| Source | us.nlm.vsac#0.11.0:null (v4.0.1) |
| resourceType | ValueSet |
| id | 2.16.840.1.113762.1.4.1078.144 |
| canonical | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1078.144 |
| version | 20230601 |
| status | active |
| publisher | Optum Steward |
| name | VirtualRealityContraindicationsSeizuresAndEpilepsy |
| title | Virtual reality contraindications Seizures and Epilepsy |
| date | 2023-06-01T01:01:19-04:00 |
| Usages | (none) |
This value set contains 365 concepts
| Code | System | Display |
| 100941000119100 | http://snomed.info/sct | Epilepsy in mother complicating pregnancy (disorder) |
| 10750951000119106 | http://snomed.info/sct | Epilepsy in mother complicating childbirth (disorder) |
| 109478007 | http://snomed.info/sct | Kohlschutter's syndrome (disorder) |
| 111498005 | http://snomed.info/sct | Extratemporal epilepsy (disorder) |
| 1163527006 | http://snomed.info/sct | Epilepsy due to disease caused by parasite (disorder) |
| 1163529009 | http://snomed.info/sct | Epilepsy due to bacterial endocarditis (disorder) |
| 1167371007 | http://snomed.info/sct | Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome (disorder) |
| 1172593006 | http://snomed.info/sct | Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome (disorder) |
| 1179282009 | http://snomed.info/sct | Severe neurodevelopmental disorder with feeding difficulties, stereotypic hand movement, bilateral cataract (disorder) |
| 1179359005 | http://snomed.info/sct | Maternal epilepsy due to perinatal stroke (disorder) |
| 1179360000 | http://snomed.info/sct | Fetal epilepsy due to perinatal stroke (disorder) |
| 1179547007 | http://snomed.info/sct | Neonatal epilepsy due to perinatal stroke (disorder) |
| 1187042007 | http://snomed.info/sct | Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome (disorder) |
| 1187278006 | http://snomed.info/sct | Spastic paraplegia, severe developmental delay, epilepsy syndrome (disorder) |
| 119001000119108 | http://snomed.info/sct | Intractable simple partial epilepsy (disorder) |
| 1197587003 | http://snomed.info/sct | Lethal neonatal spasticity, epileptic encephalopathy syndrome (disorder) |
| 1208939001 | http://snomed.info/sct | Progressive myoclonic epilepsy type 7 (disorder) |
| 1222656005 | http://snomed.info/sct | Synaptic Ras GTPase activating protein 1-related developmental and epileptic encephalopathy (disorder) |
| 1222659003 | http://snomed.info/sct | Ring finger protein 13-related severe early-onset epileptic encephalopathy (disorder) |
| 1222662000 | http://snomed.info/sct | Neonatal epileptic encephalopathy due to deficiency of glutaminase (disorder) |
| 1228857005 | http://snomed.info/sct | Progressive myoclonic epilepsy type 9 (disorder) |
| 1230376005 | http://snomed.info/sct | Contactin associated protein 2-related developmental and epileptic encephalopathy (disorder) |
| 1231282002 | http://snomed.info/sct | Benign familial neonatal-infantile seizures (disorder) |
| 1231737000 | http://snomed.info/sct | Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome (disorder) |
| 1237417007 | http://snomed.info/sct | Carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation (disorder) |
| 1237571004 | http://snomed.info/sct | Benign familial infantile epilepsy (disorder) |
| 1237619001 | http://snomed.info/sct | Fatty acyl-coenzyme A reductase 1 deficiency (disorder) |
| 13973009 | http://snomed.info/sct | Grand mal status (disorder) |
| 14401000119109 | http://snomed.info/sct | Partial frontal lobe epilepsy (disorder) |
