Chronic Neurological Disease including Significant Learning Disorder
Codelist metadata
-
Coding system
- SNOMED CT
-
Coding system release
- 36.0.0
-
Organisation
- PRIMIS Covid Vaccination Uptake Reporting
-
Codelist ID
- primis-covid19-vacc-uptake/cns_cov
-
Version Tag
- v2.5
-
Version ID
- 41fbcc17
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
References
Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.
We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.
| code | term |
|---|---|
| 10007009 | Coffin-Siris syndrome |
| 1003373003 | Microcephaly with simplified gyral pattern |
| 1003374009 | Microlissencephaly |
| 1003375005 | Metachromatic leukodystrophy due to sphingolipid activator protein I deficiency |
| 1003444000 | Type 3 lissencephaly |
| 1003445004 | Lumbosacral spina bifida aperta with hydrocephalus |
| 1003447007 | Pelizaeus-Merzbacher disease null syndrome |
| 1003448002 | Lumbosacral spina bifida aperta |
| 1003465006 | Familial spinal neurofibromatosis |
| 1003881009 | Pelizaeus-Merzbacher disease in female carrier |
| 100721000119109 | High grade astrocytoma of brain |
| 100731000119107 | Low grade astrocytoma of brain |
| 100941000119100 | Epilepsy in mother complicating pregnancy |
| 1010464002 | Agenesis of right hemisphere of cerebellum |
| 1010465001 | Agenesis of left hemisphere of cerebellum |
| 1010630006 | X-linked complicated corpus callosum dysgenesis |
| 1010642001 | Sporadic infantile bilateral striatal necrosis |
| 1010643006 | Thoracolumbosacral spina bifida aperta |
| 1010644000 | Spina bifida aperta of upper thoracic spine |
| 1010653007 | Segmental neurofibromatosis type 1 |
| 1010712009 | Autosomal dominant Emery-Dreifuss muscular dystrophy |
| 101421000119107 | Dementia due to Parkinson's disease |
| 102831000119104 | Paralytic syndrome of both lower limbs as sequela of stroke |
| 1032761000000105 | Intraventricular (nontraumatic) haemorrhage, grade 4, of fetus and newborn |
| 10349009 | Multi-infarct dementia with delirium |
| 103761000119107 | Paralytic syndrome of all four limbs as sequela of stroke |
| 103931000119102 | Hepatic coma due to hepatitis |
| 10394003 | Friedreich's ataxia |
| 104981000119104 | Oligodendroglioma of cerebrum |
| 1052243006 | Hemiparesis of left side of face |
| 1052244000 | Hemiparesis of right side of face |
| 1052326006 | Rachischisis partialis |
| 10532003 | Primary degenerative dementia of the Alzheimer type, presenile onset, with depression |
| 105421000119105 | Early onset Alzheimer's disease with behavioral disturbance |
| 1055001 | Stenosis of precerebral artery |
| 106018006 | Hereditary degenerative disease of central nervous system |
| 106021000119105 | Multi-infarct dementia due to atherosclerosis |
| 10750951000119106 | Epilepsy in mother complicating childbirth |
| 107557061000119108 | Cerebrovascular accident due to embolism of bilateral anterior cerebral arteries |
| 107581000119103 | Astrocytoma of brain stem |
| 1078001000000105 | Haemorrhagic stroke |
| 1078223005 | Thrombosis of cerebral venous sinus due to and following surgical procedure |
| 1082511000119102 | Hepatic coma due to acute hepatic failure |
| 1082621000119108 | Hepatic coma due to alcoholic liver failure |
| 1085091000119108 | Hepatic coma due to chronic hepatic failure |
| 108691000119102 | Spasticity as sequela of stroke |
| 10878002 | Aneurysm of common carotid artery |
| 1089411000000104 | Cerebral infarction due to occlusion of cerebral artery |
| 1089421000000105 | Cerebral infarction due to stenosis of cerebral artery |
| 1089501000000102 | Presenile dementia with psychosis |
| 1089521000000106 | Predominantly cortical dementia |
| 1089531000000108 | Predominantly cortical vascular dementia |
| 1092691000119109 | Hepatic coma due to subacute liver failure |
| 109478007 | Kohlschutter's syndrome |
| 109561000 | Cerebrofacial dysplasia |
| 10976711000119104 | Primary primitive neuroectodermal neoplasm of central nervous system |
| 109911004 | Overlapping malignant neoplasm of brain and other parts of the central nervous system |
| 109912006 | Overlapping malignant neoplasm of brain |
| 109915008 | Primary malignant neoplasm of meninges |
| 11045000 | Supranuclear facial nerve paralysis |
| 1105051000000102 | Subacute combined degeneration of spinal cord due to use of nitrous oxide |
| 110997000 | Fahr's syndrome |
| 111028009 | Arteriopathic granular atrophy of cerebral cortex |
| 111033008 | Circumscribed atrophy of brain |
| 111296006 | Basilar artery embolism |
| 111297002 | Nonparalytic stroke |
| 111298007 | Chronic cerebral ischemia |
| 111299004 | Atheroma of cerebral arteries |
| 111337001 | Dyke-Davidoff-Masson syndrome |
| 111383007 | Dysmorphic sialidosis, juvenile form |
| 111385000 | Tay-Sachs disease |
| 111480006 | Psychoactive substance-induced organic dementia |
| 111496009 | Syringomyelia |
| 111497000 | Arterial thrombosis of spinal cord |
| 111498005 | Extratemporal epilepsy |
| 111499002 | Déjérine-Sottas disease |
| 111501005 | Congenital hereditary muscular dystrophy |
| 111502003 | Fukuyama congenital muscular dystrophy |
| 111503008 | Merosin deficient congenital muscular dystrophy |
| 111504002 | Walker-Warburg congenital muscular dystrophy |
| 111505001 | Muscle-eye-brain disease, congenital muscular dystrophy |
| 111506000 | Distal muscular dystrophy, Miyoshi type |
| 111508004 | Emery-Dreifuss muscular dystrophy |
| 111936002 | Cerebral sarcoidosis |
| 1131000119105 | Sequela of cerebrovascular accident |
| 1137357005 | Hepatic coma due to viral hepatitis D |
| 1141661004 | Neurocutaneous melanosis |
| 1142031005 | Optic atrophy due to late congenital syphilis |
| 1142056004 | Neonatal ischemic stroke |
| 11442006 | Hereditary sensory neuropathy |
| 1144223007 | Hypoxic ischemic encephalopathy of newborn |
| 11471000224106 | Diffuse intrinsic pontine glioma |
| 1148739007 | Obstructive hydrocephalus due to entrapment of inferior horn of lateral ventricle |
| 1148758003 | Congenital microcephaly |
| 1148924004 | Dementia due to deficiency of folic acid |
| 1153543002 | Occlusion of anterior cerebral artery |
| 1153544008 | Occlusion of right anterior cerebral artery |
| 1153545009 | Occlusion of left anterior cerebral artery |
| 1153546005 | Occlusion of bilateral posterior cerebral arteries |
| 1153607003 | Occlusion of right posterior communicating artery |
| 1153608008 | Occlusion of left posterior communicating artery |
| 1153611009 | Embolism of left anterior cerebral artery |
| 1153612002 | Embolism of right anterior cerebral artery |
| 1153630009 | Embolism of left carotid artery |
| 1153631008 | Embolism of right carotid artery |
| 1153632001 | Embolism of bilateral middle cerebral arteries |
| 1153633006 | Embolism of bilateral posterior cerebral arteries |
| 1153634000 | Embolism of bilateral anterior cerebral arteries |
| 1153638002 | Occlusion of bilateral cerebellar arteries |
| 11538006 | Quadriplegia |
| 1155688007 | Embolism of bilateral carotid arteries |
| 1155689004 | Embolism of bilateral cerebellar arteries |
| 1155697006 | Embolism of left vertebral artery |
| 1155698001 | Embolism of right vertebral artery |
| 1155699009 | Embolism of bilateral vertebral arteries |
| 1155991005 | Metastatic malignant neoplasm to leptomeninges |
| 1156016006 | Thrombosis of left posterior cerebral artery |
| 1156017002 | Thrombosis of right posterior cerebral artery |
| 1156018007 | Thrombosis of left cerebellar artery |
| 1156019004 | Thrombosis of right cerebellar artery |
| 1156027008 | Thrombus of dural sinus in pregnancy |
| 1156029006 | Thrombus of dural sinus in puerperium |
| 1156340006 | Toxic encephalopathy caused by monomethyl mercury |
| 1156406005 | Anaplastic oligodendroglioma of central nervous system |
| 1156409003 | Anaplastic ependymoma of central nervous system |
| 1156410008 | Anaplastic oligoastrocytoma of central nervous system |
| 1156413005 | Gliomatosis cerebri |
| 1156414004 | Giant cell glioblastoma of brain |
| 1156415003 | Protoplasmic astrocytoma of brain |
| 1156416002 | Gemistocytic astrocytoma of brain |
| 1156417006 | Fibrillary astrocytoma of brain |
| 1156455001 | Pleomorphic xanthoastrocytoma of brain |
| 1156456000 | Pilomyxoid astrocytoma of brain |
| 1156459007 | Anaplastic ganglioglioma of central nervous system |
| 1156460002 | Desmoplastic nodular medulloblastoma of brain |
| 1156461003 | Gliosarcoma of brain |
| 1156469001 | Large cell medulloblastoma of brain |
| 1156471001 | Choroid plexus carcinoma |
| 1156472008 | Papillary tumor of pineal region |
| 1156761002 | Progressive supranuclear palsy progressive non fluent aphasia |
| 1156763004 | Progressive supranuclear palsy corticobasal syndrome |
| 1156764005 | Progressive supranuclear palsy parkinsonism syndrome |
| 1156768008 | Ovarioleukodystrophy |
| 1156789004 | Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein |
| 1156790008 | Atypical progressive supranuclear palsy syndrome |
| 1156796002 | Autosomal dominant cerebellar ataxia type 2 |
| 1156798001 | Autosomal dominant Alzheimer disease due to mutation of presenilin 2 |
| 1156800008 | Autosomal dominant Alzheimer disease due to mutation of presenilin 1 |
| 1156813002 | Gaucher disease with ophthalmoplegia and cardiovascular calcification |
| 1156822001 | Autosomal recessive familial Parkinson disease |
| 1156833003 | Germinoma of central nervous system |
| 1156835005 | Autosomal dominant Charcot-Marie-Tooth disease type 2 |
| 1156836006 | X-linked Emery-Dreifuss muscular dystrophy |
| 1156837002 | Autosomal dominant distal hereditary motor neuropathy |
| 1156840002 | X-linked distal hereditary motor neuropathy |
| 1156841003 | X-linked complex hereditary spastic paraplegia |
| 1156842005 | X-linked pure hereditary spastic paraplegia |
| 1156848009 | Autosomal recessive Emery-Dreifuss muscular dystrophy |
| 1156850001 | Autosomal recessive distal hereditary motor neuropathy |
| 1156852009 | Autosomal recessive Charcot-Marie-Tooth disease type 2 |
| 1157060001 | Diffuse astrocytoma of brain |
| 1157061002 | Gliosarcoma of central nervous system |
| 1157062009 | Giant cell glioblastoma of central nervous system |
| 1157064005 | Gemistocytic astrocytoma of central nervous system |
| 1157068008 | Fibrillary astrocytoma of central nervous system |
| 1157072007 | Gliosarcoma of spinal cord |
| 1157141006 | Astroblastoma of central nervous system |
| 1162256002 | Hydrocephalus following infectious disease |
| 1162462009 | Angelman syndrome due to maternal monosomy 15q11q13 |
| 1162839003 | XK aprosencephaly syndrome |
| 1162864000 | Familial porencephaly |
| 116288000 | Paralytic stroke |
| 1163119007 | Creutzfeldt Jakob disease following graft of dura |
| 1163149009 | Chorea due to and following encephalitis |
| 1163482004 | Hemorrhagic cerebral infarction caused by Aspergillus |
| 1163508000 | Hydrocephalus due to mycosis |
| 1163527006 | Epilepsy due to disease caused by parasite |
| 1163529009 | Epilepsy due to bacterial endocarditis |
| 1163536005 | Mycotic cerebral aneurysm caused by Aspergillus |
| 1167371007 | Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome |
| 1167373005 | Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder |
| 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 |
| 1169356004 | Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome |
| 1169358003 | Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, hydranencephaly syndrome |
| 1169361002 | Limbic encephalitis with neurexin-3 antibodies |
| 11701009 | Hemicephaly |
| 1172584005 | Childhood-onset basal ganglia degeneration syndrome |
| 1172585006 | Membrane metalloendopeptidase related autosomal dominant Charcot Marie Tooth disease type 2 |
| 1172586007 | Ocular anomalies, axonal neuropathy, developmental delay syndrome |
| 1172588008 | Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome |
| 1172590009 | Kyphoscoliosis, lateral tongue atrophy, hereditary spastic paraplegia syndrome |
| 1172593006 | Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome |
| 1172594000 | Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome |
| 1172595004 | C11ORF73-related autosomal recessive hypomyelinating leukodystrophy |
| 1172603005 | Infantile-onset generalized dyskinesia with orofacial involvement |
| 1172624000 | Arginine-glutamic acid dipeptide repeats-related neurodevelopmental syndrome |
| 1172626003 | Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder |
| 1172628002 | TBC1 domain containing kinase-related intellectual disability syndrome |
| 1172629005 | Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome |
| 1172630000 | Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome |
| 1172631001 | Autosomal recessive spastic paraplegia type 76 |
| 1172634009 | Autosomal dominant Charcot-Marie-Tooth disease type 2W |
| 1172684002 | Autosomal dominant Charcot-Marie-Tooth disease type 2 due to diacylglycerol O-acyltransferase 2 mutation |
| 1172688004 | Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome |
| 1172689007 | Prenatal-onset spinal muscular atrophy with congenital bone fractures |
| 1172691004 | Chloride voltage-gated channel 4-related X-linked intellectual disability syndrome |
| 1172694007 | Adenylosuccinate synthetase-like 1-related distal myopathy |
| 1172696009 | Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome |
| 1172698005 | Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome |
| 1172703004 | Protein O-glucosyltransferase 1-related limb girdle muscular dystrophy R21 |
| 1172705006 | Lethal hydranencephaly, diaphragmatic hernia syndrome |
| 1172838005 | Hereditary sensory and autonomic neuropathy type 8 |
| 1172839002 | Lethal left ventricular non-compaction, seizures, hypotonia, cataract, developmental delay syndrome |
| 1172841001 | Combined oxidative phosphorylation defect type 30 |
| 1172843003 | Combined oxidative phosphorylation defect type 29 |
| 1172844009 | Combined oxidative phosphorylation defect type 27 |
| 1172899000 | Peripheral myelin protein 22-retinoic acid induced 1 contiguous gene duplication syndrome |
| 1172900005 | Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome |
| 1173024006 | Typical absence seizure |
| 1173035001 | Combined oxidative phosphorylation defect type 25 |
| 1173036000 | Combined oxidative phosphorylation defect type 23 |
| 1173997008 | Pontine autosomal dominant microangiopathy with leukoencephalopathy |
| 1173998003 | Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome |
| 1177015003 | Cerebral arteritis caused by Mycobacterium tuberculosis complex |
| 1177053008 | Hydrocephalus due to suppurative infection |
| 1177054002 | Hydrocephalus due to and following infection of central nervous system |
| 1177062005 | Sporadic fatal insomnia |
| 1177122009 | Myotonic dystrophy |
| 1177165005 | Peripheral myelin protein 2-related Charcot-Marie-Tooth disease type 1 |
| 1177168007 | Autosomal recessive spastic paraplegia type 78 |
| 1177169004 | Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation |
| 1177177000 | Hyperphenylalaninemia due to DnaJ heat shock protein family (Hsp40) member C12 deficiency |
| 117776611000119102 | Cerebrovascular accident due to occlusion of left posterior communicating artery |
| 1179282009 | Severe neurodevelopmental disorder with feeding difficulties, stereotypic hand movement, bilateral cataract |
| 1179294000 | Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome |
| 1179295004 | Blood vessel epicardial substance related limb girdle muscular dystrophy |
| 1179297007 | LIM zinc finger domain containing 2-related limb girdle muscular dystrophy |
| 1179359005 | Maternal epilepsy due to perinatal stroke |
| 1179360000 | Fetal epilepsy due to perinatal stroke |
| 1179376009 | Myxedema coma due to subclinical hypothyroidism |
| 1179377000 | Adenocarcinoma of pituitary gland |
| 1179455003 | Iatrogenic myxedema coma |
| 1179508005 | Osmotic demyelination syndrome |
| 1179547007 | Neonatal epilepsy due to perinatal stroke |
| 1186710001 | Leukoencephalopathy with calcifications and cysts |
| 1186718008 | Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome |
| 1186721005 | Infantile inflammatory bowel disease with neurological involvement |
| 1186724002 | HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease |
| 1186728004 | Pediatric multiple sclerosis |
| 1186734006 | Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction |
| 1186807002 | Hereditary growth hormone deficiency |
| 1186819005 | Leukoencephalopathy due to hypocupremia |
| 1186834004 | Immunoglobulin G4 related hypophysitis |
| 1186850007 | Spinocerebellar ataxia due to vitamin E deficiency |
| 1186856001 | Atypical pantothenate kinase associated neurodegeneration |
| 1186861004 | Classical pantothenate kinase associated neurodegeneration |
| 1186877003 | Dementia due to vitamin E deficiency |
| 1186879000 | Dementia due to thiamine deficiency |
| 1186880002 | Dementia due to cobalamin deficiency |
| 1186881003 | Dementia due to niacin deficiency |
| 1186883000 | Dementia due to nutritional deficiency disorder |
| 1186887004 | Dementia caused by manganese and/or manganese compound |
| 1187004001 | Chronic traumatic encephalopathy |
| 1187042007 | Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome |
| 1187043002 | Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome |
| 1187045009 | Aicardi Goutieres syndrome type 1 |
| 1187046005 | Aicardi Goutieres syndrome type 2 |
| 1187047001 | Aicardi Goutieres syndrome type 3 |
| 1187048006 | Aicardi Goutieres syndrome type 4 |
| 1187049003 | Aicardi Goutieres syndrome type 5 |
| 1187126002 | Integral membrane protein 2B related amyloidosis |
| 1187128001 | Charcot-Marie-Tooth disease type 2T |
| 1187191003 | Autosomal recessive spastic paraplegia type 74 |
| 1187195007 | Microcephalic cortical malformations, short stature due to rotatin deficiency |
| 1187210007 | Intellectual disability, epilepsy, extrapyramidal syndrome |
| 1187249005 | VPS11 core subunit of CORVET and HOPS complexes-related autosomal recessive hypomyelinating leukodystrophy |
| 1187250005 | Seizures, scoliosis, macrocephaly syndrome |
| 1187251009 | Childhood-onset progressive contractures, limb girdle weakness, muscle dystrophy syndrome |
| 1187278006 | Spastic paraplegia, severe developmental delay, epilepsy syndrome |
| 1187279003 | Autosomal recessive hereditary spastic paraplegia |
| 1187304005 | Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome |
| 1187465008 | Autosomal dominant spastic paraplegia type 9A |
| 1187466009 | Autosomal dominant spastic paraplegia type 9B |
| 1187467000 | Autosomal recessive spastic paraplegia type 9B |
| 1187468005 | Autosomal dominant spastic paraplegia type 73 |
| 1187470001 | Autosomal recessive spastic paraplegia type 75 |
| 1187506008 | Autosomal recessive spastic paraplegia type 77 |
| 1187517009 | Maternally inherited mitochondrial myopathy |
| 1187520001 | Leigh syndrome due to cytochrome C oxidase deficiency |
| 1187538003 | Secondary systemic amyloid angiopathy of cerebrum |
| 1187539006 | Non-neuropathic heredofamilial amyloidosis angiopathy of cerebrum |
| 1187547006 | Degeneration of pituitary structure |
| 1187563003 | Autosomal recessive Charcot-Marie-Tooth disease type 2X |
| 1187564009 | Autosomal dominant Charcot-Marie-Tooth disease type 2Z |
| 1187565005 | Autosomal dominant Charcot-Marie-Tooth disease type 2Y |
| 1187566006 | Autosomal dominant Charcot-Marie-Tooth disease type 2 due to trafficking from endoplasmic reticulum to golgi regulator mutation |
| 1187567002 | Autosomal recessive intermediate Charcot-Marie-Tooth disease type D |
| 1187617004 | Charcot-Marie-Tooth disease type 2S |
| 1187618009 | Autosomal dominant Charcot-Marie-Tooth disease type 2V |
| 1187619001 | Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect |
| 1187620007 | Autosomal dominant Charcot-Marie-Tooth disease type 2DD |
| 1187621006 | DnaJ heat shock protein family (Hsp40) member B2-related Charcot-Marie-Tooth disease type 2 |
| 1187635008 | Maternally inherited mitochondrial cardiomyopathy |
| 1187643003 | Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome |
| 119001000119108 | Intractable simple partial epilepsy |
| 1196839006 | Primary embryonal carcinoma of brain |
| 1196844004 | Primary malignant astrocytoma of brain |
| 1196860000 | Primary anaplastic large cell medulloblastoma of brain |
| 1196872006 | Mitochondrial respiratory chain complex I structural subunit gene defect |
| 1196898000 | Primary malignant atypical teratoid rhabdoid neoplasm of brain |
| 1196911006 | Primary adenocarcinoma of iris neuroepithelium |
| 1196948002 | Mitochondrial respiratory chain complex I assembly gene defect |
| 1197052008 | Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form with methylmalonic aciduria |
| 1197059004 | Congenital ichthyosis, microcephalus, tetraplegia syndrome |
| 1197152005 | Distal hereditary motor neuropathy type 5 |
| 1197153000 | Typical nemaline myopathy |
| 1197154006 | Childhood-onset nemaline myopathy |
| 1197155007 | Amish nemaline myopathy |
| 1197156008 | Intermediate nemaline myopathy |
| 1197157004 | Severe congenital nemaline myopathy |
| 1197212001 | Posterior meningocele |
| 1197215004 | Microform holoprosencephaly |
| 1197277003 | Spinal cord compression due to neoplasm |
| 1197280002 | Yolk sac tumor of central nervous system |
| 1197298003 | Primary malignant germ cell neoplasm of pineal gland |
| 1197332003 | Primary malignant melanoma of central nervous system |
| 1197343006 | Primary teratoma of brain |
| 1197363004 | Pediatric arterial ischemic stroke |
| 1197429000 | Cathepsin A-related arteriopathy, strokes, leukoencephalopathy |
| 1197523001 | Autosomal dominant amyotrophic lateral sclerosis type 1 |
| 1197524007 | Autosomal recessive amyotrophic lateral sclerosis type 1 |
| 1197587003 | Lethal neonatal spasticity, epileptic encephalopathy syndrome |
| 1197588008 | X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
| 1197591008 | Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome |
| 1197758001 | Kernicterus spectrum disorder |
| 1201863001 | Amyotrophic lateral sclerosis type 1 |
| 1201947005 | Juvenile amyotrophic lateral sclerosis type 2 |
| 1201950008 | Amyotrophic lateral sclerosis type 3 |
| 1201961000 | Juvenile amyotrophic lateral sclerosis type 5 |
| 1201964008 | Congenital fiber-type disproportion myopathy due to ZAK mutation |
| 1202023003 | Congenital fiber-type disproportion myopathy due to selenoprotein N mutation |
| 1202024009 | Autosomal dominant congenital fiber-type disproportion myopathy due to selenoprotein N mutation |
| 1202025005 | Autosomal recessive congenital fiber-type disproportion myopathy due to selenoprotein N mutation |
| 1204128009 | Cholesterol atheromatous embolism of cerebrum |
| 1204147007 | Asymptomatic stenosis of middle cerebral artery |
| 1204148002 | Asymptomatic stenosis of posterior cerebral artery |
| 1204156004 | Asymptomatic stenosis of intracranial carotid artery |
| 1204158003 | Asymptomatic stenosis of extracranial carotid artery |
| 1204160001 | Asymptomatic stenosis of extracranial vertebral artery |
| 1204162009 | Asymptomatic stenosis of anterior cerebral artery |
| 1204164005 | Asymptomatic stenosis of basilar artery |
| 1204188007 | Asymptomatic occlusion of extracranial vertebral artery |
| 1204202004 | Occlusion of cerebral artery due to infection |
| 1204334005 | Amyotrophic lateral sclerosis type 6 |
| 1204349002 | Amyotrophic lateral sclerosis type 7 |
| 1204350002 | Amyotrophic lateral sclerosis type 8 |
| 1204351003 | Amyotrophic lateral sclerosis type 9 |
| 1204415006 | Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome |
| 1204463009 | Encephalopathy with sepsis |
| 1208339007 | Neuhauser Eichner Opitz syndrome |
| 1208341008 | Severe oculo-renal-cerebellar syndrome |
| 1208344000 | Fryns Smeets Thiry syndrome |
| 1208346003 | Congenital hydrocephalus, low insertion of umbilicus syndrome |
| 1208348002 | Microcephalic osteodysplastic primordial dwarfism type II |
| 1208412003 | Amyotrophic lateral sclerosis type 10 |
| 1208413008 | Congenital fiber-type disproportion myopathy due to actin alpha 1, skeletal muscle mutation |
| 1208414002 | Autosomal recessive congenital fiber-type disproportion myopathy due to actin alpha 1, skeletal muscle mutation |
| 1208415001 | Autosomal dominant congenital fiber-type disproportion myopathy due to actin alpha 1, skeletal muscle mutation |
| 1208416000 | Congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation |
| 1208417009 | Autosomal recessive congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation |
| 1208418004 | Autosomal dominant congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation |
| 1208478005 | Familial infantile bilateral striatal necrosis |
| 1208481000 | Progressive cerebello-cerebral atrophy |
| 1208483002 | Primary choriocarcinoma of central nervous system |
| 1208512000 | Spinocerebellar ataxia type 41 |
| 1208513005 | Spinocerebellar ataxia type 42 |
| 1208516002 | Spinocerebellar ataxia type 43 |
| 1208615009 | Neurogenic scapuloperoneal syndrome Kaeser type |
| 1208620009 | Multiple mitochondrial dysfunctions syndrome type 3 |
| 1208621008 | Multiple mitochondrial dysfunctions syndrome type 4 |
| 1208629005 | Myoclonic absence seizure |
| 1208720000 | Agenesis of corpus callosum, macrocephaly, hypertelorism syndrome |
| 1208727002 | Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome |
| 1208747005 | Inosine triphosphate pyrophosphohydrolase-related lethal infantile neurological disorder with cataract and cardiac involvement |
| 1208841001 | Secondary moyamoya disease |
| 1208871009 | Transient ischemic attack co-occurrent with subarachnoid hemorrhage |
| 1208880009 | Ophthalmoplegia due to abetalipoproteinemia |
| 1208887007 | Silent white matter disease due to vascular disease |
| 1208933000 | 4H leukodystrophy |
| 1208935007 | Polymicrogyria due to tubulin beta 2B class IIb mutation |
| 1208936008 | Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome |
| 1208937004 | Mitochondrial deoxyribonucleic acid depletion syndrome, encephalomyopathic form with variable craniofacial anomalies |
| 1208939001 | Progressive myoclonic epilepsy type 7 |
| 1208960007 | Motor epileptic seizure |
| 1208961006 | Non-motor epileptic seizure |
| 1208966001 | Generalized onset motor epileptic seizure |
| 1208968000 | Generalized onset atonic epileptic seizure |
| 1208969008 | Generalized onset tonic epileptic seizure |
| 1208970009 | Generalized onset clonic epileptic seizure |
| 1208971008 | Generalized onset myoclonic-atonic epileptic seizure |
| 1208972001 | Generalized onset myoclonic epileptic seizure |
