induced mood disorder |
288723005 | Acute ill-defined cerebrovascular disease |
288851000119106 | Opioid-induced mood disorder due to opioid abuse |
288861000119108 | Opioid-induced mood disorder due to opioid dependence |
29003001 | Spastic dysphonia |
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 |
290531000119102 | Intractable chronic tension headache |
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 |
290653008 | Postpartum hypopituitarism |
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 |
291665000 | Postpartum intrapituitary 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 |
29197009 | Meningoencephalomyelitis |
29212009 | Alcohol-induced organic mental disorder |
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 |
292871000119100 | Acquired pseudoporencephaly |
292921000119109 | Intraspinal granuloma |
292931000119107 | Intraspinal subdural granuloma |
292941000119103 | Intraspinal epidural granuloma |
292971000119105 | Disorder due to and following injury of thoracic spinal cord |
292991000119106 | Eaton Lambert syndrome without underlying malignancy |
29315008 | Idiopathic adductor spastic dysphonia |
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 |
29702001 | Aphasia-left parietal lobe syndrome |
297138001 | Embolus of circle of Willis |
297157005 | Intracranial venous thrombosis |
297176007 | Vertebral artery aneurysm |
297278001 | Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator |
29733004 | Opioid-induced mood disorder |
29753000 | Partial seizure |
29774004 | Vascular myelopathy |
29807001 | Brain stem contusion without open intracranial wound AND with loss of consciousness |
298282001 | Spastic quadriparesis |
2992000 | Pigmentary pallidal degeneration |
29941000119105 | Ataxia as sequela of cerebrovascular disease |
29951000119107 | Ataxic hemiparesis |
29956001 | Myelatelia |
29963001 | Dysmnesic seizure |
30023002 | Hydranencephaly |
30031007 | Cerebellar laceration without open intracranial wound |
30057005 | Polioencephalopathy |
300920004 | Carotid atherosclerosis |
300992002 | Alcohol-induced cerebellar ataxia |
300993007 | Drug-induced orofacial dyskinesia |
301643003 | Sedative, hypnotic AND/OR anxiolytic-induced persisting amnestic disorder |
301764006 | Hematoma of brain |
301765007 | Cerebellar hematoma |
302213007 | Caroticocavernous sinus fistula |
30243004 | Cerebral anoxia following molar AND/OR ectopic pregnancy |
302507002 | Sedative amnestic disorder |
30278004 | Kundrat's syndrome |
302811004 | Progressive congenital rubella encephalomyelitis |
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 |
302904002 | Infarction of visual cortex |
302909007 | Diffuse cerebrovascular disease |
303061003 | Cerebellar pyogenic abscess |
303063000 | Eclampsia in puerperium |
30310000 | Nicotine-induced organic mental disorder |
30371007 | Cerebral laceration AND contusion co-occurrent and due to open fracture of base of skull |
30400005 | Middle meningeal hemorrhage following injury |
304603007 | Variant Creutzfeldt-Jakob disease |
30491001 | Cocaine delusional disorder |
305719002 | Neuromyotonia |
30620003 | Spina bifida of dorsal region |
3072001 | Hormone-induced hypopituitarism |
307212006 | Brain ventricular shunt malfunction |
307355007 | Congenital athetosis |
307356008 | Motor epilepsy |
307357004 | Jacksonian, focal or motor epilepsy |
307359001 | Congenital agenesis of brainstem nuclei |
30736009 | Dysphonia of palatopharyngolaryngeal myoclonus |
307362003 | Intracranial venous septic embolism |
307363008 | Multiple lacunar infarcts |
30753002 | Normal pressure hydrocephalus |
307649006 | Microglioma |
307672008 | Oculopalatal myoclonus |
307680001 | Abducting nystagmus |
307756005 | Cerebral palsy, not congenital or infantile, acute |
307766002 | Left sided cerebral infarction |
307767006 | Right sided cerebral infarction |
30858001 | Cerebellar laceration with open intracranial wound |
308634000 | Spinal demyelination |
308680003 | Hypoglycemia-induced convulsion |
30871003 | Flashbacks |
308742005 | Alcohol withdrawal-induced convulsion |
30915001 | Holoprosencephaly sequence |
309279000 | Caffeine-induced organic mental disorder |
309789002 | Encephalitis caused by influenza |
31033002 | Closed fracture of T1-T6 level with posterior cord syndrome |
31076000 | Congenital ischemic atrophy of central nervous system structure |
31081000119101 | Presenile dementia with delusions |
31097004 | Post poliomyelitis syndrome |
31112008 | Tuberculous meningoencephalitis |
311191000119109 | Myelopathy co-occurrent and due to lumbosacral intervertebral disc disorder |
311825006 | Traumatic cerebral edema without open intracranial wound |
311826007 | Traumatic cerebral edema with open intracranial wound |
3119002 | Brain stem laceration with open intracranial wound AND loss of consciousness |
31216003 | Profound intellectual disability |
312215006 | Infective encephalitis |
312217003 | Infective ventriculitis, brain |
31235003 | Anterior cord syndrome co-occurrent and due to closed fracture of C5-C7 level |
312372003 | Cerebral akinetopsia |
312586003 | Intracranial thrombophlebitis |
312786001 | Spinal subluxation with cervical cord lesion |
312787005 | Spinal subluxation with thoracic cord lesion |
312788000 | Spinal subluxation with lumbar cord lesion |
31283000 | Abductor spastic dysphonia |
312837005 | Spinal dislocation with cervical cord lesion |
312838000 | Spinal dislocation with thoracic cord lesion |
312839008 | Spinal dislocation with lumbar cord lesion |
312936002 | Anxiolytic-induced organic mental disorder |
312991009 | Senile dementia of the Lewy body type |
313304007 | Non-traumatic spinal subdural hematoma |
313434001 | Residual hemiplegia |
31367003 | Postvaccinal encephalomyelitis |
31429000 | Cerebral cortical dysgenesis |
31430005 | Medication-induced postural tremor |
314950006 | Migration of spinal cord stimulator |
315046005 | Traumatic subdural hematoma without open intracranial wound |
315608004 | Cardiomyopathy in Duchenne muscular dystrophy |
31646008 | Mumps encephalitis |
31715000 | Phencyclidine delirium |
31839002 | Myasthenia gravis, adult form |
31882001 | Closed fracture of T1-T6 level with spinal cord injury |
32009006 | Hallucinogen hallucinosis |
32106001 | Cortex contusion without open intracranial wound |
32112006 | Phlebitis of inferior sagittal sinus |
32162001 | Facial hemiplegia |
322112361000132104 | Epilepsy due to scarring of brain |
32219008 | Craniorachischisis |
32232003 | Spina bifida of cervical region |
32358001 | Amphetamine delusional disorder |
32390006 | Panhypopituitarism |
32415004 | Cerebellar contusion without open intracranial wound AND with concussion |
32552001 | Psychoactive substance-induced organic delusional disorder |
32641000119107 | Exercise induced hypothalamic insufficiency |
32680009 | Nothnagel's syndrome |
32728005 | Hemorrhage due to ruptured congenital cerebral aneurysm |
32735002 | Congenital syphilitic encephalitis |
32798002 | Parkinsonism |
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 |
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 |
3298001 | Amnestic disorder |
330011000119102 | Non-traumatic cerebral edema |
330041000119103 | Congenital porencephalic cyst |
330061000119104 | Acquired cerebral ventriculomegaly |
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 |
33147008 | Open fracture of C1-C4 level with posterior cord syndrome |
33301000119105 | Sequela of cardioembolic stroke |
3331000119108 | Laryngeal dystonia |
33316007 | GM 2 gangliosidosis |
33331000119103 | Sequela of lacunar stroke |
33332005 | Brain injury without open intracranial wound AND with concussion |
33441000119100 | Transitional lipoma of spinal cord |
33559001 | Pineal hyperplasia AND diabetes mellitus syndrome |
336191000119105 | Occlusion of right central retinal artery |
3371000119106 | Refractory generalized convulsive epilepsy |
33772003 | Myelomalacia |
33871004 | Phencyclidine-induced psychotic disorder with hallucinations |
33927004 | Hypogonadotropic hypogonadism |
33941008 | Simple partial seizure with disturbance of higher cerebral function |
34041000119108 | Benign neoplasm of extramedullary spinal cord |
34101000119105 | Nocturnal myoclonus |
34139004 | Intervertebral disc disorder of lumbar region with myelopathy |
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 |
342741000119103 | Cortical blindness of right side of brain |
342751000119101 | Cortical blindness of left side of brain |
3446000 | Open fracture of T7-T12 level with spinal cord injury |
34476008 | Viral encephalitis |
3456001 | Chronic progressive non-hereditary chorea |
34601006 | Somatosensory seizure |
34663006 | Contusion of brain |
347011000119102 | Occlusion of bilateral central retinal arteries |
34781003 | Vertebral artery syndrome |
34938008 | Alcohol-induced anxiety disorder |
35111000119109 | Cystic malformation of posterior fossa |
35145002 | Uremic encephalopathy |
352818000 | Tonic-clonic epilepsy |
35386004 | Cavernous sinus syndrome |
35403005 | Closed fracture of C5-C7 level with posterior cord syndrome |
35640008 | Acute adenoviral encephalitis |
35691006 | Combined deficiency of sialidase AND beta galactosidase |
359619007 | Pinealoma |
359621002 | Acquired periventricular cysts of newborn |
359624005 | Acquired periventricular cyst |
359629000 | Progressive post hemorrhagic ventricular dilatation |
359634001 | Infantile posthemorrhagic hydrocephalus |
359686005 | Van Bogaert's sclerosing leukoencephalitis |
359824007 | Incomplete anencephaly |
36025004 | Fibrous skin tumor of tuberous sclerosis |
360353005 | Thyrotoxicosis due to pituitary thyroid hormone resistance |
360358001 | Thyrotoxicosis due to overproduction of thyroid stimulating hormone |
360361000 | Thyrotoxicosis due to inappropriate thyroid stimulating hormone secretion |
360527003 | Diplomyelia |
360530005 | Myeloschisis |
361000119103 | Paralytic syndrome on one side of the body as late effect of cerebrovascular accident |
361117008 | Female hypogonadotropic hypogonadism |
361123003 | Psychomotor epilepsy |
361151007 | Delirium due to sedative withdrawal |
361272001 | Cerebellar ataxia due to alcoholism |
361273006 | Alcoholic cerebellar degeneration |
36179005 | Reversible ischemic neurologic deficit syndrome |
36217008 | Organic personality disorder |
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 |
3652007 | Overproduction of growth hormone |
367460001 | Pituitary dwarfism |
36785009 | Aphasia-angular gyrus syndrome |
36803009 | Idiopathic generalized epilepsy |
3681008 | Thrombophlebitis of torcular Herophili |
368601000119102 | Hyperosmolar coma due to secondary diabetes mellitus |
368961000119107 | Partial nephrogenic diabetes insipidus |
370502006 | Encephalomyelopathy |
370987005 | Anaplastic astrocytoma of spinal cord |
371022006 | Seizures due to metabolic disorder |
371024007 | Senile dementia with delusion |
371026009 | Senile dementia with psychosis |
371029002 | Ischemic disorder of spinal cord |
371031006 | Staphylococcus epidermidis ventriculitis |
371040005 | Thrombotic stroke |
371041009 | Embolic stroke |
371050006 | Traumatic intracranial subdural hematoma with brief loss of consciousness |
371076006 | Congenital syringomyelia |
371077002 | Ventriculoperitoneal shunt malfunction |
371079004 | Paraplegic cerebral palsy |
371107004 | Seizures complicating intracranial hemorrhage in the newborn |
371114002 | Seizures complicating intracranial hemorrhage |
371115001 | Seizures complicating infection |
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 |
372441001 | Seizures complicating infection in the newborn |
372477008 | Post-traumatic syrinx |
37331004 | Psychoactive substance-induced organic mood disorder |
37340000 | Motor neuron disease |
37356005 | Myoclonic seizure |
373587001 | Chiari malformation type II |
373590007 | Convergence retraction nystagmus |
373606000 | Occlusive stroke |
37429009 | Hypothalamic hypothyroidism |
37650008 | Hereditary cerebellar degeneration |
37739004 | Mood disorder due to a general medical condition |
37934003 | Mitochondrial-lipid-glycogen storage myopathy |
37943007 | Multiple AND bilateral precerebral artery embolism |
37960002 | Sanger-Brown cerebellar ataxia |
38023001 | Locked in syndrome |
38115001 | Tuberculosis of spinal meninges |
38116000 | Hydromyelocele |
38228000 | Paralysis of tongue |
38353004 | Congenital porencephaly |
38403006 | Vertigo of central origin |
384993003 | Periventricular hemorrhagic venous infarct |
38523005 | Syphilitic parkinsonism |
38576000 | Nonfamilial hyperinsulinemic isolated somatotropin deficiency |
38632003 | Pharyngeal pituitary tissue |
386766007 | Marchiafava-Bignami disease |
386805003 | Mild cognitive disorder |
38742007 | Central retinal artery occlusion |
387732009 | Becker muscular dystrophy |
38795005 | Sialidosis |
38837006 | Acquired porencephaly |
389088001 | Hypoxia of brain |
389089009 | Anoxia of brain |
389098007 | Anoxic encephalopathy |
389100007 | Ischemic encephalopathy |
389101006 | Anoxic-ischemic encephalopathy |
389271000 | Spondyloenchondromatosis with basal ganglia calcification |
38941006 | Neuroleptic-induced tardive dyskinesia |
39003006 | Psychoactive substance-induced organic delirium |
39020005 | Brain injury, without skull fracture |
390936003 | Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy |
39134007 | Hematomyelia |
39150004 | Congenital anomaly of spinal meninges |
39194005 | Visual epilepsy |
392662004 | West Nile encephalitis |
39390005 | Niemann-Pick disease, type B |
39574006 | Congenital hypoplasia of inner granular layer of cerebellum |
396338004 | Metachromatic leucodystrophy |
39745004 | Chronic progressive epilepsia partialis continua |
397734008 | Hereditary sensory and autonomic neuropathy type I |
397763006 | Human immunodeficiency virus encephalopathy |
397827003 | Growth hormone deficiency |
397961002 | Encephalomyelitis caused by lymphocytic choriomeningitis virus |
398040009 | Charcot-Marie-Tooth disease, type I |
39807006 | Cannabis intoxication delirium |
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 |
398329009 | Human immunodeficiency virus encephalitis |
398432008 | Bulbar weakness |
399041003 | Chastek paralysis |
399091004 | Facioscapulohumeral muscular dystrophy |
399100005 | Disorder of hypothalamus |
39912006 | Hereditary spastic paraplegia |
399244003 | Disorder of pituitary gland |
39925003 | Juvenile myopathy, encephalopathy, lactic acidosis AND stroke |
39951001 | Cannabis-induced anxiety disorder |
39960009 | Grimaces |
40099009 | Meningoencephalitis caused by mumps |
40130009 | Spina bifida without hydrocephalus |
40135004 | Subdural hemorrhage following injury without open intracranial wound AND with no loss of consciousness |
40161000119102 | Weakness of face muscles as sequela of stroke |
40230002 | Encephalitis caused by Langat virus |