| 15523002 | http://snomed.info/sct | Benign focal epilepsy of childhood (disorder) |
| 15985351000119105 | http://snomed.info/sct | Intractable juvenile myoclonic status epilepticus (disorder) |
| 161480008 | http://snomed.info/sct | History of epilepsy (situation) |
| 192845009 | http://snomed.info/sct | Myoclonic encephalopathy (disorder) |
| 192979009 | http://snomed.info/sct | Generalized non-convulsive epilepsy (disorder) |
| 192990004 | http://snomed.info/sct | Benign myoclonic epilepsy in infancy (disorder) |
| 192999003 | http://snomed.info/sct | Partial epilepsy with impairment of consciousness (disorder) |
| 193000002 | http://snomed.info/sct | Temporal lobe epilepsy (disorder) |
| 193002005 | http://snomed.info/sct | Psychosensory epilepsy (disorder) |
| 193003000 | http://snomed.info/sct | Mesiobasal limbic epilepsy (disorder) |
| 193008009 | http://snomed.info/sct | Somatosensory epilepsy (disorder) |
| 193009001 | http://snomed.info/sct | Partial epilepsy with autonomic symptoms (disorder) |
| 193010006 | http://snomed.info/sct | Visual reflex epilepsy (disorder) |
| 193021002 | http://snomed.info/sct | Cursive (running) epilepsy (disorder) |
| 19598007 | http://snomed.info/sct | Generalized epilepsy (disorder) |
| 20121000119105 | http://snomed.info/sct | Partial occipital lobe epilepsy (disorder) |
| 21391000119102 | http://snomed.info/sct | Partial parietal lobe epilepsy (disorder) |
| 2198002 | http://snomed.info/sct | Visceral epilepsy (disorder) |
| 225931003 | http://snomed.info/sct | At risk of epileptic fits (finding) |
| 230191005 | http://snomed.info/sct | Rasmussen syndrome (disorder) |
| 230381009 | http://snomed.info/sct | Localization-related epilepsy (disorder) |
| 230382002 | http://snomed.info/sct | Benign frontal epilepsy of childhood (disorder) |
| 230383007 | http://snomed.info/sct | Benign psychomotor epilepsy of childhood (disorder) |
| 230384001 | http://snomed.info/sct | Benign atypical partial epilepsy in childhood (disorder) |
| 230386004 | http://snomed.info/sct | Childhood epilepsy with occipital paroxysms (disorder) |
| 230387008 | http://snomed.info/sct | Benign occipital epilepsy of childhood - early onset variant (disorder) |
| 230388003 | http://snomed.info/sct | Benign occipital epilepsy of childhood - late onset variant (disorder) |
| 230389006 | http://snomed.info/sct | Primary inherited reading epilepsy (disorder) |
| 230390002 | http://snomed.info/sct | Localization-related symptomatic epilepsy (disorder) |
| 230391003 | http://snomed.info/sct | Amygdalo-hippocampal epilepsy (disorder) |
| 230392005 | http://snomed.info/sct | Rhinencephalic epilepsy (disorder) |
| 230393000 | http://snomed.info/sct | Lateral temporal epilepsy (disorder) |
| 230394006 | http://snomed.info/sct | Frontal lobe epilepsy (disorder) |
| 230395007 | http://snomed.info/sct | Supplementary motor epilepsy (disorder) |
| 230396008 | http://snomed.info/sct | Cingulate epilepsy (disorder) |
| 230397004 | http://snomed.info/sct | Anterior frontopolar epilepsy (disorder) |
| 230398009 | http://snomed.info/sct | Orbitofrontal epilepsy (disorder) |
| 230399001 | http://snomed.info/sct | Dorsolateral epilepsy (disorder) |
| 230400008 | http://snomed.info/sct | Opercular epilepsy (disorder) |
| 230401007 | http://snomed.info/sct | Non-progressive Kozhevnikow syndrome (disorder) |
| 230403005 | http://snomed.info/sct | Parietal lobe epilepsy (disorder) |
| 230404004 | http://snomed.info/sct | Occipital lobe epilepsy (disorder) |