| 1208973006 | Generalized onset myoclonic-tonic-clonic epileptic seizure |
| 1208974000 | Generalized onset epileptic spasms |
| 1208991001 | Myoclonic epileptic seizure |
| 1209168005 | Congenital fiber-type disproportion myopathy due to myosin heavy chain 7 mutation |
| 1216942009 | Cerebral ventriculomegaly, cystic kidney disease |
| 1217008005 | Epileptic spasms |
| 1217013009 | Malposition of shunt in brain ventricle |
| 1217046003 | Avascular necrosis of pituitary gland |
| 1217136003 | Tonic-clonic epileptic seizure |
| 1217209006 | Generalized onset tonic-clonic epileptic seizure |
| 1217212009 | Mitochondrial pyruvate carrier deficiency |
| 1217226000 | Progressive scapulohumeroperoneal distal myopathy |
| 1217228004 | X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome |
| 1217230002 | Cerebellar ataxia with oculomotor apraxia type 4 |
| 1217367007 | Phospholipase A2 activating protein-associated neurodevelopmental disorder |
| 1217370006 | Laminin subunit alpha 5-related multisystemic syndrome |
| 1217371005 | Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome |
| 1217379007 | NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy |
| 1217381009 | Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome |
| 1217382002 | Intellectual disability, autism, speech apraxia, craniofacial dysmorphism syndrome |
| 1217383007 | RELA fusion-positive supratentorial ependymoma |
| 1217655004 | Disorder of neuromuscular junction due to Lambert-Eaton syndrome |
| 1220573009 | Primary dystonia type 27 |
| 1220574003 | Component of oligomeric golgi complex 6-congenital disorder of glycosylation |
| 1220589007 | Keppen Lubinsky syndrome |
| 1220595008 | Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome |
| 1220596009 | Microcephalic primordial dwarfism, insulin resistance syndrome |
| 1220598005 | Non-progressive predominantly posterior cavitating leukodystrophy with peripheral neuropathy |
| 1220600004 | Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy |
| 1222644009 | Autosomal dominant mitochondrial myopathy with exercise intolerance |
| 1222646006 | Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome |
| 1222655009 | Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome |
| 1222656005 | Synaptic Ras GTPase activating protein 1-related developmental and epileptic encephalopathy |
| 1222657001 | Prune exopolyphosphatase 1-related neurological syndrome |
| 1222658006 | Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome |
| 1222659003 | Ring finger protein 13-related severe early-onset epileptic encephalopathy |
| 1222660008 | Pancreatic agenesis, holoprosencephaly syndrome |
| 1222661007 | Early-onset calcifying leukoencephalopathy, skeletal dysplasia |
| 1222662000 | Neonatal epileptic encephalopathy due to deficiency of glutaminase |
| 1222672002 | 3-methylglutaconic aciduria type 9 |
| 1222704008 | Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy |
| 1222706005 | Anterior maxillary protrusion, strabismus, intellectual disability syndrome |
| 1222710008 | Neurodevelopmental disorder, craniofacial dysmorphism, cardiac defect, skeletal anomalies syndrome |
| 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 |
| 1228857005 | Progressive myoclonic epilepsy type 9 |
| 1228871002 | Proliferating cell nuclear antigen-related progressive neurodegenerative photosensitivity syndrome |
| 1229876001 | Lethal brain and heart developmental defects syndrome |
| 1229883008 | 19p13.3 microduplication syndrome |
| 1230018005 | Corticobasal syndrome |
| 1230273004 | Megaconial congenital muscular dystrophy |
| 1230308005 | Off-periods in Parkinson disease not responding to oral treatment |
| 1230343006 | Distal hereditary motor neuropathy type 2 |
| 1230376005 | Contactin associated protein 2-related developmental and epileptic encephalopathy |
| 1231168008 | Malignant middle cerebral artery syndrome |
| 1231178006 | Hereditary continuous muscle fiber activity |
| 1231188007 | Occlusion of ophthalmic artery |
| 1231203009 | Ophthalmoplegia due to neuropathy |
| 1231204003 | Ophthalmoplegia due to and following Guillain-Barré syndrome |
| 1231206001 | Meningoencephalocele of orbit |
| 1231209008 | Congenital meningocele of orbit |
| 1231267007 | Primary malignant ependymoma of optic nerve |
| 1231282002 | Benign familial neonatal-infantile seizures |
| 1231283007 | Congenital isolated adrenocorticotropic hormone deficiency |
| 1231309005 | Mitochondrial deoxyribonucleic acid depletion syndrome myopathic form |
| 1231683004 | Ophthalmoplegia due to phytanic acid storage disease |
| 1231737000 | Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome |
| 1231746006 | Isolated agenesis of cerebellar vermis |
| 12348006 | Presenile dementia |
| 1234819007 | Limb girdle muscular dystrophy due to protein O-mannose kinase deficiency |
| 12367511000119101 | Paraplegia due to and following cerebrovascular accident |
| 1236804009 | Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome |
| 1236805005 | Mitochondrial enoyl coenzyme A reductase protein-associated neurodegeneration syndrome |
| 1236807002 | Encephalopathy due to mitochondrial and peroxisomal fission defect |
| 1236845001 | DNA replication fork stabilization factor DONSON-related microcephaly, short stature, limb abnormalities spectrum |
| 1236975007 | Behavioral arrest epileptic seizure |
| 1237194006 | Myelin oligodendrocyte glycoprotein antibody-associated disease |
| 1237342004 | Lethal fetal cerebrorenogenitourinary agenesis or hypoplasia syndrome |
| 1237366005 | Aprosencephaly cerebellar dysgenesis |
| 1237413006 | Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome |
| 1237417007 | Carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation |
| 1237418002 | Spastic tetraplegia, thin corpus callosum, progressive postnatal microcephaly syndrome |
| 1237420004 | X-linked intellectual disability, global development delay, facial dysmorphism, sacral caudal remnant syndrome |
| 1237421000 | Pyrroline-5-carboxylate reductase 2 related microcephaly, progressive leukoencephalopathy |
| 1237425009 | Metastatic carcinoma to pituitary |
| 1237462006 | nudE neurodevelopment protein 1-related microhydranencephaly |
| 1237470001 | Lethal fetal brain malformation, duodenal atresia, bilateral renal hypoplasia syndrome |
| 1237475006 | Cerebellar-facial-dental syndrome |
| 1237511005 | Elastin microfibril interfacer 1 related connective tissue disease |
| 1237514002 | Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome |
| 1237515001 | Leukodystrophy due to alkaline ceramidase 3 deficiency |
| 1237571004 | Benign familial infantile epilepsy |
| 1237578005 | Primary oculocerebral non-Hodgkin lymphoma |
| 1237618009 | Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome |
| 1237619001 | Fatty acyl-coenzyme A reductase 1 deficiency |
| 1237623009 | Congenital insensitivity to pain with severe intellectual disability |
| 1237625002 | Autosomal recessive cerebellar ataxia due to CWF19 like cell cycle control factor 1 deficiency |
| 1237626001 | Congenital axonal neuropathy with encephalopathy |
| 1239331000000100 | Significant intellectual disability |
| 123950001 | Rheumatic chorea without heart involvement |
| 12454008 | Cauda equina syndrome with neurogenic bladder |
| 125081000119106 | Cerebral infarction due to occlusion of precerebral artery |
| 1251446004 | NAD(P)HX dehydratase deficiency |
| 1251447008 | NAD(P)HX epimerase deficiency |
| 1251449006 | Ubiquitin specific peptidase 18 deficiency |
| 1251456000 | Metastatic neuroblastoma to brain |
| 1251457009 | Metastatic neuroblastoma to central nervous system |
| 1251484005 | Metastatic adenocarcinoma to pituitary gland |
| 1254650002 | Microcephaly, corpus callosum hypoplasia, intellectual disability, facial dysmorphism syndrome |
| 1254651003 | Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome |
| 1254941001 | Hereditary sensory autonomic neuropathy type IIC |
| 1255268002 | Oculocerebrodental syndrome |
| 1255271005 | Juvenile-onset diabetes mellitus, central and peripheral neurodegeneration syndrome |
| 1255274002 | Congenital myopathy with reduced type 2 muscle fibers |
| 1255278004 | X-linked myotubular myopathy, abnormal genitalia syndrome |
| 1255323007 | Spastic ataxia, dysarthria due to glutaminase deficiency |
| 1258933008 | Arteriovenous fistula of carotid artery and internal jugular vein |
| 1259038005 | Autosomal dominant complex hereditary spastic paraplegia |
| 1259039002 | Demyelination of central nervous system due to Whipple disease |
| 1259042008 | Demyelination of central nervous system due to Lyme borreliosis |
| 1259051000 | Brachial variant of chronic immune demyelinating polyradiculoneuropathy |
| 1259062000 | Acute toxicity due to and following early brain irradiation |
| 1259068001 | Alexander disease adult form |
| 1259083006 | Disorder of autonomic nervous system due to multiple sclerosis |
| 1259086003 | Autoimmune inflammation of cerebellum |
| 1259087007 | Autoimmune encephalitis caused by N-methyl-D-aspartate receptor antibody |
| 1259088002 | Autoimmune degeneration of cerebellum |
| 1259089005 | Autoimmune acquired autonomic encephalomyelitis |
| 1259106002 | Alexander disease infantile form |
| 1259108001 | Alexander disease juvenile form |
| 1259121008 | Amyotrophic lateral sclerosis, parkinsonism, dementia complex of West New Guinea |
| 1259122001 | Amyotrophic lateral sclerosis with parkinsonism |
| 1259123006 | Amyotrophic lateral sclerosis, parkinsonism, dementia complex of Kii Peninsula |
| 1259124000 | Amyotrophic lateral sclerosis with frontotemporal dementia |
| 1259125004 | Amyotrophic lateral sclerosis with multiple system atrophy |
| 1259126003 | Amyotrophic lateral sclerosis with autonomic dysfunction |
| 1259127007 | Amyotrophic lateral sclerosis with cerebellar dysfunction |
| 1259128002 | Alzheimer disease with psychosis |
| 1259129005 | Amyotrophic lateral sclerosis with spinocerebellar ataxia |
| 125921000119106 | Hepatic coma due to acute hepatitis C |
| 1259425005 | Primary neuroblastoma of brain |
| 1259456002 | Primary ganglioneuroblastoma of central nervous system |
| 1259457006 | Primary neuroblastoma of central nervous system |
| 1259465009 | Dementia due to hepatic failure |
| 1259467001 | Dementia due to hypercalcemia |
| 1259469003 | Dementia due to Gerstmann Straussler Scheinker syndrome |
| 1259471003 | Dementia due to Hashimoto encephalopathy |
| 1259473000 | Dementia due to fragile X syndrome |
| 1259476008 | Dementia due to genetic disease |
| 1259478009 | Dementia due to familial Creutzfeldt-Jakob disease |
| 1259480003 | Dementia due to fatal familial insomnia |
| 1259485008 | Dementia due to cerebral vasculitis |
| 1259488005 | Dementia due to cerebral amyloid angiopathy |
| 1259492003 | Dementia due to metastatic malignant neoplasm to brain |
| 1259494002 | Dementia due to leukodystrophy |
| 1259496000 | Dementia due to Lyme disease |
| 1259499007 | Dementia due to hemorrhagic cerebral infarction due to hypertension |
| 1259501004 | Dementia due to kuru |
| 1259503001 | Dementia due to iatrogenic Creutzfeldt-Jakob disease |
| 1259511006 | Dementia due to Wilson disease |
| 1259513009 | Dementia due to Whipple disease |
| 1259517005 | Dementia due to systemic lupus erythematosus |
| 1259519008 | Dementia due to subacute sclerosing panencephalitis |
| 1259522005 | Dementia due to variant Creutzfeldt-Jakob disease |
| 1259524006 | Dementia due to trypanosomiasis |
| 1259529001 | Dementia due to sporadic Creutzfeldt-Jakob disease |
| 1259531005 | Dementia due to hypertensive encephalopathy |
| 1259552002 | Cerebrovascular disease due to late-delayed irradiation of brain |
| 1259554001 | Anoxic encephalopathy due to respiratory arrest |
| 1259556004 | Anoxic encephalopathy due to cardiac arrest |
| 1259558003 | Anoxic encephalopathy due to asphyxiation |
| 1259560001 | Congenital multi-minicore disease with external ophthalmoplegia |
| 1259565006 | Chorea caused by oral contraceptive |
| 1259579003 | Dementia due to Behcet syndrome |
| 1259581001 | Dementia due to celiac disease |
| 1259584009 | Dementia due to and following dialysis |
| 1259586006 | Dementia due to autoimmune encephalitis |
| 1259588007 | Delayed disorder of cerebral white matter due to and following hypoxia of brain |
| 1259591007 | Dementia due to acquired hypothyroidism |
| 1259629009 | Primary adenocarcinoma of pituitary gland |
| 1259636005 | Chronic inflammatory demyelinating disease of peripheral nervous system and central nervous system |
| 1259656006 | Dementia due to renal failure |
| 1259661008 | Dementia due to inflammatory disorder of musculoskeletal system |
| 1259663006 | Dementia due to polyarteritis nodosa |
| 1259665004 | Dementia due to progressive subcortical gliosis |
| 1259667007 | Dementia due to paraneoplastic encephalitis |
| 1259673008 | Dementia due to neurofilament inclusion body disease |
| 1259675001 | Dementia due to obstructive hydrocephalus |
| 1259677009 | Dementia due to multiple system atrophy |
| 1259679007 | Dementia due to atypical pantothenate kinase associated neurodegeneration |
| 1259685000 | Chorea due to Huntington disease-like 3 |
| 1259689006 | Chorea due to Huntington disease-like 2 |
| 1259692005 | Primary gliosarcoma of brain |
| 1259693000 | Primary gliosarcoma of spinal cord |
| 1259694006 | Chorea due to Huntington disease-like 1 |
| 1259720004 | Primary malignant glioma of brain |
| 1259721000 | Primary malignant glioma of spinal cord |
| 1259722007 | Primary glioblastoma multiforme of brain |
| 1259723002 | Primary glioblastoma multiforme of spinal cord |
| 1259724008 | Primary anaplastic astrocytoma of brain |
| 1259725009 | Primary medulloblastoma of cerebellum |
| 1259730008 | Primary oligodendroglioma of brain |
| 1259731007 | Primary astrocytoma of spinal cord |
| 1259732000 | Primary oligodendroglioma of spinal cord |
| 1259733005 | Primary malignant astrocytoma of optic nerve |
| 1259734004 | Primary malignant meningioma of optic nerve sheath |
| 1259739009 | Primary malignant glioma of hypothalamus |
| 1259740006 | Primary malignant glioma of cerebellum |
| 1259742003 | Primary malignant glioma of cerebrum |
| 1259743008 | Primary astrocytoma of brain stem |
| 1259744002 | Primary glioblastoma multiforme of central nervous system |
| 1259745001 | Primary malignant glioma of central nervous system |
| 1259749007 | Primary malignant meningioma of meninges of brain |
| 1259750007 | Primary astrocytoma of cerebrum |
| 1259762006 | Primary malignant optic glioma of adulthood |
| 1259764007 | Primary supratentorial primitive neuroectodermal tumor |
| 1259765008 | Primary classic medulloblastoma |
| 1259769002 | Primary malignant glioma of brainstem |
| 1259770001 | Primary anaplastic glioma of brain |
| 1259773004 | Primary anaplastic astrocytoma of spinal cord |
| 1259787004 | Primary malignant optic glioma |
| 1259798003 | Primary oligodendroglioma of cerebrum |
| 1259812009 | Primary astroblastoma of brain |
| 1259813004 | Primary anaplastic oligoastrocytoma of central nervous system |
| 1259814005 | Primary gemistocytic astrocytoma of brain |
| 1259815006 | Primary giant cell glioblastoma of brain |
| 1259816007 | Primary fibrillary astrocytoma of brain |
| 1259817003 | Primary pleomorphic xanthoastrocytoma of brain |
| 1259818008 | Primary pilomyxoid astrocytoma of brain |
| 1259819000 | Primary anaplastic ganglioglioma of central nervous system |
| 1259827009 | Primary mixed germ cell neoplasm of central nervous system |
| 1259990004 | Dementia due to classical pantothenate kinase associated neurodegeneration |
| 1260097007 | Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome |
| 126011000119107 | Acquired caroticocavernous sinus fistula |
| 1260128008 | Tryptophanyl tRNA synthetase 2, mitochondrial-related combined oxidative phosphorylation defect |
| 1260129000 | Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome |
| 1260134001 | Spastic paraplegia, intellectual disability, nystagmus, obesity syndrome |
| 1260143005 | Megalencephaly, severe kyphoscoliosis, overgrowth syndrome |
| 1260271009 | Hemorrhagic cerebral infarction due to hypertension |
| 1260337002 | Hydrocephalus ex vacuo due to cerebrovascular disease |
| 1260338007 | Hydrocephalus ex vacuo due to and following radiation therapy |
| 1260340002 | Hydrocephalus ex vacuo due to injury of brain |
| 1260342005 | Hydrocephalus ex vacuo due to degenerative brain disorder |
| 1260344006 | Hydrocephalus ex vacuo due to aging |
| 1260357003 | Injury of brain due to early brain irradiation |
| 1260374003 | Epilepsy due to congenital infectious disease |
| 1260375002 | Epilepsy due to glucose transporter protein type 1 deficiency syndrome |
| 1260377005 | Epilepsy due to congenital anomaly of brain |
| 1260449002 | Polyendocrine polyneuropathy syndrome |
| 1260450002 | Infantile multisystem neurologic, endocrine, pancreatic disease |
| 1263449003 | Isolated encephalocele |
| 126944002 | Brain disorder resulting from a period of impaired oxygen delivery to the brain |
| 126945001 | Perinatal anoxic-ischemic brain injury |
| 127551000119100 | Congenital hypoplasia of brain |
| 128171000119104 | Spontaneous caroticocavernous sinus fistula |
| 128188000 | Cerebral palsy |
| 128190004 | Inherited metabolic disorder of nervous system |
| 128203003 | Hereditary motor and sensory neuropathy with optic atrophy |
| 128204009 | Hereditary motor and sensory neuropathy with retinitis pigmentosa |
| 128205005 | Hereditary sensory and autonomic neuropathy |
| 128206006 | Congenital sensory neuropathy with selective loss of small myelinated fibers |
| 128207002 | Giant axonal neuropathy |
| 128209004 | Chronic inflammatory demyelinating polyradiculoneuropathy |
| 128212001 | Spinal muscular atrophy, type II |
| 128213006 | Neuromuscular junction disorder |
| 128218002 | Disorder of intracranial venous sinus |
| 12853006 | Embolism of torcular Herophili |
| 128608001 | Cerebral arterial aneurysm |
| 128609009 | Intracranial aneurysm |
| 129608008 | Progressive pyramidopallidal degeneration |
| 129609000 | Spinocerebellar ataxia |
| 129614001 | Paralysis of vagus, spinal accessory and hypoglossal nerves |
| 129620000 | Scapuloperoneal muscular dystrophy |
| 129621001 | Nemaline myopathy, early onset type |
| 129622008 | Nemaline myopathy, late onset type |
| 130121000119104 | Dementia due to Rett's syndrome |
| 13092008 | Pick's disease |
| 133301000119102 | Degenerative brain disorder caused by alcohol |
| 133981000119106 | Dysarthria as late effects of cerebrovascular disease |
| 133991000119109 | Fluency disorder as sequela of cerebrovascular disease |
| 134771000119108 | Alteration of sensation as late effect of stroke |
| 134811000119108 | Severe hypoxic ischemic encephalopathy of newborn |
| 134821000119101 | Moderate hypoxic ischemic encephalopathy of newborn |
| 134831000119103 | Mild hypoxic ischemic encephalopathy of newborn |
| 135491000119100 | Myelopathy due to benign neoplastic disease |
| 135511000119105 | Myelopathy due to malignant neoplastic disease |
| 135761000119101 | Cerebral degeneration due to alcoholism |
| 135781000119105 | Cerebral degeneration due to hypothyroidism |
| 135811000119107 | Lewy body dementia with behavioral disturbance |
| 137991000119103 | Seizure disorder as sequela of stroke |
| 13920009 | Hepatic encephalopathy |
| 13973009 | Grand mal status |
| 140281000119108 | Hemiparesis as late effect of cerebrovascular disease |
| 14055002 | Hydrocephalus ex vacuo |
| 14070001 | Multi-infarct dementia with depression |
| 140881000119109 | Compression of brain co-occurrent and due to spontaneous cerebral hemorrhage |
| 140911000119109 | Ischemic stroke with coma |
| 140921000119102 | Ischemic stroke without coma |
| 141991000119109 | Delusions in Alzheimer's disease |
| 142001000119106 | Depressed mood in Alzheimer's disease |
| 142011000119109 | Alzheimer's disease co-occurrent with delirium |
| 142031000119104 | Visual field defect due to and following cerebrovascular accident |
| 14210003 | Lipofuscinosis |
| 14246007 | Embolism of intracranial venous sinus |
| 142851000119103 | Spontaneous cerebellar hemorrhage |
| 14309005 | Anterior choroidal artery syndrome |
| 143521000119103 | Nontraumatic intraparenchymal cerebral hemorrhage |
| 14401000119109 | Partial frontal lobe epilepsy |
| 14447001 | Dandy-Walker syndrome |
| 145741000119101 | Apraxia as late effect of cerebrovascular disease |
| 14637005 | Late-infantile neuronal ceroid lipofuscinosis |
| 146371000119104 | Hepatic coma due to chronic hepatitis C |
| 147101000119108 | Primary malignant astrocytoma of central nervous system |
| 147131000119101 | Glioblastoma multiforme of central nervous system |
| 148871000119109 | Weakness as a late effect of cerebrovascular accident |
| 14977000 | Multiple AND bilateral precerebral artery thrombosis |
| 149821000119103 | Cerebral infarction due to carotid artery occlusion |
| 15080006 | Myotubular myopathy with type I atrophy |
| 15139001 | Chronic brain-hydrocephalus syndrome |
| 15182000 | Coffin-Lowry syndrome |
| 152148641000119104 | Cerebrovascular accident due to embolism of bilateral carotid arteries |
| 153091000119109 | Hepatic coma due to chronic hepatitis B with delta agent |
| 15523002 | Benign focal epilepsy of childhood |
| 15552004 | Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts |
| 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 |
| 1581000119101 | Dementia of the Alzheimer type with behavioral disturbance |
| 1591000119103 | Dementia with behavioral disturbance |
| 1593000 | Infantile hemiplegia |
| 15978431000119106 | Thrombosis of right vertebral artery |
| 15978471000119109 | Thrombosis of left vertebral artery |
| 15978631000119109 | Occlusion of bilateral vertebral arteries |
| 15982271000119104 | Weakness of right facial muscle due to and following cerebrovascular disease |
| 15982311000119104 | Weakness of left facial muscle due to and following cerebrovascular disease |
| 15984951000119108 | Neonatal spontaneous cerebellar hemorrhage |
| 15985031000119102 | Neonatal non-traumatic intraventricular hemorrhage |
| 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 |
| 16260551000119106 | Dysphasia due to and following cerebrovascular accident |
| 16276361000119109 | Vascular dementia without behavioral disturbance |
| 16279401000119108 | Occlusion of right cilioretinal artery |
| 16279441000119105 | Occlusion of left cilioretinal artery |
| 163601006 | On examination - hemiplegia |
| 163604003 | On examination - paraplegia |
| 163605002 | On examination - quadriplegia |
| 163606001 | On examination - diplegia |
| 16371781000119100 | Cerebellar stroke |
| 16415361000119105 | Radiologically isolated syndrome |
| 16415791000119104 | Myasthenia gravis in remission |
| 16418006 | Embolism of basilar sinus |
| 16476641000119100 | Acquired arteriovenous fistula of dura of cerebrum |
| 16517004 | Cerebral lipidosis |
| 16520041000119104 | Congenital fenestration of basilar artery |
| 166071000000101 | Congenital dilated lateral ventricles of brain |
| 16644681000119102 | Cerebrovascular accident due to occlusion of bilateral pontine arteries |
| 16652001 | Fabry's disease |
| 16661931000119102 | Cerebrovascular accident due to stenosis of bilateral vertebral arteries |
| 16661971000119104 | Cerebrovascular accident due to stenosis of bilateral carotid arteries |
| 16662331000119106 | Aneurysm of right vertebral artery |
| 16662371000119109 | Aneurysm of left vertebral artery |
| 1670004 | Cerebral hemiparesis |
| 16703491000119101 | Memory deficit due to and following spontaneous intracerebral hemorrhage |
| 16703551000119107 | Memory deficit due to and following cerebrovascular disease |
| 16703661000119105 | Memory deficit due to and following cerebrovascular accident |
| 16703711000119100 | Memory deficit due to and following embolic cerebrovascular accident |
| 16703761000119102 | Memory deficit due to and following ischemic cerebrovascular accident |
| 16703821000119101 | Memory deficit due to and following hemorrhagic cerebrovascular accident |
| 16709811000119106 | Spontaneous hemorrhage of subarachnoid space from anterior communicating artery |
| 16818591000119108 | Calcification of basal ganglia |
| 16845301000119108 | Primary glioblastoma multiforme of cerebellum |
| 16845341000119105 | Primary glioblastoma multiforme of brainstem |
| 16851005 | Mitochondrial myopathy |
| 168747591000119109 | Cerebrovascular accident due to embolism of bilateral posterior cerebral arteries |
| 16891111000119104 | Cryptogenic stroke |
| 171822009 | Acute atrophic spinal paralysis |
| 172069000 | Congenital meningocele |
| 17258002 | Chronic anoxic encephalopathy |
| 17409003 | Facial hemiparesis |
| 17761000119109 | High lumbar myelomeningocele |
| 17771000119103 | Low lumbar myelomeningocele |
| 17944005 | Cerebral calcification |
| 18058007 | Phlebitis of intracranial venous sinus |
| 18191000 | Salaam spasm |
| 182960891000119101 | Cerebrovascular accident due to occlusion of left anterior cerebral artery |
| 182961000119101 | Acute disseminated encephalomyelitis following infectious disease |
| 18322005 | Thrombosis of torcular Herophili |
| 1845001 | Paraparesis |
| 186317009 | Listerial cerebral arteritis |
| 186476008 | Acute paralytic non-bulbar poliomyelitis |
| 186478009 | Acute paralytic poliomyelitis, vaccine-associated |
| 186479001 | Acute paralytic poliomyelitis, wild virus, imported |
| 186480003 | Acute paralytic poliomyelitis, wild virus, indigenous |
| 186624004 | Hepatic coma due to acute hepatitis B with delta agent |
| 186628001 | Hepatic coma due to viral hepatitis C |
| 186831000119104 | Apraxia due to and following cerebrovascular accident |
| 186893003 | Rupture of syphilitic cerebral aneurysm |
| 18756002 | Juvenile GM1 gangliosidosis |
| 188174841000119103 | Cerebrovascular accident due to occlusion of bilateral middle cerebral arteries |
| 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 | Metastatic malignant neoplasm to brain and spinal cord |
| 18927009 | Niemann-Pick disease, type D |
| 190492009 | Diencephalic syndrome secondary to tumor |
| 190823004 | Westphal-Strumpell syndrome |
| 19091006 | Pallidoluysian degeneration |
| 191449005 | Uncomplicated senile dementia |
| 191451009 | Uncomplicated presenile dementia |
| 191452002 | Presenile dementia with delirium |
| 191454001 | Presenile dementia with paranoia |
| 191455000 | Presenile dementia with depression |
| 191457008 | Senile dementia with depressive or paranoid features |
| 191458003 | Senile dementia with paranoia |