402460000 | Familial amyloid polyneuropathy with cutaneous amyloidosis |
40259002 | Progressive sensory ataxia of Charolais |
402732001 | Habit tic |
402733006 | Habit tic affecting skin |
402735004 | Habit tic affecting hair |
40276003 | Embolism of precerebral artery |
40354009 | De Lange syndrome |
403595006 | Pinocchio syndrome |
403815003 | Axillary freckling due to neurofibromatosis |
403816002 | Multiple café-au-lait macules due to neurofibromatosis |
403817006 | Multiple neurofibromas in neurofibromatosis |
403819009 | Elephantiasis neurofibromatosa |
40405003 | Illegal abortion with cerebral anoxia |
404235004 | Jamestown Canyon virus encephalitis |
40425004 | Postconcussion syndrome |
40450001 | Embolism of superior sagittal sinus |
404664002 | Malignant optic glioma |
404689008 | Alternating hemiplegia |
404906000 | Post-operative confusion |
40571009 | Hallucinogen intoxication delirium |
405754008 | Cervical spinal cord injury |
405755009 | Anterior cervical spinal cord injury at C1-C4 level without spinal bone injury |
405756005 | Anterior cervical spinal cord injury, without spinal bone injury, C5-7 |
405757001 | Central cervical cord injury, without spinal bony injury, C1-4 |
405758006 | Central cervical cord injury, without spinal bony injury, C5-7 |
405759003 | Cervical spinal cord injury without spinal bone injury |
405760008 | Complete cervical cord injury, without spinal bone injury, C1-4 |
405761007 | Complete cervical cord injury, without spinal bone injury, C5-7 |
405764004 | Posterior cervical spinal cord injury without spinal bone injury, C5-7 |
405765003 | Posterior cervical spinal cord injury, without spinal bone injury, C1-4 |
4061000119104 | Myelomeningocele without hydrocephalus |
40632002 | Charcot-Marie-Tooth disease, type IA |
406573001 | Primary encephalitis |
40673001 | Post-encephalitic syndrome |
4069002 | Anoxic brain damage during AND/OR resulting from a procedure |
40700009 | Severe intellectual disability |
40720005 | Cerebral cyst |
407472000 | Nairoviral encephalitis |
407675009 | Complex partial epileptic seizure |
40781006 | Hypopituitarism due to pituitary tumor |
40802007 | Metachromatic leukodystrophy, congenital type |
40816002 | Retropulsion petit mal |
408664007 | Pontine artery occlusion |
408665008 | Pontine artery thrombosis |
4088009 | Acquired hydrocephalus |
40946000 | Hepatic coma due to viral hepatitis |
409556004 | Q fever encephalitis |
40980002 | Spastic paralysis due to birth injury |
410014007 | Post-traumatic communicating hydrocephalus |
410015008 | Post-traumatic non-communicating hydrocephalus |
41009006 | Progressive cerebellar tremor |
41022003 | Intervertebral disc disorder of thoracic region with myelopathy |
4103001 | Complex partial seizure with impairment of consciousness |
41040004 | Complete trisomy 21 syndrome |
41075004 | Fungal infection of brain |
41083005 | Alcohol-induced sleep disorder |
4113009 | Arrested hydrocephalus |
41133002 | Closed fracture of T7-T12 level with posterior cord syndrome |
41142009 | Globoid cell leukodystrophy, late-onset |
41222005 | Brain stem laceration with open intracranial wound AND concussion |
41283003 | Cerebro-oculo-facio-skeletal syndrome |
413099000 | Cyst of pineal gland |
413100008 | Akinetic rigid syndrome |
413101007 | Stress-induced epilepsy |
413102000 | Infarction of basal ganglia |
413638006 | Benign neonatal sleep myoclonus |
41370002 | Myelitis |
413758000 | Cardioembolic stroke |
413807008 | Cerebellar hernia |
413808003 | Cerebral ventriculomegaly |
413924001 | Cortical visual impairment |
414400006 | Hernia of cerebellar tonsil into foramen magnum |
414667000 | Meningomyelocele |
414927004 | Ocular myasthenia with strabismus |
415347009 | Rio Bravo viral encephalitis |
415525005 | Encephalitis caused by Siberian tick-borne encephalitis virus |
41574007 | Paramyotonia congenita |
41590007 | Familial amyloid polyneuropathy, Jewish type |
416073003 | Long duration flashbacks |
416123004 | Complaining of akathisia |
416265003 | Tuberculoma of brain |
416714005 | Episodic flashbacks |
416780008 | Primary degenerative dementia of the Alzheimer type, presenile onset |
416792008 | Vein of Galen malformation |
416903004 | Tuberculoma of spinal cord |
416975007 | Primary degenerative dementia of the Alzheimer type, senile onset |
417017003 | Acute cerebellar syndrome |
417075004 | Neuroinvasive California encephalitis virus infection |
41713005 | Benedikt's syndrome |
417143004 | Short duration flashbacks |
417360004 | Duplicative flashbacks |
417484006 | Tuberculous abscess of spinal cord |
417607009 | Neuroinvasive Saint Louis encephalitis virus infection |
417658006 | Holoanencephaly |
417872000 | Neuroinvasive Cache Valley encephalitis virus infection |
418143002 | Cerebral degeneration |
4183003 | Charcot-Marie-Tooth disease, type IC |
418455000 | Encephalitis caused by protozoa |
418480000 | Eosinophilic meningoencephalitis caused by Angiostrongylus cantonensis |
418531007 | California serogroup virus neuroinvasive disease |
41870008 | Cortex laceration with open intracranial wound AND loss of consciousness |
419868009 | Encephalitis caused by rickettsia |
42012007 | Neuronal ceroid lipofuscinosis |
420146005 | Cerebral degeneration associated with generalized lipidosis |
42021008 | Familial diabetes insipidus |
420244003 | Encephalitis associated with acquired immunodeficiency syndrome |
420351005 | Adult-onset growth hormone deficiency |
420452002 | Myelopathy associated with acquired immunodeficiency syndrome |
420499009 | Hypogonadotropic hypogonadism due to isolated gonadotropin deficiency |
420554003 | Progressive multifocal leukoencephalopathy associated with acquired immunodeficiency syndrome |
420614009 | Organic dementia associated with acquired immunodeficiency syndrome |
420662003 | Coma due to diabetes mellitus |
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 |
420996007 | Coma due to malnutrition-related diabetes mellitus |
421019006 | Hypogonadotropic hypogonadism due to follicle-stimulating hormone deficiency |
421023003 | Presenile dementia associated with acquired immunodeficiency syndrome |
421075007 | Ketoacidotic coma due to type 1 diabetes mellitus |
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 |
421437000 | Hypoglycemic coma due to type 1 diabetes mellitus |
421529006 | Dementia associated with acquired immunodeficiency syndrome |
421684006 | Adult growth hormone deficiency |
421725003 | Hypoglycemic coma due to diabetes mellitus |
421821002 | Hypogonadotropic hypogonadism due to luteinizing hormone deficiency |
421827003 | Encephalopathy associated with acquired immunodeficiency syndrome |
421847006 | Ketoacidotic coma due to type 2 diabetes mellitus |
421931005 | Adult growth hormone deficiency with onset in childhood |
421966007 | Non-ketotic non-hyperosmolar coma due to diabetes mellitus |
421998001 | Central nervous disorder associated with acquired immunodeficiency syndrome |
422089004 | Encephalomyelitis associated with acquired immunodeficiency syndrome |
422126006 | Hyperosmolar coma due to diabetes mellitus |
422240004 | Gonadotropin releasing factor deficiency |
4223005 | Parkinsonism caused by drug |
422474003 | Partial absence of septum pellucidum |
422504002 | Ischemic stroke |
422513000 | Epilepsy, not refractory |
422527005 | Refractory infantile spasms |
422724001 | Refractory localization-related epilepsy |
422873003 | Refractory epilepsia partialis continua |
42295001 | Familial amyloid polyneuropathy |
423086004 | Simple partial status epilepticus |
423144007 | Multifactorial encephalopathy |
423279000 | Refractory migraine without aura |
423361002 | Lipoma of dorsal spinal cord |
42344001 | Alcohol-induced psychosis |
42365007 | Atonic seizure |
423683008 | Refractory migraine with aura |
42369001 | Pallidopontonigral degeneration |
42376006 | Occipital encephalocele |
423771003 | Acquired neuromuscular ptosis |
424099008 | Hepatic coma due to acute hepatitis B |
424151006 | Anaplastic glioma of brain |
424271007 | Hysterical cataplexy |
424276002 | Malignant glioma of brainstem |
42429001 | Cerebromeningeal hemorrhage |
424334007 | Malignant tumor of spinal cord, intramedullary |
424340000 | Hepatic coma due to chronic hepatitis B |
42440009 | Partial seizure with illusions and hallucinations |
424549003 | Malignant tumor of spinal cord, extramedullary |
424699007 | Migraine variants, not intractable |
424761009 | Paraneoplastic encephalomyelitis |
424795008 | Non dystrophic myotonia |
424911007 | Paraneoplastic encephalitis |
425007008 | Migraine without aura, not refractory |
425054007 | Refractory occipital lobe epilepsy |
425219008 | Progressive spinal ataxia |
425237009 | Refractory frontal lobe epilepsy |
425349008 | Refractory parietal lobe epilepsy |
425365009 | Refractory migraine variants |
425390006 | Dementia associated with Parkinson's Disease |
425420004 | Thrombosis of internal carotid artery |
425476007 | Non-organic parasomnia |
425492002 | Generalized dystonia |
425500002 | Secondary progressive multiple sclerosis |
425522009 | Hyperammonemic encephalopathy |
425687007 | Spina bifida aperta of cervical spine |
425756000 | Idiopathic transverse myelitis |
425805004 | Cognitive developmental delay |
425868004 | Benign papilloma of choroid plexus |
425882004 | Paralytic syndrome as late effect of stroke |
425919003 | Chronic organic mental disorder |
425932008 | Thrombosis of posterior communicating artery |
425936006 | Intractable ophthalmic migraine |
42594001 | Organic mood disorder of depressed type |
425957003 | Non-traumatic intracerebral ventricular hemorrhage |
4260009 | Sacral spinal cord injury without bone injury |
426033005 | Dysphagia as a late effect of cerebrovascular accident |
426055002 | Spinal arachnoiditis |
426107000 | Acute lacunar infarction |
426187002 | Myoclonus of stapedius muscle |
4262001 | Phlebitis of superior sagittal sinus |
426266003 | Post-infective myelitis |
426373005 | Relapsing remitting multiple sclerosis |
426470009 | Lipoma of conus medullaris |
426510004 | Schwannoma of spinal cord |
426592006 | Ballism |
426599002 | Myelitis caused by herpes simplex |
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 |
427086003 | Bickerstaff's brainstem encephalitis |
427111000 | Non-epileptic myoclonus |
427216002 | Spina bifida aperta of thoracic spine |
427232004 | Hemidystonia |
427296003 | Thalamic infarction |
427432001 | Paralytic syndrome as late effect of thalamic stroke |
427488005 | On - off phenomenon |
42769004 | Diffuse Lewy body disease with spongiform cortical change |
427789001 | Myoclonus of tensor tympani muscle |
427796004 | Encephalitis caused by human herpes simplex virus |
427945008 | Segmental dystonia |
428061005 | Malignant neoplasm of brain |
428175000 | Primary amebic encephalitis caused by Naegleria fowleri |
428259005 | Acquired tethered cord syndrome |
428544003 | Abscess of medulla oblongata |
428635007 | Primary viral encephalitis |
428638009 | Encephalitis caused by Herpesvirus |
428668000 | Apraxia due to cerebrovascular accident |
428687006 | Nightmares associated with chronic post-traumatic stress disorder |
428700003 | Primary progressive multiple sclerosis |
428703001 | Transient organic mental disorder |
428753007 | Low grade glioma of cerebellum |
428960009 | Low grade glioma of brainstem |
428964000 | Low grade glioma of cerebrum |
428965004 | Low grade glioma of thalamus |
429033009 | Malignant neoplasm of cerebrum |
429306002 | Benign neoplasm of spinal intradural intramedullary space |
429408002 | Low grade glioma of brain |
429436007 | Post-immunization myelitis |
429458009 | Dementia due to Creutzfeldt Jakob disease |
429466000 | Spina bifida aperta of lumbar spine |
429514007 | Growth hormone deficiency after bone marrow transplant |
429565004 | Germ cell tumor of the brain |
429691007 | Benign neoplasm of intradural space of spine |
42970005 | Nonpyogenic thrombosis of intracranial venous sinus |
429765002 | Benign neoplasm of medulla oblongata |
42986003 | Charcot-Marie-Tooth disease, type IB |
429998004 | Vascular dementia |
43019009 | Nelson syndrome |
430399004 | Infection of spinal cord caused by Histoplasma |
430404002 | Abscess of medulla of spinal cord caused by Histoplasma |
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 |
431034009 | Torsion dystonia |
43105007 | Choreoathetosis |
431265009 | Fetal microcephaly |
431266005 | Intraparenchymal hematoma of brain |
431468008 | Slit ventricle syndrome |
431520004 | Inflammation of spinal cord caused by toxin |
432249006 | Infarction of spinal cord |
432504007 | Cerebral infarction |
432616009 | Infection of ventriculoperitoneal shunt |
43262000 | Subdural hemorrhage following injury with open intracranial wound AND concussion |
433183000 | Neurogenic bladder as late effect of cerebrovascular accident |
433493000 | Acquired torsion dystonia |
43405004 | Anterior cord syndrome co-occurrent and due to open fracture of C5-C7 level |
434541000124109 | Benign childhood epilepsy with centrotemporal spikes, refractory |
434551000124106 | Benign childhood epilepsy with centrotemporal spikes, non-refractory |
43486001 | Hemiplegic cerebral palsy |
43497001 | Amphetamine-induced mood disorder |
43532007 | Hereditary oculoleptomeningeal amyloid angiopathy |
43647007 | Juvenile paralysis agitans of Hunt |
43658003 | Vertebral artery obstruction |
438113009 | Convulsive syncope |
438481007 | Postoperative tethered cord syndrome |
438511000 | Benign multiple sclerosis |
438513002 | Cerebral degeneration due to Parkinson's disease |
438583008 | Congenital bilateral perisylvian syndrome |
439567002 | Malignant multiple sclerosis |
439732004 | Myoclonic dystonia |
43977004 | Corticostriatal-spinal degeneration |
44031002 | Postseizure confusion |
44145005 | Benign Rolandic epilepsy |
441460004 | Cysticercosis of brain |
441512004 | Encephalitis caused by human herpesvirus 6 infection |
441526008 | Infarct of cerebrum due to iatrogenic cerebrovascular accident |
441529001 | Dysphasia as late effect of cerebrovascular disease |
441604003 | Myoclonus associated with fever |
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 |
441806004 | Abscess of brain |
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 |
442001 | Secondary hypopituitarism |
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 |
44248001 | Raymond-Cestan syndrome |
442481002 | Epilepsy characterized by intractable complex partial seizures |
442512002 | Nonconvulsive status epilepticus |
442536003 | Fungal infection of cerebrum |
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 |
442964000 | Conus medullaris syndrome |
443153007 | Inflammation of brain and spinal cord caused by toxic substance |
443265004 | Cognitive disorder |
443333004 | Medulloblastoma |
443352005 | Dystonia of head |
44341005 | Cortex laceration without open intracranial wound |
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 |