| 230405003 | http://snomed.info/sct | Chronic progressive epilepsia partialis continua of childhood (disorder) |
| 230406002 | http://snomed.info/sct | Localization-related symptomatic epilepsy with specific precipitant (disorder) |
| 230407006 | http://snomed.info/sct | Hemiplegia-hemiconvulsion-epilepsy syndrome (disorder) |
| 230408001 | http://snomed.info/sct | Localization-related cryptogenic epilepsy (disorder) |
| 230410004 | http://snomed.info/sct | Benign neonatal familial convulsions (disorder) |
| 230411000 | http://snomed.info/sct | Benign non-familial neonatal convulsions (disorder) |
| 230412007 | http://snomed.info/sct | Myoclonic epilepsy of early childhood (disorder) |
| 230413002 | http://snomed.info/sct | Juvenile absence epilepsy (disorder) |
| 230414008 | http://snomed.info/sct | Epilepsy with grand mal seizures on awakening (disorder) |
| 230415009 | http://snomed.info/sct | Cryptogenic generalized epilepsy (disorder) |
| 230416005 | http://snomed.info/sct | Cryptogenic West syndrome (disorder) |
| 230417001 | http://snomed.info/sct | Symptomatic West syndrome (disorder) |
| 230418006 | http://snomed.info/sct | Lennox-Gastaut syndrome (disorder) |
| 230419003 | http://snomed.info/sct | Cryptogenic Lennox-Gastaut syndrome (disorder) |
| 230420009 | http://snomed.info/sct | Symptomatic Lennox-Gastaut syndrome (disorder) |
| 230421008 | http://snomed.info/sct | Myoclonic astatic epilepsy (disorder) |
| 230422001 | http://snomed.info/sct | Myoclonic absence epilepsy (disorder) |
| 230423006 | http://snomed.info/sct | Unverricht-Lundborg syndrome (disorder) |
| 230425004 | http://snomed.info/sct | Lafora disease (disorder) |
| 230426003 | http://snomed.info/sct | Myoclonic epilepsy with ragged red fibers (disorder) |
| 230427007 | http://snomed.info/sct | Cryptogenic myoclonic epilepsy (disorder) |
| 230428002 | http://snomed.info/sct | Idiopathic myoclonic epilepsy (disorder) |
| 230429005 | http://snomed.info/sct | Early infantile epileptic encephalopathy with suppression bursts (disorder) |
| 230430000 | http://snomed.info/sct | Symptomatic myoclonic epilepsy (disorder) |
| 230435005 | http://snomed.info/sct | Epilepsy undetermined whether focal or generalized (disorder) |
| 230437002 | http://snomed.info/sct | Severe myoclonic epilepsy in infancy (disorder) |
| 230438007 | http://snomed.info/sct | Acquired epileptic aphasia (disorder) |
| 230439004 | http://snomed.info/sct | Epilepsy with continuous spike wave during slow-wave sleep (disorder) |
| 230440002 | http://snomed.info/sct | Secondary reading epilepsy (disorder) |
| 230441003 | http://snomed.info/sct | Drug-induced epilepsy (disorder) |
| 230443000 | http://snomed.info/sct | Narcotic withdrawal epilepsy (disorder) |
| 230444006 | http://snomed.info/sct | Menstrual epilepsy (disorder) |
| 230445007 | http://snomed.info/sct | Nocturnal epilepsy (disorder) |
| 230448009 | http://snomed.info/sct | Writing epilepsy (disorder) |
| 230450001 | http://snomed.info/sct | Eating epilepsy (disorder) |
| 230452009 | http://snomed.info/sct | Toothbrushing epilepsy (disorder) |
| 230453004 | http://snomed.info/sct | Decision-making epilepsy (disorder) |
| 230454005 | http://snomed.info/sct | Aquagenic epilepsy (disorder) |
| 230455006 | http://snomed.info/sct | Self-induced non-photosensitive epilepsy (disorder) |
| 230456007 | http://snomed.info/sct | Status epilepticus (disorder) |
| 230459000 | http://snomed.info/sct | Non-convulsive simple partial status epilepticus (disorder) |
| 230460005 | http://snomed.info/sct | Complex partial status epilepticus (disorder) |