| 191459006 | Senile dementia with depression |
| 191461002 | Senile dementia with delirium |
| 191463004 | Uncomplicated arteriosclerotic dementia |
| 191464005 | Arteriosclerotic dementia with delirium |
| 191465006 | Arteriosclerotic dementia with paranoia |
| 191466007 | Arteriosclerotic dementia with depression |
| 191471000 | Korsakov's alcoholic psychosis with peripheral neuritis |
| 191475009 | Chronic alcoholic brain syndrome |
| 191493005 | Dementia caused by drug |
| 191519005 | Dementia associated with another disease |
| 192673008 | Sarcoid meningitis |
| 192685000 | Subacute sclerosing panencephalitis |
| 192730008 | Toxic encephalitis |
| 192754003 | Embolism cavernous sinus |
| 192755002 | Embolism superior longitudinal sinus |
| 192756001 | Embolism lateral sinus |
| 192757005 | Embolism transverse sinus |
| 192759008 | Cerebral venous sinus thrombosis |
| 192760003 | Thrombosis of superior longitudinal sinus |
| 192761004 | Thrombosis transverse sinus |
| 192764007 | Phlebitis cavernous sinus |
| 192765008 | Phlebitis of superior longitudinal sinus |
| 192769002 | Thrombophlebitis of central nervous system venous sinuses |
| 192770001 | Thrombophlebitis of cavernous sinus |
| 192771002 | Thrombophlebitis of superior longitudinal venous sinus |
| 192772009 | Thrombophlebitis lateral venous sinus |
| 192781003 | Leukodystrophy |
| 192782005 | Galactosylceramide beta-galactosidase deficiency |
| 192787004 | B variant hexosaminidase A deficiency |
| 192788009 | Retinal dystrophy in cerebroretinal lipidosis |
| 192791009 | Cerebral degeneration in Gaucher's disease |
| 192792002 | Cerebral degeneration in Niemann-Pick disease |
| 192794001 | Cerebral degeneration associated with another disorder |
| 192795000 | Cerebral degeneration in Hunter's disease |
| 192796004 | Cerebral degeneration in mucopolysaccharidosis |
| 192805000 | Acquired communicating hydrocephalus |
| 192811002 | Alcoholic encephalopathy |
| 192812009 | Cerebral degeneration due to beriberi |
| 192813004 | Cerebral degeneration due to cerebrovascular disease |
| 192814005 | Cerebral degeneration due to congenital hydrocephalus |
| 192815006 | Cerebral degeneration due to neoplastic disease |
| 192816007 | Myxedema encephalopathy |
| 192817003 | Cerebral degeneration due to vitamin B12 deficiency |
| 192818008 | Cerebral degeneration due to Creutzfeldt-Jakob disease |
| 192819000 | Cerebral degeneration due to progressive multifocal leukoencephalopathy |
| 192845009 | Myoclonic encephalopathy |
| 192871008 | Early onset cerebellar ataxia with myoclonus |
| 192874000 | Cerebellar ataxia associated with another disorder |
| 192876003 | Myxedema cerebellar degeneration |
| 192877007 | Paraneoplastic cerebellar degeneration |
| 192894009 | Syringomyelia and syringobulbia |
| 192897002 | Myelopathy due to acute infarction of spinal cord |
| 192898007 | Myelopathy due to arterial thrombosis of spinal cord |
| 192900009 | Myelopathy due to hematomyelia |
| 192904000 | Myelopathy due to another disorder |
| 192906003 | Myelopathy due to neoplastic disease |
| 192926004 | Multiple sclerosis of the brainstem |
| 192927008 | Multiple sclerosis of the spinal cord |
| 192928003 | Generalized multiple sclerosis |
| 192929006 | Exacerbation of multiple sclerosis |
| 192933004 | Acute and subacute hemorrhagic leukoencephalitis [Hurst] |
| 192949002 | Congenital paraplegia |
| 192958009 | Hypotonic cerebral palsy |
| 192964002 | Flaccid tetraplegia |
| 192965001 | Spastic tetraplegia |
| 192966000 | Flaccid paraplegia |
| 192967009 | Spastic paraplegia |
| 192976002 | Progressive supranuclear palsy |
| 192979009 | Generalized non-convulsive epilepsy |
| 192981006 | Atonic epileptic seizure |
| 192982004 | Epileptic seizures - akinetic |
| 192990004 | Benign myoclonic epilepsy in infancy |
| 192991000 | Clonic epileptic seizure |
| 192993002 | Tonic epileptic seizure |
| 192999003 | Partial epilepsy with impairment of consciousness |
| 193000002 | Temporal lobe epilepsy |
| 193002005 | Psychosensory epilepsy |
| 193003000 | Mesiobasal limbic epilepsy |
| 193008009 | Somatosensory epilepsy |
| 193009001 | Partial epilepsy with autonomic symptoms |
| 193010006 | Visual reflex epilepsy |
| 193021002 | Cursive (running) epilepsy |
| 193022009 | Localization-related(focal)(partial)idiopathic epilepsy and epileptic syndromes with seizures of localized onset |
| 193069004 | Intracranial hypotension following ventricular shunting |
| 193165008 | Neuropathy in association with hereditary ataxia |
| 193195000 | Sarcoid neuropathy |
| 193207007 | Juvenile or adult myasthenia gravis |
| 193209005 | Myasthenic syndrome due to another disorder |
| 193212008 | Myasthenic syndrome due to hypothyroidism |
| 193213003 | Myasthenic syndrome due to pernicious anemia |
| 193214009 | Myasthenic syndrome due to thyrotoxicosis |
| 193216006 | Congenital and developmental myasthenia |
| 193225000 | Hereditary progressive muscular dystrophy |
| 193227008 | Pelvic muscular dystrophy |
| 193230001 | Distal muscular dystrophy with juvenile onset |
| 193237003 | Myotonic disorder |
| 193238008 | Infantile myotonia |
| 195154000 | Ruptured berry aneurysm |
| 195160000 | Intracranial subarachnoid hemorrhage from vertebral artery |
| 195165005 | Basal ganglia hemorrhage |
| 195167002 | External capsule hemorrhage |
| 195168007 | Intracerebral hemorrhage with intraventricular hemorrhage |
| 195169004 | Intracerebral hemorrhage, multiple localized |
| 195180004 | Basilar artery occlusion |
| 195182007 | Vertebral artery occlusion |
| 195183002 | Multiple and bilateral precerebral arterial occlusion |
| 195185009 | Cerebral infarct due to thrombosis of precerebral arteries |
| 195186005 | Cerebral infarction due to embolism of precerebral arteries |
| 195189003 | Cerebral infarction due to thrombosis of cerebral arteries |
| 195190007 | Cerebral infarction due to embolism of cerebral arteries |
| 195199008 | Vertebrobasilar artery syndrome |
| 195200006 | Carotid artery syndrome hemispheric |
| 195205001 | Impending cerebral ischemia |
| 195206000 | Intermittent cerebral ischemia |
| 195209007 | Middle cerebral artery syndrome |
| 195210002 | Anterior cerebral artery syndrome |
| 195211003 | Posterior cerebral artery syndrome |
| 195212005 | Brainstem stroke syndrome |
| 195213000 | Cerebellar stroke syndrome |
| 195216008 | Left sided cerebral hemisphere cerebrovascular accident |
| 195217004 | Right sided cerebral hemisphere cerebrovascular accident |
| 195229008 | Non-pyogenic venous sinus thrombosis |
| 195230003 | Cerebral infarction due to cerebral venous thrombosis, non-pyogenic |
| 195232006 | Occlusion and stenosis of middle cerebral artery |
| 195233001 | Occlusion and stenosis of anterior cerebral artery |
| 195234007 | Occlusion and stenosis of posterior cerebral artery |
| 195235008 | Occlusion and stenosis of cerebellar arteries |
| 195236009 | Occlusion and stenosis of multiple and bilateral cerebral arteries |
| 195239002 | Late effects of cerebrovascular disease |
| 195241001 | Sequelae of intracerebral hemorrhage |
| 195243003 | Sequelae of cerebral infarction |
| 195373009 | Anterior spinal and vertebral artery compression syndromes |
| 19598007 | Generalized epilepsy |
| 199451000000106 | Simple partial epileptic seizure |
| 19972008 | Postencephalitic parkinsonism |
| 20022000 | Hemiparesis |
| 200258006 | Obstetric cerebral venous thrombosis |
| 200259003 | Cerebral venous thrombosis in pregnancy |
| 200260008 | Cerebral venous thrombosis in puerperium |
| 200330000 | Puerperal cerebrovascular disorder - delivered |
| 200331001 | Puerperal cerebrovascular disorder - delivered with postnatal complication |
| 200332008 | Puerperal cerebrovascular disorder with antenatal complication |
| 200333003 | Puerperal cerebrovascular disorder with postnatal complication |
| 20059004 | Occlusion of cerebral artery |
| 20121000119105 | Partial occipital lobe epilepsy |
| 20305008 | Congenital myotonia, autosomal recessive form |
| 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 |
| 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 |
| 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 |
| 204021005 | Encephalomyelocele |
| 204022003 | Hydromeningocele - cranial |
| 204036008 | Lissencephaly |
| 204040004 | Agenesis of cerebrum |
| 204042007 | Congenital malformation of corpus callosum |
| 204043002 | Hypoplasia of corpus callosum |
| 204044008 | Aplasia of corpus callosum |
| 204049003 | Aplasia of cerebellum |
| 204052006 | Cebocephaly |
| 20415001 | Progressive sclerosing poliodystrophy |
| 20447006 | Plasma cell dyscrasia with polyneuropathy |
| 204493007 | Arteriovenous malformation of precerebral vessels |
| 204501003 | Congenital stricture of cerebral artery |
| 204745000 | Total intestinal aganglionosis |
| 20484008 | Prion disease |
| 20544001 | Secondarily generalized seizures |
| 205615000 | Trisomy 21- meiotic nondisjunction |
| 205616004 | Trisomy 21- mitotic nondisjunction mosaicism |
| 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 |
| 206196005 | Cerebral hemorrhage due to birth injury |
| 206398001 | Intraventricular hemorrhage due to birth injury |
| 20725005 | Familial visceral neuropathy |
| 20908003 | Subcortical cerebral hemorrhage |
| 21007002 | Wernicke's disease |
| 21086008 | Cockayne syndrome |
| 21111006 | Complete trisomy 13 syndrome |
| 21201006 | Sporadic cerebellar degeneration |
| 21258007 | Thrombosis of lateral venous sinus |
| 21263006 | Myxedema coma |
| 213044006 | Mechanical complication of carotid artery bypass |
| 213208008 | Anoxic brain damage complication |
| 213209000 | Cerebral anoxia complication |
| 21361000119109 | Paraneoplastic peripheral neuropathy |
| 21391000119102 | Partial parietal lobe epilepsy |
| 21601000119103 | Hypoxic ischemic encephalopathy due to birth trauma |
| 21634003 | Borjeson-Forssman-Lehmann syndrome |
| 21921000119103 | Dementia co-occurrent and due to Pick's disease |
| 2198002 | Visceral epilepsy |
| 22126005 | Hereditary neuraxial edema |
| 22255007 | Progressive multifocal leukoencephalopathy |
| 223176004 | Cerebellar disorder |
| 22381000119105 | Primary degenerative dementia |
| 22386003 | Syphilitic optic atrophy |
| 224186005 | Cerebellar deficiency syndrome |
| 22443004 | Vestibulocerebellar ataxia |
| 22471005 | Hemispheric cerebellar agenesis |
| 22811006 | Leukoencephalopathy |
| 22881000119100 | Quadriplegia with quadriparesis |
| 230156002 | Malignant meningitis |
| 230180003 | Human immunodeficiency virus leukoencephalopathy |
| 230191005 | Rasmussen syndrome |
| 230193008 | Neurosarcoidosis |
| 230202002 | Vacuolar myelopathy |
| 230220006 | Intracranial septic embolism |
| 230221005 | Intracranial arterial septic embolism |
| 230222003 | Septic thrombophlebitis of straight sinus |
| 230223008 | Septic thrombophlebitis of sigmoid sinus |
| 230224002 | Septic thrombophlebitis of cortical vein |
| 230225001 | Septic thrombophlebitis of great cerebral vein |
| 230226000 | System disorder of the nervous system |
| 230227009 | Early onset cerebellar ataxia |
| 230228004 | Early onset cerebellar ataxia with retained tendon reflexes |
| 230229007 | Early onset cerebellar ataxia with hypogonadism |
| 230230002 | Early onset cerebellar ataxia with retinitis pigmentosa and optic atrophy |
| 230231003 | Early onset cerebellar ataxia with essential tremor |
| 230232005 | Late onset cerebellar ataxia |
| 230233000 | Progressive cerebellar ataxia |
| 230234006 | Periodic ataxia |
| 230235007 | Olivopontocerebellar atrophy with slow eye movement |
| 230236008 | Olivopontocerebellar atrophy with blindness |
| 230237004 | Progressive spinocerebellar ataxia with decreased tendon reflexes |
| 230238009 | Progressive spinocerebellar ataxia with retained tendon reflexes |
| 230239001 | Progressive cerebellar ataxia with palatal myoclonus |
| 230240004 | Progressive cerebellar ataxia with hypogonadism |
| 230241000 | Secondary cerebellar degeneration |
| 230242007 | Drug-induced cerebellar ataxia |
| 230243002 | Cerebellar ataxia caused by toxin |
| 230244008 | Disorder primarily affecting the motor pathways |
| 230246005 | Progressive bulbar palsy of childhood |
| 230247001 | Distal spinal muscular atrophy |
| 230248006 | Scapuloperoneal spinal muscular atrophy |
| 230249003 | Facioscapulohumeral spinal muscular atrophy |
| 230250003 | Facioscapulohumeral spinal muscular atrophy with sensory loss |
| 230251004 | Scapulohumeral spinal muscular atrophy |
| 230252006 | Oculopharyngeal spinal muscular atrophy |
| 230253001 | Bulbospinal neuronopathy |
| 230254007 | Western Pacific motor neurone disease |
| 230255008 | Madras-type motor neurone disease |
| 230257000 | Paraneoplastic motor neurone disease |
| 230258005 | Amyotrophic lateral sclerosis with dementia |
| 230260007 | Pure hereditary spastic paraplegia |
| 230261006 | Complicated hereditary spastic paraplegia |
| 230263009 | Autosomal dominant spastic paraplegia type 17 |
| 230264003 | Troyer syndrome |
| 230265002 | Familial Alzheimer's disease of early onset |
| 230266001 | Non-familial Alzheimer's disease of early onset |
| 230267005 | Familial Alzheimer's disease of late onset |
| 230268000 | Non-familial Alzheimer's disease of late onset |
| 230269008 | Focal Alzheimer's disease |
| 230270009 | Frontotemporal dementia |
| 230271008 | Pick's disease with Pick bodies |
| 230272001 | Pick's disease with Pick cells and no Pick bodies |
| 230273006 | Frontotemporal degeneration |
| 230274000 | Frontal lobe degeneration with motor neurone disease |
| 230278002 | Progressive aphasia |
| 230279005 | Non-Alzheimer's progressive dysphasia |
| 230280008 | Progressive aphasia in Alzheimer's disease |
| 230281007 | Argyrophilic grain disease |
| 230282000 | Post-traumatic dementia |
| 230283005 | Punch drunk syndrome |
| 230284004 | Spongiform encephalopathy |
| 230285003 | Vascular dementia of acute onset |
| 230286002 | Subcortical vascular dementia |
| 230287006 | Mixed cortical and subcortical vascular dementia |
| 230288001 | Semantic dementia |
| 230289009 | Patchy dementia |
| 230291001 | Juvenile Parkinson's disease |
| 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 |
| 230311004 | Basal ganglia degeneration with calcification |
| 230312006 | Aicardi Goutieres syndrome |
| 230313001 | Autosomal dominant late onset basal ganglia degeneration |
| 230319002 | Autosomal dominant idiopathic familial dystonia |
| 230320008 | Autosomal recessive idiopathic familial dystonia |
| 230329009 | Posthemiplegic dystonia |
| 230352008 | Encephalopathy due to vitamin deficiency |
| 230353003 | Morel laminar sclerosis |
| 230354009 | Drug-induced encephalopathy |
| 230355005 | Encephalopathy caused by heavy metal |
| 230357002 | Urate encephalopathy |
| 230359004 | Secondary amyloid encephalopathy |
| 230360009 | Encephalopathy caused by radiation damage |
| 230363006 | Progressive neuronal degeneration of childhood |
| 230364000 | Progressive neuronal degeneration without liver cirrhosis |
| 230365004 | Neuroaxonal dystrophy |
| 230366003 | Late infantile and juvenile neuroaxonal dystrophy |
| 230367007 | Neuroaxonal leukodystrophy |
| 230368002 | Type III transitional Pelizaeus-Merzbacher disease |
| 230369005 | Type IV adult Pelizaeus-Merzbacher disease |
| 230370006 | Type V atypical Pelizaeus-Merzbacher disease |
| 230371005 | Type VI Cockayne Pelizaeus-Merzbacher disease |
| 230372003 | Acute relapsing multiple sclerosis |
| 230373008 | Chronic progressive multiple sclerosis |
| 230375001 | Subacute hemorrhagic leukoencephalitis |
| 230377009 | Extrapontine myelinolysis |
| 230379007 | Subacute necrotizing myelitis |
| 230380005 | Balo concentric sclerosis |
| 230381009 | Localization-related epilepsy |
| 230382002 | Benign frontal epilepsy of childhood |
| 230383007 | Benign psychomotor epilepsy of childhood |
| 230384001 | Benign atypical partial epilepsy in childhood |
| 230386004 | Childhood epilepsy with occipital paroxysms |
| 230387008 | Benign occipital epilepsy of childhood - early onset variant |
| 230388003 | Benign occipital epilepsy of childhood - late onset variant |
| 230389006 | Primary inherited reading epilepsy |
| 230390002 | Localization-related symptomatic epilepsy |
| 230391003 | Amygdalo-hippocampal epilepsy |
| 230392005 | Rhinencephalic epilepsy |
| 230393000 | Lateral temporal epilepsy |
| 230394006 | Frontal lobe epilepsy |
| 230395007 | Supplementary motor epilepsy |
| 230396008 | Cingulate epilepsy |
| 230397004 | Anterior frontopolar epilepsy |
| 230398009 | Orbitofrontal epilepsy |
| 230399001 | Dorsolateral epilepsy |
| 230400008 | Opercular epilepsy |
| 230401007 | Non-progressive Kozhevnikow syndrome |
| 230403005 | Parietal lobe epilepsy |
| 230404004 | Occipital lobe epilepsy |
| 230405003 | Chronic progressive epilepsia partialis continua of childhood |
| 230406002 | Localization-related symptomatic epilepsy with specific precipitant |
| 230407006 | Hemiplegia-hemiconvulsion-epilepsy syndrome |
| 230408001 | Localization-related cryptogenic epilepsy |
| 230412007 | Myoclonic epilepsy of early childhood |
| 230413002 | Juvenile absence epilepsy |
| 230414008 | Epilepsy with grand mal seizures on awakening |
| 230415009 | Cryptogenic generalized epilepsy |
| 230416005 | Cryptogenic West syndrome |
| 230417001 | Symptomatic West syndrome |
| 230418006 | Lennox-Gastaut syndrome |
| 230419003 | Cryptogenic Lennox-Gastaut syndrome |
| 230420009 | Symptomatic Lennox-Gastaut syndrome |
| 230421008 | Myoclonic astatic epilepsy |
| 230422001 | Myoclonic absence epilepsy |
| 230423006 | Unverricht-Lundborg syndrome |
| 230425004 | Lafora disease |
| 230426003 | Myoclonic epilepsy with ragged red fibers |
| 230427007 | Cryptogenic myoclonic epilepsy |
| 230428002 | Idiopathic myoclonic epilepsy |
| 230429005 | Early infantile epileptic encephalopathy with suppression bursts |
| 230430000 | Symptomatic myoclonic epilepsy |
| 230435005 | Epilepsy undetermined whether focal or generalized |
| 230437002 | Severe myoclonic epilepsy in infancy |
| 230438007 | Acquired epileptic aphasia |
| 230439004 | Epilepsy with continuous spike wave during slow-wave sleep |
| 230440002 | Secondary reading epilepsy |
| 230444006 | Menstrual epilepsy |
| 230445007 | Nocturnal epilepsy |
| 230447004 | Absence seizure with eyelid myoclonia |
| 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 |
| 230466004 | Alternating hemiplegia of childhood |
| 230518009 | Infarction of optic tract |
| 230521006 | Optic radiation disorder |
| 230522004 | Inflammatory disorder of optic radiation |
| 230523009 | Infarction of optic radiation |
| 230525002 | Compression of optic radiation |
| 230552007 | X-linked hereditary motor and sensory neuropathy |
| 230553002 | Autosomal dominant sensory neuropathy |
| 230556005 | X-linked recessive sensory neuropathy |
| 230557001 | Hereditary dysautonomia with motor neuropathy |
| 230558006 | Hereditary liability to pressure palsies |
| 230559003 | Hereditary hypertrophic neuropathy with paraproteinemia |
| 230561007 | Congenital neuropathy with arthrogryposis multiplex congenita |
| 230562000 | Congenital hypomyelinating neuropathy |
| 230564004 | Chronic inflammatory demyelinating polyradiculoneuropathy with central nervous system demyelination |
| 230586003 | Neuropathy due to multiple myeloma |
| 230594005 | Critical illness polyneuropathy |
| 230666006 | Paraneoplastic autonomic dysfunction |
| 230669004 | Genetically determined myasthenia |
| 230670003 | Familial infantile myasthenia |
| 230671004 | Acetylcholine resynthesis deficiency |
| 230672006 | Congenital myasthenic syndrome |
| 230673001 | Congenital end-plate acetylcholine receptor deficiency |
| 230674007 | Pseudomyopathic myasthenia |
| 230675008 | Slow channel syndrome |
| 230676009 | Putative defect in acetylcholine synthesis or packaging |
| 230677000 | Congenital end-plate acetylcholinesterase deficiency |
| 230678005 | Decrease of motor end-plate potential amplitude without acetylcholine receptor deficiency |
| 230679002 | Abnormality of synaptic vesicles |
| 230684008 | Ocular myasthenia |
| 230685009 | Myasthenia gravis associated with thymoma |
| 230686005 | Generalized myasthenia |
| 230687001 | Myopathy in myasthenia gravis |
| 230690007 | Cerebrovascular accident |
| 230691006 | Cerebrovascular accident due to occlusion of cerebral artery |
| 230692004 | Infarction - precerebral |
| 230693009 | Anterior cerebral circulation infarction |
| 230694003 | Total anterior cerebral circulation infarction |
| 230695002 | Partial anterior cerebral circulation infarction |
| 230696001 | Posterior cerebral circulation infarction |
| 230698000 | Lacunar infarction |
| 230699008 | Pure motor lacunar infarction |
| 230700009 | Pure sensory lacunar infarction |
| 230701008 | Pure sensorimotor lacunar infarction |
| 230702001 | Lacunar ataxic hemiparesis |
| 230703006 | Dysarthria-clumsy hand syndrome |
| 230704000 | Multi-infarct state |
| 230706003 | Hemorrhagic cerebral infarction |
| 230707007 | Anterior cerebral circulation hemorrhagic infarction |
| 230708002 | Posterior cerebral circulation hemorrhagic infarction |
| 230709005 | Massive supratentorial cerebral hemorrhage |
| 230710000 | Lobar cerebral hemorrhage |
| 230711001 | Thalamic hemorrhage |
| 230712008 | Lacunar hemorrhage |
| 230713003 | Stroke of uncertain pathology |
| 230714009 | Anterior circulation stroke of uncertain pathology |
| 230715005 | Posterior circulation stroke of uncertain pathology |
| 230716006 | Carotid territory transient ischemic attack |
| 230717002 | Vertebrobasilar territory transient ischemic attack |
| 230720005 | Cerebral venous thrombosis of straight sinus |
| 230721009 | Cerebral venous thrombosis of sigmoid sinus |
| 230722002 | Cerebral venous thrombosis of cortical vein |
| 230723007 | Cerebral venous thrombosis of great cerebral vein |
| 230724001 | Cerebral amyloid angiopathy |
| 230725000 | Sporadic cerebral amyloid angiopathy |
| 230730001 | Dissection of vertebral artery |
| 230731002 | Cerebral arteritis in systemic vasculitis |
| 230732009 | Cerebral arteritis in giant cell arteritis |
| 230735006 | Syphilitic cerebral arteritis |
| 230738008 | Asymptomatic cerebrovascular disease |
| 230739000 | Spinal cord stroke |
| 230741004 | Venous infarction of spinal cord |
| 230745008 | Hydrocephalus |
| 230746009 | Obstructive hydrocephalus |
| 230747000 | Isolated fourth ventricle hydrocephalus |
| 230748005 | Intermittently raised pressure hydrocephalus |
| 230749002 | Hydrocephalus due to and following meningitis |
| 230751003 | Hydrocephalus following traumatic injury |
| 230752005 | Hydrocephalus due to cerebrospinal fluid absorption defect |
| 230753000 | Hydrocephalus due to cerebrospinal fluid overproduction |
| 230769007 | Periventricular leukomalacia |
| 230773005 | Spastic cerebral palsy |
| 230780007 | Dyskinetic cerebral palsy |
| 230781006 | Dystonic/rigid cerebral palsy |
| 230784003 | Congenital pseudobulbar palsy |
| 230806005 | Brain ventricular shunt infection |
| 230807001 | Brain ventricular shunt displacement |
| 230808006 | Brain ventricular shunt obstruction |
| 23150001 | Proteus syndrome |
| 232036006 | Cilioretinal artery occlusion |
| 232059000 | Laurence-Moon syndrome |
| 23276006 | Ventricular hemorrhage |
| 233718008 | Pulmonary tuberous sclerosis |
| 23374007 | Atypical absence seizure |
| 233964008 | Internal carotid artery stenosis |
| 233983001 | Ruptured cerebral aneurysm |
| 233988005 | Carotid artery aneurysm |
| 234142008 | Cerebral arteriovenous malformation |
| 234149004 | Congenital arteriovenous fistula of brain |
| 23501004 | Arginase deficiency |
| 2355008 | Rud's syndrome |
| 236529001 | Prune belly syndrome with pulmonic stenosis, intellectual disability and deafness |
| 23671000119107 | Sequela of ischemic cerebral infarction |
| 23728006 | Partial bilateral paralysis |
| 23732000 | Primary cerebellar degeneration |
| 237611007 | Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus |
| 237612000 | Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction |
| 237683004 | X-linked panhypopituitarism |
| 237701005 | Pituitary apoplexy |
| 237702003 | Pituitary hemorrhage |
| 237706000 | Autoimmune hypophysitis |
| 237733001 | Diencephalic syndrome |
| 237867001 | Hereditary cerebrovascular amyloidosis |
| 237960000 | D-2-hydroxyglutaric aciduria |
| 237961001 | L-2-hydroxyglutaric aciduria |
| 237988006 | Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency |
| 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 |
| 238069004 | Acyl-coenzyme A oxidase deficiency |
| 23808003 | Rolandic vein occlusion syndrome |
| 23819000 | Embolism of cavernous venous sinus |
| 23849003 | Sandhoff disease |
| 238826008 | de Barsy syndrome |
| 23931000119104 | Hydrocephalus due to Arnold Chiari malformation type 2 |
| 23941000119108 | Arnold Chiari type 2 without hydrocephalus |
| 239965291000119107 | Cerebrovascular accident due to occlusion of basilar artery |
| 240046001 | Muscular dystrophy with predominantly proximal limb girdle distribution |
| 240047005 | X-linked muscular dystrophy with limb girdle distribution |
| 240048000 | X-linked muscular dystrophy with abnormal dystrophin |
| 240049008 | Intermediate X-linked muscular dystrophy |
| 240050008 | Manifesting female carrier of X-linked muscular dystrophy |
| 240051007 | X-linked limb girdle muscular dystrophy with normal dystrophin |
| 240052000 | Ji muscular dystrophy |
| 240053005 | Hereditary myopathy limited to females |
| 240054004 | Autosomal recessive muscular dystrophy with limb girdle distribution |
| 240055003 | Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein |
| 240056002 | Severe autosomal recessive muscular dystrophy of childhood - North African type |
| 240057006 | Autosomal recessive muscular dystrophy with gene located at 15q |
| 240058001 | Reunion-Indiana Amish type muscular dystrophy |
| 240059009 | Congenital muscular dystrophy |
| 240060004 | Western type of congenital muscular dystrophy |
| 240061000 | Congenital muscular dystrophy with arthrogryposis multiplex congenita |
| 240062007 | Ullrich congenital muscular dystrophy |
| 240063002 | Eichsfeld type congenital muscular dystrophy |
| 240064008 | Hutterite type of muscular dystrophy |
| 240065009 | Adult onset autosomal recessive muscular dystrophy with normal dystrophin |
| 240067001 | Autosomal dominant muscular dystrophy with limb girdle distribution |
| 240068006 | Autosomal dominant muscular dystrophy with gene located at 5q31 |
| 240069003 | Late onset proximal muscular dystrophy with dysarthria |