44423001 | Early myoclonic encephalopathy |
44433009 | Recurrent transient tic disorder |
44434003 | Closed fracture of thoracic spine with spinal cord injury |
444545003 | Glioma of brainstem |
444657001 | Superior cerebellar artery syndrome |
444860006 | Meningomyelocele of lumbosacral spine |
444957003 | Bacterial meningomyelitis |
444980006 | Sporadic olivopontocerebellar atrophy |
445006008 | Focal dystonia |
445014002 | Paraneoplastic limbic encephalitis |
445109004 | Isolation of left common carotid artery |
445116003 | Encephalocele of vertex |
445158000 | Colloid cyst of pituitary gland |
445166009 | Cystic degeneration of brain |
445252005 | Glucose transporter protein type 1 deficiency syndrome |
445307009 | Spina bifida of sacral region |
445308004 | Split spinal cord malformation |
445322004 | Migraine variant with headache |
445349004 | Isolation of right common carotid artery |
445355009 | Refractory epilepsy |
445359003 | Bacterial meningoencephalitis |
445423005 | Paraneoplastic subacute necrotic myelopathy |
445475001 | Paraneoplastic sensorimotor neuropathy |
445779008 | Traumatic injury of spinal cord at T7-T12 level |
445897006 | Incomplete transverse lesion of thoracic spinal cord |
4463009 | Familial amyloid polyneuropathy, type II |
446311006 | Acute bulbar poliomyelitis caused by Human poliovirus 2 |
446495002 | Ependymal cyst of spinal meninges |
446644006 | Traumatic injury of spinal cord at T1-T6 level |
446712002 | Thromboembolus of precerebral artery |
446835008 | Traumatic injury of sacral spinal cord |
446940004 | Ependymal cyst of spinal cord |
446945009 | Invasive pituitary adenoma |
446957000 | Acute bulbar poliomyelitis caused by Human poliovirus 1 |
446958005 | Acute paralytic poliomyelitis caused by Human poliovirus 1 |
446995005 | Shuddering attacks |
447012002 | Tuberculosis of spinal cord |
447232008 | Ependymal cyst of ventricle of brain |
447262002 | Acute paralytic poliomyelitis caused by Human poliovirus 2 |
447292006 | Mitochondrial encephalomyopathy |
4473006 | Migraine with aura |
447351004 | Vanishing white matter disease |
447378002 | Acute paralytic poliomyelitis caused by Human poliovirus 3 |
447396006 | Concussion injury of cerebrum |
447464004 | Complete spinal cord injury at T7-T12 level |
447575003 | Complete spinal cord injury at T1-T6 level |
447655002 | Benign neoplastic cyst of brain |
4477007 | Juvenile myopathy AND lactate acidosis |
448045004 | Fragile X associated tremor ataxia syndrome |
448054001 | Adult onset autosomal dominant leukodystrophy |
448135004 | Benign teratoma of pineal region |
448148000 | Functioning pituitary neoplasm |
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 |
448563005 | Functionless pituitary neoplasm |
448705004 | Mesial temporal lobe sclerosis |
448788000 | Open fracture of lumbar spine with incomplete lesion of lumbar 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 |
44913001 | Athetosis |
449203004 | Focal seizure with experiential sensory symptoms |
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 |
449795002 | Hemorrhage into subdural space of spine |
449799008 | Subependymal giant cell astrocytoma |
44983007 | Intervertebral disc disorder with myelopathy |
449901005 | Hepatic encephalopathy in fulminant hepatic failure |
449902003 | Portal systemic encephalopathy |
449903008 | Dural arteriovenous fistula of spinal cord |
449904002 | Intramedullary glomus arteriovenous malformation of spinal cord |
449905001 | Intramedullary and extramedullary arteriovenous malformation of spinal cord |
449906000 | Perimedullary arteriovenous fistula of spinal cord |
450363003 | Hemorrhage into subarachnoid space of spine |
450569000 | Traumatic brain injury with loss of consciousness one hour or more |
450886002 | Posterior reversible encephalopathy syndrome |
451036001 | Hemorrhage into subpial space of spinal cord |
451037005 | Hemorrhage in globus pallidus |
451038000 | Hemorrhage in caudate nucleus |
451039008 | Hemorrhage in putamen |
45163000 | Congenital pontocerebellar hypoplasia |
45170000 | Encephalitis |
4523006 | Babinski-Nageotte syndrome |
45369008 | Neurohypophyseal diabetes insipidus |
45639009 | Hereditary cerebral amyloid angiopathy, Icelandic type |
45659008 | Subdural hemorrhage following injury with open intracranial wound AND loss of consciousness |
45740001 | Diencephalic syndrome of infancy |
45814002 | Birnbaum's syndrome |
45853006 | Roussy-Lévy syndrome |
45864009 | Senile degeneration of brain |
45897005 | Jervis' syndrome |
45912004 | Organic hallucinosis |
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 |
46138007 | Tropical ataxic neuropathy |
4619009 | Generalized-onset seizures |
462165005 | Fetal choroid plexus cyst |
46229002 | Severe mixed bipolar I disorder without psychotic features |
46251005 | Corticospinal motor disease |
46263000 | Cataplexy |
46421000119102 | Behavior disorder as sequela of cerebral infarction |
4645000 | Senile brain amyloidosis |
46549005 | Multiple spinal cord injuries without spinal bone injury |
46659004 | Von Hippel-Lindau syndrome |
46721000 | Psychoactive substance-induced organic personality disorder |
46804001 | Severe x-linked myotubular myopathy |
46826000 | Rheumatic chorea |
46963008 | Compression of brain |
46966000 | Cerebral compression due to injury |
46975003 | Cocaine-induced organic mental disorder |
46995009 | Closed fracture of C5-C7 level with spinal cord injury |
47000000 | Acute transverse myelitis |
47032000 | Congenital hydrocephalus |
472320005 | Maternally inherited mitochondrial cardiomyopathy and myopathy |
472746006 | Cerebrovascular disorder due to paradoxical embolus |
472916000 | Toxic metabolic encephalopathy |
47311000119103 | Static encephalopathy |
473429002 | Tuberculoma of spinal cord confirmed |
47362003 | Medication-induced movement disorder |
47391000119107 | Primary generalized absence epilepsy |
47664006 | Sedative, hypnotic AND/OR anxiolytic-induced psychotic disorder with hallucinations |
47683004 | Metachromatic leukodystrophy, late infantile type |
47924005 | Motor cortical disorder |
48090007 | Neurologic adductor spastic dysphonia |
48163001 | Triparesis |
4817008 | Primary degenerative dementia of the Alzheimer type, senile onset, with delirium |
48248005 | Thrombophlebitis of inferior sagittal sinus |
48376004 | Congenital pseudoporencephaly |
48518008 | Subarachnoid hemorrhage following injury with open intracranial wound AND concussion |
48522003 | Spinal cord disorder |
48601000119107 | Paralytic syndrome on one side of the body as effect of cerebrovascular accident |
48601002 | Thrombosis of precerebral artery |
4863002 | Phencyclidine mood disorder |
48662007 | Cerebral paraplegia |
48721008 | Quadriplegic cerebral palsy |
48956000 | Open fracture of lumbar vertebra with spinal cord injury |
49049000 | Parkinson's disease |
49386006 | Orofacial dyskinesia |
49422009 | Cortical hemorrhage |
4945003 | Microgyria |
49453006 | Cerebral herniation |
49481000 | Postseizure delirium |
49497005 | Anterior cord syndrome co-occurrent and due to open fracture of T1-T6 level |
4952001 | Cerebral irritability in newborn |
49562005 | Adult chronic GM 2 gangliosidosis |
49644006 | Simple partial onset seizure followed by impaired consciousness |
49692006 | Schilder's disease |
49747005 | Closed fracture of lumbar vertebra with spinal cord injury |
49776008 | Centrencephalic epilepsy |
49793008 | Hereditary motor neuron disease |
49949003 | Paroxysmal choreoathetosis |
50026000 | Psychoactive substance-induced organic anxiety disorder |
50122000 | Metabolic encephalopathy |
50320000 | Hallucinogen intoxication |
50429003 | Congenital stenosis of aqueduct of Sylvius |
50541007 | Bruns' syndrome |
50582007 | Hemiplegia |
50722006 | Phencyclidine delusional disorder |
50776006 | Allergic encephalomyelitis |
508171000000105 | Severe learning disability |
50866000 | Childhood absence epilepsy |
50888000 | Closed fracture of C1-C4 level with central cord syndrome |
50933003 | Hallucinogen delusional disorder |
509341000000107 | Petit-mal epilepsy |
50967008 | Gangliosidosis |
51004007 | Herniation under falx cerebri |
5102002 | Agenesis of corpus callosum |
51075009 | Complex partial seizure evolving to generalized seizure |
5120006 | Cortex laceration without open intracranial wound AND with concussion |
51258005 | Open fracture of T7-T12 level with posterior cord syndrome |
5134006 | Familial amyloid polyneuropathy, type VI |
51371005 | Pituitary dwarfism with normal somatotropin level AND low somatomedin |
51399001 | Toxic encephalopathy caused by lead |
51443000 | Amphetamine-induced psychotic disorder with hallucinations |
51493001 | Cocaine-induced anxiety disorder |
51495008 | Cerebral anoxia following anesthesia AND/OR sedation in labor AND/OR delivery |
51500006 | Complete trisomy 18 syndrome |
51514006 | Closed fracture of C1-C4 level with posterior cord syndrome |
51568001 | Brain stem vertigo |
5158005 | Gilles de la Tourette's syndrome |
51638003 | Thogoto virus disease |
51742006 | Disorder of anterior pituitary |
51887003 | Tonic seizure |
51928006 | General paresis - neurosyphilis |
51984006 | Dysmorphic sialidosis, infantile form |
52008007 | Organic writer's cramp |
5202009 | Brain injury with open intracranial wound AND concussion |
52125007 | Gustatory seizure |
52165006 | Niemann-Pick disease, type A |
5217008 | Stiff-man syndrome |
52186006 | Dysmorphic sialidosis |
52201006 | Internal capsule hemorrhage |
52274002 | Dystonia lenticularis |
52281009 | Meningoencephalitis caused by Naegleria |
52289006 | Closed fracture of T1-T6 level with central cord syndrome |
52330001 | Meningoencephalocele |
52448006 | Dementia |
52522001 | Degenerative brain disorder |
5262007 | Spinal muscular atrophy |
52677002 | Deficiency of N-acetylgalactosamine-4-sulfatase |
52713000 | Infantile neuroaxonal dystrophy |
52859009 | Rathke's pouch cyst |
52866005 | Opioid intoxication delirium |
52888005 | Brain stem contusion without open intracranial wound |
52913008 | Brain stem contusion with open intracranial wound AND no loss of consciousness |
52947006 | Japanese encephalitis virus disease |
530041000000105 | Lumbar spina bifida without mention of hydrocephalus |
53050002 | Hallucinogen-induced organic mental disorder |
53194005 | Posthemiplegic athetosis |
53267002 | Brain injury without open intracranial wound AND with loss of consciousness |
53318002 | Spina bifida with hydrocephalus |
53521000119106 | First generalized onset seizure |
53622003 | Cerebral malaria |
53633000 | Peutz-Jeghers polyps of small bowel |
53776005 | Encephalocystocele |
53810004 | Injury at T1-T6 level with spinal cord injury AND without bone injury |
53857003 | Heredofamilial brachial plexus paralysis syndrome |
53868003 | Anterior cord syndrome co-occurrent and due to closed fracture of C1-C4 level |
53936005 | Alcohol-induced mood disorder |
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 |
5444000 | Sedative, hypnotic AND/OR anxiolytic intoxication delirium |
54502004 | Primary degenerative dementia of the Alzheimer type, presenile onset, with delusions |
54519002 | Basilar artery stenosis |
54794009 | Ectopic gray matter in centrum ovale |
55004003 | Syndrome of inappropriate vasopressin secretion |
55009008 | Primary degenerative dementia of the Alzheimer type, senile onset, with delusions |
55016009 | Congenital muscular hypertrophy-cerebral syndrome |
55051001 | Myasthenia gravis, juvenile form |
5510009 | Organic delusional disorder |
55234004 | Pyogranulomatous meningoencephalomyelitis |
55382008 | Cerebral atherosclerosis |
55481000 | Limbic disorder |
55489003 | Eosinophilic meningoencephalitis |
55623006 | Toxic encephalopathy caused by mercury |
55637002 | Spinal hemiplegia |
55702009 | Laceration of brain without open intracranial wound |
55709000 | Ethmocephalus |
55734000 | Endophlebitis of basilar sinus |
55776008 | Symptomatic torsion dystonia |
5582005 | Posterior fossa compression syndrome |
55967005 | Phencyclidine-induced anxiety disorder |
55999004 | Encephalocele |
56097005 | Migraine without aura |
56155002 | Hemispheric cerebral agenesis |
56194001 | Caffeine-induced sleep disorder |
56267009 | Multi-infarct dementia |
56271007 | Hypothermia-sweating syndrome |
56384000 | Embolism of inferior sagittal sinus |
56453003 | Hereditary cerebral amyloid angiopathy, Dutch type |
56509006 | Adductor spastic dysphonia of organic voice tremor |
56529007 | Adenoviral encephalitis |
56531003 | Ulegyria |
56573006 | Transient tic disorder |
568005 | Tic disorder |
56989000 | Eaton-Lambert syndrome |
57148006 | Congenital anomaly of brain |
57739006 | Cerebellar contusion without open intracranial wound |
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 |
58329000 | Organic mood disorder of manic type |
5842009 | Spinal cord dysplasia |
58459009 | Sphingomyelin/cholesterol lipidosis |
58557008 | Spina bifida aperta |
58638006 | Pseudoporencephaly |
58756001 | Huntington's chorea |
58762006 | Encephalomalacia |
58766009 | Granulomatous meningoencephalomyelitis |
58795000 | Distal muscular dystrophy |
590005 | Congenital aneurysm of anterior communicating artery |
59026006 | Blepharospasm |
59103002 | Cerebral paralysis with homolateral ataxia |
59178007 | Menkes kinky-hair syndrome |
59292006 | Hemiplegic migraine |
59457001 | Simple partial seizure evolving to secondary generalized seizure |
59572000 | Necrosis of pituitary |
5963005 | Subacute neuronopathic Gaucher's disease |
59636002 | Pelizaeus-Merzbacher disease, connatal variant |
59651006 | Sedative, hypnotic AND/OR anxiolytic-induced persisting dementia |
59748008 | Cortex laceration with open intracranial wound |
59918000 | Cerebellar laceration with open intracranial wound AND concussion |
60146005 | Bailey-Cushing syndrome |
60192008 | Lethal multiple pterygium syndrome |
60338000 | Partial seizure with multiple symptoms |
60342002 | Movement disorder |
60389000 | Paraplegia |
60404007 | Cerebral abscess |
60576007 | Subacute combined degeneration of spinal cord |
60706008 | Phlebitis of torcular Herophili |
608817003 | Pituicytoma |
608874000 | Eaton Lambert syndrome with underlying malignancy |
609218006 | Paroxysmal nonkinesigenic dyskinesia |
609221008 | Paroxysmal kinesigenic dyskinesia |
60935008 | Paramyoclonus multiplex |
609461007 | Induced termination of pregnancy complicated by cerebral anoxia |
609528003 | Posterior fossa arachnoid cyst |
609529006 | Persistent Blake's pouch cyst |
609553000 | Paralytic syndrome of both lower limbs |
609554006 | Paralytic syndrome of all four limbs |
609557004 | Paralytic syndrome on one side of the body |
609558009 | Essential tremor |
61091005 | Aneurysm of external carotid artery |
61104008 | Inhalant-induced organic mental disorder |
61144001 | Alcohol-induced psychotic disorder with delusions |