| 241006 | http://snomed.info/sct | Epilepsia partialis continua (disorder) |
| 267581004 | http://snomed.info/sct | Progressive myoclonic epilepsy (disorder) |
| 267592003 | http://snomed.info/sct | Motor cortex epilepsy (disorder) |
| 278510009 | http://snomed.info/sct | Localization-related idiopathic epilepsy (disorder) |
| 28055006 | http://snomed.info/sct | West syndrome (disorder) |
| 290671000119100 | http://snomed.info/sct | Status epilepticus due to complex partial epileptic seizure (disorder) |
| 290681000119102 | http://snomed.info/sct | Status epilepticus due to refractory complex partial seizures (disorder) |
| 290691000119104 | http://snomed.info/sct | Status epilepticus due to generalized idiopathic epilepsy (disorder) |
| 290711000119101 | http://snomed.info/sct | Status epilepticus due to intractable idiopathic generalized epilepsy (disorder) |
| 290721000119108 | http://snomed.info/sct | Status epilepticus due to refractory epilepsy (disorder) |
| 290731000119106 | http://snomed.info/sct | Idiopathic partial status epilepticus (disorder) |
| 290741000119102 | http://snomed.info/sct | Intractable idiopathic partial epilepsy (disorder) |
| 290761000119103 | http://snomed.info/sct | Status epilepticus due to refractory simple partial epilepsy (disorder) |
| 290871000119101 | http://snomed.info/sct | Infantile spasms co-occurrent with status epilepticus (disorder) |
| 290881000119103 | http://snomed.info/sct | Refractory infantile spasms co-occurrent with status epilepticus (disorder) |
| 291311000119108 | http://snomed.info/sct | Status epilepticus in benign Rolandic epilepsy (disorder) |
| 307356008 | http://snomed.info/sct | Motor epilepsy (disorder) |
| 307357004 | http://snomed.info/sct | Jacksonian, focal or motor epilepsy (disorder) |
| 322112361000132104 | http://snomed.info/sct | Epilepsy due to scarring of brain (disorder) |
| 329991000119104 | http://snomed.info/sct | Intractable atypical absence epilepsy (disorder) |
| 3371000119106 | http://snomed.info/sct | Refractory generalized convulsive epilepsy (disorder) |
| 352818000 | http://snomed.info/sct | Tonic-clonic epilepsy (disorder) |
| 361123003 | http://snomed.info/sct | Psychomotor epilepsy (disorder) |
| 361268000 | http://snomed.info/sct | Alcohol-induced epilepsy (disorder) |
| 36803009 | http://snomed.info/sct | Idiopathic generalized epilepsy (disorder) |
| 38281008 | http://snomed.info/sct | Benign neonatal convulsions (disorder) |
| 39194005 | http://snomed.info/sct | Visual epilepsy (disorder) |
| 39745004 | http://snomed.info/sct | Chronic progressive epilepsia partialis continua (disorder) |
| 413101007 | http://snomed.info/sct | Stress-induced epilepsy (disorder) |
| 422513000 | http://snomed.info/sct | Epilepsy, not refractory (disorder) |
| 422724001 | http://snomed.info/sct | Refractory localization-related epilepsy (disorder) |
| 422873003 | http://snomed.info/sct | Refractory epilepsia partialis continua (disorder) |
| 425054007 | http://snomed.info/sct | Refractory occipital lobe epilepsy (disorder) |
| 425237009 | http://snomed.info/sct | Refractory frontal lobe epilepsy (disorder) |
| 425349008 | http://snomed.info/sct | Refractory parietal lobe epilepsy (disorder) |
| 430811000124100 | http://snomed.info/sct | Benign familial neonatal seizures, refractory (disorder) |
| 430821000124108 | http://snomed.info/sct | Benign familial neonatal seizures, non-refractory (disorder) |
| 431071000124107 | http://snomed.info/sct | Early infantile epileptic encephalopathy, refractory (disorder) |