| 240070002 | Muscular dystrophy not predominantly limb girdle in distribution |
| 240071003 | X-linked muscular dystrophy not predominantly limb girdle |
| 240072005 | Benign scapuloperoneal muscular dystrophy with cardiomyopathy |
| 240073000 | Autosomal recessive muscular dystrophy not predominantly limb girdle |
| 240074006 | Scapulohumeral muscular dystrophy |
| 240075007 | Autosomal dominant muscular dystrophy not predominantly limb girdle |
| 240076008 | Benign scapuloperoneal muscular dystrophy |
| 240077004 | Severe scapuloperoneal muscular dystrophy with cardiomyopathy |
| 240078009 | Benign congenital muscular dystrophy with finger flexion contractures |
| 240081004 | Autosomal recessive centronuclear myopathy |
| 240082006 | Myopathy with abnormality of histochemical fiber type |
| 240083001 | Myopathy with type I hypotrophy |
| 240084007 | Congenital myopathy with fiber type disproportion |
| 240085008 | Congenital myopathy with uniform fiber type |
| 240086009 | Myopathy with cytoplasmic inclusions |
| 240087000 | Myopathy with tubular aggregates |
| 240104008 | Congenital myotonic dystrophy |
| 240460008 | Acute paralytic poliomyelitis |
| 24059009 | Acute cerebellar ataxia caused by varicella |
| 241006 | Epilepsia partialis continua |
| 2421000119107 | Hallucinations co-occurrent and due to late onset dementia |
| 24326000 | Metachromatic leukodystrophy, adult type |
| 24473007 | Persistent vegetative state |
| 24624008 | Aneurysm of internal carotid artery |
| 24654003 | Weber-Gubler syndrome |
| 246545002 | Generalized onset epileptic seizure |
| 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 |
| 2495006 | Congenital cerebral arteriovenous aneurysm |
| 249892007 | Progressive pseudobulbar palsy |
| 25044007 | Neuromyelitis optica |
| 25133001 | Completed stroke |
| 251770561000119107 | Cerebrovascular accident due to embolism of left anterior cerebral artery |
| 253098009 | Neural tube defect |
| 253100009 | Congenital endaural hernia |
| 253101008 | Congenital cerebral hernia |
| 253103006 | Frontal encephalocele |
| 253104000 | Frontoethmoidal encephalocele |
| 253106003 | Nasofrontal encephalocele |
| 253107007 | Nasopharyngeal encephalocele |
| 253108002 | Temporal encephalocele |
| 253109005 | Parietal encephalocele |
| 253113003 | Rachischisis with hydrocephalus |
| 253114009 | Myelocele with hydrocephalus |
| 253115005 | Hydromyelocele with hydrocephalus |
| 253116006 | Fissured spine with hydrocephalus |
| 253118007 | Thoracolumbar spina bifida with hydrocephalus - closed |
| 253119004 | Hemimyelocele |
| 253120005 | Lipomeningocele |
| 253131002 | Hydrocephalus associated with late onset aqueduct stenosis |
| 253132009 | External hydrocephalus |
| 253133004 | Hydrocephalus with anomaly of aqueduct of Sylvius |
| 253136007 | Lobar holoprosencephaly |
| 253137003 | Alobar holoprosencephaly |
| 253138008 | Semi-lobar holoprosencephaly |
| 253139000 | Agenesis of corpus callosum with lipoma |
| 253140003 | Partial agenesis of corpus callosum |
| 253142006 | Atrophy of corpus callosum |
| 253143001 | Absence of septum pellucidum |
| 253147000 | Type 1 lissencephaly |
| 253148005 | Miller Dieker syndrome |
| 253149002 | Type 2 lissencephaly |
| 253158009 | Hydranencephaly with proliferative vasculopathy |
| 253159001 | Schizencephaly |
| 253160006 | Colpocephaly |
| 253166000 | Lateral meningocele |
| 253172000 | Agenesis of cerebellum |
| 253174004 | Aplasia of the vermis |
| 253175003 | Familial aplasia of the vermis |
| 253176002 | Gillespie syndrome |
| 253178001 | Granular cell hypoplasia |
| 253180007 | Dysgenesis of the brainstem |
| 253181006 | Olive dysplasia |
| 253183009 | Olivary heterotopia |
| 253186001 | Chiari malformation type III |
| 253194008 | Aneurysm of the vein of Galen |
| 253203003 | Hypoplasia of brain gyri |
| 25362006 | Phytanic acid storage disease |
| 253699002 | Isolation of common carotid artery |
| 25397008 | Aqueduct of Sylvius anomaly |
| 254092004 | Saldino-Mainzer dysplasia |
| 254132000 | Endosteal hyperostoses with cerebellar hypoplasia |
| 254243001 | Ash leaf spot, tuberous sclerosis |
| 254775002 | Bregeat's syndrome |
| 254938000 | Astrocytoma of brain |
| 254940005 | Oligodendroglioma of brain |
| 254948003 | Astrocytoma of spinal cord |
| 254950006 | Oligodendroglioma of spinal cord |
| 254955001 | Pituitary carcinoma |
| 254969001 | Malignant tumor of olfactory tract |
| 254972008 | Malignant tumor of optic nerve and sheath |
| 254973003 | Malignant astrocytoma of optic nerve |
| 254974009 | Malignant tumor of optic nerve sheath |
| 254975005 | Malignant meningioma of optic nerve sheath |
| 255112006 | Malignant tumor of pituitary and hypothalamus |
| 256321009 | Disorder of neuromuscular transmission |
| 257277002 | Combined disorder of muscle AND peripheral nerve |
| 25772007 | Multi-infarct dementia with delusions |
| 2584003 | Cerebral degeneration in childhood |
| 2593002 | Dubowitz's syndrome |
| 26015003 | Maroteaux-Lamy syndrome, intermediate form |
| 26021000119107 | Vertigo as sequela of cerebrovascular disease |
| 261808007 | Neonatal cerebral hemorrhage |
| 26206000 | Hepatic coma due to viral hepatitis B |
| 262692002 | Burst lobe of brain |
| 262711004 | Transection of cervical cord |
| 26594006 | Syringobulbia |
| 26595007 | Congenital absence of part of brain |
| 266253001 | Precerebral arterial occlusion |
| 266254007 | Occlusion of carotid artery |
| 266257000 | Transient ischemic attack |
| 267581004 | Progressive myoclonic epilepsy |
| 267592003 | Motor cortex epilepsy |
| 267604001 | Myasthenic syndrome due to diabetic mellitus |
| 268143001 | Spina bifida with hydrocephalus - open |
| 268146009 | Spina bifida without hydrocephalus - open |
| 26852004 | Primary degenerative dementia of the Alzheimer type, senile onset, with depression |
| 268612007 | Senile and presenile organic psychotic conditions |
| 26929004 | Alzheimer's disease |
| 26954004 | Thrombophlebitis of superior sagittal sinus |
| 27148008 | Hereditary motor end-plate disease |
| 271569006 | Communicating hydrocephalus |
| 271986005 | Disorder of brain ventricular shunt |
| 274100004 | Cerebral hemorrhage |
| 275363001 | Rupture of superficial cerebral vein |
| 275434003 | Stroke in the puerperium |
| 275468009 | Congenital quadriplegia |
| 276219001 | Occipital cerebral infarction |
| 276220007 | Foville syndrome |
| 276221006 | Millard-Gubler syndrome |
| 276222004 | Top of basilar syndrome |
| 27642008 | Dysmorphic sialidosis, congenital form |
| 276594006 | Perinatal rupture of superficial cerebral vein |
| 276599001 | Cerebral leukomalacia |
| 276648002 | Intraventricular hemorrhage of prematurity |
| 276650005 | Perinatal subependymal hemorrhage |
| 276651009 | Perinatal subependymal hemorrhage with intraventricular extension |
| 276652002 | Perinatal subependymal hemorrhage with intraventricular and intracerebral extension |
| 276706004 | Perinatal cerebral ischemia |
| 276722003 | Intracerebellar and posterior fossa hemorrhage |
| 276826005 | Malignant glioma of brain |
| 276827001 | Malignant glioma of spinal cord |
| 276828006 | Glioblastoma multiforme of brain |
| 276829003 | Glioblastoma multiforme of spinal cord |
| 276836002 | Primary cerebral lymphoma |
| 277196008 | Berry aneurysm |
| 277299009 | Ruptured cerebral arteriovenous malformation |
| 277315000 | Ruptured aneurysm of anterior cerebral artery |
| 277316004 | Ruptured aneurysm of middle cerebral artery |
| 277319006 | Ruptured aneurysm of posterior cerebral artery |
| 277320000 | Ruptured aneurysm of anterior communicating artery |
| 277322008 | Ruptured aneurysm of posterior communicating artery |
| 277324009 | Ruptured aneurysm of basilar artery |
| 277325005 | Ruptured aneurysm of posterior inferior cerebellar artery |
| 277330009 | Ruptured internal carotid bifurcation aneurysm |
| 277373000 | Severe childhood autosomal recessive muscular dystrophy |
| 277461004 | Anaplastic astrocytoma of brain |
| 277505007 | Medulloblastoma of cerebellum |
| 277526007 | Diffuse melanosis of meninges |
| 277530005 | Malignant melanoma of meninges |
| 277922001 | Aprosencephaly |
| 277949001 | Combined malformation of central nervous system and skeletal muscle |
| 277950001 | Muscle eye brain disease |
| 278284007 | Right hemiplegia |
| 278285008 | Left hemiplegia |
| 278286009 | Right hemiparesis |
| 278287000 | Left hemiparesis |
| 278510009 | Localization-related idiopathic epilepsy |
| 278512001 | Ataxic cerebral palsy |
| 278849000 | Cerebral atrophy |
| 278855005 | Frontal lobe degeneration |
| 278857002 | Dementia of frontal lobe type |
| 279982005 | Cerebral degeneration presenting primarily with dementia |
| 28055006 | West syndrome |
| 281004 | Dementia associated with alcoholism |
| 281240008 | Extension of cerebrovascular accident |
| 281411007 | Spastic diplegia |
| 281560004 | Neuroblastoma of brain |
| 281899002 | Congenital hydrocephalus caused by toxoplasmosis |
| 28318001 | Basilar hemorrhage |
| 28366008 | Cerebral arteritis |
| 28394000 | Toxic encephalopathy |
| 284811000119102 | Aneurysm of extracranial portion of internal carotid artery |
| 284821000119109 | Aneurysm of intracranial portion of internal carotid artery |
| 284861000119104 | Atherosclerosis of bilateral carotid arteries |
| 284871000119105 | Atherosclerosis of left carotid artery |
| 284881000119108 | Atherosclerosis of right carotid artery |
| 285161000119105 | Occlusion of left carotid artery |
| 285171000119104 | Occlusion of right carotid artery |
| 285191000119103 | Stenosis of left carotid artery |
| 285201000119100 | Stenosis of right carotid artery |
| 28534004 | Spastic paralysis due to intracranial birth injury |
| 285641009 | Metastasis to brain of unknown primary |
| 28634005 | Cerebral ataxia |
| 286742002 | Impending cerebrovascular accident |
| 287731003 | Cerebral ischemia |
| 28778005 | Phrenic nerve paralysis as birth trauma |
| 28790007 | Obstruction of precerebral artery |
| 288276001 | Fetal cerebral hemorrhage |
| 288631000119104 | Vascular dementia with behavioral disturbance |
| 28978003 | Progressive supranuclear ophthalmoplegia |
| 290401000119108 | Complete paraplegia |
| 290411000119106 | Incomplete paraplegia |
| 290461000119109 | Spastic hemiplegia of left dominant side |
| 290471000119103 | Spastic hemiplegia of left nondominant side |
| 290481000119100 | Spastic hemiplegia of right dominant side |
| 290491000119102 | Spastic hemiplegia of right nondominant side |
| 290581000119101 | Ataxia due to and following cerebrovascular accident |
| 290621000119101 | Cognitive deficit due to and following cerebrovascular disease |
| 290631000119103 | Dysarthria due to and following cerebrovascular accident |
| 290641000119107 | Dysphagia due to and following non-traumatic intracerebral hemorrhage |
| 290671000119100 | Status epilepticus due to complex partial epileptic seizure |
| 290681000119102 | Status epilepticus due to refractory complex partial seizures |
| 290691000119104 | Status epilepticus due to generalized idiopathic epilepsy |
| 290711000119101 | Status epilepticus due to intractable idiopathic generalized epilepsy |
| 290721000119108 | Status epilepticus due to refractory epilepsy |
| 290741000119102 | Intractable idiopathic partial epilepsy |
| 290761000119103 | Status epilepticus due to refractory simple partial epilepsy |
| 290791000119105 | Fluency disorder due to and following cerebrovascular accident |
| 290871000119101 | Infantile spasms co-occurrent with status epilepticus |
| 290881000119103 | Refractory infantile spasms co-occurrent with status epilepticus |
| 29093005 | Crossed hemiparesis |
| 291311000119108 | Status epilepticus in benign Rolandic epilepsy |
| 291351000119109 | Spontaneous hemorrhage of subarachnoid space from basilar artery |
| 291371000119100 | Spontaneous hemorrhage of subarachnoid space from intracranial artery |
| 291411000119104 | Spontaneous hemorrhage of subarachnoid space from left posterior communicating artery |
| 291481000119105 | Spontaneous haemorrhage of subarachnoid space from right posterior communicating artery |
| 291511000119103 | Spontaneous hemorrhage of deep cerebral hemisphere |
| 291521000119105 | Spontaneous hemorrhage of cortical intracerebral hemisphere |
| 291531000119108 | Spontaneous hemorrhage of cerebral hemisphere |
| 291541000119104 | Spontaneous hemorrhage of brain stem |
| 291571000119106 | Spontaneous cerebral hemorrhage |
| 29159009 | Familial dysautonomia |
| 291621000119109 | Cognitive deficit due to and following nontraumatic subarachnoid hemorrhage |
| 291631000119107 | Aphasia due to and following non-traumatic subarachnoid hemorrhage |
| 291665000 | Postpartum intrapituitary hemorrhage |
| 291681000119108 | Dysphagia due to and following non-traumatic subarachnoid hemorrhage |
| 291711000119109 | Cognitive deficit due to and following nontraumatic intracerebral hemorrhage |
| 291721000119102 | Aphasia due to and following non-traumatic intracerebral hemorrhage |
| 29188005 | Complete bilateral paralysis |
| 292621000119100 | Occlusion of right vertebral artery |
| 292631000119102 | Occlusion of left vertebral artery |
| 292661000119105 | Cerebrovascular accident due to stenosis of right vertebral artery |
| 292671000119104 | Cerebrovascular accident due to stenosis of left vertebral artery |
| 292681000119101 | Cerebrovascular accident due to occlusion of right vertebral artery |
| 292691000119103 | Cerebrovascular accident due to occlusion of left vertebral artery |
| 292851000119109 | Lacunar ataxic hemiparesis of right dominant side |
| 292861000119106 | Lacunar ataxic hemiparesis of left dominant side |
| 292991000119106 | Eaton Lambert syndrome without underlying malignancy |
| 29322000 | Acute cerebrovascular insufficiency |
| 293671000119109 | Behavioral disturbance due to multi-infarct dementia |
| 293811000119100 | Cerebral infarction due to vertebral artery stenosis |
| 293831000119105 | Cerebral infarction due to stenosis of precerebral artery |
| 294041000119107 | Flaccid hemiplegia of left dominant side |
| 294051000119109 | Flaccid hemiplegia of left nondominant side |
| 294061000119106 | Flaccid hemiplegia of right dominant side |
| 294071000119100 | Flaccid hemiplegia of right nondominant side |
| 294101000119109 | Hemiplegia of left dominant side |
| 294111000119107 | Hemiplegia of left nondominant side |
| 294121000119100 | Hemiplegia of right dominant side |
| 294131000119102 | Hemiplegia of right nondominant side |
| 29426003 | Paralytic syndrome |
| 29570005 | Leigh's disease |
| 29618004 | Striatonigral degeneration |
| 297138001 | Embolus of circle of Willis |
| 297157005 | Thrombus of intracranial vein |
| 297176007 | Vertebral artery aneurysm |
| 297278001 | Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator |
| 29774004 | Vascular myelopathy |
| 298282001 | Spastic quadriparesis |
| 2992000 | Pigmentary pallidal degeneration |
| 29941000119105 | Ataxia as sequela of cerebrovascular disease |
| 29951000119107 | Ataxic hemiparesis |
| 30023002 | Hydranencephaly |
| 300920004 | Carotid atherosclerosis |
| 300992002 | Alcohol-induced cerebellar ataxia |
| 301764006 | Hematoma of brain |
| 301765007 | Cerebellar hematoma |
| 302213007 | Caroticocavernous sinus fistula |
| 30278004 | Kundrat's syndrome |
| 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 |
| 302887008 | Neuropathy in secondary amyloidosis |
| 302902003 | Infarction of optic chiasm |
| 302904002 | Infarction of visual cortex |
| 302909007 | Diffuse cerebrovascular disease |
| 30400005 | Middle meningeal hemorrhage following injury |
| 304603007 | Variant Creutzfeldt-Jakob disease |
| 305719002 | Neuromyotonia |
| 307212006 | Brain ventricular shunt malfunction |
| 307356008 | Motor epilepsy |
| 307357004 | Jacksonian, focal or motor epilepsy |
| 307359001 | Congenital agenesis of brainstem nuclei |
| 307360006 | Leucodystrophy without a known biochemical basis |
| 307362003 | Intracranial venous septic embolism |
| 307363008 | Multiple lacunar infarcts |
| 30753002 | Normal pressure hydrocephalus |
| 307649006 | Microglioma |
| 307756005 | Cerebral palsy, not congenital or infantile, acute |
| 307766002 | Left sided cerebral infarction |
| 307767006 | Right sided cerebral infarction |
| 308634000 | Spinal demyelination |
| 30915001 | Holoprosencephaly sequence |
| 31076000 | Congenital ischemic atrophy of central nervous system structure |
| 31081000119101 | Presenile dementia with delusions |
| 31097004 | Post poliomyelitis syndrome |
| 31216003 | Profound intellectual disability |
| 312586003 | Intracranial thrombophlebitis |
| 312991009 | Senile dementia of the Lewy body type |
| 313307000 | Epileptic seizure |
| 313434001 | Residual hemiplegia |
| 315608004 | Cardiomyopathy in Duchenne muscular dystrophy |
| 31839002 | Myasthenia gravis, adult form |
| 32112006 | Phlebitis of inferior sagittal sinus |
| 32162001 | Facial hemiplegia |
| 322112361000132104 | Epilepsy due to scarring of brain |
| 32680009 | Nothnagel's syndrome |
| 32728005 | Hemorrhage due to ruptured congenital cerebral aneurysm |
| 32875003 | Inhalant-induced persisting dementia |
| 329361000119107 | Cerebrovascular accident due to occlusion of right middle cerebral artery by embolus |
| 329371000119101 | Cerebrovascular accident due to occlusion of left middle cerebral artery by embolus |
| 329421000119107 | Cerebrovascular accident due to occlusion of right posterior cerebral artery by embolus |
| 329431000119105 | Cerebrovascular accident due to occlusion of left posterior cerebral artery by embolus |
| 329451000119104 | Cerebrovascular accident due to occlusion of right cerebellar artery by embolus |
| 329461000119102 | Cerebrovascular accident due to occlusion of left cerebellar artery by embolus |
| 329481000119106 | Occlusion of right middle cerebral artery |
| 329491000119109 | Occlusion of left middle cerebral artery |
| 329501000119102 | Occlusion of bilateral middle cerebral arteries |
| 329541000119100 | Occlusion of bilateral anterior cerebral arteries |
| 329561000119101 | Occlusion of right posterior cerebral artery |
| 329571000119107 | Occlusion of left posterior cerebral artery |
| 329641000119104 | Cerebrovascular accident due to thrombus of basilar artery |
| 329651000119102 | Cerebrovascular accident due to thrombus of right carotid artery |
| 329671000119106 | Traumatic subarachnoid hemorrhage with loss of consciousness |
| 330411000119109 | Lacunar ataxic hemiparesis of left nondominant side |
| 330421000119102 | Lacunar ataxic hemiparesis of right nondominant side |
| 330791000119108 | Cerebrovascular accident due to thrombus of left carotid artery |
| 33301000119105 | Sequela of cardioembolic stroke |
| 33316007 | GM2 gangliosidosis |
| 33331000119103 | Sequela of lacunar stroke |
| 336191000119105 | Occlusion of right central retinal artery |
| 3371000119106 | Refractory generalized convulsive epilepsy |
| 341551000000108 | Cerebral degeneration in Parkinson's disease |
| 341801000119101 | Occlusion of left central retinal artery |
| 34181000119102 | Cerebral infarction due to occlusion of basilar artery |
| 34184002 | Corpus callosum syndrome |
| 34191000119104 | Cerebral infarction due to vertebral artery occlusion |
| 34209003 | Cerebral hemiplegia |
| 3456001 | Chronic progressive non-hereditary chorea |
| 346674811000119104 | Cerebrovascular accident due to occlusion of bilateral cerebellar arteries |
| 347011000119102 | Occlusion of bilateral central retinal arteries |
| 34781003 | Vertebral artery syndrome |
| 35145002 | Uremic encephalopathy |
| 352818000 | Tonic-clonic epilepsy |
| 352911000119101 | Primary malignant neoplasm of left optic nerve |
| 352921000119108 | Primary malignant neoplasm of right optic nerve |
| 35386004 | Cavernous sinus syndrome |
| 35691006 | Combined deficiency of sialidase AND beta galactosidase |
| 359629000 | Progressive post hemorrhagic ventricular dilatation |
| 359634001 | Infantile posthemorrhagic hydrocephalus |
| 359686005 | Van Bogaert's sclerosing leukoencephalitis |
| 36010004 | Congenital cerebral meningocele |
| 36025004 | Fibrous skin tumor of tuberous sclerosis |
| 360353005 | Thyrotoxicosis due to pituitary thyroid hormone resistance |
| 361000119103 | Paralytic syndrome on one side of the body as late effect of cerebrovascular accident |
| 361123003 | Psychomotor epilepsy |
| 361272001 | Cerebellar ataxia due to alcoholism |
| 361273006 | Alcoholic cerebellar degeneration |
| 36179005 | Reversible ischemic neurologic deficit syndrome |
| 363235000 | Hereditary disorder of nervous system |
| 363467004 | Malignant neoplasm of frontal lobe |
| 363468009 | Malignant neoplasm of temporal lobe |
| 363469001 | Malignant neoplasm of parietal lobe |
| 363470000 | Malignant neoplasm of occipital lobe |
| 363471001 | Malignant neoplasm of cerebral ventricles |
| 363473003 | Malignant neoplasm of brainstem |
| 363474009 | Malignant neoplasm of cerebral meninges |
| 363475005 | Malignant tumor of spinal cord |
| 363476006 | Malignant neoplasm of spinal meninges |
| 363482009 | Malignant tumor of pituitary gland |
| 363483004 | Malignant tumor of pineal gland |
| 363497007 | Malignant tumor of meninges |
| 363498002 | Malignant tumor of optic nerve |
| 36803009 | Idiopathic generalized epilepsy |
| 3681008 | Thrombophlebitis of torcular Herophili |
| 370987005 | Anaplastic astrocytoma of spinal cord |
| 371024007 | Senile dementia with delusion |
| 371026009 | Senile dementia with psychosis |
| 371029002 | Ischemic disorder of spinal cord |
| 371040005 | Thrombotic stroke |
| 371041009 | Embolic stroke |
| 371045000 | Translocation Down syndrome |
| 371076006 | Congenital syringomyelia |
| 371077002 | Ventriculoperitoneal shunt malfunction |
| 371079004 | Paraplegic cerebral palsy |
| 371116000 | Posthemorrhagic hydrocephalus |
| 371120001 | Quadriplegic spinal paralysis |
| 371121002 | Neonatal stroke |
| 371129000 | Paralysis from birth trauma |
| 371158002 | Disorder of basilar artery |
| 371160000 | Disorder of carotid artery |
| 371313002 | Congenital cerebellar cortical atrophy |
| 372062007 | Malignant neoplasm of central nervous system |
| 372310001 | Paralysis due to lesion of spinal cord |
| 372477008 | Post-traumatic syrinx |
| 37340000 | Motor neuron disease |
| 37356005 | Myoclonic seizure |
| 373587001 | Chiari malformation type II |
| 373606000 | Occlusive stroke |
| 37650008 | Hereditary cerebellar degeneration |
| 37934003 | Mitochondrial-lipid-glycogen storage myopathy |
| 37943007 | Embolism of multiple and bilateral precerebral arteries |
| 37960002 | Sanger-Brown cerebellar ataxia |
| 38023001 | Locked in syndrome |
| 380941000000104 | Progressive encephalopathy with oedema, hypsarrhythmia and optic atrophy syndrome |
| 38116000 | Hydromyelocele |
| 384430101000119103 | Cerebrovascular accident due to embolism of right carotid artery |
| 384993003 | Periventricular hemorrhagic venous infarct |
| 38523005 | Syphilitic parkinsonism |
| 38595071000119104 | Cerebrovascular accident due to thrombosis of right posterior cerebral artery |
| 386766007 | Marchiafava-Bignami disease |
| 38742007 | Central retinal artery occlusion |
| 387732009 | Becker muscular dystrophy |
| 38795005 | Sialidosis |
| 389098007 | Anoxic encephalopathy |
| 389100007 | Ischemic encephalopathy |
| 389101006 | Anoxic-ischemic encephalopathy |
| 389271000 | Spondyloenchondromatosis with basal ganglia calcification |
| 390936003 | Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy |
| 39194005 | Visual epilepsy |
| 39390005 | Niemann-Pick disease, type B |
| 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 |
| 398040009 | Charcot-Marie-Tooth disease, type I |
| 398100001 | Hereditary motor and sensory neuropathy |
| 398148000 | Hereditary sensory and autonomic neuropathy type II |
| 398187000 | Charcot-Marie-Tooth disease, type II |
| 398229007 | Amyloid polyneuropathy type I |
| 398432008 | Bulbar weakness |
| 399091004 | Facioscapulohumeral muscular dystrophy |
| 39912006 | Hereditary spastic paraplegia |
| 39925003 | Juvenile myopathy, encephalopathy, lactic acidosis AND stroke |
| 40161000119102 | Weakness of face muscles as sequela of stroke |
| 402460000 | Familial amyloid polyneuropathy with cutaneous amyloidosis |
| 40259002 | Progressive sensory ataxia of Charolais |
| 40276003 | Embolism of precerebral artery |
| 40354009 | De Lange syndrome |
| 403815003 | Axillary freckling due to neurofibromatosis |
| 403816002 | Multiple café-au-lait macules due to neurofibromatosis |
| 403817006 | Multiple neurofibromas in neurofibromatosis |
| 403819009 | Elephantiasis neurofibromatosa |
| 403856000 | Port-wine stain in proteus syndrome |
| 40450001 | Embolism of superior sagittal sinus |
| 404664002 | Malignant optic glioma |
| 404689008 | Alternating hemiplegia |
| 4061000119104 | Myelomeningocele without hydrocephalus |
| 40632002 | Charcot-Marie-Tooth disease, type IA |
| 4069002 | Anoxic brain damage during AND/OR resulting from a procedure |
| 40700009 | Severe intellectual disability |
| 40802007 | Metachromatic leukodystrophy, congenital type |
| 408371000000100 | [X]Cerebral palsy and other paralytic syndromes |
| 408581000000109 | [X]Extrapyramidal and movement disorders |
| 408664007 | Pontine artery occlusion |
| 408665008 | Pontine artery thrombosis |
| 4088009 | Acquired hydrocephalus |
| 40946000 | Hepatic coma due to viral hepatitis |
| 40980002 | Spastic paralysis due to birth injury |
| 410014007 | Communicating hydrocephalus following traumatic injury |
| 410015008 | Obstructive hydrocephalus following traumatic injury |
| 410057002 | Hereditary AND/OR degenerative disease of central nervous system |
| 41040004 | Complete trisomy 21 syndrome |
| 4113009 | Arrested hydrocephalus |
| 41142009 | Globoid cell leukodystrophy, late-onset |
| 41283003 | Cerebro-oculo-facio-skeletal syndrome |
| 413101007 | Stress-induced epilepsy |
| 413102000 | Infarction of basal ganglia |
| 413758000 | Cardioembolic stroke |
| 414667000 | Meningomyelocele |
| 414927004 | Ocular myasthenia with strabismus |
| 415713009 | Thoracic hydromeningocele |
| 41574007 | Paramyotonia congenita |
| 41590007 | Familial amyloid polyneuropathy, Jewish type |
| 416780008 | Primary degenerative dementia of the Alzheimer type, presenile onset |
| 416792008 | Vein of Galen malformation |
| 416975007 | Primary degenerative dementia of the Alzheimer type, senile onset |
| 417017003 | Acute cerebellar syndrome |
| 41713005 | Benedikt's syndrome |
| 418143002 | Cerebral degeneration |
| 4183003 | Charcot-Marie-Tooth disease, type IC |
| 418856006 | Paraneoplastic optic neuropathy |