61165007 | Hereditary nephrogenic diabetes insipidus |
6118003 | Demyelinating disease of central nervous system |
61200008 | Pallidonigroluysian degeneration |
61337004 | Electric chorea |
61386002 | Open fracture of C1-C4 level with central cord syndrome |
61407009 | Protozoal myelitis |
61484000 | Simple partial seizure evolving to generalized seizure |
61663001 | Juvenile neuronal ceroid lipofuscinosis |
61687004 | Endophlebitis of inferior sagittal sinus |
61701006 | Lymphocytic hypopituitarism |
61819007 | Rachischisis |
61927004 | Auditory seizure |
62009002 | Adult neuronal ceroid lipofuscinosis |
6204001 | Juvenile myoclonic epilepsy |
62106007 | Concussion with no loss of consciousness |
62158001 | Status marmoratus |
62206004 | Abscess of pituitary |
62440002 | Infantile GM 2 gangliosidosis |
62564004 | Concussion with loss of consciousness |
62702001 | Cerebral vein occlusion |
62732009 | Alien limb phenomenon |
62904009 | Spastic pseudobulbar dysphonia |
62914000 | Cerebrovascular disease |
62950007 | Encephalomyelitis |
62985007 | Hereditary insensitivity to pain with anhidrosis |
62999006 | Adiposogenital dystrophy |
63081009 | Acute infarction of spinal cord |
63135006 | Amyotonia congenita |
6348008 | Cocaine-induced psychotic disorder with hallucinations |
63576006 | Mixed flaccid-spastic pseudobulbar dysphonia |
63649001 | Cannabis delusional disorder |
63795001 | Thrombosis of intracranial venous sinus of pregnancy AND/OR puerperium |
63814006 | Abnormal cerebral signs in the newborn |
63819001 | Open fracture of T1-T6 level with central cord syndrome |
63903007 | Incomplete spinal cord lesion at T7-T12 level without bone injury |
63983005 | Inhalant-induced psychotic disorder with hallucinations |
63986002 | Brain stem herniation |
64009001 | Basilar artery syndrome |
64228003 | Paralysis of diaphragm |
64383006 | Werdnig-Hoffmann disease |
64586002 | Carotid artery stenosis |
64624009 | Hypoglycemic encephalopathy |
64678009 | Non-pregnancy related A-G syndrome |
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 |
65144005 | Congenital spinal meningocele |
65260001 | Cervical spondylosis with myelopathy |
65312002 | Cerebral arteriosclerosis |
6537000 | Ectopic pituitary tissue |
65433005 | Mechanical complication of ventricular communicating shunt |
65455002 | Nasal encephalocele |
65587001 | Congenital anomaly of cerebrovascular system |
65605001 | Edema of spinal cord |
65705009 | Porencephalic cyst |
65764006 | Pseudo-Hurler polydystrophy |
6594005 | Cerebrovascular disorder in the puerperium |
66010009 | Supranuclear paralysis |
66020004 | Open fracture of C5-C7 level with posterior cord syndrome |
6607004 | Syringoencephalomyelia |
66108005 | Primary degenerative dementia of the Alzheimer type, senile onset, uncomplicated |
66158003 | Closed fracture of C5-C7 level with incomplete spinal cord lesion |
66393002 | Brain stem contusion with open intracranial wound AND loss of consciousness |
66454007 | Murray valley encephalitis |
66521008 | Deficiency of cerebroside-sulfatase |
66637005 | Hemiballism |
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 |
67305007 | Familial essential myoclonus |
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 |
67437007 | Lumbar spondylosis with myelopathy |
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 |
674481000119100 | Spontaneous hematoma of spinal cord |
67531005 | Spina bifida |
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 |
67873006 | Isolated prolactin deficiency |
67876003 | Congenital obstruction of aqueduct of Sylvius |
67930001 | Syringoencephalia |
67975003 | Fibrocartilagenous emboli of spinal cord |
67992007 | Multiple AND bilateral precerebral artery obstruction |
68061000119109 | Partial diabetes insipidus |
6807001 | Central pontine myelinolysis |
68091000119102 | Intractable absence seizures |
68107009 | Cerebral paresis with homolateral ataxia |
68116008 | Dentatorubropallidoluysian degeneration |
68186003 | Congenital myopathy with abnormal subcellular organelles |
68267002 | Benign intracranial hypertension |
68390005 | Sphingolipid activator protein 1 deficiency |
684911000119105 | Primary glioblastoma multiforme of frontal lobe |
68504005 | Ataxia-telangiectasia syndrome |
68574006 | Cortical blindness |
68577004 | Acute necrotizing myelitis |
68618008 | Rett's disorder |
68761002 | Epileptic vertigo |
69017006 | Cortical vertigo |
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 |
69233001 | Paradoxical facial movements |
69463008 | Maroteaux-Lamy syndrome |
69482004 | Korsakoff's psychosis |
6955002 | Negishi encephalitis |
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 |
698404009 | Injury at T7 - T12 level with central cord syndrome |
698500002 | Spinal cord injury due to birth trauma |
698616008 | Loss of consciousness co-occurrent and due to closed fracture of vault of skull |
698617004 | Concussion co-occurrent and due to closed fracture of vault of skull |
698618009 | Loss of consciousness co-occurrent and due to open fracture of vault of skull |
698619001 | Concussion co-occurrent and due to open fracture of vault of skull |
698620007 | Closed fracture of base of skull with loss of consciousness |
698621006 | Concussion co-occurrent and due to closed fracture of base of skull |
698624003 | Dementia associated with cerebral lipidosis |
698625002 | Dementia associated with normal pressure hydrocephalus |
698626001 | Dementia associated with multiple sclerosis |
698627005 | Postoperative phlebitis and thrombophlebitis of intracranial sinuses |
698687007 | Post-traumatic dementia with behavioral change |
698691002 | Cognitive disorder in remission |
698725008 | Dementia associated with neurosyphilis |
698726009 | Dementia associated with viral encephalitis |
698736001 | Postoperative communicating hydrocephalus |
698737005 | Postmeningitic obstructive hydrocephalus |
698738000 | Brainstem myoclonus |
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 |
69875006 | Cortex laceration with open intracranial wound AND concussion |
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 |
698783004 | Injury at T7-T12 level with anterior cord syndrome |
698835006 | Cerebral cortex myoclonus |
698836007 | Spinal cord myoclonus |
698837003 | Posttraumatic porencephalic cyst of brain |
698838008 | Benign intracranial hypertension due to drug |
698839000 | Benign intracranial hypertension due to hypervitaminosis A |
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 |
698958008 | Delirium in remission |
698999002 | Congenital atresia of aqueduct of Sylvius |
69909000 | Eclampsia added to pre-existing hypertension |
699184009 | Perry syndrome |
699190008 | Paroxysmal extreme pain disorder |
699299001 | Neuroferritinopathy |
699314009 | Migraine with persistent visual aura |
699318007 | Supratentorial primitive neuroectodermal tumor |
699328003 | Myoclonic epilepsy myopathy sensory ataxia |
699331002 | Granular cell tumor of neurohypophysis |
699688008 | Generalized epilepsy with febrile seizures plus |
699704002 | Classic medulloblastoma |
699706000 | Embolism of middle cerebral artery |
699812002 | Subependymal nodular heterotopia |
699813007 | Xanthogranuloma of choroid plexus |
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 |
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 |
7025000 | Subchronic undifferentiated schizophrenia with acute exacerbations |
702575003 | Retinocochleocerebral vasculopathy |
702611008 | Congenital brain aplasia |
702628006 | Congenital anomaly of cerebrum |
702753003 | Complete partial seizure of uncertain origin |
702949005 | Proopiomelanocortin deficiency syndrome |
703041000 | Dysexecutive syndrome |
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 |
70328006 | Cocaine delirium |
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 |
703850002 | Delirium due to benzodiazepine withdrawal |
703862003 | Spinal subdural hematoma |
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 |
7052005 | Alcohol hallucinosis |
70528007 | Mucolipidosis |
70534000 | Occult spinal dysraphism sequence |
70576008 | Enteroviral encephalomyelitis |
70607008 | Thrombosis of superior sagittal sinus |
70655008 | Caffeine-induced anxiety disorder |
70835005 | Disorder of basal ganglia |
708728007 | Traumatic brain injury of unknown intent |
70884002 | Allergic encephalitis |
709073001 | Neurocognitive disorder |
709281006 | Rippling muscle disease |
70932007 | Amphetamine-induced sexual dysfunction |
70936005 | Multi-infarct dementia, uncomplicated |
709415008 | Mitochondrial membrane protein associated neurodegeneration |
709469005 | Periodontitis co-occurrent with Down syndrome |
71003000 | Ateleiotic dwarfism |
710046001 | Refractory idiopathic generalized epilepsy |
710575003 | Transient ischemic attack due to embolism |
71105005 | Ilheus virus encephalitis |
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 |
711487002 | Methyl-cytosine phosphate guanine binding protein 2 related severe neonatal encephalopathy |
71178008 | Congenital spinal hydromeningocele |
7125002 | Meningoencephalitis |
71253000 | Tay-Sachs disease, variant AB |
712637001 | Ribonucleic acid polymerase III-related leukodystrophy |
712647003 | Spasmodic torticollis due to infection |
712820006 | Cerebral pseudoatrophy |
71286001 | Spinal cord compression |
712986001 | Encephalitis caused by tick-borne encephalitis virus |
713035000 | Dissection of precerebral artery |
713060000 | Sporadic Creutzfeldt-Jakob disease |
713081000 | Dissection of cerebral artery |
713260006 | Subacute adenoviral encephalitis co-occurrent with human immunodeficiency virus infection |
713265001 | Nontraumatic ruptured cerebral aneurysm |
71328000 | Opioid-induced sexual dysfunction |
713325002 | Primary cerebral lymphoma co-occurrent with human immunodeficiency virus infection |
713327005 | Malignant meningioma of meninges of brain |
713341001 | Myelitis co-occurrent with human immunodeficiency virus infection |
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 |
713491003 | Organic brain syndrome co-occurrent with human immunodeficiency virus infection |
713503007 | Disorder of spinal cord 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 |
713956000 | Spasmodic torticollis as late effect of trauma |
714279000 | Myelopathy caused by Human T-lymphotropic virus 1 |
71444005 | Cerebral arterial thrombosis |
71460009 | Trypanosomiasis with encephalitis |
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 |
715425000 | Benign focal seizure of adolescence |
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 |
715533002 | Microcephaly, microphthalmia, ectrodactyly of lower limbs and prognathism syndrome |
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 |
715627004 | Primary progressive freezing gait 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 |
715668008 | Pituitary deficiency due to empty sella turcica syndrome |
715726000 | Spinocerebellar ataxia type 7 |
715727009 | Pituitary stalk interruption syndrome |
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 |
715902009 | Primary orthostatic tremor |
715904005 | Pineal parenchymal tumor of intermediate differentiation |
715905006 | Unilateral polymicrogyria |
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 |
716592003 | Liponeurocytoma of cerebellum |
716662004 | Autosomal dominant late onset Parkinson disease |
716664003 | Primary dystonia 21 |
716667005 | Right temporal atrophy variant frontotemporal dementia |
716684004 | Limbic encephalitis with N-methyl-D-aspartate receptor antibodies |
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 |
716771000 | Chronic hiccup |
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 |
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 |
717939009 | Anencephaly without rachischisis |
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 |
718178006 | Autosomal dominant limb girdle muscular dystrophy type 1B |
718179003 | Autosomal recessive limb girdle muscular dystrophy type 2B |
718180000 | Autosomal recessive limb girdle muscular dystrophy type 2I |
718182008 | Combined pituitary hormone deficiency genetic form |
718210003 | Deficiency of monoamine oxidase A |
718212006 | Mitochondrial encephalocardiomyopathy due to transmembrane protein 70 mutation |
718219002 | Congenital lactic acidosis Saguenay-Lac-Saint-Jean type |
71831005 | Symptomatic generalized epilepsy |
718362003 | Functional movement disorder |
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 |
719162001 | Radioulnar synostosis with microcephaly and scoliosis 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 |
719216001 | Hypoglycemic coma due to type 2 diabetes mellitus |
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 |
719521002 | Benign paroxysmal torticollis of infancy |
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 |
719986000 | Autosomal dominant limb girdle muscular dystrophy type 1C |
719987009 | Autosomal dominant limb girdle muscular dystrophy type 1D |
719988004 | Autosomal dominant limb girdle muscular dystrophy type 1E |
719989007 | Autosomal dominant limb girdle muscular dystrophy type 1F |
719990003 | Autosomal dominant limb girdle muscular dystrophy type 1G |
720010009 | Microphthalmia with brain atrophy 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 |
720632004 | Central bilateral macrogyria |
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 |
72103000 | Simple partial seizure with special sensory symptoms |
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 |
721211008 | Encephalopathy caused by methylmercury |
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 |
721244002 | Infection causing myelitis |
721245001 | Myelitis caused by bacterium |
721246000 | Myelitis caused by fungus |
721247009 | Parasitic infection causing myelitis |
721248004 | Myelitis caused by virus |
721249007 | Infection causing encephalomyelitis |
721250007 | Abscess of spinal cord caused by bacterium |
721255002 | Acquired prion disease |
721288009 | Hypopituitarism following procedure |
721297008 | Galloway Mowat syndrome |
721330006 | Diffuse injury of cerebrum |
721331005 | Diffuse injury of cerebellum |
721332003 | Diffuse injury of brainstem |
721333008 | Crush injury of brain |
721362009 | Complete lesion of cervical spinal cord |
721363004 | Complete lesion of spinal cord at first cervical level |
721364005 | Complete lesion of spinal cord at second cervical level |
721365006 | Complete lesion of spinal cord at third cervical level |
721366007 | Complete lesion of spinal cord at fourth cervical level |
721367003 | Complete lesion of spinal cord at fifth cervical level |
721368008 | Complete lesion of spinal cord at sixth cervical level |
721369000 | Complete lesion of spinal cord at seventh cervical level |
721370004 | Complete lesion of spinal cord at eighth cervical level |
721371000 | Central cord syndrome of cervical spinal cord |
721372007 | Central cord syndrome of spinal cord at first cervical level |
721373002 | Central cord syndrome of spinal cord at second cervical level |
721374008 | Central cord syndrome of spinal cord at third cervical level |
721375009 | Central cord syndrome of spinal cord at fourth cervical level |
721376005 | Central cord syndrome of spinal cord at fifth cervical level |
721377001 | Central cord syndrome of spinal cord at sixth cervical level |
721378006 | Central cord syndrome of spinal cord at seventh cervical level |
721379003 | Central cord syndrome of spinal cord at eighth cervical level |
721380000 | Anterior cord syndrome of cervical spinal cord |
721381001 | Anterior cord syndrome of spinal cord at first cervical level |
721382008 | Anterior cord syndrome of spinal cord at second cervical level |
721383003 | Anterior cord syndrome of spinal cord at third cervical level |
721384009 | Anterior cord syndrome of spinal cord at fourth cervical level |
721385005 | Anterior cord syndrome of spinal cord at fifth cervical level |
721386006 | Anterior cord syndrome of spinal cord at sixth cervical level |
721387002 | Anterior cord syndrome of spinal cord at seventh cervical level |
721388007 | Anterior cord syndrome of spinal cord at eighth cervical level |
721389004 | Posterior cord syndrome of cervical spinal cord |
721390008 | Posterior cord syndrome of spinal cord at first cervical level |
721391007 | Posterior cord syndrome of spinal cord at second cervical level |
721392000 | Posterior cord syndrome of spinal cord at third cervical level |
721393005 | Posterior cord syndrome of spinal cord at fourth cervical level |
721394004 | Posterior cord syndrome of spinal cord at fifth cervical level |
721395003 | Posterior cord syndrome of spinal cord at sixth cervical level |
721396002 | Posterior cord syndrome of spinal cord at seventh cervical level |
721397006 | Posterior cord syndrome of spinal cord at eighth cervical level |
721398001 | Brown-Sequard syndrome of cervical spinal cord |
721399009 | Brown-Sequard syndrome at first cervical level |
721400002 | Brown-Sequard syndrome at second cervical level |
721401003 | Brown-Sequard syndrome at third cervical level |
721402005 | Brown-Sequard syndrome at fourth cervical level |
721403000 | Brown-Sequard syndrome at fifth cervical level |
721404006 | Brown-Sequard syndrome at sixth cervical level |
721405007 | Brown-Sequard syndrome at seventh cervical level |
721406008 | Brown-Sequard syndrome at eighth cervical level |
721428008 | Injury of thoracic spinal cord |
721429000 | Complete lesion of thoracic spinal cord |
721430005 | Complete lesion of spinal cord at first thoracic level |
721431009 | Complete lesion of spinal cord at second thoracic level |
721432002 | Complete lesion of spinal cord at third thoracic level |
721433007 | Complete lesion of spinal cord at fourth thoracic level |
721434001 | Complete lesion of spinal cord at fifth thoracic level |
721435000 | Complete lesion of spinal cord at sixth thoracic level |
721436004 | Complete lesion of spinal cord at seventh thoracic level |
721437008 | Complete lesion of spinal cord at eighth thoracic level |
721438003 | Complete lesion of spinal cord at ninth thoracic level |
721439006 | Complete lesion of spinal cord at tenth thoracic level |
721440008 | Complete lesion of spinal cord at eleventh thoracic level |
721441007 | Complete lesion of spinal cord at twelfth thoracic level |
721442000 | Central cord syndrome of thoracic spinal cord |
721443005 | Central cord syndrome of spinal cord at first thoracic level |
721444004 | Central cord syndrome of spinal cord at second thoracic level |
721445003 | Central cord syndrome of spinal cord at third thoracic level |
721446002 | Central cord syndrome of spinal cord at fourth thoracic level |
721447006 | Central cord syndrome of spinal cord at fifth thoracic level |
721448001 | Central cord syndrome of spinal cord at sixth thoracic level |
721449009 | Central cord syndrome of spinal cord at seventh thoracic level |
721450009 | Central cord syndrome of spinal cord at eighth thoracic level |
721451008 | Central cord syndrome of spinal cord at ninth thoracic level |
721452001 | Central cord syndrome of spinal cord at tenth thoracic level |
721453006 | Central cord syndrome of spinal cord at eleventh thoracic level |
721454000 | Central cord syndrome of spinal cord at twelfth thoracic level |
721455004 | Anterior cord syndrome of thoracic spinal cord |
721456003 | Anterior cord syndrome of spinal cord at first thoracic level |
721457007 | Anterior cord syndrome of spinal cord at second thoracic level |
721458002 | Anterior cord syndrome of spinal cord at third thoracic level |
721459005 | Anterior cord syndrome of spinal cord at fourth thoracic level |
721460000 | Anterior cord syndrome of spinal cord at fifth thoracic level |
721461001 | Anterior cord syndrome of spinal cord at sixth thoracic level |
721462008 | Anterior cord syndrome of spinal cord at seventh thoracic level |
721463003 | Anterior cord syndrome of spinal cord at eighth thoracic level |
721464009 | Anterior cord syndrome of spinal cord at ninth thoracic level |
721465005 | Anterior cord syndrome of spinal cord at tenth thoracic level |
721466006 | Anterior cord syndrome of spinal cord at eleventh thoracic level |
721467002 | Anterior cord syndrome of spinal cord at twelfth thoracic level |
721468007 | Posterior cord syndrome of thoracic spinal cord |
721469004 | Posterior cord syndrome of spinal cord at first thoracic level |
721470003 | Posterior cord syndrome of spinal cord at second thoracic level |
721471004 | Posterior cord syndrome of spinal cord at third thoracic level |
721472006 | Posterior cord syndrome of spinal cord at fourth thoracic level |
721473001 | Posterior cord syndrome of spinal cord at fifth thoracic level |
721474007 | Posterior cord syndrome of spinal cord at sixth thoracic level |
721475008 | Posterior cord syndrome of spinal cord at seventh thoracic level |
721476009 | Posterior cord syndrome of spinal cord at eighth thoracic level |
721477000 | Posterior cord syndrome of spinal cord at ninth thoracic level |
721478005 | Posterior cord syndrome of spinal cord at tenth thoracic level |
721479002 | Posterior cord syndrome of spinal cord at eleventh thoracic level |
721480004 | Posterior cord syndrome of spinal cord at twelfth thoracic level |
721481000 | Brown-Séquard syndrome of thoracic spinal cord |
721482007 | Brown-Séquard syndrome at first thoracic level |
721483002 | Brown-Séquard syndrome at second thoracic level |
721484008 | Brown-Séquard syndrome at third thoracic level |
721485009 | Brown-Séquard syndrome at fourth thoracic level |
721486005 | Brown-Séquard syndrome at fifth thoracic level |
721487001 | Brown-Séquard syndrome at sixth thoracic level |
721488006 | Brown-Séquard syndrome at seventh thoracic level |
721489003 | Brown-Séquard syndrome at eighth thoracic level |
721490007 | Brown-Séquard syndrome at ninth thoracic level |
721491006 | Brown-Séquard syndrome at tenth thoracic level |
721492004 | Brown-Séquard syndrome at eleventh thoracic level |
721493009 | Brown-Séquard syndrome at twelfth thoracic level |
721499008 | Complete lesion of lumbar spinal cord |
721500004 | Complete lesion of spinal cord at first lumbar level |
721501000 | Complete lesion of spinal cord at second lumbar level |
721502007 | Complete lesion of spinal cord at third lumbar level |
721503002 | Complete lesion of spinal cord at fourth lumbar level |
721504008 | Complete lesion of spinal cord at fifth lumbar level |
721505009 | Central cord syndrome of lumbar spinal cord |
721506005 | Central cord syndrome of spinal cord at first lumbar level |
721507001 | Central cord syndrome of spinal cord at second lumbar level |
721508006 | Central cord syndrome of spinal cord at third lumbar level |
721509003 | Central cord syndrome of spinal cord at fourth lumbar level |
721510008 | Central cord syndrome of spinal cord at fifth lumbar level |
721511007 | Anterior cord syndrome of lumbar spinal cord |
721512000 | Anterior cord syndrome of spinal cord at first lumbar level |
721513005 | Anterior cord syndrome of spinal cord at second lumbar level |
721514004 | Anterior cord syndrome of spinal cord at third lumbar level |
721515003 | Anterior cord syndrome of spinal cord at fourth lumbar level |
721516002 | Anterior cord syndrome of spinal cord at fifth lumbar level |
721517006 | Posterior cord syndrome of lumbar spinal cord |
721518001 | Posterior cord syndrome of spinal cord at first lumbar level |
721519009 | Posterior cord syndrome of spinal cord at second lumbar level |
721520003 | Posterior cord syndrome of spinal cord at third lumbar level |
721521004 | Posterior cord syndrome of spinal cord at fourth lumbar level |
721522006 | Posterior cord syndrome of spinal cord at fifth lumbar level |
721523001 | Brown-Séquard syndrome of lumbar spinal cord |
721524007 | Brown-Séquard syndrome at first lumbar level |
721525008 | Brown-Séquard syndrome at second lumbar level |
721526009 | Brown-Séquard syndrome at third lumbar level |
721527000 | Brown-Séquard syndrome at fourth lumbar level |
721528005 | Brown-Séquard syndrome at fifth lumbar level |
721529002 | Complete injury of sacral spinal cord |
721535002 | Central neurocytoma of brain |
721766005 | Encephalitis caused by Alphavirus |
721776008 | Encephalitis caused by Polyoma virus |
721788005 | Encephalitis caused by Rubulavirus |
721790006 | Encephalitis caused by Hendra virus |
721791005 | Encephalitis caused by Nipah virus |
721815007 | Encephalitis caused by Trypanosoma brucei |
721818009 | Encephalitis caused by Schistosoma |
721819001 | Encephalitis caused by Schistosoma haematobium |
721820007 | Encephalitis caused by Schistosoma mansoni |
721821006 | Encephalitis caused by Schistosoma japonicum |
721823009 | Encephalitis caused by Echinococcus granulosus |
721825002 | Encephalitis caused by Taenia solium |
721826001 | Encephalitis caused by Coenurus cerebralis |
721842008 | Hypogonadotropic hypogonadism with frontoparietal alopecia 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 |
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 |
722556003 | Parkinsonism co-occurrent and due to acute infection |
722557007 | Parkinsonism due to human immunodeficiency virus infection |
722558002 | Parkinsonism following infection |
722576009 | Injury of brain stem due to birth trauma |
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 |
722614006 | Focal non-hemorrhagic contusion of cerebrum |
722615007 | Focal hemorrhagic contusion of cerebrum |
722616008 | Focal laceration of cerebrum |
722617004 | Multiple focal injuries of cerebrum |
722618009 | Focal non-hemorrhagic contusion of cerebellum |
722622004 | Focal non-hemorrhagic contusion of brainstem |
722625002 | Focal laceration of brainstem |
722626001 | Multiple focal injuries of cerebellum |
722627005 | Focal injury of brainstem |
722633001 | Multiple traumatic hemorrhages of brain tissue |
722653002 | Injury of lumbar spinal cord |
722654008 | Incomplete injury of sacral spinal cord |
722660008 | Radiation injury of brain caused by ionizing radiation following radiotherapy procedure |
722671009 | Metastatic malignant neoplasm of meninges |
722702007 | Focal laceration of cerebellum |
722718001 | Primary malignant meningioma |
722762005 | Ganglioside GM3 synthase deficiency |
722763000 | Infantile dystonia parkinsonism |
722907006 | Contusion of cerebellum due to birth trauma |
722908001 | Contusion of brain due to birth trauma |
722914008 | Central neonatal apnea |
722929005 | Perinatal arterial ischemic stroke |
722931001 | Neonatal compression of brain |
722943000 | Macroprolactinemia |
722944006 | Congenital hypogonadotropic hypogonadism |
722961009 | Delirium caused by substance or medication |
722962002 | Amnestic disorder caused by substance |
722964001 | Atypical Parkinsonism |
722965000 | Parkinsonism due to heredodegenerative disorder |
722966004 | Chorea due to heredodegenerative disorder |
722967008 | Ataxia due to mitochondrial mutations |
722968003 | Acquired ataxia |
722969006 | Tremor due to metabolic disorder |
722970007 | Tremor due to substance abuse |
722972004 | Secondary tic disorder |
722973009 | Tic due to developmental disorder |
722974003 | Segmental myoclonus |
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 |
722981005 | Infrequent episodic tension-type headache |
722982003 | Frequent episodic tension-type headache |
722984002 | Myelopathy due to metabolic disorder |
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 |
722995008 | Concussion of sacral spinal cord |
722997000 | Inherited autonomic nervous system disorder |
723082006 | Silent cerebral infarct |
723083001 | Late effects of cerebral ischemic stroke |
723084007 | Sequela of non-traumatic intracerebral hemorrhage |
723122006 | Primary tic disorder |
723123001 | Ischemic vascular dementia |
723124007 | Primary progressive apraxia of speech |
723125008 | Epileptic encephalopathy |
723129002 | Spinal cord compression due to degenerative disorder of spinal column |
723137005 | Crush injury of brain without coma |
723151005 | Permanent vegetative state |
723155001 | Injury of spinal cord caused by ionizing radiation following radiotherapy procedure |
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 |
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 |
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 |
723830005 | Keratosis follicularis, dwarfism, cerebral atrophy syndrome |
723857007 | Silent micro-hemorrhage of brain |
723926008 | Perceptual disturbances and seizures co-occurrent and due to alcohol withdrawal |
723927004 | Psychotic disorder caused by alcohol with schizophreniform symptoms |
723928009 | Mood disorder with depressive symptoms caused by alcohol |
723929001 | Mood disorder with manic symptoms caused by alcohol |
723930006 | Mood disorder with mixed manic and depressive symptoms caused by alcohol |
723936000 | Psychotic disorder caused by cannabis |
723937009 | Sleep disorder caused by cannabis |
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 |
724072002 | Paroxysmal exertion-induced dyskinesia |
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 |
724174003 | Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome |
724207001 | Kleefstra syndrome |
724226009 | Infantile osteopetrosis with neuroaxonal dysplasia syndrome |
724227000 | Infantile onset spinocerebellar ataxia |
724228005 | Infantile choroidocerebral calcification syndrome |
724281002 | Hyposmia, nasal and ocular hypoplasia, hypogonadotropic hypogonadism syndrome |
724283004 | Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum |
724351008 | Hereditary hyperekplexia |
724357007 | Hereditary cerebral hemorrhage with amyloidosis |
724383002 | Hemidystonia hemiatrophy syndrome |
724385009 | Growth delay due to insulin-like growth factor type 1 deficiency |