| 42012007 | Neuronal ceroid lipofuscinosis |
| 420146005 | Cerebral degeneration associated with generalized lipidosis |
| 420244003 | Encephalitis with acquired immunodeficiency syndrome |
| 420452002 | Myelopathy with acquired immunodeficiency syndrome |
| 420554003 | Progressive multifocal leukoencephalopathy with acquired immunodeficiency syndrome |
| 420614009 | Organic dementia with acquired immunodeficiency syndrome |
| 420675003 | Supranuclear gaze palsy |
| 420718004 | Central nervous system demyelinating disease with acquired immunodeficiency syndrome |
| 420774007 | Organic brain syndrome with acquired immunodeficiency syndrome |
| 420788006 | Intraocular non-Hodgkin malignant lymphoma |
| 421023003 | Presenile dementia with acquired immunodeficiency syndrome |
| 421283008 | Primary lymphoma of brain with acquired immunodeficiency syndrome |
| 421315006 | Myelitis with acquired immunodeficiency syndrome |
| 421415007 | Subacute adenoviral encephalitis with acquired immunodeficiency syndrome |
| 421529006 | Dementia with acquired immunodeficiency syndrome |
| 421827003 | Encephalopathy with acquired immunodeficiency syndrome |
| 421998001 | Central nervous disorder with acquired immunodeficiency syndrome |
| 422089004 | Encephalomyelitis with acquired immunodeficiency syndrome |
| 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 |
| 423144007 | Multifactorial encephalopathy |
| 42365007 | Atonic seizure |
| 42369001 | Pallidopontonigral degeneration |
| 423771003 | Acquired neuromuscular ptosis |
| 424099008 | Hepatic coma due to acute hepatitis B |
| 424151006 | Anaplastic glioma of brain |
| 424276002 | Malignant glioma of brainstem |
| 42429001 | Cerebromeningeal hemorrhage |
| 424334007 | Malignant tumor of spinal cord, intramedullary |
| 424340000 | Hepatic coma due to chronic hepatitis B |
| 424549003 | Malignant tumor of spinal cord, extramedullary |
| 424761009 | Paraneoplastic encephalomyelitis |
| 424795008 | Non dystrophic myotonia |
| 425054007 | Refractory occipital lobe epilepsy |
| 425219008 | Progressive spinal ataxia |
| 425237009 | Refractory frontal lobe epilepsy |
| 425349008 | Refractory parietal lobe epilepsy |
| 425390006 | Dementia associated with Parkinson's Disease |
| 425420004 | Thrombosis of internal carotid artery |
| 425500002 | Secondary progressive multiple sclerosis |
| 425522009 | Hyperammonemic encephalopathy |
| 425687007 | Spina bifida aperta of cervical spine |
| 425882004 | Paralytic syndrome as late effect of stroke |
| 425919003 | Chronic organic mental disorder |
| 425932008 | Thrombosis of posterior communicating artery |
| 425957003 | Non-traumatic intracerebral ventricular hemorrhage |
| 426033005 | Dysphagia as a late effect of cerebrovascular accident |
| 426107000 | Acute lacunar infarction |
| 4262001 | Phlebitis of superior sagittal sinus |
| 426373005 | Relapsing remitting multiple sclerosis |
| 426651005 | Occlusion of bilateral carotid arteries |
| 426788002 | Vertigo as late effect of stroke |
| 426814001 | Transient cerebral ischemia due to atrial fibrillation |
| 426983002 | Infarction of medulla oblongata |
| 427020007 | Cerebral vasculitis |
| 427216002 | Spina bifida aperta of thoracic spine |
| 427296003 | Thalamic infarction |
| 427432001 | Paralytic syndrome as late effect of thalamic stroke |
| 42769004 | Diffuse Lewy body disease with spongiform cortical change |
| 427943001 | Ophthalmoplegia due to diabetes mellitus |
| 428061005 | Malignant neoplasm of brain |
| 428241007 | Ventricular hemorrhage of fetus |
| 428700003 | Primary progressive multiple sclerosis |
| 429033009 | Malignant neoplasm of cerebrum |
| 429458009 | Dementia due to Creutzfeldt Jakob disease |
| 429466000 | Spina bifida aperta of lumbar spine |
| 42970005 | Nonpyogenic thrombosis of intracranial venous sinus |
| 42986003 | Charcot-Marie-Tooth disease, type IB |
| 429998004 | Vascular dementia |
| 430947007 | Paralytic syndrome of nondominant side as late effect of stroke |
| 430959006 | Paralytic syndrome of dominant side as late effect of stroke |
| 43100002 | Late cortical cerebellar atrophy |
| 431266005 | Intraparenchymal hematoma of brain |
| 431421000124103 | Arteriosclerosis of carotid artery |
| 432249006 | Infarction of spinal cord |
| 432504007 | Cerebral infarction |
| 432616009 | Infection of ventriculoperitoneal shunt |
| 433183000 | Neurogenic bladder as late effect of cerebrovascular accident |
| 434541000124109 | Benign childhood epilepsy with centrotemporal spikes, refractory |
| 434551000124106 | Benign childhood epilepsy with centrotemporal spikes, non-refractory |
| 43486001 | Hemiplegic cerebral palsy |
| 43532007 | Hereditary oculoleptomeningeal amyloid angiopathy |
| 43647007 | Juvenile paralysis agitans of Hunt |
| 43658003 | Vertebral artery obstruction |
| 438156004 | Anoxic epileptic seizure |
| 438511000 | Benign multiple sclerosis |
| 438513002 | Cerebral degeneration due to Parkinson's disease |
| 439567002 | Malignant multiple sclerosis |
| 43977004 | Corticostriatal-spinal degeneration |
| 44145005 | Benign Rolandic epilepsy |
| 441526008 | Infarct of cerebrum due to iatrogenic cerebrovascular accident |
| 441529001 | Dysphasia as late effect of cerebrovascular disease |
| 441630004 | Aphasia as late effect of cerebrovascular disease |
| 441678004 | Refractory generalized nonconvulsive epilepsy |
| 441688003 | Incomplete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra |
| 441705005 | Complete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra |
| 441717007 | Hemiplegia of nondominant side |
| 441722007 | Spastic hemiplegia of nondominant side |
| 441735003 | Sensory disorder as a late effect of cerebrovascular disease |
| 441759008 | Abnormal vision as a late effect of cerebrovascular disease |
| 441794001 | Incomplete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra |
| 441892008 | Spastic hemiplegia of dominant side |
| 441960006 | Speech and language deficit as late effect of cerebrovascular accident |
| 441980007 | Complete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra |
| 441991000 | Hemiparesis as late effect of cerebrovascular accident |
| 442020005 | Flaccid hemiplegia of dominant side |
| 442024001 | Hemiplegia as late effect of cerebrovascular disease |
| 442077006 | Flaccid hemiplegia of nondominant side |
| 442155009 | Hemiplegia of dominant side |
| 442212003 | Residual cognitive deficit as late effect of cerebrovascular accident |
| 442300000 | Rhombencephalosynapsis |
| 442344002 | Dementia due to Huntington chorea |
| 442481002 | Epilepsy characterized by intractable complex partial seizures |
| 442511009 | Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome |
| 442512002 | Nonconvulsive status epilepticus |
| 442617003 | Aphasia as late effect of cerebrovascular accident |
| 442668000 | Hemiplegia of nondominant side as late effect of cerebrovascular disease |
| 442676003 | Hemiplegia of dominant side as late effect of cerebrovascular disease |
| 442733008 | Hemiplegia as late effect of cerebrovascular accident |
| 443153007 | Inflammation of brain and spinal cord caused by toxic substance |
| 443333004 | Medulloblastoma |
| 44359008 | Metachromatic leukodystrophy, juvenile type |
| 443929000 | Small vessel cerebrovascular disease |
| 44395000 | Spastic tetraplegia with rigidity syndrome |
| 444024002 | Multiple system atrophy, cerebellar variant |
| 444172003 | Recurrent transient cerebral ischemic attack |
| 444197004 | Multiple system atrophy, Parkinson variant |
| 444657001 | Superior cerebellar artery syndrome |
| 444860006 | Meningomyelocele of lumbosacral spine |
| 444980006 | Sporadic olivopontocerebellar atrophy |
| 445095002 | Epileptic seizure witnessed by provider of history other than subject |
| 445109004 | Isolation of left common carotid artery |
| 445116003 | Encephalocele of vertex |
| 445166009 | Cystic degeneration of brain |
| 445252005 | Glucose transporter protein type 1 deficiency syndrome |
| 445349004 | Isolation of right common carotid artery |
| 445355009 | Refractory epilepsy |
| 445423005 | Paraneoplastic subacute necrotic myelopathy |
| 445475001 | Paraneoplastic sensorimotor neuropathy |
| 4463009 | Familial amyloid polyneuropathy, type II |
| 446311006 | Acute bulbar poliomyelitis caused by Human poliovirus 2 |
| 446712002 | Thromboembolus of precerebral artery |
| 446957000 | Acute bulbar poliomyelitis caused by Human poliovirus 1 |
| 446958005 | Acute paralytic poliomyelitis caused by Human poliovirus 1 |
| 447262002 | Acute paralytic poliomyelitis caused by Human poliovirus 2 |
| 447292006 | Mitochondrial encephalomyopathy |
| 447351004 | Vanishing white matter disease |
| 447378002 | Acute paralytic poliomyelitis caused by Human poliovirus 3 |
| 4477007 | Juvenile myopathy AND lactate acidosis |
| 448045004 | Fragile X associated tremor ataxia syndrome |
| 448054001 | Adult onset autosomal dominant leukodystrophy |
| 448218008 | Malignant neoplasm of cerebellopontine angle |
| 448227009 | X-linked periventricular heterotopia |
| 448248006 | Malignant neoplasm of axial suprasellar region of brain |
| 448250003 | Malignant teratoma of pineal region |
| 448254007 | Non-Hodgkin's lymphoma of central nervous system |
| 448314007 | Malignant epithelial neoplasm of spinal cord |
| 448863000 | Malignant epithelial neoplasm of pineal gland |
| 448989001 | Malignant epithelial neoplasm of brain |
| 448995000 | Follicular non-Hodgkin's lymphoma of central nervous system |
| 449020009 | Intraparenchymal hemorrhage of brain |
| 449221001 | Diffuse non-Hodgkin's lymphoma of central nervous system |
| 449253005 | Malignant epithelial neoplasm of hypothalamus |
| 449305009 | Paraneoplastic sensory neuropathy |
| 449420002 | Malignant neoplasm of cerebellum |
| 449901005 | Hepatic encephalopathy in fulminant hepatic failure |
| 449902003 | Portal systemic encephalopathy |
| 449903008 | Dural arteriovenous fistula of spinal cord |
| 450886002 | Posterior reversible encephalopathy syndrome |
| 451037005 | Hemorrhage in globus pallidus |
| 451038000 | Hemorrhage in caudate nucleus |
| 451039008 | Hemorrhage in putamen |
| 45163000 | Congenital pontocerebellar hypoplasia |
| 45502001 | Cerebrovascular amyloidosis |
| 45639009 | Hereditary cerebral amyloid angiopathy, Icelandic type |
| 45740001 | Diencephalic syndrome of infancy |
| 45814002 | Birnbaum's syndrome |
| 45853006 | Roussy-Lévy syndrome |
| 45864009 | Senile degeneration of brain |
| 45897005 | Jervis' syndrome |
| 460307002 | Systemic to pulmonary collateral artery from right carotid artery |
| 460312001 | Systemic to pulmonary collateral artery from left carotid artery |
| 460880006 | Arteriovenous fistula of great cerebral vein of Galen |
| 460890003 | Anomalous common origin of brachiocephalic artery and left common carotid artery |
| 460899002 | Anomalous origin of left common carotid artery from brachiocephalic artery |
| 461326001 | Anomalous separate origins of internal carotid arteries and external carotid arteries from single aortic arch |
| 46251005 | Corticospinal motor disease |
| 46421000119102 | Behavior disorder as sequela of cerebral infarction |
| 4645000 | Senile brain amyloidosis |
| 46659004 | Von Hippel-Lindau syndrome |
| 46804001 | Severe X-linked myotubular myopathy |
| 46808003 | Marie's cerebellar ataxia |
| 46826000 | Rheumatic chorea |
| 47032000 | Congenital hydrocephalus |
| 472320005 | Maternally inherited mitochondrial cardiomyopathy and myopathy |
| 472746006 | Cerebrovascular disorder due to paradoxical embolus |
| 472916000 | Toxic metabolic encephalopathy |
| 47391000119107 | Primary generalized absence epilepsy |
| 47683004 | Metachromatic leukodystrophy, late infantile type |
| 48163001 | Triparesis |
| 4817008 | Primary degenerative dementia of the Alzheimer type, senile onset, with delirium |
| 48248005 | Thrombophlebitis of inferior sagittal sinus |
| 48522003 | Spinal cord disorder |
| 48601000119107 | Paralytic syndrome on one side of the body as effect of cerebrovascular accident |
| 48601002 | Thrombosis of precerebral artery |
| 48662007 | Cerebral paraplegia |
| 48721008 | Quadriplegic cerebral palsy |
| 49049000 | Parkinson's disease |
| 49422009 | Cortical hemorrhage |
| 49562005 | Adult chronic GM2 gangliosidosis |
| 496369931000119104 | Cerebrovascular accident due to thrombosis of right cerebellar artery |
| 49692006 | Schilder's disease |
| 49776008 | Centrencephalic epilepsy |
| 49793008 | Hereditary motor neuron disease |
| 50122000 | Metabolic encephalopathy |
| 50429003 | Congenital stenosis of aqueduct of Sylvius |
| 50582007 | Hemiplegia |
| 508171000000105 | Severe learning disability |
| 50866000 | Childhood absence epilepsy |
| 509341000000107 | Petit-mal epilepsy |
| 50967008 | Gangliosidosis |
| 5102002 | Agenesis of corpus callosum |
| 511452481000119102 | Cerebrovascular accident due to thrombosis of right vertebral artery |
| 5134006 | Familial amyloid polyneuropathy, type VI |
| 51399001 | Toxic encephalopathy caused by lead |
| 51500006 | Complete trisomy 18 syndrome |
| 517253051000119105 | Cerebrovascular accident due to embolism of left vertebral artery |
| 51887003 | Tonic seizure |
| 51928006 | General paresis - neurosyphilis |
| 51984006 | Dysmorphic sialidosis, infantile form |
| 52165006 | Niemann-Pick disease, type A |
| 52186006 | Dysmorphic sialidosis |
| 52201006 | Internal capsule hemorrhage |
| 52330001 | Meningoencephalocele |
| 52448006 | Dementia |
| 52522001 | Degenerative brain disorder |
| 5262007 | Spinal muscular atrophy |
| 52677002 | Deficiency of N-acetylgalactosamine-4-sulfatase |
| 52713000 | Infantile neuroaxonal dystrophy |
| 53318002 | Spina bifida with hydrocephalus |
| 53633000 | Peutz-Jeghers polyps of small bowel |
| 53776005 | Encephalocystocele |
| 53857003 | Heredofamilial brachial plexus paralysis syndrome |
| 54099005 | Diplegia of upper limbs |
| 54200006 | Tonic-clonic seizure |
| 54265003 | Congenital anomaly of cerebral artery |
| 54280009 | Kugelberg-Welander disease |
| 54304004 | Progressive bulbar palsy |
| 54411001 | Peutz-Jeghers syndrome |
| 54502004 | Primary degenerative dementia of the Alzheimer type, presenile onset, with delusions |
| 54519002 | Basilar artery stenosis |
| 54794009 | Ectopic gray matter in centrum ovale |
| 54954004 | Aspartylglucosaminuria |
| 55009008 | Primary degenerative dementia of the Alzheimer type, senile onset, with delusions |
| 55016009 | Congenital muscular hypertrophy-cerebral syndrome |
| 55051001 | Myasthenia gravis, juvenile form |
| 55382008 | Cerebral atherosclerosis |
| 55623006 | Toxic encephalopathy caused by mercury |
| 55637002 | Spinal hemiplegia |
| 55709000 | Ethmocephalus |
| 5571000124103 | Cerebrovascular accident with intracranial hemorrhage |
| 55734000 | Endophlebitis of basilar sinus |
| 55999004 | Encephalocele |
| 56155002 | Hemispheric cerebral agenesis |
| 56267009 | Multi-infarct dementia |
| 56384000 | Embolism of inferior sagittal sinus |
| 56453003 | Hereditary cerebral amyloid angiopathy, Dutch type |
| 56989000 | Eaton-Lambert syndrome |
| 57803009 | Rheumatic chorea with heart involvement |
| 57917004 | Seckel syndrome |
| 57938005 | Congenital myotonia, autosomal dominant form |
| 57981008 | Progressing stroke |
| 58173271000119101 | Cerebrovascular accident due to embolism of bilateral cerebellar arteries |
| 58193001 | Diplegic cerebral palsy |
| 5822000 | Athetosis with spastic paraplegia |
| 58258004 | Infantile neuronal ceroid lipofuscinosis |
| 58263000 | Maroteaux-Lamy syndrome, severe form |
| 58459009 | Sphingomyelin/cholesterol lipidosis |
| 58557008 | Spina bifida aperta |
| 58756001 | Huntington's chorea |
| 58795000 | Distal muscular dystrophy |
| 590005 | Congenital aneurysm of anterior communicating artery |
| 59103002 | Cerebral paralysis with homolateral ataxia |
| 59178007 | Menkes kinky-hair syndrome |
| 595899961000119100 | Cerebrovascular accident of basal ganglia |
| 5963005 | Subacute neuronopathic Gaucher's disease |
| 59636002 | Pelizaeus-Merzbacher disease, connatal variant |
| 59651006 | Sedative, hypnotic AND/OR anxiolytic-induced persisting dementia |
| 60146005 | Bailey-Cushing syndrome |
| 60192008 | Lethal multiple pterygium syndrome |
| 60389000 | Paraplegia |
| 60576007 | Subacute combined degeneration of spinal cord |
| 60706008 | Phlebitis of torcular Herophili |
| 608874000 | Eaton Lambert syndrome with underlying malignancy |
| 60935008 | Paramyoclonus multiplex |
| 609553000 | Paralytic syndrome of bilateral lower limbs |
| 609554006 | Paralytic syndrome of all four limbs |
| 609557004 | Paralytic syndrome on one side of the body |
| 61091005 | Aneurysm of external carotid artery |
| 61165007 | Hereditary nephrogenic diabetes insipidus |
| 6118003 | Demyelinating disease of central nervous system |
| 61200008 | Pallidonigroluysian degeneration |
| 61663001 | Juvenile neuronal ceroid lipofuscinosis |
| 61687004 | Endophlebitis of inferior sagittal sinus |
| 61819007 | Rachischisis |
| 62009002 | Adult neuronal ceroid lipofuscinosis |
| 6204001 | Juvenile myoclonic epilepsy |
| 6208003 | Clonic seizure |
| 62158001 | Status marmoratus |
| 62239001 | Parkinson-dementia complex of Guam |
| 62440002 | Infantile GM2 gangliosidosis |
| 62702001 | Cerebral vein occlusion |
| 62914000 | Cerebrovascular disease |
| 62985007 | Hereditary insensitivity to pain with anhidrosis |
| 63081009 | Acute infarction of spinal cord |
| 63135006 | Amyotonia congenita |
| 64009001 | Basilar artery syndrome |
| 64383006 | Werdnig-Hoffmann disease |
| 64586002 | Carotid artery stenosis |
| 64624009 | Hypoglycemic encephalopathy |
| 6475002 | Primary degenerative dementia of the Alzheimer type, presenile onset, uncomplicated |
| 64764001 | Acute paralytic poliomyelitis, bulbar |
| 64775002 | Vertebral artery thrombosis |
| 6481005 | Diplegia |
| 64855000 | Pelizaeus-Merzbacher disease |
| 65017003 | Hereditary peripheral neuropathy |
| 65084004 | Vertebral artery embolism |
| 65096006 | Primary degenerative dementia of the Alzheimer type, presenile onset, with delirium |
| 65120008 | Generalized convulsive epilepsy |
| 65144005 | Congenital spinal meningocele |
| 652287331000119104 | Cerebrovascular accident of brainstem |
| 65312002 | Cerebral arteriosclerosis |
| 65433005 | Mechanical complication of ventricular communicating shunt |
| 65455002 | Nasal encephalocele |
| 655081461000119101 | Cerebrovascular accident due to occlusion of right anterior cerebral artery |
| 65587001 | Congenital anomaly of cerebrovascular system |
| 65764006 | Pseudo-Hurler polydystrophy |
| 6594005 | Cerebrovascular disorder in the puerperium |
| 66010009 | Supranuclear paralysis |
| 66108005 | Primary degenerative dementia of the Alzheimer type, senile onset, uncomplicated |
| 66521008 | Deficiency of cerebroside-sulfatase |
| 66751000 | Niemann-Pick disease, type C |
| 66881004 | Choreoacanthocytosis |
| 67155006 | Gerstmann-Straussler-Scheinker syndrome |
| 672441000119103 | Hemiplegia of nondominant side due to and following ischemic cerebrovascular accident |
| 672461000119104 | Hemiplegia of dominant side due to and following ischemic cerebrovascular accident |
| 672501000119104 | Dysarthria due to and following ischemic cerebrovascular accident |
| 672511000119101 | Dysarthria due to and following hemorrhagic cerebrovascular accident |
| 672521000119108 | Dysphasia due to and following ischemic cerebrovascular accident |
| 672531000119106 | Dysphasia due to and following hemorrhagic cerebrovascular accident |
| 672541000119102 | Aphasia due to and following ischemic cerebrovascular accident |
| 672551000119100 | Aphasia due to and following hemorrhagic cerebrovascular accident |
| 672561000119103 | Cognitive deficit due to and following ischemic cerebrovascular accident |
| 672571000119109 | Cognitive deficit due to and following hemorrhagic cerebrovascular accident |
| 6729006 | Cerebral-retinal arteriovenous aneurysm |
| 674091000119108 | Vertigo due to and following ischemic cerebrovascular accident |
| 674111000119100 | Ataxia due to and following ischemic cerebrovascular accident |
| 674121000119107 | Ataxia due to and following hemorrhagic cerebrovascular accident |
| 674361000119104 | Apraxia due to and following ischemic cerebrovascular accident |
| 674381000119108 | Weakness of facial muscle due to and following ischemic cerebrovascular accident |
| 674391000119106 | Speech and language deficit due to and following hemorrhagic cerebrovascular accident |
| 674401000119108 | Speech and language deficit due to and following ischemic cerebrovascular accident |
| 67761004 | Olivopontocerebellar degeneration |
| 67854007 | Maroteaux-Lamy syndrome, mild form |
| 67855008 | Niemann-Pick disease, type C, subacute form |
| 67876003 | Congenital obstruction of aqueduct of Sylvius |
| 67992007 | Multiple AND bilateral precerebral artery obstruction |
| 6807001 | Central pontine myelinolysis |
| 68107009 | Cerebral paresis with homolateral ataxia |
| 68116008 | Dentatorubropallidoluysian degeneration |
| 68186003 | Congenital myopathy with abnormal subcellular organelles |
| 682221000119103 | Primary anaplastic astrocytoma of cerebrum |
| 682231000119100 | Primary anaplastic astrocytoma of frontal lobe |
| 682241000119109 | Primary anaplastic astrocytoma of occipital lobe |
| 682251000119106 | Primary anaplastic astrocytoma of parietal lobe |
| 682261000119108 | Primary anaplastic astrocytoma of temporal lobe |
| 682441000119105 | Primary astrocytoma of cerebral ventricle |
| 682451000119107 | Primary astrocytoma of frontal lobe |
| 682461000119109 | Primary astrocytoma of occipital lobe |
| 682471000119103 | Primary astrocytoma of parietal lobe |
| 682481000119100 | Primary astrocytoma of temporal lobe |
| 683761000119107 | Primary ependymoma of brain ventricle |
| 683791000119100 | Primary ependymoma of parietal lobe |
| 68390005 | Sphingolipid activator protein 1 deficiency |
| 684901000119107 | Primary glioblastoma multiforme of cerebrum |
| 684911000119105 | Primary glioblastoma multiforme of frontal lobe |
| 684921000119103 | Primary glioblastoma multiforme of occipital lobe |
| 684931000119100 | Primary glioblastoma multiforme of parietal lobe |
| 684941000119109 | Primary glioblastoma multiforme of temporal lobe |
| 68504005 | Ataxia-telangiectasia syndrome |
| 68618008 | Rett's disorder |
| 686431000119100 | Primary malignant glioma of frontal lobe |
| 686441000119109 | Primary malignant glioma of occipital lobe |
| 686451000119106 | Primary malignant glioma of parietal lobe |
| 686461000119108 | Primary malignant glioma of temporal lobe |
| 687331000119109 | Primary oligodendroglioma of frontal lobe |
| 687351000119103 | Primary oligodendroglioma of parietal lobe |
| 687361000119101 | Primary oligodendroglioma of temporal lobe |
| 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 |
| 69463008 | Maroteaux-Lamy syndrome |
| 69482004 | Korsakoff's psychosis |
| 69798007 | Carotid artery obstruction |
| 698021005 | Autosomal dominant nocturnal frontal lobe epilepsy |
| 698279003 | X-linked dystonia parkinsonism |
| 698291007 | Acute paraplegia |
| 698292000 | Chronic paraplegia |
| 698363002 | Postoperative thromboembolus of precerebral artery |
| 698624003 | Dementia associated with cerebral lipidosis |
| 698625002 | Dementia associated with normal pressure hydrocephalus |
| 698626001 | Dementia associated with multiple sclerosis |
| 698687007 | Post-traumatic dementia with behavioral change |
| 698725008 | Dementia associated with neurosyphilis |
| 698726009 | Dementia associated with viral encephalitis |
| 698736001 | Postoperative communicating hydrocephalus |
| 698737005 | Obstructive hydrocephalus due to and following meningitis |
| 698741009 | Acute complete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra |
| 698742002 | Chronic incomplete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra |
| 698743007 | Acute complete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra |
| 698744001 | Chronic incomplete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra |
| 698754002 | Chronic paralysis due to lesion of spinal cord |
| 698755001 | Acute paralysis due to lesion of spinal cord |
| 698760002 | Generalized non-convulsive absence epilepsy |
| 698761003 | Refractory juvenile myoclonic epilepsy |
| 698762005 | Refractory myoclonic epilepsy |
| 698763000 | Postoperative status epilepticus |
| 698764006 | Post infectious grand mal epilepsy |
| 698767004 | Post-cerebrovascular accident epilepsy |
| 698781002 | Dementia associated with cerebral anoxia |
| 698846009 | Tibial muscular dystrophy |
| 698870008 | 2-hydroxyglutaric aciduria |
| 698948009 | Vascular dementia in remission |
| 698949001 | Dementia in remission |
| 698954005 | Primary degenerative dementia of the Alzheimer type, senile onset in remission |
| 698955006 | Primary degenerative dementia of the Alzheimer type, presenile onset in remission |
| 698999002 | Congenital atresia of aqueduct of Sylvius |
| 699184009 | Perry syndrome |
| 699190008 | Paroxysmal extreme pain disorder |
| 699299001 | Neuroferritinopathy |
| 699318007 | Supratentorial primitive neuroectodermal tumor |
| 699328003 | Myoclonic epilepsy myopathy sensory ataxia |
| 699688008 | Generalized epilepsy with febrile seizures plus |
| 699704002 | Classic medulloblastoma |
| 699706000 | Embolism of middle cerebral artery |
| 699866005 | Progressive bulbar palsy with sensorineural deafness |
| 700063005 | Megalencephaly capillary malformation |
| 700150001 | Congenital leptin deficiency |
| 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 |
| 702349003 | Actin accumulation myopathy |
| 702354007 | X-linked intellectual developmental disorder Christianson type |
| 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 |
| 702426001 | GRN-related frontotemporal dementia |
| 702427005 | Hereditary diffuse leukoencephalopathy with spheroids |
| 702429008 | Frontotemporal dementia with parkinsonism-17 |
| 702433001 | Congenital cataracts, facial dysmorphism and neuropathy |
| 702437000 | Amish lethal microcephaly |
| 702439002 | Agenesis of corpus callosum with peripheral neuropathy |
| 702441001 | Fatal X-linked ataxia with deafness and loss of vision |
| 702442008 | Ataxia with vitamin E deficiency |
| 702445005 | Autosomal recessive spastic ataxia of Charlevoix-Saguenay |
| 702448007 | Dystonia 6 |
| 702450004 | FOXG1 syndrome |
| 702463005 | Paralytic syndrome of two limbs |
| 702464004 | Paralytic syndrome of three limbs |
| 702465003 | Paralytic syndrome on both sides of the body |
| 702575003 | Retinocochleocerebral vasculopathy |