72442006 | Disorder of posterior pituitary |
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 |
724508005 | Late-onset central hypoventilation co-occurrent and due to hypothalamic dysfunction |
724542001 | Encephalitis caused by Venezuelan equine encephalomyelitis virus |
724543006 | Infection causing multiple abscesses of brain |
724544000 | Infection causing tic |
724545004 | Tic due to and following infection |
724546003 | Infection causing parkinsonism |
724549005 | Epilepsy due to infectious disease of central nervous system |
724561002 | Encephalopathy due to nutritional deficiency |
724562009 | Myelopathy due to nutritional deficiency |
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 |
724654009 | Anxiety disorder caused by opioid |
724655005 | Psychotic disorder caused by opioid |
724668002 | Seizure co-occurrent and due to sedative withdrawal |
724669005 | Seizure co-occurrent and due to hypnotic withdrawal |
724670006 | Seizure co-occurrent and due to anxiolytic withdrawal |
724671005 | Perceptual disturbances and seizures co-occurrent and due to sedative withdrawal |
724672003 | Perceptual disturbances and seizures co-occurrent and due to hypnotic withdrawal |
724673008 | Psychotic disorder caused by sedative |
724674002 | Psychotic disorder caused by hypnotic |
724675001 | Psychotic disorder caused by anxiolytic |
724679007 | Mood disorder with manic symptoms caused by sedative |
724680005 | Mood disorder with manic symptoms caused by hypnotic |
724681009 | Mood disorder with manic symptoms caused by anxiolytic |
724682002 | Mood disorder with mixed depressive and manic symptoms caused by sedative |
724683007 | Mood disorder with mixed depressive and manic symptoms caused by hypnotic |
724684001 | Mood disorder with mixed depressive and manic symptoms caused by anxiolytic |
724685000 | Amnestic disorder caused by sedative |
724686004 | Amnestic disorder caused by hypnotic |
724687008 | Amnestic disorder caused by anxiolytic |
724689006 | Psychotic disorder caused by cocaine |
724690002 | Mood disorder with depressive symptoms caused by cocaine |
724691003 | Mood disorder with manic symptoms caused by cocaine |
724692005 | Mood disorder with mixed depressive and manic symptoms caused by cocaine |
724693000 | Obsessive compulsive disorder caused by cocaine |
724696008 | Psychotic disorder caused by hallucinogen |
724702008 | Psychotic disorder caused by volatile inhalant |
724705005 | Delirium caused by methylenedioxymethamphetamine |
724706006 | Psychotic disorder caused by methylenedioxymethamphetamine |
724707002 | Mood disorder caused by methylenedioxymethamphetamine |
724708007 | Anxiety disorder caused by methylenedioxymethamphetamine |
724716003 | Delirium caused by ketamine |
724717007 | Delirium caused by dissociative drug |
724718002 | Psychotic disorder caused by dissociative drug |
724719005 | Psychotic disorder caused by ketamine |
724720004 | Mood disorder caused by dissociative drug |
724721000 | Mood disorder caused by ketamine |
724722007 | Anxiety disorder caused by dissociative drug |
724723002 | Anxiety disorder caused by ketamine |
724725009 | Psychoactive substance withdrawal without complication |
724726005 | Perceptual disturbances co-occurrent and due to psychoactive substance withdrawal |
724727001 | Seizure co-occurrent and due to psychoactive substance withdrawal |
724728006 | Perceptual disturbances and seizures co-occurrent and due to psychoactive substance withdrawal |
724746000 | Delirium due to multiple etiological factors |
724747009 | Amnestic disorder due to multiple etiological factors |
724761004 | Sporadic Parkinson disease |
724762006 | Parkinsonism due to and following injury of head |
724763001 | Parkinsonism due to mass lesion of brain |
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 |
724788009 | Epilepsy due to and following traumatic brain injury |
724789001 | Epilepsy due to intracranial tumor |
724792002 | Incomplete cord syndrome of thoracic spinal cord |
724793007 | Incomplete cord syndrome of lumbar spinal cord |
724813004 | Autonomic nervous system disorder co-occurrent and due to neurodegenerative disorder |
724819000 | Functional paraparesis |
724820006 | Functional hemiparesis |
724822003 | Functional dystonia |
724823008 | Functional parkinsonism |
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 |
725012004 | Incomplete cord syndrome of cervical spinal cord |
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 |
72513001 | Closed fracture of T7-T12 level with spinal cord injury |
725132001 | Ischemic stroke without residual deficits |
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 |
72585000 | Parkinsonian syndrome associated with idiopathic orthostatic hypotension |
725898002 | Delirium co-occurrent with dementia |
725907002 | Autosomal recessive limb girdle muscular dystrophy type 2Y |
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 |
72820004 | Parkinsonism caused by neuroleptic drug |
72836002 | Hepatic coma |
72858000 | Speech cortex disorder |
72880002 | Oropouche virus disease |
73020009 | Cerebral hemisphere hemorrhage |
73064001 | Thyrotropin overproduction |
73097000 | Alcohol amnestic disorder |
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 |
732931006 | Autosomal recessive limb girdle muscular dystrophy type 2R |
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 |
733168003 | Invasive aspergillosis of brain |
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 |
733198005 | Encephalopathy due to and following cardiopulmonary bypass |
733199002 | Multifocal cerebral infarction due to and following procedure on cardiovascular system |
73331006 | Hemimyelia |
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 |
73413009 | Cortex contusion with open intracranial wound AND concussion |
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 |
73462009 | Chronic vocal tic disorder |
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 |
735235000 | Seizure co-occurrent and due to drug withdrawal |
735421004 | Leukoencephalopathy with brain stem and spinal cord involvement and high lactate syndrome |
735537007 | Hyperosmolar hyperglycemic coma due to diabetes mellitus without ketoacidosis |
735555003 | Deep abscess of cerebral hemisphere |
735556002 | Abscess of corpus callosum |
735558001 | Parasitic infection causing granuloma of cerebrum |
735560004 | Infection causing granuloma of spinal cord |
735749005 | Myelomeningocele co-occurrent with hydrocephalus |
735750005 | Psychotic disorder with schizophreniform symptoms caused by cocaine |
735757008 | Primary ganglioneuroblastoma of brain |
736321008 | Injury of both visual cortices |
73663008 | Neurologic xeroderma pigmentosum |
737159004 | Aneurysm of basilar artery |
737160009 | Dissection of basilar artery |
737225007 | Secondary psychotic syndrome with hallucinations and delusions |
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 |
737233008 | Concussion of cervical spinal cord |
737234002 | Traumatic edema of cervical spinal cord |
737236000 | Concussion of thoracic spinal cord |
737237009 | Traumatic edema of thoracic spinal cord |
737238004 | Concussion of lumbar spinal cord |
737239007 | Traumatic edema of lumbar spinal cord |
737338002 | Synthetic cannabinoid withdrawal |
737339005 | Delirium caused by synthetic cannabinoid |
737341006 | Anxiety disorder caused by synthetic cannabinoid |
737582007 | Hemiparkinsonism hemiatrophy syndrome |
7379000 | Pseudobulbar palsy |
73935008 | Toxic encephalopathy caused by hydroxyquinoline |
739665005 | Complete spinal cord injury |
739666006 | Incomplete spinal cord injury |
74012004 | Congenital anomaly of pituitary gland |
74073002 | Cerebellar hemangioblastomatosis |
74107003 | Acromegaly |
74267005 | Toxic encephalopathy caused by carbon tetrachloride |
74333002 | Spasmodic torticollis |
74351001 | Reye's syndrome |
74360009 | Open fracture of C5-C7 level with central cord syndrome |
7454002 | Simple partial seizure with autonomic dysfunction |
74644004 | Influenza with encephalopathy |
74728003 | Hypopituitarism |
74737003 | Complex partial seizure + impairment consciousness at onset |
74772000 | Meningomyelitis |
74810008 | Premotor cortex syndrome |
74934004 | Psychoactive substance-induced withdrawal syndrome |
75019001 | Athetoid cerebral palsy |
75023009 | Post-traumatic epilepsy |
75038005 | Cerebellar hemorrhage |
75046006 | Combined pyramidal-extrapyramidal syndrome |
75072002 | Nemaline myopathy |
75122001 | Inhalant-induced psychotic disorder with delusions |
751371000000107 | Personal history of transient ischaemic attack |
75138007 | Endophlebitis of superior sagittal sinus |
75143000 | Toxic encephalitis caused by thallium |
75299005 | Spastic spinal syphilitic paralysis |
75467001 | Intervertebral disc disorder of cervical region with myelopathy |
75491005 | Amyotrophia congenita |
75507000 | Subarachnoid hemorrhage following injury with open intracranial wound AND loss of consciousness |
75543006 | Cerebral embolism |
75837004 | Mood disorder with depressive features due to general medical condition |
758664007 | Isolated follicle stimulating hormone deficiency |
75968004 | Sotos' syndrome |
7611002 | Septo-optic dysplasia sequence |
76156000 | Juvenile cerebellar degeneration AND myoclonus |
762287001 | Mixed neonatal apnea |
762294003 | Transient infantile hyperthyrotropinemia |
762295002 | Congenital obstructive hydrocephalus |
762297005 | White matter disorder due to vitamin B12 deficiency |
762299008 | Myelopathy due to toxicity of substance |
762300000 | Movement disorder due to toxicity of substance |
762320004 | Mood disorder with manic symptoms caused by opioid |
762321000 | Mood disorder with depressive symptoms caused by opioid |
762322007 | Mood disorder with mixed depressive and manic symptoms caused by opioid |
762324008 | Delirium caused by stimulant |
762325009 | Psychotic disorder caused by stimulant |
762326005 | Psychotic disorder with hallucinations caused by stimulant |
762327001 | Psychotic disorder with delusions caused by stimulant |
762328006 | Mood disorder caused by stimulant |
762329003 | Mood disorder with depressive symptoms caused by stimulant |
762330008 | Mood disorder with mixed depressive and manic symptoms caused by stimulant |
762331007 | Anxiety disorder caused by stimulant |
762335003 | Mood disorder with manic symptoms caused by hallucinogen |
762336002 | Mood disorder with depressive symptoms caused by hallucinogen |
762337006 | Mood disorder with mixed depressive and manic symptoms caused by hallucinogen |
762338001 | Mood disorder with manic symptoms caused by volatile inhalant |
762339009 | Mood disorder with depressive symptoms caused by volatile inhalant |
762340006 | Mood disorder with mixed depressive and manic symptoms caused by volatile inhalant |
762344002 | Mood disorder with manic symptoms caused by dissociative drug |
762345001 | Mood disorder with depressive symptoms caused by dissociative drug |
762346000 | Mood disorder with mixed depressive and manic symptoms caused by dissociative drug |
762350007 | Dementia due to prion disease |
762351006 | Dementia due to and following injury of head |
762352004 | Demyelination due to systemic vasculitis |
76236006 | Atypical tic disorder |
762436001 | Injury of left visual cortex |
762457009 | Astroblastoma of brain |
762506007 | Delirium caused by synthetic cathinone |
762507003 | Psychotic disorder caused by synthetic cathinone |
762508008 | Psychotic disorder with hallucinations caused by synthetic cathinone |
762509000 | Psychotic disorder with delusions caused by synthetic cathinone |
762510005 | Psychotic disorder with schizophreniform symptoms caused by synthetic cathinone |
762511009 | Mood disorder caused by synthetic cathinone |
762512002 | Mood disorder with depressive symptoms caused by synthetic cathinone |
762513007 | Mood disorder with manic symptoms caused by synthetic cathinone |
762514001 | Mood disorder with mixed depressive and manic symptoms caused by synthetic cathinone |
762515000 | Anxiety disorder caused by synthetic cathinone |
762516004 | Obsessive compulsive disorder caused by synthetic cathinone |
762617003 | Injury of right visual cortex |
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 |
762663009 | Mesencephalic light-near dissociation |
762672001 | Synthetic cathinone withdrawal |
762707000 | Subcortical dementia |
763065008 | Ataxia telangiectasia variant |
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 |
763127004 | Benign paroxysmal tonic upgaze of childhood with ataxia |
763130006 | Cleft palate, large ears, small head syndrome |
763135001 | Charcot-Marie-Tooth disease type 4E |
763136000 | Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome |
763280005 | Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome |
763310000 | Acute necrotizing encephalopathy of childhood |
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 |
76349003 | Extrapyramidal disease |
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 |
763717004 | Sporadic fetal brain disruption sequence |
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 |
763793004 | Limbic encephalitis with contactin-associated protein-like 2 antibodies |
763794005 | Limbic encephalitis with leucine-rich glioma-inactivated 1 antibodies |
763797003 | Agenesis of corpus callosum and abnormal genitalia syndrome |
763798008 | Microcephalus, complex motor and sensory axonal neuropathy syndrome |
763802009 | Micturition induced epilepsy |
763803004 | Morvan syndrome |
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 |
763869003 | Myelitis caused by ionizing radiation following radiotherapy |
763889002 | Spina bifida and hypospadias syndrome |
763895001 | Myosclerosis |
76402003 | Carotid artery insufficiency syndrome |
764095005 | Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome |
76418009 | Concussion with mental confusion AND/OR disorientation without loss of consciousness |
76435008 | Open fracture of C1-C4 level with spinal cord injury |
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 |
764661000000103 | Cervical spinal cord injury, without spinal bone injury, C5-7 |
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 |
764734003 | Autosomal recessive spastic paraplegia type 21 |
764736001 | Autosomal recessive spastic paraplegia type 43 |
76474001 | Herpetic acute necrotizing encephalitis |
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 |
764993001 | Encephalitis caused by Mycoplasma pneumoniae |
764998005 | Non-herpetic acute limbic encephalitis |
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 |
765151006 | Asphyxiophilia |
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 |
765751002 | Autoimmune encephalopathy with parasomnia and obstructive sleep apnea |
765753004 | Autosomal recessive spastic paraplegia type 45 |
765756007 | Benign infantile seizure with mild gastroenteritis syndrome |