| 702611008 | Congenital brain aplasia |
| 703156006 | Deep hemispheric cerebral hemorrhage |
| 703163006 | Secondary cerebrovascular disease |
| 703166003 | Dural arteriovenous fistula |
| 703176000 | Ruptured aneurysm of vertebral artery |
| 703180005 | Asymptomatic occlusion of extracranial carotid artery |
| 703184001 | Asymptomatic occlusion of intracranial carotid artery |
| 703205008 | Asymptomatic occlusion of posterior cerebral artery |
| 703206009 | Asymptomatic occlusion of basilar artery |
| 703207000 | Asymptomatic occlusion of anterior cerebral artery |
| 703208005 | Asymptomatic occlusion of middle cerebral artery |
| 703218000 | Cerebral vasoconstriction syndrome |
| 703219008 | Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy |
| 703221003 | Congenital intracranial vascular malformation |
| 703226008 | Familial cerebral saccular aneurysm |
| 703266007 | Cerebrofacial arteriovenous metameric syndrome |
| 703267003 | Cerebrofacial arteriovenous metameric syndrome type 1 |
| 703268008 | Cerebrofacial arteriovenous metameric syndrome type 3 |
| 703300001 | Hypoxic ischemic encephalopathy |
| 7033004 | Absence status epilepticus |
| 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 |
| 703527003 | TK2-related mitochondrial deoxyribonucleic acid depletion syndrome myopathic form |
| 703535000 | Mowat-Wilson syndrome |
| 703536004 | Megalencephalic leukoencephalopathy with subcortical cysts |
| 703537008 | Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation |
| 703542000 | Retinal detachment and occipital encephalocele |
| 703543005 | Infantile ascending hereditary spastic paralysis |
| 703544004 | Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia |
| 705066004 | Dissection of internal carotid artery |
| 705128004 | Cerebral infarction due to embolism of middle cerebral artery |
| 705129007 | Thrombosis of middle cerebral artery |
| 705130002 | Cerebral infarction due to thrombosis of middle cerebral artery |
| 70528007 | Mucolipidosis |
| 70607008 | Thrombosis of superior sagittal sinus |
| 70611002 | Perinatal intraventricular hemorrhage |
| 709281006 | Rippling muscle disease |
| 70936005 | Multi-infarct dementia, uncomplicated |
| 709415008 | Mitochondrial membrane protein associated neurodegeneration |
| 710046001 | Refractory idiopathic generalized epilepsy |
| 710575003 | Transient ischemic attack due to embolism |
| 711151004 | Hypomagnesemia with secondary hypocalcemia |
| 711158005 | Spinocerebellar ataxia type 36 |
| 711403001 | Cerebral folate transport deficiency |
| 711406009 | Autosomal recessive axonal neuropathy with neuromyotonia |
| 711409002 | 3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome |
| 711482008 | Cerebroretinal microangiopathy with calcifications and cysts |
| 711483003 | Spinal muscular atrophy with respiratory distress type 1 |
| 71253000 | Tay-Sachs disease, variant AB |
| 712637001 | Ribonucleic acid polymerase III-related leukodystrophy |
| 713035000 | Dissection of precerebral artery |
| 713060000 | Sporadic Creutzfeldt-Jakob disease |
| 713081000 | Dissection of cerebral artery |
| 713265001 | Nontraumatic ruptured cerebral aneurysm |
| 713325002 | Primary cerebral lymphoma co-occurrent with human immunodeficiency virus infection |
| 713327005 | Malignant meningioma of meninges of brain |
| 713401006 | Combined D-2-hydroxyglutaric aciduria and L-2-hydroxyglutaric aciduria |
| 713425003 | Spinal cord compression due to metastasis to spine |
| 713487008 | Progressive multifocal leukoencephalopathy co-occurrent with human immunodeficiency virus infection |
| 713488003 | Presenile dementia co-occurrent with human immunodeficiency virus infection |
| 713543002 | Demyelinating disease of central nervous system co-occurrent with human immunodeficiency virus infection |
| 713844000 | Dementia co-occurrent with human immunodeficiency virus infection |
| 71444005 | Cerebral arterial thrombosis |
| 715317001 | Proximal myotonic myopathy |
| 715338007 | Fatal infantile lactic acidosis co-occurrent with methylmalonic aciduria |
| 715340002 | Autosomal recessive limb girdle muscular dystrophy type 2D |
| 715341003 | Autosomal recessive limb girdle muscular dystrophy type 2A |
| 715344006 | Neurofibromatosis Noonan syndrome |
| 715345007 | Young onset Parkinson disease |
| 715366004 | Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 |
| 715369006 | Autosomal recessive cerebelloparenchymal disorder type 3 |
| 715371006 | Cerebellar ataxia co-occurrent with ectodermal dysplasia |
| 715406003 | Isolated lissencephaly type 1 without known genetic defect |
| 715415005 | Richards-Rundle syndrome |
| 715419004 | Lethal congenital contracture syndrome type 2 |
| 715422002 | Craniotelencephalic dysplasia |
| 715429006 | Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome |
| 715434005 | Holoprosencephaly craniosynostosis syndrome |
| 715436007 | Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration |
| 715462003 | Microcephalus co-occurrent with cervical spine fusion anomaly |
| 715463008 | Congenital pontocerebellar hypoplasia type 2 |
| 715464002 | Microcephalus microcornea syndrome of Seemanova type |
| 715465001 | Spinocerebellar degeneration co-occurrent with macular corneal dystrophy |
| 715482004 | Microcephalic primordial dwarfism of Toriello type |
| 715483009 | Olivopontocerebellar atrophy co-occurrent with sensorineural hearing loss |
| 715491000 | Autosomal recessive spastic paraplegia type 11 |
| 715504003 | Spastic paraparesis co-occurrent with deafness |
| 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 |
| 715629001 | Generalized epilepsy and paroxysmal dyskinesia syndrome |
| 715645004 | Hereditary thermosensitive neuropathy |
| 715646003 | Desmin related myopathy with Mallory body-like inclusions |
| 715662009 | Iatrogenic Jakob-Creutzfeldt disease |
| 715665006 | Hereditary motor and sensory neuropathy Okinawa type |
| 715666007 | Charcot-Marie-Tooth disease type IE |
| 715726000 | Spinocerebellar ataxia type 7 |
| 715737004 | Parkinsonism co-occurrent with dementia of Guadeloupe |
| 715748006 | Spinocerebellar ataxia type 1 |
| 715751004 | Spinocerebellar ataxia type 2 |
| 715752006 | Spinocerebellar ataxia type 6 |
| 715753001 | Spinocerebellar ataxia type 8 |
| 715754007 | Spinocerebellar ataxia type 10 |
| 715755008 | Spinocerebellar ataxia type 4 |
| 715768000 | Autosomal dominant dopa responsive dystonia |
| 715776003 | Spastic paraplegia type 7 |
| 715777007 | Primary dystonia type 2 |
| 715780008 | Lissencephaly type 1 due to doublecortin gene mutation |
| 715794009 | Progressive encephalopathy with severe infantile anorexia |
| 715795005 | Charcot-Marie-Tooth disease type 4 |
| 715796006 | Charcot-Marie-Tooth disease type 4A |
| 715797002 | Charcot-Marie-Tooth disease type 4C |
| 715798007 | Charcot-Marie-Tooth disease type 4D |
| 715799004 | Charcot-Marie-Tooth disease type 4G |
| 715800000 | Charcot-Marie-Tooth disease type 4B2 |
| 715801001 | Charcot-Marie-Tooth disease type 4F |
| 715802008 | Charcot-Marie-Tooth disease type 4H |
| 715803003 | Charcot-Marie-Tooth disease type 4B1 |
| 715807002 | Familial Creutzfeldt-Jakob |
| 715817007 | Lissencephaly co-occurrent with congenital cerebellar hypoplasia |
| 715819005 | Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B |
| 715820004 | Lissencephaly co-occurrent with congenital cerebellar hypoplasia type C |
| 715821000 | Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D |
| 715822007 | Lissencephaly co-occurrent with congenital cerebellar hypoplasia type F |
| 715824008 | Spinocerebellar ataxia type 28 |
| 715825009 | Spinocerebellar ataxia type 29 |
| 715826005 | Spinocerebellar ataxia type 31 |
| 715827001 | Autosomal recessive dopa responsive dystonia |
| 715904005 | Pineal parenchymal tumor of intermediate differentiation |
| 715951007 | Acrocallosal syndrome |
| 715952000 | Waardenburg Shah syndrome |
| 715980003 | Encephalopathy due to sulfite oxidase deficiency |
| 715981004 | Autosomal recessive primary microcephaly |
| 715984007 | Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome |
| 715990006 | Agenesis of cerebellum and hydrocephalus syndrome |
| 716023007 | Prominent glabella with microcephaly and hypogenitalism syndrome |
| 716051003 | Cerebrovascular accident during surgery |
| 716091000 | Holoprosencephaly and postaxial polydactyly syndrome |
| 716107009 | Early onset parkinsonism and intellectual disability syndrome |
| 716108004 | Macrocephaly with spastic paraplegia and dysmorphism syndrome |
| 716112005 | Microcephaly with deafness and intellectual disability syndrome |
| 716169009 | Holoprosencephaly sequence with hypokinesia and congenital joint contracture syndrome |
| 716198008 | Growth delay with hydrocephalus and lung hypoplasia syndrome |
| 716200002 | Nephrogenic diabetes insipidus and intracranial calcification syndrome |
| 716233007 | Steinfeld syndrome |
| 716243005 | Deafness with malformation of ear and facial palsy syndrome |
| 716278005 | Jeavons syndrome |
| 716281000 | Primary progressive non fluent aphasia |
| 716335003 | Congenital suprabulbar paresis |
| 716380002 | Logopenic progressive aphasia |
| 716662004 | Autosomal dominant late onset Parkinson disease |
| 716664003 | Primary dystonia 21 |
| 716667005 | Right temporal atrophy variant frontotemporal dementia |
| 716696006 | Autosomal dominant centronuclear myopathy |
| 716706009 | Female restricted epilepsy with intellectual disability syndrome |
| 716724006 | Spinocerebellar ataxia type 15/16 |
| 716745004 | Livedo reticularis and cerebrovascular accident syndrome |
| 716994006 | Behavioral variant of frontotemporal dementia |
| 716996008 | Hypoplasia of corpus callosum, intellectual disability, adducted thumbs, spasticity, hydrocephalus syndrome |
| 716997004 | Joubert syndrome |
| 716998009 | Joubert syndrome with ocular defect |
| 716999001 | Joubert syndrome with renal defect |
| 717008005 | Autosomal dominant Charcot-Marie-Tooth disease type 2B |
| 717010007 | Autosomal dominant Charcot-Marie-Tooth disease type 2C |
| 717011006 | Autosomal dominant Charcot-Marie-Tooth disease type 2D |
| 717012004 | Autosomal dominant Charcot-Marie-Tooth disease type 2E |
| 717013009 | Autosomal dominant Charcot-Marie-Tooth disease type 2I |
| 717014003 | Autosomal dominant Charcot-Marie-Tooth disease type 2J |
| 717016001 | Autosomal dominant Charcot-Marie-Tooth disease type 2A1 |
| 717042001 | Pelizaeus Merzbacher like disease |
| 717052002 | Maternally inherited Leigh syndrome |
| 717054001 | Maternally inherited mitochondrial dystonia |
| 717185008 | Deficiency of leukotriene C4 synthase |
| 717223008 | X-linked epilepsy with learning disability and behavior disorder syndrome |
| 717225001 | Benign adult familial myoclonic epilepsy |
| 717266001 | Sensory ataxic neuropathy with dysarthria and ophthalmoparesis syndrome |
| 717276003 | Folinic acid responsive seizure syndrome |
| 717332007 | Cerebellar ataxia Cayman type |
| 717632002 | X-linked lissencephaly with agenesis of corpus callosum and genital anomaly syndrome |
| 71779008 | X-linked hydrocephalus syndrome |
| 717812000 | Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome |
| 717822006 | Goldberg Shprintzen megacolon syndrome |
| 717825008 | Hereditary sensory and autonomic neuropathy type 1B |
| 717826009 | Hereditary sensory and autonomic neuropathy with deafness and global delay |
| 717827000 | Hereditary sensory and autonomic neuropathy with spastic paraplegia |
| 717859007 | Hydrocephalus, cardiac malformation, dense bone syndrome |
| 717942003 | Brain dopamine-serotonin vesicular transport disease |
| 717943008 | Brain malformation, congenital heart disease, postaxial polydactyly syndrome |
| 717964007 | Juvenile primary lateral sclerosis |
| 717968005 | Melanoma and neural system tumor syndrome |
| 717977003 | Lissencephaly syndrome Norman Roberts type |
| 718103001 | Hereditary geniospasm |
| 718174008 | Infantile striatonigral degeneration |
| 718176005 | Autosomal recessive limb girdle muscular dystrophy type 2C |
| 718177001 | Autosomal recessive limb girdle muscular dystrophy type 2F |
| 718179003 | Autosomal recessive limb girdle muscular dystrophy type 2B |
| 718180000 | Autosomal recessive limb girdle muscular dystrophy type 2I |
| 718182008 | Combined pituitary hormone deficiency genetic form |
| 718210003 | Deficiency of monoamine oxidase A |
| 718212006 | Mitochondrial encephalocardiomyopathy due to transmembrane protein 70 mutation |
| 718214007 | Mitochondrial neurogastrointestinal encephalomyopathy syndrome |
| 718219002 | Congenital lactic acidosis Saguenay-Lac-Saint-Jean type |
| 718221007 | Behr syndrome |
| 71831005 | Symptomatic generalized epilepsy |
| 718551002 | Moyamoya disease with early onset achalasia |
| 718555006 | Juvenile amyotrophic lateral sclerosis |
| 718556007 | Cranio-cerebello-cardiac dysplasia syndrome |
| 718572004 | Bethlem myopathy |
| 718573009 | Achalasia microcephaly syndrome |
| 718576001 | Hydrocephalus with cleft palate and joint contracture syndrome |
| 718605009 | Congenital pontocerebellar hypoplasia type 7 |
| 718606005 | Congenital pontocerebellar hypoplasia type 6 |
| 718607001 | Congenital pontocerebellar hypoplasia type 5 |
| 718608006 | Congenital pontocerebellar hypoplasia type 4 |
| 718609003 | Congenital pontocerebellar hypoplasia type 3 |
| 718610008 | Congenital pontocerebellar hypoplasia type 1 |
| 718611007 | Congenital pontocerebellar hypoplasia type 8 |
| 718685006 | Orthostatic hypotension co-occurrent and due to Parkinson's disease |
| 718713000 | Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome |
| 718719001 | Lissencephaly type 3 familial fetal akinesia sequence syndrome |
| 718720007 | Lissencephaly type 3 metacarpal bone dysplasia syndrome |
| 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 |
| 718845002 | X-linked intellectual disability with ataxia and apraxia syndrome |
| 718847005 | X-linked neurodegenerative syndrome Hamel type |
| 718848000 | Fried syndrome |
| 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 |
| 719102004 | Congenital cataract with ataxia and deafness 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 |
| 719156006 | X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration 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 |
| 719249005 | Spinocerebellar ataxia type 17 |
| 719250005 | Spinocerebellar ataxia type 18 |
| 719251009 | Spinocerebellar ataxia type 19 |
| 719252002 | Spinocerebellar ataxia type 27 |
| 719253007 | Spinocerebellar ataxia type 30 |
| 719254001 | Spinocerebellar ataxia type 32 |
| 719255000 | Spinocerebellar ataxia type 34 |
| 719267003 | Progressive cavitating leukoencephalopathy |
| 719276005 | Primary dystonia type 4 |
| 719278006 | Primary dystonia type 13 |
| 719300001 | Spinocerebellar ataxia type 35 |
| 719301002 | Spinocerebellar ataxia type 37 |
| 719302009 | Spinocerebellar ataxia type 5 |
| 719377004 | Microcephalus with albinism and digital anomaly syndrome |
| 719378009 | Microcephalus with brachydactyly and kyphoscoliosis syndrome |
| 719379001 | Microcephalus with cardiac defect and lung malsegmentation syndrome |
| 719380003 | Microcephalus cardiomyopathy syndrome |
| 719394002 | Microcephalus cleft palate syndrome |
| 719395001 | Microcephalus facio-cardio-skeletal syndrome Hadziselimovic type |
| 719403003 | Leukoencephalopathy co-occurrent with bilateral anterior temporal lobe cysts |
| 719405005 | Leukoencephalopathy with metaphyseal chondrodysplasia syndrome |
| 719510006 | Autosomal dominant Charcot-Marie-Tooth disease type 2F |
| 719511005 | Autosomal dominant Charcot-Marie-Tooth disease type 2G |
| 719512003 | Autosomal dominant Charcot-Marie-Tooth disease type 2K |
| 719513008 | Autosomal dominant Charcot-Marie-Tooth disease type 2L |
| 719514002 | Autosomal dominant Charcot-Marie-Tooth disease type 2M |
| 719515001 | Autosomal dominant Charcot-Marie-Tooth disease type 2N |
| 719516000 | Autosomal dominant focal dystonia DYT25 type |
| 719717006 | Psychosis co-occurrent and due to Parkinson's disease |
| 719810000 | X-linked intellectual disability with seizure and psoriasis syndrome |
| 719815005 | X-linked myopathy with excessive autophagy |
| 719816006 | X-linked sideroblastic anemia with spinocerebellar ataxia |
| 719817002 | X-linked spinocerebellar ataxia type 3 |
| 719818007 | X-linked spinocerebellar ataxia type 4 |
| 719819004 | Xeroderma pigmentosum and Cockayne syndrome complex |
| 719824001 | Vici syndrome |
| 719826004 | X-linked intellectual disability with acromegaly and hyperactivity syndrome |
| 719827008 | X-linked immunoneurologic disorder |
| 719833004 | Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome |
| 719836007 | X-linked distal arthrogryposis multiplex congenita |
| 719838008 | X-linked hereditary sensory and autonomic neuropathy with deafness |
| 7199000 | Tuberous sclerosis syndrome |
| 719947004 | Craniofacial dysmorphism with coloboma of eye and corpus callosum agenesis syndrome |
| 719979008 | Charcot-Marie-Tooth disease type ID |
| 719980006 | Charcot-Marie-Tooth disease type IF |
| 719981005 | Charcot-Marie-Tooth disease type 2B2 |
| 719985001 | Autosomal dominant limb girdle muscular dystrophy type 1A |
| 719987009 | Autosomal dominant limb girdle muscular dystrophy type 1D |
| 719988004 | Autosomal dominant limb girdle muscular dystrophy type 1E |
| 719989007 | Autosomal dominant limb girdle muscular dystrophy type 1F |
| 719990003 | Autosomal dominant limb girdle muscular dystrophy type 1G |
| 720010009 | Microphthalmia with brain atrophy syndrome |
| 720261501000119107 | Cerebrovascular accident due to occlusion of bilateral anterior cerebral arteries |
| 720410001 | Acrootoocular syndrome |
| 720466001 | Adult-onset dystonia parkinsonism |
| 720494009 | Anonychia with microcephaly syndrome |
| 720498007 | Aphalangy and syndactyly with microcephaly syndrome |
| 720517001 | Ataxia with deafness and intellectual disability syndrome |
| 720518006 | Athabaskan brainstem dysgenesis syndrome |
| 720519003 | Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome |
| 720522001 | Autosomal recessive limb girdle muscular dystrophy type 2G |
| 720523006 | Autosomal recessive limb girdle muscular dystrophy type 2K |
| 720576001 | Brain calcification Rajab type |
| 720626009 | Dissection of carotid artery |
| 720634003 | Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome |
| 720637005 | Charcot-Marie-Tooth disease type 2H |
| 720638000 | Charcot-Marie-Tooth disease type 4J |
| 720750004 | Spinocerebellar degeneration and corneal dystrophy syndrome |
| 720809000 | Dissection of external carotid artery |
| 720813007 | Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome |
| 720815000 | Capra DeMarco syndrome |
| 720816004 | Craniosynostosis and intracranial calcification syndrome |
| 720819006 | Curry Jones syndrome |
| 720825005 | Cystic leukoencephalopathy without megalencephaly |
| 720830009 | Neuronal ceroid lipofuscinosis due to deficiency of cathepsin D |
| 720852000 | Cervical hypertrichosis and peripheral neuropathy syndrome |
| 720855003 | Cerebrooculonasal syndrome |
| 720864008 | Encephalopathy due to prosaposin deficiency |
| 720954000 | Filippi syndrome |
| 721008000 | Hall Riggs syndrome |
| 721015008 | Hydrocephalus with endocardial fibroelastosis and cataract syndrome |
| 721072003 | Short stature, pituitary and cerebellar defect and small sella turcica syndrome |
| 721088003 | Developmental delay, epilepsy, neonatal diabetes syndrome |
| 721092005 | Developmental malformation, deafness, dystonia syndrome |
| 721165001 | Variably protease sensitive prionopathy |
| 721200000 | Early-onset X-linked optic atrophy |
| 721207002 | Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome |
| 721219005 | Familial Alzheimer-like prion disease |
| 721221000 | Hirschsprung disease with deafness and polydactyly syndrome |
| 721222007 | Hirschsprung disease with type D brachydactyly syndrome |
| 721223002 | Hirschsprung disease with nail hypoplasia and dysmorphism |
| 721228006 | Huntington disease-like 2 |
| 721229003 | Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome |
| 721231007 | Hydrocephalus with obesity and hypogonadism syndrome |
| 721255002 | Acquired prion disease |
| 721297008 | Galloway Mowat syndrome |
| 721842008 | Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome |
| 721843003 | Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome |
| 721846006 | Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome |
| 721847002 | Joubert syndrome with congenital hepatic fibrosis |
| 721862000 | Joubert syndrome with oculorenal defect |
| 721873007 | Joubert syndrome with orofaciodigital defect |
| 721903007 | Microcephaly, hypogammaglobulinemia, abnormal immunity syndrome |
| 721974000 | Lowry MacLean syndrome |
| 721975004 | Epiphyseal dysplasia, microcephalus, nystagmus syndrome |
| 721979005 | Lymphedema and cerebral arteriovenous anomaly syndrome |
| 722004001 | Agenesis of internal carotid artery |
| 722006004 | Isotretinoin embryopathy-like syndrome |
| 722033000 | Macrocephaly, short stature, paraplegia syndrome |
| 722036008 | Megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome |
| 722055008 | Oculopalatocerebral syndrome |
| 722056009 | Oculocerebrofacial syndrome Kaufman type |
| 722064003 | Odontoleukodystrophy |
| 722110003 | Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome |
| 722201004 | Median cleft of upper lip, corpus callosum lipoma, cutaneous polyp syndrome |
| 722209002 | Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome |
| 722212004 | Severe X-linked mitochondrial encephalomyopathy |
| 722213009 | Severe X-linked intellectual disability Gustavson type |
| 722281001 | Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome |
| 722282008 | Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome |
| 722283003 | Agnathia, holoprosencephaly, situs inversus syndrome |
| 722293005 | Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome |
| 722294004 | Autosomal dominant intermediate Charcot-Marie-Tooth disease type E |
| 722377004 | Paraganglioma and gastric stromal sarcoma syndrome |
| 722380003 | Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome |
| 722381004 | Congenital cataract, nephropathy, encephalopathy syndrome |
| 722385008 | Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma syndrome |
| 722386009 | Celiac disease with epilepsy and cerebral calcification syndrome |
| 722389002 | Congenital hereditary facial paralysis with variable hearing loss syndrome |
| 722390006 | Congenital intrauterine infection-like syndrome |
| 722432000 | Duane anomaly, myopathy, scoliosis syndrome |
| 722435003 | Dystonia 16 |
| 722451006 | Gomez Lopez Hernandez syndrome |
| 722453009 | Cutaneous mastocytosis, short stature, hearing loss syndrome |
| 722455002 | Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome |
| 722456001 | Intellectual disability, developmental delay, contracture syndrome |
| 722488009 | Neurodegeneration due to 3-hydroxyisobutyryl coenzyme A hydrolase deficiency |
| 722493007 | Familial caudal dysgenesis |
| 722575008 | Traumatic hemorrhage of cerebellum 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 |
| 722615007 | Focal hemorrhagic contusion of cerebrum |
| 722633001 | Multiple traumatic hemorrhages of brain tissue |
| 722671009 | Metastatic malignant neoplasm of meninges |
| 722718001 | Primary malignant meningioma |
| 722762005 | Ganglioside GM3 synthase deficiency |
| 722763000 | Infantile dystonia parkinsonism |
| 722929005 | Perinatal arterial ischemic stroke of fetus and/or neonate |
| 722964001 | Atypical Parkinsonism |
| 722966004 | Chorea due to heredodegenerative disorder |
| 722977005 | Dementia co-occurrent and due to neurocysticercosis |
| 722978000 | Dementia caused by toxin |
| 722979008 | Dementia due to metabolic abnormality |
| 722980006 | Dementia due to chromosomal anomaly |
| 722985001 | Acute venous infarction of spinal cord |
| 722986000 | Chronic venous infarction of spinal cord |
| 722987009 | Amyotrophic lateral sclerosis plus syndrome |
| 722992006 | Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi |
| 722997000 | Inherited autonomic nervous system disorder |
| 723082006 | Silent cerebral infarct |
| 723083001 | Late effects of cerebral ischemic stroke |
| 723084007 | Sequela of non-traumatic intracerebral hemorrhage |
| 723123001 | Ischemic vascular dementia |
| 723124007 | Primary progressive apraxia of speech |
| 723125008 | Epileptic encephalopathy |
| 723151005 | Permanent vegetative state |
| 723156000 | Flaccid diplegia of upper limbs |
| 723157009 | Spastic diplegia of upper limbs |
| 723158004 | Diplegia of lower limbs |
| 723304001 | Microcephaly, seizure, intellectual disability, heart disease syndrome |
| 723306004 | Facial onset sensory and motor neuronopathy syndrome |
| 723307008 | Ethylmalonic encephalopathy |
| 723308003 | Epidermolysis bullosa simplex with muscular dystrophy |
| 723309006 | Endocrine-cerebro-osteodysplasia syndrome |
| 723359002 | Familial acute necrotizing encephalopathy |
| 723366001 | Macrostomia, preauricular tag, external ophthalmoplegia syndrome |
| 723390000 | Rapidly progressive dementia |
| 723404002 | Microcephalic osteodysplastic dysplasia Saul Wilson type |
| 723405001 | Microlissencephaly micromelia syndrome |
| 723441001 | Non-progressive cerebellar ataxia with intellectual disability |
| 723452007 | Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome |
| 723497003 | Peripheral neuropathy with sensorineural hearing impairment syndrome |
| 723557004 | Thiamine-responsive encephalopathy |
| 723612001 | Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome |
| 723621000 | Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome |
| 723622007 | X-linked spastic paraplegia type 2 |
| 723675006 | Sialidosis type 1 |
| 723676007 | Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome |
| 723819007 | Autosomal dominant spastic paraplegia type 36 |
| 723820001 | Autosomal dominant spastic paraplegia type 4 |
| 723821002 | Autosomal recessive spastic paraplegia type 44 |
| 723822009 | Autosomal recessive spastic paraplegia type 46 |
| 723823004 | Autosomal recessive spastic paraplegia type 53 |
| 723824005 | Autosomal recessive spastic paraplegia type 54 |
| 723825006 | Autosomal recessive spastic paraplegia type 55 |
| 723826007 | Autosomal recessive spastic paraplegia type 57 |
| 723830005 | Keratosis follicularis, dwarfism, cerebral atrophy syndrome |
| 723857007 | Silent micro-hemorrhage of brain |
| 723992000 | Kufor Rakeb syndrome |
| 723999009 | Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome |
| 724002003 | Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome |
| 724065003 | Autosomal recessive posterior column ataxia and retinitis pigmentosa |
| 724067006 | Permanent neonatal diabetes mellitus with cerebellar agenesis syndrome |
| 724091002 | Neuroectodermal melanolysosomal disease |
| 724097003 | Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome |
| 724138007 | Mitochondrial myopathy with sideroblastic anemia syndrome |
| 724141003 | Microcephalic primordial dwarfism due to zinc finger protein 335 deficiency |
| 724146008 | Metaphyseal chondromatosis co-occurrent with D-2 hydroxyglutaric aciduria |
| 724172004 | McLeod neuroacanthocytosis syndrome |
| 724207001 | Kleefstra syndrome |
| 724226009 | Infantile osteopetrosis with neuroaxonal dysplasia syndrome |
| 724227000 | Infantile onset spinocerebellar ataxia |
| 724228005 | Infantile choroidocerebral calcification syndrome |
| 724283004 | Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum |
| 724349009 | Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome |
| 724351008 | Hereditary hyperekplexia |
| 724357007 | Hereditary cerebral hemorrhage with amyloidosis |
| 724385009 | Growth delay due to insulin-like growth factor type 1 deficiency |
| 724424009 | Cerebral ischemic stroke due to small artery occlusion |
| 724425005 | Cerebral ischemic stroke due to intracranial large artery atherosclerosis |
| 724426006 | Cerebral ischemic stroke due to extracranial large artery atherosclerosis |
| 724427002 | Asymptomatic stenosis of intracranial artery |
| 724428007 | Asymptomatic stenosis of extracranial artery |
| 724429004 | Stroke co-occurrent with migraine |
| 724549005 | Epilepsy due to infectious disease of central nervous system |
| 724565006 | White matter disorder due to nutritional deficiency |
| 724572007 | Neuromuscular junction disorder caused by organic phosphorus compound ingestion |
| 724576005 | Pyridoxal 5-phosphate dependent epilepsy |
| 724643004 | Transient abnormal myelopoiesis co-occurrent with Down syndrome |
| 724644005 | Myeloid leukemia co-occurrent with Down syndrome |
| 724761004 | Sporadic Parkinson disease |
| 724764007 | Chorea co-occurrent and due to Huntington disease-like condition |
| 724765008 | Chorea co-occurrent and due to dentatorubropallidoluysian degeneration |
| 724766009 | Chorea co-occurrent and due to Wilson disease |
| 724769002 | Ataxia co-occurrent and due to phytanic acid storage disease |
| 724770001 | Ataxia co-occurrent and due to abetalipoproteinemia |
| 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 |
| 724786008 | Epilepsy due to perinatal anoxic-ischemic brain injury |
| 724787004 | Epilepsy due to cerebrovascular accident |
| 724789001 | Epilepsy due to intracranial tumor |
| 724813004 | Autonomic nervous system disorder co-occurrent and due to neurodegenerative disorder |
| 724819000 | Functional paraparesis |
| 724820006 | Functional hemiparesis |
| 72488000 | Niemann-Pick disease, type C, chronic form |
| 724988000 | Epilepsy co-occurrent and due to degenerative brain disorder |
| 724989008 | Epilepsy co-occurrent and due to mesial temporal sclerosis |
| 724990004 | Epilepsy due to immune disorder |
| 724991000 | Epilepsy co-occurrent and due to demyelinating disorder |
| 724992007 | Epilepsy co-occurrent and due to dementia |
| 724993002 | Cerebral ischemic stroke due to occlusion of extracranial large artery |
| 724994008 | Cerebral ischemic stroke due to stenosis of extracranial large artery |
| 725001004 | Idiopathic syringomyelia |
| 725042001 | Autosomal recessive limb girdle muscular dystrophy type 2J |
| 725043006 | Autosomal recessive limb girdle muscular dystrophy type 2O |
| 725047007 | Autosomal recessive Charcot-Marie-Tooth disease with hoarseness |
| 725048002 | Charcot-Marie-Tooth disease type 2B1 |
| 725097006 | Crisponi syndrome |
| 725132001 | Ischemic stroke without residual deficits |
| 725139005 | Spastic paraplegia, optic atrophy, neuropathy syndrome |
| 725146001 | Atypical juvenile parkinsonism |
| 725163002 | X-linked spasticity, intellectual disability, epilepsy syndrome |
| 725296006 | Mucolipidosis type IV |
| 725392005 | Autosomal dominant striatal neurodegeneration |
| 725394006 | Autosomal recessive ataxia due to ubiquinone deficiency |
| 725408001 | Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 |
| 725413002 | Febrile infection related epilepsy syndrome |
| 725420009 | Congenital muscular dystrophy Paradas type |
| 725433003 | Autosomal recessive cerebellar ataxia Beauce type |
| 725461009 | Microcephalic osteodysplastic primordial dwarfism types I and III |
| 725464001 | Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy |
| 72585000 | Parkinsonian syndrome with idiopathic orthostatic hypotension |
| 725898002 | Delirium co-occurrent with dementia |
| 725907002 | Autosomal recessive limb girdle muscular dystrophy type 2Y |
| 726031001 | Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome |
| 726051002 | Myotonia congenita |
| 726083008 | Congenital sacral meningocele with conotruncal heart defect syndrome |
| 726107008 | Distal myopathy Welander type |
| 72655000 | Alternating hypoglossal hemiplegia |
| 726606003 | Autosomal recessive spastic paraplegia type 32 |
| 726607007 | Autosomal recessive spastic paraplegia type 26 |
| 726608002 | Autosomal recessive spastic paraplegia type 23 |
| 726609005 | Autosomal recessive spastic paraplegia type 64 |
| 726610000 | Autosomal recessive spastic paraplegia type 63 |
| 726611001 | Autosomal recessive spastic paraplegia type 61 |
| 726614009 | Autosomal recessive limb girdle muscular dystrophy type 2P |
| 726615005 | Autosomal recessive limb girdle muscular dystrophy type 2Q |
| 726616006 | Autosomal recessive limb girdle muscular dystrophy type 2L |
| 726617002 | Autosomal recessive limb girdle muscular dystrophy type 2N |
| 726618007 | Autosomal recessive limb girdle muscular dystrophy type 2M |
| 726622002 | Spastic paraplegia with Paget disease of bone syndrome |
| 726669007 | Central nervous system calcification, deafness, tubular acidosis, anemia syndrome |
| 726702005 | Epileptic encephalopathy with global cerebral demyelination |
| 726704006 | Cataract, congenital heart disease, neural tube defect syndrome |
| 72836002 | Hepatic coma |
| 72986009 | Acute hemorrhagic leukoencephalitis |
| 73020009 | Cerebral hemisphere hemorrhage |
| 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 |
| 732330391000119107 | Cerebrovascular accident due to embolism of bilateral vertebral arteries |
| 732923001 | Hemorrhage of medulla oblongata |
| 732926009 | Hydrocephalus, tall stature, joint laxity syndrome |
| 732927000 | Split hand, obstructive uropathy, spina bifida, diaphragmatic defect syndrome |
| 732929002 | Autosomal recessive limb girdle muscular dystrophy type 2S |
| 732930007 | Autosomal recessive limb girdle muscular dystrophy type 2T |
| 732932004 | Autosomal recessive spastic paraplegia type 18 |
| 732933009 | Autosomal recessive spastic paraplegia type 25 |
| 732948003 | Autosomal dominant spastic paraplegia type 10 |
| 732949006 | Autosomal dominant spastic paraplegia type 6 |
| 732951005 | Mitochondrial myopathy, lactic acidosis, deafness syndrome |
| 732958004 | Spastic paraplegia with precocious puberty syndrome |
| 732959007 | Beta-propeller protein-associated neurodegeneration |
| 73297009 | Muscular dystrophy |
| 733028000 | Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome |
| 733029008 | Autosomal dominant spastic paraplegia type 29 |
| 733031004 | Epilepsy, microcephaly, skeletal dysplasia syndrome |
| 733032006 | Epilepsy telangiectasia syndrome |
| 733033001 | Spinocerebellar ataxia dysmorphism syndrome |
| 733044009 | Dermatoleukodystrophy |
| 733049004 | Encephalopathy, intracerebral calcification, retinal degeneration syndrome |
| 733065003 | Myoclonus, cerebellar ataxia, deafness syndrome |
| 733068001 | Absent tibia, polydactyly, arachnoid cyst syndrome |
| 733071009 | Deafness, small bowel diverticulosis, neuropathy syndrome |
| 733072002 | Alaninuria, microcephaly, dwarfism, enamel hypoplasia, diabetes mellitus syndrome |
| 733082001 | Early-onset Lafora body disease |
| 733086003 | Pseudoprogeria syndrome |
| 733089005 | Spastic paraplegia, nephritis, deafness syndrome |
| 733091002 | Isolated hereditary congenital facial paralysis |
| 733092009 | Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
| 733094005 | Dandy-Walker malformation with postaxial polydactyly syndrome |
| 733096007 | Thyrocerebrorenal syndrome |
| 733113002 | Hypogonadotropic hypogonadism retinitis pigmentosa syndrome |
| 733184002 | Dementia caused by heavy metal exposure |
| 733185001 | Dementia following injury caused by exposure to ionizing radiation |
| 733190003 | Dementia due to primary malignant neoplasm of brain |
| 733191004 | Dementia due to chronic subdural hematoma |
| 733192006 | Dementia due to herpes encephalitis |
| 733193001 | Dementia co-occurrent and due to progressive multifocal leukoencephalopathy |
| 733194007 | Dementia co-occurrent and due to Down syndrome |
| 733195008 | Epilepsy of infancy with migrating focal seizures |
| 733199002 | Multifocal cerebral infarction due to and following procedure on cardiovascular system |
| 733417008 | Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome |
| 733418003 | Joubert syndrome with Jeune asphyxiating thoracic dystrophy |
| 733422008 | Prion protein systemic amyloidosis |
| 733452000 | Leukoencephalopathy, dystonia, motor neuropathy syndrome |
| 733455003 | Spastic paraplegia, glaucoma, intellectual disability syndrome |
| 733469003 | Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome |
| 733472005 | Microcephalus, glomerulonephritis, marfanoid habitus syndrome |
| 733489002 | Distal myopathy with posterior leg and anterior hand involvement |
| 733599009 | Adult-onset multiple mitochondrial deoxyribonucleic acid deletion syndrome due to deoxyguanosine kinase deficiency |
| 733604003 | Microcephalus, lymphedema, chorioretinopathy syndrome |
| 733623005 | Autism spectrum disorder, epilepsy, arthrogryposis syndrome |
| 733630004 | Deficiency of alpha-ketoglutarate dehydrogenase |
| 733636005 | 3-phosphoglycerate dehydrogenase deficiency juvenile form |
| 733637001 | 3-phosphoglycerate dehydrogenase deficiency infantile form |
| 733650000 | Adult familial nephronophthisis with spastic quadriparesia syndrome |
| 73390009 | Endophlebitis of cavernous venous sinus |
| 733926004 | Ganglioneuroblastoma of central nervous system |
| 734017008 | Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome |
| 734020000 | Spinocerebellar ataxia type 40 |
| 734021001 | Spinocerebellar ataxia type 38 |
| 734023003 | Sporadic adult-onset ataxia of unknown etiology |
| 734031008 | Congenital absence of optic chiasma |
| 734066005 | Diffuse large B-cell lymphoma of central nervous system |
| 734099007 | Neuroblastoma of central nervous system |
| 734326000 | Stenosis of left vertebral artery |
| 734327009 | Stenosis of right vertebral artery |
| 734374000 | Thrombosis of left carotid artery |
| 734382000 | Thrombosis of right carotid artery |
| 734383005 | Thrombosis of left middle cerebral artery |
| 734384004 | Thrombosis of right middle cerebral artery |
| 734396006 | Spontaneous rupture of left posterior communicating artery |
| 734397002 | Spontaneous rupture of right posterior communicating artery |
| 734434007 | Pyridoxine-dependent epilepsy |
| 734879002 | Ruptured aneurysm of right posterior communicating artery |
| 734880004 | Ruptured aneurysm of left posterior communicating artery |
| 73495003 | Dyssynergia cerebellaris myoclonica |
| 734959006 | Embolus of left cerebellar artery |
| 734960001 | Embolus of right cerebellar artery |
| 734961002 | Embolus of left posterior cerebral artery |
| 734963004 | Embolus of right posterior cerebral artery |
| 734964005 | Embolus of left middle cerebral artery |
| 734965006 | Embolus of right middle cerebral artery |
| 735114006 | Occlusion of right pontine artery |
| 735115007 | Occlusion of left pontine artery |
| 735131004 | Occlusion of left cerebellar artery |
| 735132006 | Occlusion of right cerebellar artery |
| 735206008 | Communicating hydrocephalus due to and following traumatic hemorrhage |
| 735421004 | Leukoencephalopathy with brain stem and spinal cord involvement and high lactate syndrome |
| 735556002 | Abscess of corpus callosum |
| 735749005 | Myelomeningocele co-occurrent with hydrocephalus |
| 735757008 | Primary ganglioneuroblastoma of brain |
| 73663008 | Neurologic xeroderma pigmentosum |
| 737159004 | Aneurysm of basilar artery |
| 737160009 | Dissection of basilar artery |
| 737227004 | Autosomal dominant hereditary spastic paraplegia |
| 737228009 | Progressive focal cortical atrophy |
| 737229001 | White matter disorder due to vascular abnormality |
| 737230006 | White matter disorder due to ischemia |
| 737231005 | Traumatic hemorrhage of thalamus |
| 737232003 | Traumatic hemorrhage of basal ganglia |
| 7379000 | Pseudobulbar palsy |
| 73935008 | Toxic encephalopathy caused by hydroxyquinoline |
| 74073002 | Cerebellar hemangioblastomatosis |
| 74267005 | Toxic encephalopathy caused by carbon tetrachloride |
| 74351001 | Reye's syndrome |
| 75019001 | Athetoid cerebral palsy |
| 75023009 | Post-traumatic epilepsy |
| 75038005 | Cerebellar hemorrhage |
| 75046006 | Combined pyramidal-extrapyramidal syndrome |
| 75072002 | Nemaline myopathy |
| 751371000000107 | Personal history of transient ischaemic attack |
| 75138007 | Endophlebitis of superior sagittal sinus |
| 75143000 | Toxic encephalitis caused by thallium |
| 75299005 | Spastic spinal syphilitic paralysis |
| 75491005 | Amyotrophia congenita |
| 75543006 | Cerebral embolism |
| 758664007 | Isolated follicle stimulating hormone deficiency |
| 75968004 | Sotos' syndrome |
| 759950981000119101 | Cerebrovascular accident due to thrombosis of left vertebral artery |
| 76043009 | Hereditary sensory-motor neuropathy, type V |
| 7611002 | Septo-optic dysplasia sequence |
| 76156000 | Juvenile cerebellar degeneration AND myoclonus |
| 762295002 | Congenital obstructive hydrocephalus |
| 762297005 | White matter disorder due to vitamin B12 deficiency |
| 762350007 | Dementia due to prion disease |
| 762351006 | Dementia due to and following injury of head |
| 762352004 | Demyelination due to systemic vasculitis |
| 762457009 | Astroblastoma of brain |
| 762629007 | Occlusion of right middle cerebral artery by embolus |
| 762630002 | Occlusion of left middle cerebral artery by embolus |
| 762632005 | Occlusion of left cerebellar artery by embolus |
| 762633000 | Occlusion of right cerebellar artery by embolus |
| 762648006 | Stenosis of right cerebellar artery |
| 762649003 | Stenosis of left cerebellar artery |
| 762651004 | Occlusion of right posterior cerebral artery by embolus |
| 762652006 | Occlusion of left posterior cerebral artery by embolus |
| 762707000 | Subcortical dementia |
| 763067000 | Autosomal dominant congenital benign spinal muscular atrophy |
| 763068005 | Autosomal dominant spastic paraplegia type 31 |
| 763069002 | Autosomal dominant spastic paraplegia type 41 |
| 763070001 | Autosomal dominant spastic paraplegia type 42 |
| 763130006 | Cleft palate, large ears, small head syndrome |
| 763135001 | Charcot-Marie-Tooth disease type 4E |
| 763136000 | Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome |
| 763280005 | Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome |
| 763312008 | Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome |
| 763314009 | Congenital muscular dystrophy with hyperlaxity |
| 763315005 | Congenital myopathy with myasthenic-like onset |
| 763344007 | Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome |
| 763345008 | Charcot-Marie-Tooth disease type 4B3 |
| 763347000 | X-linked Charcot-Marie-Tooth disease type 6 |
| 763348005 | Autosomal recessive cerebellar ataxia with late-onset spasticity |
| 763349002 | Progressive myoclonic epilepsy with dystonia |
| 763350002 | Intellectual disability, obesity, brain malformation, facial dysmorphism syndrome |
| 763351003 | Spectrin-associated autosomal recessive cerebellar ataxia |
| 763352005 | Familial dyskinesia and facial myokymia |
| 763366000 | Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome |
| 763367009 | Autosomal recessive spastic paraplegia type 48 |
| 763369007 | Autosomal dominant spastic paraplegia type 37 |
| 763370008 | X-linked spastic paraplegia type 34 |
| 763373005 | Autosomal recessive spastic paraplegia type 5A |
| 763374004 | Autosomal dominant spastic paraplegia type 12 |
| 763375003 | Autosomal dominant spastic paraplegia type 19 |
| 763376002 | Autosomal recessive spastic paraplegia type 28 |
| 763377006 | Autosomal spastic paraplegia type 30 |
| 763400005 | X-linked Charcot-Marie-Tooth disease type 4 |
| 763402002 | Spastic paraplegia, neuropathy, poikiloderma syndrome |
| 763403007 | Spastic paraplegia, facial cutaneous lesion syndrome |
| 763455008 | X-linked Charcot-Marie-Tooth disease type 1 |
| 763457000 | X-linked Charcot-Marie-Tooth disease type 2 |
| 763458005 | X-linked Charcot-Marie-Tooth disease type 3 |
| 763460007 | X-linked Charcot-Marie-Tooth disease type 5 |
| 763533003 | Distal hereditary motor neuropathy Jerash type |
| 763534009 | Hot water reflex epilepsy |
| 763597000 | Hereditary ataxia |
| 763622006 | Thinking epilepsy |
| 763632004 | Startle epilepsy |
| 763669001 | Spastic ataxia with congenital miosis |
| 763688008 | Deafness, encephaloneuropathy, obesity, valvulopathy syndrome |
| 763715007 | Familial hyperprolactinemia |
| 763718009 | Finnish upper limb onset distal myopathy |
| 763721006 | Hypermethioninemia encephalopathy due to deficiency of adenosine kinase |
| 763722004 | Hypotonia, speech impairment, severe cognitive delay syndrome |
| 763743003 | Intellectual disability, spasticity, ectrodactyly syndrome |
| 763770005 | Familial myoclonus of cerebral cortex |
| 763776004 | Kelch like family member 9 related early-onset distal myopathy |
| 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 |
| 763821001 | Porencephaly, cerebellar hypoplasia, internal malformations syndrome |
| 763827002 | Orgasm induced epilepsy |
| 763829004 | Oculopharyngodistal myopathy |
| 763837007 | Oro-facial digital syndrome type 14 |
| 763861000 | Pachygyria, intellectual disability, epilepsy syndrome |
| 763895001 | Myosclerosis |
| 76402003 | Carotid artery insufficiency syndrome |
| 764095005 | Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome |
| 764453009 | Action myoclonus renal failure syndrome |
| 764456001 | Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency |
| 764522009 | Familial focal epilepsy with variable foci |
| 764525006 | Cylindrical spirals myopathy |
| 764686003 | Autosomal recessive spastic paraplegia type 15 |
| 764688002 | Autosomal recessive spastic paraplegia type 35 |
| 764730007 | Autosomal dominant Charcot-Marie-Tooth disease type 2 due to kinesin family member 5A mutation |
| 764732004 | Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome |
| 764733009 | Progressive external ophthalmoplegia, myopathy, emaciation syndrome |
| 764734003 | Autosomal recessive spastic paraplegia type 21 |
| 764736001 | Autosomal recessive spastic paraplegia type 43 |
| 764812008 | Autosomal recessive myogenic arthrogryposis multiplex congenita |
| 764850002 | Autosomal dominant Charcot-Marie-Tooth disease type 2A2 |
| 764854006 | Autosomal dominant slowed nerve conduction velocity |
| 764859001 | Laing early-onset distal myopathy |
| 764944006 | Congenital muscular dystrophy type 1B |
| 764945007 | Congenital myopathy with internal nuclei and atypical cores |
| 764959000 | Intellectual disability, myopathy, short stature, endocrine defect syndrome |
| 764962002 | Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 |
| 765045003 | Autosomal recessive spastic paraplegia type 62 |
| 765046002 | Autosomal dominant Charcot-Marie-Tooth disease type 2U |
| 765047006 | SURF1, cytochrome c oxidase assembly factor related Charcot-Marie-Tooth disease type 4 |
| 765089003 | Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome |
| 765091006 | Spinocerebellar ataxia with axonal neuropathy type 1 |
| 765093009 | Rolandic epilepsy, speech dyspraxia syndrome |
| 765100000 | Ribonucleotide reductase regulatory TP53 inducible subunit M2B-related mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form with renal tubulopathy |
| 765170001 | Sodium voltage-gated channel alpha subunit 8-related epilepsy with encephalopathy |
| 765197008 | Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier |
| 765202001 | Familial multiple benign meningioma |
| 765216006 | Audiogenic epilepsy |
| 765325002 | Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease |
| 765331004 | Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis |
| 765401006 | Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form |
| 765403009 | F-box and leucine rich repeat protein 4 related mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form |
| 765434008 | Human immunodeficiency virus type I enhancer binding protein 2 related intellectual disability |
| 765744006 | Autosomal dominant intermediate Charcot-Marie-Tooth disease type A |
| 765745007 | Autosomal dominant intermediate Charcot-Marie-Tooth disease type B |
| 765746008 | Autosomal dominant intermediate Charcot-Marie-Tooth disease type C |
| 765747004 | Autosomal dominant intermediate Charcot-Marie-Tooth disease type D |
| 765751002 | Autoimmune encephalopathy with parasomnia and obstructive sleep apnea |
| 765753004 | Autosomal recessive spastic paraplegia type 45 |
| 765758008 | Microcephalic primordial dwarfism Montreal type |
| 766032007 | Holoprosencephaly, ectrodactyly, cleft lip, cleft palate syndrome |
| 766044005 | Acute encephalopathy with biphasic seizures and late reduced diffusion |
| 766246000 | Marburg acute multiple sclerosis |
| 766251006 | Lethal infantile mitochondrial myopathy |
| 76628006 | Post-hemiplegic chorea |
| 76670001 | Duchenne muscular dystrophy |
| 766709000 | Isolated hypoplasia of cerebellar vermis |
| 766752000 | Neurolymphomatosis |
| 766753005 | Nijmegen breakage syndrome-like disorder |
| 766764008 | X-linked distal spinal muscular atrophy type 3 |
| 766767001 | Autosomal recessive spastic paraplegia type 67 |
| 766814006 | Autosomal recessive cerebellar ataxia with saccadic intrusion syndrome |
| 766815007 | Perioral myoclonia with absences |
| 766818009 | X-linked non progressive cerebellar ataxia |
| 766871009 | Diencephalic mesencephalic junction dysplasia |
| 766931003 | Hypomyelination neuropathy arthrogryposis syndrome |
| 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 |
| 769023031000119104 | Cerebrovascular accident of thalamus |
| 769065000 | Tubulin beta 4A class IVa related leukodystrophy |
| 77015008 | Crossed hemiplegia |
| 770404004 | Autosomal recessive chorioretinopathy and microcephaly syndrome |
| 770430000 | Autosomal recessive distal spinal muscular atrophy type 3 |
| 770431001 | Early-onset epileptic encephalopathy and intellectual disability due to glutamate receptor, ionotropic, N-methyl-D-aspartate, subunit 2A mutation |
| 770438007 | Infantile spasm and broad thumb syndrome |
| 770560008 | Lissencephaly due to LIS1 mutation |
| 770564004 | Microcephalic primordial dwarfism Alazami type |
| 770565003 | Microcephalic primordial dwarfism Dauber type |
| 770596007 | Rippling muscle disease with myasthenia gravis |
| 770604006 | X-linked cerebral, cerebellar, coloboma syndrome |
| 770623004 | Benign occipital lobe epilepsy |
| 770624005 | Benign partial epilepsy of infancy with complex partial seizures |
| 770625006 | Combined immunodeficiency with faciooculoskeletal anomalies syndrome |
| 770626007 | Congenital Horner syndrome |
| 770627003 | Desmin-related myofibrillar myopathy |
| 770628008 | Diffuse leptomeningeal melanocytosis |
| 770630005 | Distal hereditary motor neuropathy type 1 |
| 770643005 | Mesial temporal lobe epilepsy with hippocampal sclerosis |
| 770655004 | Microcephalus, brain defect, spasticity, hypernatremia syndrome |
| 770678005 | Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome |
| 770683002 | Secondary syringomyelia |
| 770720005 | Autosomal recessive spastic paraplegia type 58 |
| 770721009 | Microcephaly, thin corpus callosum, intellectual disability syndrome |
| 770722002 | Proximal myopathy with extrapyramidal signs |
| 770723007 | Optic atrophy, intellectual disability syndrome |
| 770724001 | Autosomal recessive spastic paraplegia type 70 |
| 770725000 | Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly |
| 770727008 | Spinal muscular atrophy with respiratory distress type 2 |
| 770751003 | Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome |
| 770755007 | Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome |
| 770757004 | X-linked parkinsonism with spasticity syndrome |
| 770758009 | New-onset refractory status epilepticus |
| 770759001 | Autosomal dominant intermediate Charcot-Marie-Tooth disease type F |
| 770786001 | Hereditary inclusion body myopathy type 4 |
| 770792007 | Adult-onset distal myopathy due to valosin containing protein mutation |
| 770898002 | Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency |
| 770939009 | Huntington disease-like 3 |
| 770941005 | Alopecia, progressive neurological defect, endocrinopathy syndrome |
| 77097004 | Oculopharyngeal muscular dystrophy |
| 771074000 | Microcephaly, short stature, intellectual disability, facial dysmorphism syndrome |
| 771081007 | Distal hereditary motor neuropathy type 7 |
| 771141002 | Benign partial epilepsy with secondarily generalized seizures in infancy |
| 771142009 | Cortical dysplasia with focal epilepsy syndrome |
| 771143004 | Hereditary motor and sensory neuropathy type 5 |
| 771144005 | Hereditary motor and sensory neuropathy with acrodystrophy |
| 771146007 | Holoprosencephaly with caudal dysgenesis syndrome |
| 771147003 | Isolated arhinencephaly |
| 771148008 | X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome |
| 771179007 | Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome |
| 771184001 | Leukoencephalopathy, palmoplantar keratoderma syndrome |
| 771223000 | Infantile epileptic dyskinetic encephalopathy |
| 771234002 | Isolated bilateral hemispheric cerebellar hypoplasia |
| 771238004 | Spinal atrophy, ophthalmoplegia, pyramidal syndrome |
| 771261002 | Digital extensor muscle aplasia with polyneuropathy |
| 771263004 | Ptosis and vocal cord paralysis syndrome |
| 771267003 | Congenital muscular dystrophy with integrin alpha-7 deficiency |
| 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 |
| 771336003 | Polymicrogyria with optic nerve hypoplasia |
| 771448004 | Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency |
| 771469002 | Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome |
| 771470001 | Jawad syndrome |
| 771471002 | Optic nerve edema, splenomegaly syndrome |
| 771475006 | Young adult-onset distal hereditary motor neuropathy |
| 771476007 | Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome |
| 771509001 | Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial deoxyribonucleic acid mutation |
| 771514002 | Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome |
| 771516000 | Solute carrier family 35 member A2 congenital disorder of glycosylation |
| 772129007 | Autosomal dominant childhood-onset proximal spinal muscular atrophy |
| 772224009 | Warburg micro syndrome |
| 772225005 | RAB18, member RAS oncogene family deficiency |
| 773230003 | Cyclin-dependent kinase-like 5 deficiency |
| 773280009 | Hydrocephalus, blue sclera, nephropathy syndrome |
| 773305003 | Microcephaly, polymicrogyria, corpus callosum agenesis syndrome |
| 773306002 | Congenital lethal myopathy Compton North type |
| 773307006 | Zechi Ceide syndrome |
| 773308001 | Autosomal recessive intermediate Charcot-Marie-Tooth disease type A |
| 773330000 | Autosomal recessive intermediate Charcot-Marie-Tooth disease type B |
| 773393001 | Autosomal dominant Charcot-Marie-Tooth disease type 2Q |
| 773394007 | Autosomal recessive frontotemporal pachygyria |
| 773398005 | Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome |
| 773414009 | Autosomal recessive intermediate Charcot-Marie-Tooth disease type C |
| 773415005 | Contiguous ABCD1 DXS1357E deletion syndrome |
| 773421009 | Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression |
| 773425000 | Autosomal recessive spastic paraplegia type 59 |
| 773492007 | Childhood-onset spasticity with hyperglycinemia |
| 773497001 | Partial corpus callosum agenesis, cerebellar vermis hypoplasia with posterior fossa cysts syndrome |
| 773498006 | Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency |
| 773548008 | Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome |
| 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 |
| 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 |
| 773729007 | X-linked myopathy with postural muscle atrophy |
| 773737004 | Nephrocystin 3-related Meckel-like syndrome |
| 774069007 | Protein kinase cAMP-dependent type I regulatory subunit beta-related neurodegenerative dementia with intermediate filaments |
| 774070008 | Fibulin 1-related developmental delay, central nervous system anomaly, syndactyly syndrome |
| 774147002 | Charcot-Marie-Tooth disease type 2R |
| 774149004 | Severe intellectual disability, progressive postnatal microcephaly, midline stereotypic hand movements syndrome |
| 774150004 | Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome |
| 774151000 | Ferro-cerebro-cutaneous syndrome |
| 774205007 | Growth and developmental delay, hypotonia, vision impairment, lactic acidosis syndrome |
| 774206008 | Fatal post-viral neurodegenerative disorder |
| 77461000119109 | Myasthenia gravis with exacerbation |
| 77471000119103 | Myasthenia gravis without exacerbation |
| 775907000 | Congenital pontocerebellar hypoplasia type 9 |
| 776087007 | Autosomal recessive cerebral atrophy |
| 77659000 | Paraneoplastic neuropathy |
| 777999008 | Hypomyelination with brain stem and spinal cord involvement and leg spasticity |
| 778001003 | Potassium voltage-gated channel subfamily Q member 2 related epileptic encephalopathy |
| 778003000 | Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain |
| 778011005 | Severe intellectual disability and progressive spastic paraplegia |
| 778027003 | Primary CD59 deficiency |
| 778029000 | FAST kinase domains 2-related infantile mitochondrial encephalomyopathy |
| 778030005 | Autosomal recessive spastic paraplegia type 27 |
| 778047006 | Myoclonic epilepsy in non-progressive encephalopathy |
| 778048001 | Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial spastic paraplegia |
| 778060000 | Collagen type IV alpha 1 chain related familial vascular leukoencephalopathy |
| 778063003 | Cryptogenic late-onset epileptic spasms |
| 778070003 | Autosomal dominant primary microcephaly |
| 77817004 | Neu-Laxova syndrome |
| 77956009 | Steinert myotonic dystrophy syndrome |
| 78071008 | Hydromicrocephaly |
| 780827006 | Synaptic Ras GTPase activating protein 1- related intellectual disability |
| 782432008 | Acquired hydrocephalus of newborn |
| 782670003 | Autosomal dominant spastic paraplegia type 3 |
| 782675008 | Distal myopathy with anterior tibial onset |
| 782690007 | Gemignani syndrome |
| 782695002 | Primary dystonia DYT17 type |
| 782696001 | Recessive mitochondrial ataxia syndrome |
| 782718007 | Dystonia aphonia syndrome |
| 782719004 | Autosomal recessive cerebellar ataxia due to STIP1 homology and U-box containing protein 1 deficiency |
| 782720005 | Congenital pontocerebellar hypoplasia type 10 |
| 782721009 | Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUN and cysteine rich domain containing beclin 1 interacting protein deficiency |
| 782723007 | Severe intellectual disability, progressive spastic diplegia syndrome |
| 782725000 | Autosomal recessive spastic paraplegia type 69 |
| 782726004 | Autosomal recessive spastic paraplegia type 71 |
| 782727008 | Autosomal spastic paraplegia type 72 |
| 782737003 | Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome |
| 782739000 | Male emopamil-binding protein disorder with neurological defect |
| 782742006 | Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons |
| 782743001 | Huntington disease-like syndrome due to chromosome 9 open reading frame 72 expansions |
| 782744007 | Lipoic acid synthetase deficiency |
| 782746009 | Autosomal recessive spastic paraplegia type 60 |
| 782747000 | Autosomal recessive spastic paraplegia type 66 |
| 782752005 | Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome |
| 782753000 | Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome |
| 782754006 | Foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis syndrome |
| 782755007 | Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome |
| 782757004 | Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome |
| 782771007 | Mitochondrial deoxyribonucleic acid depletion syndrome hepatocerebrorenal form |
| 782772000 | Congenital muscular dystrophy with intellectual disability and severe epilepsy |
| 782822006 | Infantile cerebellar and retinal degeneration |
| 782824007 | Sodium channelopathy-related small fiber neuropathy |
| 782825008 | Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome |
| 782826009 | Charcot-Marie-Tooth disease type 2P |
| 782829002 | Autosomal dominant Charcot-Marie-Tooth disease type 2O |
| 782879004 | Occipital pachygyria and polymicrogyria |
| 782881002 | Hereditary sensorimotor neuropathy with hyperelastic skin |
| 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 |
| 782945001 | Ophthalmoplegia, intellectual disability, lingua scrotalis syndrome |
| 782951006 | Thoracic dysplasia and hydrocephalus syndrome |
| 783005002 | Severe microbrachycephaly, intellectual disability, athetoid cerebral palsy syndrome |
| 783012006 | Parkinsonian pyramidal syndrome |
| 783055005 | Progressive myoclonic epilepsy type 5 |
| 783057002 | DNA replication helicase/nuclease 2-related mitochondrial deoxyribonucleic acid deletion syndrome |
| 783060009 | Autosomal recessive cerebellar ataxia, psychomotor delay syndrome |
| 78306007 | Epidural ascending spinal paralysis |
| 783062001 | Progressive myoclonic epilepsy type 6 |
| 783064000 | Progressive myoclonic epilepsy type 3 |
| 783091003 | 46,XY gonadal dysgenesis, motor and sensory neuropathy syndrome |
| 783094006 | Autosomal recessive spastic paraplegia type 14 |
| 783139000 | Progressive myoclonic epilepsy type 8 |
| 783148005 | Distal nebulin myopathy |
| 783157004 | Leigh syndrome with nephrotic syndrome |
| 783160006 | Hereditary gelsolin amyloidosis |
| 783161005 | Familial dementia British type |
| 783166000 | Distal anoctaminopathy |
| 783174004 | Congenital muscular dystrophy with intellectual disability |
| 783175003 | Congenital muscular dystrophy without intellectual disability |
| 783176002 | Congenital muscular dystrophy with cerebellar involvement |
| 783179009 | Cranio-cervical dystonia with laryngeal and upper limb involvement |
| 783203003 | Ataxia with tapetoretinal degeneration syndrome |
| 783242003 | Adult-onset cervical dystonia DYT23 type |
| 783258000 | Familial dementia Danish type |
| 783413008 | Multiple aneurysms of cerebral artery |
| 783415001 | Aneurysm of internal carotid bifurcation |
| 783416000 | Aneurysm of anterior cerebral artery |
| 783417009 | Aneurysm of posterior inferior cerebellar artery |
| 783418004 | Aneurysm of anterior communicating artery |
| 783419007 | Aneurysm of posterior cerebral artery |
| 783420001 | Aneurysm of middle cerebral artery |
| 783421002 | Aneurysm of posterior communicating artery |
| 783422009 | Aneurysm of internal carotid-anterior communicating artery zone |
| 783423004 | Aneurysm of internal carotid-posterior communicating artery zone |
| 783550006 | Hereditary sensory and autonomic neuropathy type 7 |
| 783554002 | Autosomal recessive limb girdle muscular dystrophy type 2U |
| 783558004 | Combined oxidative phosphorylation defect type 11 |
| 783618006 | Lower motor neuron syndrome with late-adult onset |
| 783622001 | Autosomal dominant spastic paraplegia type 38 |
| 783629005 | Congenital aneurysm of cerebral artery |
| 783630000 | Congenital aneurysm of precerebral artery |
| 783697000 | X-linked spastic paraplegia type 16 |
| 783698005 | Autosomal dominant spastic paraplegia type 13 |
| 783701002 | Port-wine nevi, mega cisterna magna, hydrocephalus syndrome |
| 783703004 | White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome |
| 783707003 | Cerebral aneurysm due to dissection of cerebral artery |
| 783716004 | Acquired aneurysm of cerebral artery |
| 783722008 | Myopathy and diabetes mellitus |
| 783731008 | Fibromuscular dysplasia of wall of carotid artery |
| 783733006 | Fibromuscular dysplasia of wall of bilateral carotid arteries |
| 783734000 | Mitochondrial deoxyribonucleic acid depletion syndrome, hepatocerebral form due to deoxyguanosine kinase deficiency |
| 783739005 | Familial temporal lobe epilepsy |
| 783764008 | Autosomal recessive spastic paraplegia type 56 |
| 783787000 | Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations |
| 784341001 | Amyotrophic lateral sclerosis type 4 |
| 784342008 | Familial infantile myoclonic epilepsy |
| 784343003 | Autosomal recessive spastic ataxia with leukoencephalopathy |
| 784344009 | Cortical dysgenesis with pontocerebellar hypoplasia due to tubulin beta 3 class III mutation |
| 784345005 | Malignant migrating partial seizures of infancy |
| 784346006 | Navajo neurohepatopathy |
| 784347002 | Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome |
| 784348007 | Familial congenital mirror movements |
| 784352007 | X-linked scapuloperoneal muscular dystrophy |
| 784370005 | Mitochondrial myopathy with reversible cytochrome C oxidase deficiency |
| 784371009 | Huntington disease-like 1 |
| 784372002 | Familial mesial temporal lobe epilepsy with febrile seizures |
| 784377008 | Autosomal dominant epilepsy with auditory features |
| 784380009 | Autosomal dominant spastic ataxia type 1 |
| 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 |
| 787172004 | Childhood-onset autosomal recessive myopathy with external ophthalmoplegia |
| 787174003 | Intellectual disability, hyperkinetic movement, truncal ataxia syndrome |
| 788417006 | Alopecia, epilepsy, intellectual disability syndrome Moynahan type |
| 788454002 | Stenosis of bilateral vertebral arteries |
| 788455001 | Occlusion of bilateral pontine arteries |
| 788880006 | Cerebral ischemic stroke due to dissection of artery |
| 788881005 | Cerebral ischemic stroke due to aortic arch embolism |
| 788882003 | Cerebral ischemic stroke due to global hypoperfusion with watershed infarct |
| 788883008 | Cerebral ischemic stroke due to hypercoagulable state |
| 788884002 | Cerebral ischemic stroke due to subarachnoid hemorrhage |
| 788898005 | Dementia caused by volatile inhalant |
| 788899002 | Dementia due to pellagra |
| 788916009 | Encephalopathy caused by ammonia |
| 789063000 | Primary hyperaldosteronism, seizures, neurological abnormalities syndrome |
| 789170003 | Disinhibited behavior due to dementia |
| 789187001 | X-linked acrogigantism due to Xq26 microduplication |
| 789657008 | ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis |
| 789674008 | Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder |
| 791000124107 | 2-methyl-3-hydroxybutyric aciduria |
| 792004 | Jakob-Creutzfeldt disease |
| 7931000119101 | Anterior choroidal artery thrombosis |
| 79341000119107 | Mixed dementia |
| 79385002 | Lowe syndrome |
| 79591004 | Spastic paralysis due to spinal birth injury |
| 79631006 | Absence seizure |
| 79633009 | Spastic hemiplegia |
| 79745005 | Reflex epilepsy |
| 80098002 | Diffuse Lewy body disease |
| 80180004 | Pallidonigral degeneration |
| 80328002 | Progressive cone-rod dystrophy |
| 80544005 | Spongy degeneration of central nervous system |
| 80606009 | Carotid artery embolism |
| 806161651000119106 | Cerebrovascular accident due to embolism of right vertebral artery |
| 80651009 | Aicardi's syndrome |
| 80690008 | Degenerative disease of the central nervous system |
| 80734006 | Marinesco-Sjögren syndrome |
| 80758005 | Embolism of lateral venous sinus |
| 80901002 | Endophlebitis of torcular Herophili |
| 80935004 | Flaccid hemiplegia |
| 80976008 | Myasthenic crisis |
| 81211007 | Primary lateral sclerosis |
| 81308009 | Disorder of brain |
| 813921000000104 | Spastic hemiplegic cerebral palsy |
| 816067005 | Diabetes, hypogonadism, deafness, intellectual disability syndrome |
| 816068000 | Periventricular nodular heterotopia |
| 816205008 | Malignant pituitary blastoma |
| 8166000 | Thrombophlebitis of basilar sinus |
| 816984002 | Progressive multiple sclerosis |
| 81780002 | Beckwith-Wiedemann syndrome |
| 81854007 | Alexander's disease |
| 81896006 | Dysmorphic sialidosis with renal involvement |
| 818967003 | Medulloepithelioma of central nervous system |
| 82058009 | Myelocele |
| 82077006 | Myotubular myopathy |
| 82346000 | Acquired obstructive hydrocephalus |
| 82351000119105 | Altered behavior due to Pick's disease |
| 82361000119107 | Altered behavior in dementia due to Huntington chorea |
| 82371000119101 | Dementia due to multiple sclerosis with altered behavior |
| 82381000119103 | Epileptic dementia with behavioral disturbance |
| 82501000119102 | Anaplastic astrocytoma of central nervous system |
| 8269002 | Cerebrospinal angiopathy |
| 827172005 | X-linked progressive cerebellar ataxia |
| 8291000119107 | Atonic epilepsy |
| 82959004 | Dementia paralytica juvenilis |
| 83157008 | Fatal familial insomnia |
| 83304000 | Dubini's chorea |
| 833326008 | Cortical vascular dementia |
| 838275008 | Stenosis of cerebral artery |
| 838276009 | Amyotrophic lateral sclerosis, parkinsonism, dementia complex |
| 838308007 | Fibromuscular dysplasia of wall of intracranial artery |
| 838309004 | Cerebrovascular abnormality due to Takayasu disease |
| 83832001 | Metachromatic leukodystrophy without arylsulfatase deficiency |
| 838339009 | Basal encephalocele |
| 838383000 | Chorea caused by toxin |
| 838441009 | Intellectual disability, aphasia, shuffling gait, adducted thumbs syndrome |
| 83942000 | Acute disseminated encephalomyelitis |
| 840419005 | Dissection of extracranial carotid artery |
| 840420004 | Dissection of extracranial vertebral artery |
| 840422007 | Dissection of anterior cerebral artery |
| 840434004 | Dissection of posterior cerebral artery |
| 840436002 | Dissection of middle cerebral artery |
| 840437006 | Dissection of multiple cerebral arteries |
| 840438001 | Dissection of intracranial vertebral artery |
| 840439009 | Dissection of intracranial carotid artery |
| 840441005 | Dissection of intracranial artery |
| 840452004 | Classical sporadic Creutzfeldt-Jakob disease |
| 840464007 | Dementia due to carbon monoxide poisoning |
| 840465008 | Dementia due to iron deficiency |
| 840471002 | Hydrocephalus due to Dandy-Walker malformation |
| 840505007 | Down syndrome co-occurrent with leukemoid reaction associated transient neonatal pustulosis |
| 84160009 | Laryngeal hemiplegia |
| 84161000119100 | Partial epileptic seizure of parietal lobe with impairment of consciousness |
| 84171000119106 | Partial epileptic seizure of frontal lobe with impairment of consciousness |
| 84181000119109 | Partial epileptic seizure of occipital lobe with impairment of consciousness |
| 84191000119107 | Partial epileptic seizure of temporal lobe with impairment of consciousness |
| 84201000119105 | Intractable partial temporal lobe epilepsy with impairment of consciousness |
| 84211000119108 | Intractable partial parietal lobe epilepsy with impairment of consciousness |
| 84221000119101 | Intractable partial frontal lobe epilepsy with impairment of consciousness |
| 84231000119103 | Intractable partial occipital lobe epilepsy with impairment of consciousness |
| 84438001 | Pure autonomic failure |
| 84455002 | Spinal paraplegia |
| 84590007 | Lower motor neuron disease |
| 84757009 | Epilepsy |
| 849488701000119104 | Cerebrovascular accident due to embolism of right anterior cerebral artery |
| 849579281000119106 | Cerebrovascular accident due to occlusion of right posterior communicating artery |
| 85102008 | Cerebellar ataxia |
| 851365731000119106 | Cerebrovascular accident due to thrombosis of left posterior cerebral artery |
| 85505000 | Adult spinal muscular atrophy |
| 85592008 | Primary progressive cerebellar degeneration |
| 8563000 | Cholinergic crisis |
| 85641006 | Hemianencephaly |
| 85672005 | Anterior horn cell disease |
| 859422751000119101 | Cerebrovascular accident due to embolism of left carotid artery |
| 86003009 | Carotid artery thrombosis |
| 86044005 | Amyotrophic lateral sclerosis |
| 860802009 | Ex-vacuo hydrocephalus due to infection |
| 860803004 | Hydrocephalus due to tuberculosis of brain |
| 860804005 | Epilepsy due to infectious encephalitis |
| 860806007 | Epilepsy due to infectious meningitis |
| 860807003 | Hereditary autonomic neuropathy |
| 860809000 | Hereditary sensory autonomic neuropathy type IIA |
| 860810005 | Hereditary sensory autonomic neuropathy type IIB |
| 860811009 | Hereditary sensory autonomic neuropathy type ID |
| 860812002 | Hereditary sensory autonomic neuropathy type IE |
| 860813007 | Hereditary sensory autonomic neuropathy type IA |
| 860814001 | Hereditary sensory autonomic neuropathy type IC |
| 860815000 | Epilepsy due to neonatal central nervous system infection |
| 860826006 | Creutzfeldt-Jakob Disease caused by human growth hormone |
| 860881004 | Flaccid diplegia of lower extremities |
| 86188000 | Kuru |
| 86444004 | Niemann-Pick disease, type C, acute form |
| 864471000000106 | Anterior opercular syndrome |
| 86553761000119103 | Cerebrovascular accident due to occlusion of bilateral posterior cerebral arteries |
| 866050001 | Mixed germ cell neoplasm of central nervous system |
| 866051002 | Motor neuron disease due to lead intoxication |
| 866053004 | Middle interhemispheric variant of holoprosencephaly |
| 870284000 | Pelizaeus Merzbacher like disease due to HSPD1 mutation |
| 870285004 | Pelizaeus Merzbacher like disease due to SLC16A2 mutation |
| 870286003 | Pelizaeus Merzbacher like disease due to AIMP1 mutation |
| 870287007 | Pelizaeus Merzbacher like disease due to GJC2 mutation |
| 870319003 | Optic atrophy due to late syphilis |
| 870345007 | Compression of spinal cord due to cavernous hemangioma |
| 870544005 | Occlusion of distal basilar artery |
| 870566003 | Occlusion of anterior choroidal artery |
| 870579007 | Occlusion of branch of basilar artery |
| 870637009 | Dissection of cervical artery |
| 87091000119101 | Malignant glioma of cerebrum |
| 87111000119109 | Malignant glioma of hypothalamus |
| 87121000119102 | Malignant glioma of cerebellum |
| 87141000119108 | Primary malignant neoplasm of intramedullary spinal cord |
| 87151000119105 | Malignant glioma of central nervous system |
| 871637001 | Thrombosis of multiple cerebral veins |
| 87235005 | Dialysis disequilibrium syndrome |
| 87551000119101 | Visual disturbance as sequela of cerebrovascular disease |
| 87555007 | Claude's syndrome |
| 87607002 | Pelizaeus-Merzbacher disease, classic form |
| 87842000 | Generalized neuromuscular exhaustion syndrome |
| 878808006 | Nongerminomatous germ cell tumor of central nervous system |
| 87937009 | Endophlebitis of intracranial venous sinus |
| 879937000 | Alpha-N-acetylgalactosaminidase deficiency type 1 |
| 880065001 | Alpha-N-acetylgalactosaminidase deficiency type 2 |
| 880066000 | Alpha-N-acetylgalactosaminidase deficiency type 3 |
| 880093002 | 17q11 deletion syndrome |
| 88032003 | Amaurosis fugax |
| 881694631000119107 | Cerebrovascular accident of medulla oblongata |
| 88174006 | Basilar artery thrombosis |
| 88518009 | Wilson's disease |
| 885831000000109 | Choreoathetoid cerebral palsy |
| 88755007 | Phlebitis of lateral venous sinus |
| 88922007 | Thrombosis of basilar sinus |
| 88923002 | Progressive muscular atrophy |
| 890118006 | Mowat-Wilson syndrome due to monosomy 2q22 |
| 890286007 | Bilateral frontoparietal polymicrogyria |
| 890346002 | Holoprosencephaly co-occurrent with congenital nasal pyriform aperture stenosis |
| 890368007 | Congenital muscular dystrophy type 1C due to fukutin related protein gene mutation |
| 890395002 | Congenital muscular dystrophy type 1D large gene mutation |
| 890422008 | Cervicothoracic spina bifida aperta with hydrocephalus |
| 890430009 | Complete agenesis of vermis |
| 890432001 | Cockayne syndrome type 3 |
| 890433006 | Cockayne syndrome type 1 |
| 890434000 | Cockayne syndrome type 2 |
| 89142007 | Progressive intracranial arterial occlusion |
| 894125007 | Cervicothoracic spina bifida aperta |
| 89437009 | Cerebral paraparesis |
| 89576007 | Pallidonigrospinal degeneration |
| 898941951000119108 | Cerebrovascular accident due to occlusion of bilateral vertebral arteries |
| 89980009 | Thrombosis of cavernous venous sinus |
| 90099008 | Subcortical leukoencephalopathy |
| 90253000 | Progressive subcortical gliosis |
| 903741000000102 | Uhthoff phenomenon |
| 904531000000100 | Bilateral spastic cerebral palsy |
| 90520006 | Vertebral artery stenosis |
| 90791004 | Posthemiplegic ataxia |
| 90811000119100 | Low grade malignant glioma of brain |
| 90831000119105 | Grade 4 malignant glioma of brain |
| 91327001 | Quadriparesis |
| 9133005 | Familial amyloid polyneuropathy, Iowa type |
| 91502009 | Spinocerebellar disease |
| 915141931000119109 | Cerebrovascular accident due to embolism of basilar artery |
| 91601000119109 | Sequela of thrombotic stroke |
| 91637004 | Myasthenia gravis |
| 91952008 | Azorean disease |
| 91953003 | Azorean disease, type I |
| 91954009 | Azorean disease, type II |
| 91955005 | Azorean disease, type III |
| 91956006 | Azorean disease, type IV |
| 92341000119107 | Weakness of extremities as sequela of stroke |
| 92503002 | Neurofibromatosis type 2 |
| 92824003 | Neurofibromatosis type 1 |
| 92962004 | Congenital absence of carotid artery |
| 92997002 | Congenital anomaly of carotid artery |
| 93054001 | Congenital dilatation of carotid artery |
| 93153005 | Limb-girdle muscular dystrophy |
| 93249003 | Congenital hypoplasia of cerebrum |
| 93312006 | Congenital malposition of carotid artery |
| 93396008 | Congenital stenosis of carotid artery |
| 9345005 | Dialysis dementia |
| 93557001 | Holorachischisis |
| 936271000000100 | Congenital anomaly of precerebral vessel |
| 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 |
| 939885431000119109 | Cerebrovascular accident due to embolism of bilateral middle cerebral arteries |
| 94068003 | Primary malignant neoplasm of spinal cord |
| 94069006 | Primary malignant neoplasm of spinal meninges |
| 94086000 | Primary malignant neoplasm of temporal lobe |
| 94224009 | Metastatic malignant neoplasm to brain stem |
| 94225005 | Metastatic malignant neoplasm to brain |
| 94243009 | Metastatic malignant neoplasm to central nervous system |
| 94245002 | Metastatic malignant neoplasm to cerebellum |
| 94246001 | Metastatic malignant neoplasm to cerebral meninges |
| 94247005 | Metastatic malignant neoplasm to cerebral ventricle |
| 94248000 | Metastatic malignant neoplasm to cerebrum |
| 94267001 | Metastatic malignant neoplasm to craniopharyngeal duct |
| 94309003 | Metastatic malignant neoplasm to frontal lobe |
| 943181000000103 | Degenerative disease of basal ganglia |
| 94448002 | Metastatic malignant neoplasm to occipital lobe |
| 94452002 | Metastatic malignant neoplasm to optic nerve |
| 94471000 | Metastatic malignant neoplasm to parietal lobe |
| 94489004 | Metastatic malignant neoplasm to pineal gland |
| 94491007 | Metastatic malignant neoplasm to pituitary gland |
| 94600009 | Metastatic malignant neoplasm to spinal cord |
| 94601008 | Metastatic malignant neoplasm to spinal meninges |
| 94622002 | Metastatic malignant neoplasm to temporal lobe |
| 95208000 | Photogenic epilepsy |
| 95235009 | Retroesophageal carotid artery |
| 9537004 | Juvenile GM2 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 |
| 95643007 | Autoimmune encephalitis |
| 95644001 | Systemic lupus erythematosus encephalitis |
| 95646004 | Cerebellar degeneration |
| 95647008 | Upper motor neuron disease |
| 95650006 | Transient hemiplegia |
| 95651005 | Chronic progressive paraparesis |
| 957319791000119104 | Cerebrovascular accident due to thrombosis of left cerebellar artery |
| 95830009 | Pituitary infarction |
| 9611000119107 | Symptomatic carotid artery stenosis |
| 96981000119102 | Primary malignant neoplasm of rectosigmoid junction metastatic to brain |
| 97381000119100 | Neurogenic bladder due to quadriplegia |
| 97391000119102 | Paraplegia with neurogenic bladder |
| 9753004 | Triplegia |
| 97751000119108 | Altered behavior in Alzheimer's disease |
| 984681000000101 | Profound learning disability |
| 9901000119100 | Occlusion of cerebral artery with stroke |
| 99131000119108 | Astrocytoma of cerebrum |
| 99451000119105 | Cerebral infarction due to stenosis of carotid artery |
Codes not in the full codelist are in faint grey.