765757003 | Bilateral polymicrogyria |
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 |
766709000 | Isolated hypoplasia of cerebellar vermis |
766710005 | Isolated focal cortical dysplasia |
76675006 | Cerebellar laceration without open intracranial wound AND with concussion |
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 |
766872002 | Parkinsonism caused by cyanide |
766931003 | Hypomyelination neuropathy arthrogryposis syndrome |
766932005 | Hypothalamic hamartoma with gelastic seizure |
766934006 | Isolated unilateral hemispheric cerebellar hypoplasia |
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 |
76889003 | Failed attempted abortion with cerebral anoxia |
768939009 | Primary tethered cord syndrome |
769065000 | Tubulin beta 4A class IVa related leukodystrophy |
76916001 | Spina bifida occulta |
76938004 | Infantile encephalopathy AND lactic acidosis |
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 |
770626007 | Congenital Horner syndrome |
770627003 | Desmin-related myofibrillar myopathy |
770630005 | Distal hereditary motor neuropathy type 1 |
770643005 | Mesial temporal lobe epilepsy with hippocampal sclerosis |
770655004 | Microcephalus, brain defect, spasticity, hypernatremia syndrome |
770664009 | Neonatal brainstem dysfunction |
770678005 | Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome |
770680004 | Prader-Willi-like syndrome |
770682007 | Rosette-forming glioneuronal neoplasm |
770683002 | Secondary syringomyelia |
770720005 | Autosomal recessive spastic paraplegia type 58 |
770721009 | Microcephaly, thin corpus callosum, intellectual disability syndrome |
770722002 | Proximal myopathy with extrapyramidal signs |
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 |
771076003 | Leptomyelolipoma |
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 |
771234002 | Isolated bilateral hemispheric cerebellar hypoplasia |
771261002 | Digital extensor muscle aplasia with polyneuropathy |
771263004 | Ptosis and vocal cord paralysis syndrome |
771267003 | Congenital muscular dystrophy with integrin alpha-7 deficiency |
771271000 | Steroid-responsive encephalopathy associated with autoimmune thyroiditis |
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 |
771418002 | Delirium following surgical procedure |
771419005 | Hyperactive delirium following surgical procedure |
771420004 | Hypoactive delirium following surgical procedure |
771421000 | Mixed hyperactive hypoactive delirium following surgical procedure |
771448004 | Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency |
771469002 | Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome |
771470001 | Jawad 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 |
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 |
77224008 | Spina bifida of lumbar region |
77274005 | Idiopathic diabetes insipidus |
773230003 | Cyclin-dependent kinase-like 5 deficiency |
773275000 | Acute limbic encephalitis following transplant |
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 |
773395008 | Limbic encephalitis with dipeptidyl-peptidase 6 antibodies |
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 |
77355000 | Cannabis-induced organic mental disorder |
773552008 | Intellectual disability, feeding difficulties, developmental delay, microcephaly 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 |
773663004 | Rapid-onset childhood obesity, hypothalamic dysfunction, hypoventilation, autonomic dysregulation 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 |
773688007 | Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids |
773699009 | Pitt Hopkins-like syndrome |
773737004 | Nephrocystin 3-related Meckel-like syndrome |
77375009 | Adductor spastic dysphonia of conversion reaction |
773989002 | Late-onset isolated adrenocorticotropic hormone deficiency |
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 |
77486005 | Mood disorder with major depressive-like episode due to general medical condition |
77553008 | Opticocochleodentate degeneration |
77575005 | Secondary hyperprolactinemia due to prolactin-secreting tumor |
775907000 | Congenital pontocerebellar hypoplasia type 9 |
77600008 | Bing-Neel syndrome |
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 |
778002005 | Sodium voltage-gated channel alpha subunit 2 encephalopathy |
778003000 | Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain |
778005007 | Duplication of pituitary gland |
778011005 | Severe intellectual disability and progressive spastic paraplegia |
778027003 | Primary CD59 deficiency |
778029000 | FAST kinase domains 2-related infantile mitochondrial encephalomyopathy |
778030005 | Autosomal recessive spastic paraplegia type 27 |
778046002 | Somatomammotropinoma |
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 |
7794004 | Chronic motor tic disorder |
77956009 | Steinert myotonic dystrophy syndrome |
78028004 | Brain stem contusion with open intracranial wound AND concussion |
78071008 | Hydromicrocephaly |
780822000 | Desmoplastic infantile astrocytoma and ganglioglioma |
780827006 | Synaptic Ras GTPase activating protein 1- related intellectual disability |
78085003 | Open fracture of T7-T12 level with incomplete spinal cord lesion |
78157002 | Closed fracture of C5-C7 level with central cord syndrome |
7819003 | Intracranial hemorrhage following injury with open intracranial wound AND no loss of consciousness |
78211006 | Open fracture of thoracic spine with spinal cord injury |
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 |
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 |
782884005 | Pontine tegmental cap dysplasia |
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 |
782951006 | Thoracic dysplasia and hydrocephalus syndrome |
783005002 | Severe microbrachycephaly, intellectual disability, athetoid cerebral palsy syndrome |
783008000 | Pituitary dermoid and epidermoid cysts |
783009008 | Pituitary deficiency due to Rathke cleft cysts |
783012006 | Parkinsonian pyramidal syndrome |
783016009 | Panhypophysitis |
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 |
783158009 | Infundibulo neurohypophysitis |
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 |
783243008 | Adenohypophysitis |
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 |
78358001 | Amphetamine withdrawal |
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 |
783705006 | Sporadic hyperekplexia |
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 |
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 |
78693004 | Congenital hypoplasia of part of brain |
787037000 | Congenital muscular dystrophy type 1A |
787044009 | Stenosis of bilateral carotid arteries |
787174003 | Intellectual disability, hyperkinetic movement, truncal ataxia syndrome |
78784005 | Amyelia |
788417006 | Alopecia, epilepsy, intellectual disability syndrome Moynahan type |
788454002 | Stenosis of bilateral vertebral arteries |
788455001 | Occlusion of bilateral pontine arteries |
788756004 | Spindle cell oncocytoma of posterior pituitary gland |
788757008 | Pituicytoma of posterior pituitary gland |
788758003 | Sellar ependymoma of posterior pituitary gland |
78879009 | Intracranial hemorrhage following injury with open intracranial wound AND concussion |
788863007 | Amnestic disorder caused by psychoactive substance |
788864001 | Amnestic disorder caused by volatile solvent |
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 |
788908000 | Dissociative neurological symptom disorder co-occurrent with dystonia |
788911004 | Dissociative neurological symptom disorder co-occurrent with Parkinsonism |
788915008 | Encephalitis caused by Henipavirus |
788916009 | Encephalopathy caused by ammonia |
788930004 | Focal contusion of brain |
788931000 | Focal contusion of occipital lobe |
788932007 | Focal contusion of parietal lobe |
788933002 | Focal contusion of temporal lobe |
788934008 | Focal laceration of brain |
788983007 | Mood disorder caused by cannabis |
789005009 | Paralysis of uvula after diphtheria |
789046004 | Sleep-related movement disorder caused by drug |
789047008 | Sleep-related movement disorder caused by substance |
789053008 | Transient motor tic |
789063000 | Primary hyperaldosteronism, seizures, neurological abnormalities syndrome |
789120001 | Neurenteric cyst |
78914008 | Laceration of brain |
789187001 | X-linked acrogigantism due to Xq26 microduplication |
789657008 | ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis |
78968003 | Brain stem contusion with open intracranial wound |
791000124107 | 2-methyl-3-hydroxybutyric aciduria |
792004 | Jakob-Creutzfeldt disease |
79220008 | Brain stem contusion without open intracranial wound AND with concussion |
79267007 | Retinal migraine |
7931000119101 | Anterior choroidal artery thrombosis |
79341000119107 | Mixed dementia |
79348005 | Simple partial seizure, consciousness not impaired |
79385002 | Lowe syndrome |
79591004 | Spastic paralysis due to spinal birth injury |
79631006 | Absence seizure |
79633009 | Spastic hemiplegia |
79745005 | Reflex epilepsy |
79897009 | Cerebellar abscess |
7990002 | Immunoglobulinemia with isolated somatotropin deficiency |
80098002 | Diffuse Lewy body disease |
80180004 | Pallidonigral degeneration |
80328002 | Progressive cone-rod dystrophy |
80381005 | Adductor spastic dysphonia of dystonia |
80495009 | Sleep walking disorder |
80544005 | Spongy degeneration of central nervous system |
80599001 | Isolated corticotropin deficiency |
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 |
80849007 | Gigantism |
80868005 | Cocaine withdrawal |
80901002 | Endophlebitis of torcular Herophili |
80935004 | Flaccid hemiplegia |
80976008 | Myasthenic crisis |
80980003 | Open fracture of C5-C7 level with spinal cord injury |
81042008 | Congenital anomaly of spinal cord |
81211007 | Primary lateral sclerosis |
81308009 | Disorder of brain |
813921000000104 | Spastic hemiplegic cerebral palsy |
81412002 | Cortex contusion with open intracranial wound AND loss of consciousness |
81442004 | Closed fracture of cervical region with spinal cord injury |
81475007 | Acquired nephrogenic diabetes insipidus |
81526008 | Hydromeningomyelocele |
816067005 | Diabetes, hypogonadism, deafness, intellectual disability syndrome |
816068000 | Periventricular nodular heterotopia |
816205008 | Malignant pituitary blastoma |
81642009 | Late effect of spinal cord injury |
8166000 | Thrombophlebitis of basilar sinus |
816984002 | Progressive multiple sclerosis |
81780002 | Beckwith-Wiedemann syndrome |
8183009 | Closed fracture of T7-T12 level with central cord syndrome |
81854007 | Alexander's disease |
81896006 | Dysmorphic sialidosis with renal involvement |
818967003 | Medulloepithelioma of central nervous system |
82058009 | Myelocele |
82077006 | Myotubular myopathy |
822021000000103 | Acute encephalitis |
82339009 | Amphetamine-induced anxiety disorder |
82344002 | Cerebellar contusion with open intracranial wound |
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 |
82401000 | Simple partial seizure with motor dysfunction |
82501000119102 | Anaplastic astrocytoma of central nervous system |
82547005 | Acute adenoviral meningoencephalitis |
82598004 | Secondary hypothyroidism |
8269002 | Cerebrospinal angiopathy |
827172005 | X-linked progressive cerebellar ataxia |
82793005 | Hypothalamic obesity |
82800008 | Dipsogenic diabetes insipidus |
8291000119107 | Atonic epilepsy |
82959004 | Dementia paralytica juvenilis |
830015009 | Dermoid cyst of spinal cord |
830032008 | Dermoid cyst of occipital lobe |
830033003 | Dermoid cyst of brain |
8301004 | Caudal dysplasia sequence |
83157008 | Fatal familial insomnia |
83159006 | Cytomegalovirus encephalitis |
83168008 | Psychoactive substance-induced organic amnestic disorder |
83304000 | Dubini's chorea |
833326008 | Cortical vascular dementia |
83351003 | Basilar migraine |
83367009 | Amphetamine-induced organic mental disorder |
83465002 | Neuroleptic-induced acute dystonia |
83501007 | Organic mood disorder of mixed type |
836301008 | Amnestic mild cognitive disorder |
83716008 | Traumatic spinal cord compression |
83759003 | Adductor spastic dysphonia of musculoskeletal tension reaction |
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 |
838315004 | Encephalomyelitis caused by Burkholderia |
83832001 | Metachromatic leukodystrophy without arylsulfatase deficiency |
838323002 | Autoimmune opsoclonus myoclonus |
838331007 | Ataxia due to chronic infection of central nervous system |
838332000 | Abscess of brainstem |
838339009 | Basal encephalocele |
838351006 | Acute seizure due to infection of central nervous system |
838371002 | Abscess of cerebral hemisphere lobe |
838373004 | Abscess of frontal lobe |
838383000 | Chorea caused by toxin |
838390005 | Abscess of spinal cord caused by fungus |
838392002 | Abscess of parietal lobe |
838393007 | Abscess of pons cerebri |
838394001 | Abscess of midbrain |
838395000 | Abscess of occipital lobe |
838441009 | Mental retardation, adducted thumbs, shuffling gait, aphasia syndrome |
838528007 | Mood disorder with manic symptoms caused by amfetamine and amfetamine derivative |
838529004 | Mood disorder with mixed depressive and manic symptoms caused by amfetamine and amfetamine derivative |
838530009 | Mood disorder with depressive symptoms caused by amfetamine and amfetamine derivative |
83942000 | Acute disseminated encephalomyelitis |
83982007 | Subacute necrotic myelopathy |
83991006 | Incomplete spinal cord lesion at C5-C7 level without bone injury |
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 |
840440006 | Encephalitis caused by Leptospira species |
840441005 | Dissection of intracranial artery |
840442003 | Encephalitis caused by human immunodeficiency virus type 2 |
840449007 | Cognitive impairment caused by ingestible alcohol |
840452004 | Classical sporadic Creutzfeldt-Jakob disease |
840454003 | Cyst of spinal cord caused by parasite |
840464007 | Dementia due to carbon monoxide poisoning |
840465008 | Dementia due to iron deficiency |
840471002 | Hydrocephalus due to Dandy-Walker malformation |
840496004 | Encephalitis caused by Borrelia species |
840498003 | Encephalitis caused by human immunodeficiency virus type 1 |
840501003 | Dystonia caused by toxin |
840505007 | Down syndrome co-occurrent with leukemoid reaction associated transient neonatal pustulosis |
840511005 | Compression of spinal cord due to intraspinal abscess |
840721004 | Incomplete spinal cord syndrome |
84160009 | Laryngeal hemiplegia |
84161000119100 | Partial epileptic seizure of parietal lobe with impairment of consciousness |
84170006 | Contusion of brain with open intracranial wound |
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 |
843004 | Poliomyelomalacia |
84455002 | Spinal paraplegia |
84461004 | Exencephaly |
84590007 | Lower motor neuron disease |
8459005 | Closed fracture of C1-C4 level with incomplete cord lesion |
846680003 | Functional hypogonadotropic hypogonadism |
84757009 | Epilepsy |
84900008 | Cerebellar laceration with open intracranial wound AND loss of consciousness |
85039006 | Postpartum amenorrhea-galactorrhea syndrome |
85102008 | Cerebellar ataxia |
8511007 | Transient tic disorder, single episode |
85262003 | Open fracture of T1-T6 level with posterior cord syndrome |
8528005 | Acute ascending myelitis |
85505000 | Adult spinal muscular atrophy |
8551000119100 | Benign neoplasm of spinal intradural extramedullary space |
85561006 | Uncomplicated alcohol withdrawal |
85592008 | Primary progressive cerebellar degeneration |
8563000 | Cholinergic crisis |
85641006 | Hemianencephaly |
85672005 | Anterior horn cell disease |
85821003 | Acute non-psychotic brain syndrome |
85861002 | Subchronic undifferentiated schizophrenia |
86003009 | Carotid artery thrombosis |
86044005 | Amyotrophic lateral sclerosis |
86073008 | Hypersomatotropic gigantism |
860799000 | Encephalopathy due to folate deficiency |
860802009 | Ex-vacuo hydrocephalus due to infection |
860803004 | Hydrocephalus due to tuberculosis of brain |
860804005 | Epilepsy due to infectious encephalitis |
860805006 | Encephalomyelitis caused by Neisseria meningitidis |
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 |
860822008 | Encephalitis caused by Nocardia |
860826006 | Creutzfeldt-Jakob Disease caused by human growth hormone |
860834000 | Granuloma of brain caused by Schistosoma |
860840007 | Granuloma of brain caused by Schistosoma japonicum |
860841006 | Encephalomyelitis caused by bacterium |
860842004 | Encephalomyelitis caused by Coxiella burnetii |
860849008 | Granuloma of spinal cord caused by fungus |
860851007 | Granuloma of cerebral hemispheric lobe |
860852000 | Granuloma of brainstem |
860864008 | Granuloma of brain caused by Schistosoma haematobium |
860865009 | Encephalitis caused by Trypanosoma brucei gambiense |
860866005 | Encephalitis caused by Trypanosoma brucei rhodesiense |
860868006 | Encephalitis caused by Me Tri virus |
860881004 | Flaccid diplegia of lower extremities |
860886009 | Granuloma of brain caused by Schistosoma mansoni |
86125000 | Cerebellar contusion with open intracranial wound AND concussion |
86188000 | Kuru |
8635005 | Alcohol withdrawal delirium |
864171000000103 | Non-epileptic attack disorder |
86444004 | Niemann-Pick disease, type C, acute form |
864471000000106 | Anterior opercular syndrome |
86558004 | Cerebellar pressure cone |
866045007 | Myelitis caused by Actinomyces |
866050001 | Mixed germ cell neoplasm of central nervous system |
866051002 | Motor neuron disease due to lead intoxication |
866053004 | Middle interhemispheric variant of holoprosencephaly |
866055006 | Myelitis caused by Enterovirus |
866056007 | Myelitis caused by Epstein-Barr virus |
866057003 | Myelitis caused by Dengue virus |
866058008 | Myelitis caused by Human echovirus |
866059000 | Myelitis caused by Human coxsackievirus A |
866060005 | Myelitis caused by Cytomegalovirus |
866061009 | Myelitis caused by Coccidioides |
866062002 | Myelitis caused by Coenurus cerebralis |
866063007 | Myelitis caused by Mycoplasma pneumoniae |
866064001 | Myelitis caused by Aspergillus |
866065000 | Myelitis caused by Schistosoma mansoni |
866066004 | Myelitis caused by Borrelia burgdorferi |
866067008 | Myelitis caused by Schistosoma japonicum |
866090003 | Meningomyelitis caused by Treponema pallidum |
866121005 | Myelitis caused by Schistosoma |
866123008 | Myelitis caused by Schistosoma haematobium |
866124002 | Myelitis caused by human poliovirus |
866125001 | Myelitis caused by Retroviridae |
866126000 | Myelitis caused by Influenza A virus |
866127009 | Myelitis caused by Plasmodium |
866128004 | Myelitis caused by Roseolovirus |
866129007 | Myelitis caused by human T-lymphotropic virus type 1 |
866130002 | Myelitis caused by Herpes simplex type 2 |
866131003 | Myelitis caused by Human herpes virus |
866132005 | Myelitis caused by Herpes simplex type 1 |
866251007 | Myelitis caused by Human coxsackievirus B |
86842008 | Iatrogenic pituitary disorder |
870262000 | Pervasive developmental disorder with disorder of intellectual development without loss of previously acquired skills |
870264004 | Pervasive developmental disorder with disorder of intellectual development and pervasive impairment of functional language without loss of previously acquired skills |
870265003 | Pervasive developmental disorder with disorder of intellectual development with loss of previously acquired skills |
870266002 | Pervasive developmental disorder with disorder of intellectual development and marked impairment of functional language with loss of previously acquired skills |
870267006 | Pervasive developmental disorder with disorder of intellectual development and marked impairment of functional language without loss of previously acquired skills |
870268001 | Pervasive developmental disorder with disorder of intellectual development and complete impairment of functional language without loss of previously acquired skills |
870269009 | Pervasive developmental disorder with disorder of intellectual development and absence of functional language with loss of previously acquired skills |
870270005 | Pervasive developmental disorder with disorder of intellectual development and complete impairment of functional language with loss of previously acquired skills |
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 |
870288002 | Parkinsonism caused by methanol |
870290001 | Myelopathy due to vitamin B12 deficiency |
870291002 | Myelopathy due to lathyrism |
870293004 | Myelitis caused by Treponema pallidum |
870294005 | Myelitis caused by Toxoplasma gondii |
870295006 | Parkinsonism caused by carbon disulfide |
870305003 | Pervasive developmental disorder with cognitive developmental delay and marked impairment of functional language |
870308001 | Pervasive developmental disorder with cognitive developmental delay and complete impairment of functional language |
870340002 | Granuloma of spinal cord caused by Mycobacterium |
870341003 | Granuloma of spinal cord caused by parasite |
870342005 | Compression of spinal cord due to granulomatous disorder |
870343000 | Granuloma of spinal cord caused by bacterium |
870345007 | Compression of spinal cord due to cavernous hemangioma |
870364001 | Traumatic anterior cord syndrome |
87043009 | Cerebral anoxia after obstetrical surgery AND/OR other procedure including delivery |
870540001 | Contusion of hindbrain |
870544005 | Occlusion of distal basilar artery |
870548008 | Closed fracture of skull with cerebral laceration |
870549000 | Closed fracture of skull with cerebral contusion |
870550000 | Closed fracture of base of skull with cerebral laceration |
870551001 | Closed fracture of base of skull with cerebral contusion |
870553003 | Open fracture of vault of skull with cerebral laceration |
870554009 | Open fracture of vault of skull with cerebral contusion |
870555005 | Open fracture of skull with cerebral contusion |
870556006 | Open fracture of skull with cerebral laceration |
870563006 | Contusion of cerebrum with open intracranial wound |
870565004 | Contusion of hindbrain with open intracranial wound |
870566003 | Occlusion of anterior choroidal artery |
870579007 | Occlusion of branch of basilar artery |
870637009 | Dissection of cervical artery |
87091000119101 | Malignant glioma of cerebrum |
87095001 | Olfactory seizure |
87111000119109 | Malignant glioma of hypothalamus |
87121000119102 | Malignant glioma of cerebellum |
87132004 | Opioid withdrawal |
87151000119105 | Malignant glioma of central nervous system |
871637001 | Thrombosis of multiple cerebral veins |
87227007 | Cerebral depression in newborn |
87235005 | Dialysis disequilibrium syndrome |
87476004 | Convulsions in the newborn |
87551000119101 | Visual disturbance as sequela of cerebrovascular disease |
87555007 | Claude's syndrome |
87607002 | Pelizaeus-Merzbacher disease, classic form |
87842000 | Generalized neuromuscular exhaustion syndrome |
87888006 | Cortex contusion with open intracranial wound |
87937009 | Endophlebitis of intracranial venous sinus |
88032003 | Amaurosis fugax |
88174006 | Basilar artery thrombosis |
88269008 | Thalamic syndrome |
8829008 | Isolated lutropin deficiency |
8837000 | Amphetamine delirium |
8840000 | Closed fracture of C1-C4 level with spinal cord injury |
88405003 | Open fracture of T7-T12 level with central cord syndrome |
88518009 | Wilson's disease |
885831000000109 | Choreoathetoid cerebral palsy |
88755007 | Phlebitis of lateral venous sinus |
88845000 | Explosive type organic personality disorder |
88922007 | Thrombosis of basilar sinus |
88923002 | Progressive muscular atrophy |
89142007 | Progressive intracranial arterial occlusion |
89261000 | Isolated thyrotropin deficiency |
89369001 | Anencephalus |
8939001 | Incomplete spinal cord lesion at C1-C4 level without bone injury |
89392001 | Prader-Willi syndrome |
89437009 | Cerebral paraparesis |
89441000119109 | Ventriculitis of the brain |
89451009 | Inhalant-induced mood disorder |
89476005 | Pituitary cachexia |
89525009 | Gelastic seizure |
89576007 | Pallidonigrospinal degeneration |
89601008 | Tic of organic origin |
89980009 | Thrombosis of cavernous venous sinus |
90011000119105 | Organic sleep related movement disorder |
90099008 | Subcortical leukoencephalopathy |
9015001 | Brain injury without open intracranial wound |
90162006 | Syringopontia |
90182005 | Hypophysectomy-induced hypopituitarism |
90253000 | Progressive subcortical gliosis |
903741000000102 | Uhthoff phenomenon |
90429009 | Cerebellar laceration without open intracranial wound AND with loss of consciousness |
904531000000100 | Bilateral spastic cerebral palsy |
90520006 | Vertebral artery stenosis |
90584004 | Spinal cord injury |
90755006 | Nicotine withdrawal |
90768003 | Contusion of brain without open intracranial wound |
90791004 | Posthemiplegic ataxia |
90811000119100 | Low grade malignant glioma of brain |
90831000119105 | Grade 4 malignant glioma of brain |
91012008 | Repeated concussion of brain |
91187007 | Pituitary dwarfism with small sella turcica |
91327001 | Quadriparesis |
9133005 | Familial amyloid polyneuropathy, Iowa type |
91377003 | Transient hyperprolactinemia |
91483004 | Tuberculous encephalitis |
91502009 | Spinocerebellar disease |
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 |
92029009 | Benign neoplasm of brain stem |
92030004 | Benign neoplasm of brain |
92050000 | Benign neoplasm of cerebellum |
92052008 | Benign neoplasm of cerebral ventricle |
92072003 | Benign neoplasm of craniopharyngeal duct |
92114009 | Benign neoplasm of frontal lobe |
92253009 | Benign neoplasm of occipital lobe |
92276007 | Benign neoplasm of parietal lobe |
92294001 | Benign neoplasm of pineal gland |
92296004 | Benign neoplasm of pituitary gland |
92341000119107 | Weakness of extremities as sequela of stroke |
92405007 | Benign neoplasm of spinal cord |
92406008 | Benign neoplasm of spinal meninges |
92427003 | Benign neoplasm of temporal lobe |
92503002 | Neurofibromatosis type 2 |
92573003 | Carcinoma in situ of craniopharyngeal duct |
92682003 | Carcinoma in situ of pineal gland |
92683008 | Carcinoma in situ of pituitary gland |
92824003 | Neurofibromatosis type 1 |
92904001 | Congenital abnormal shape of cerebellum |
92905000 | Congenital abnormal shape of cerebrum |
92962004 | Congenital absence of carotid artery |
92997002 | Congenital anomaly of carotid artery |
93054001 | Congenital dilatation of carotid artery |
93249003 | Congenital hypoplasia of cerebrum |
93312006 | Congenital malposition of carotid artery |
93396008 | Congenital stenosis of carotid artery |
93433003 | Drug-induced dyskinesia, acute onset |
9345005 | Dialysis dementia |
93557001 | Holorachischisis |
936271000000100 | Congenital anomaly of precerebral vessel |
9366002 | Palatal myoclonus |
93681000119102 | Insomnia co-occurrent and due to nocturnal myoclonus |
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 |
943121000000104 | Psychoactive substance-induced psychosis |
943151000000109 | Volatile inhalant-induced psychosis |
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 |
94766006 | Neoplasm of uncertain behavior of brain stem |
94767002 | Neoplasm of uncertain behavior of brain |
94786005 | Neoplasm of uncertain behavior of cerebellum |
94788006 | Neoplasm of uncertain behavior of cerebral ventricle |
94789003 | Neoplasm of uncertain behavior of cerebrum |
94808000 | Neoplasm of uncertain behavior of craniopharyngeal duct |
94847003 | Neoplasm of uncertain behavior of frontal lobe |
94968001 | Neoplasm of uncertain behavior of occipital lobe |
94986003 | Neoplasm of uncertain behavior of parietal lobe |
95002008 | Neoplasm of uncertain behavior of pineal gland |
95004009 | Neoplasm of uncertain behavior of pituitary gland |
95108005 | Neoplasm of uncertain behavior of spinal cord |
95109002 | Neoplasm of uncertain behavior of spinal meninges |
95126008 | Neoplasm of uncertain behavior of temporal lobe |
9520006 | Dissociated nystagmus |
95208000 | Photogenic epilepsy |
95235009 | Retroesophageal carotid artery |
9526000 | Pineal gland dysfunction |
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 |
95478002 | Congenital sacral meningocele |
95569006 | Uremic coma |
95610008 | Congenital brain damage |
95628005 | Neonatal encephalopathy |
95631006 | Drowsiness of the newborn |
95635002 | Caffeine withdrawal |
95638000 | Localized cranial lesion |
95640005 | Disorder of brain stem |
95641009 | Disorder of midbrain |
95643007 | Autoimmune encephalitis |
95644001 | Systemic lupus erythematosus encephalitis |
95646004 | Cerebellar degeneration |
95647008 | Upper motor neuron disease |
95650006 | Transient hemiplegia |
95651005 | Chronic progressive paraparesis |
95655001 | Ophthalmic migraine |
95815000 | Central positional vertigo |
95830009 | Pituitary infarction |
9611000119107 | Symptomatic carotid artery stenosis |
963741000000101 | Bacterial meningoencephalomyelitis |
9678009 | Herpetic meningoencephalitis |
96981000119102 | Malignant neoplasm of rectosigmoid junction metastatic to brain |
97381000119100 | Neurogenic bladder due to quadriplegia |
97391000119102 | Paraplegia with neurogenic bladder |
9740002 | Macroencephaly |
9753004 | Triplegia |
97751000119108 | Altered behavior in Alzheimer's disease |
984681000000101 | Profound learning disability |
98541000119101 | Herpes zoster myelitis |
98811000119103 | Subacute dyskinesia caused by drug |
9901000119100 | Occlusion of cerebral artery with stroke |
99131000119108 | Astrocytoma of cerebrum |
99451000119105 | Cerebral infarction due to stenosis of carotid artery |
9971000119105 | Myelopathy co-occurrent and due to spinal stenosis of cervical region |
Codes not in the full codelist are in faint grey.