| 431081000124105 | http://snomed.info/sct | Early infantile epileptic encephalopathy, non-refractory (disorder) |
| 431091000124108 | http://snomed.info/sct | Benign myoclonic epilepsy in infancy, refractory (disorder) |
| 431101000124102 | http://snomed.info/sct | Benign myoclonic epilepsy in infancy, non-refractory (disorder) |
| 431111000124104 | http://snomed.info/sct | Lennox-Gastaut syndrome, refractory (disorder) |
| 431121000124107 | http://snomed.info/sct | Lennox-Gastaut syndrome, non-refractory (disorder) |
| 431131000124105 | http://snomed.info/sct | Myoclonic absence epilepsy, refractory (disorder) |
| 431141000124100 | http://snomed.info/sct | Myoclonic absence epilepsy, non-refractory (disorder) |
| 431151000124103 | http://snomed.info/sct | Childhood absence epilepsy, refractory (disorder) |
| 431161000124101 | http://snomed.info/sct | Childhood absence epilepsy, non-refractory (disorder) |
| 431461000124109 | http://snomed.info/sct | Juvenile absence epilepsy, refractory (disorder) |
| 431471000124102 | http://snomed.info/sct | Juvenile absence epilepsy, non-refractory (disorder) |
| 431961000124104 | http://snomed.info/sct | Benign occipital epilepsy of childhood - late onset, refractory (disorder) |
| 431971000124106 | http://snomed.info/sct | Benign occipital epilepsy of childhood - late onset, non-refractory (disorder) |
| 432031000124101 | http://snomed.info/sct | Infantile spasms, non-refractory (disorder) |
| 432151000124107 | http://snomed.info/sct | Myoclonic seizure, non-refractory (disorder) |
| 432161000124109 | http://snomed.info/sct | Severe myoclonic epilepsy in infancy, non-refractory (disorder) |
| 432171000124102 | http://snomed.info/sct | Severe myoclonic epilepsy in infancy, refractory (disorder) |
| 432291000124105 | http://snomed.info/sct | Temporal lobe epilepsy, non-refractory (disorder) |
| 432461000124101 | http://snomed.info/sct | Post-traumatic epilepsy, refractory (disorder) |
| 432471000124108 | http://snomed.info/sct | Post-traumatic epilepsy, non-refractory (disorder) |
| 432501000124101 | http://snomed.info/sct | Atonic seizure, refractory (disorder) |
| 432541000124104 | http://snomed.info/sct | Epilepsia partialis continua, non-refractory (disorder) |
| 434201000124105 | http://snomed.info/sct | Grand mal status epilepticus, refractory (disorder) |
| 434211000124108 | http://snomed.info/sct | Grand mal status epilepticus, non-refractory (disorder) |
| 434291000124103 | http://snomed.info/sct | Myoclonic seizure, refractory (disorder) |
| 434491000124104 | http://snomed.info/sct | Idiopathic generalized epilepsy, non-refractory (disorder) |
| 434501000124107 | http://snomed.info/sct | Complex partial status epilepticus, refractory (disorder) |
| 434511000124105 | http://snomed.info/sct | Complex partial status epilepticus, non-refractory (disorder) |
| 434541000124109 | http://snomed.info/sct | Benign childhood epilepsy with centrotemporal spikes, refractory (disorder) |
| 434551000124106 | http://snomed.info/sct | Benign childhood epilepsy with centrotemporal spikes, non-refractory (disorder) |
| 435321000124106 | http://snomed.info/sct | Acquired epileptic aphasia, non-refractory (disorder) |
| 435331000124109 | http://snomed.info/sct | Acquired epileptic aphasia, refractory (disorder) |
| 435341000124104 | http://snomed.info/sct | Rasmussen syndrome, refractory (disorder) |
| 435361000124100 | http://snomed.info/sct | Juvenile myoclonic epilepsy, non-refractory (disorder) |
| 438411000124101 | http://snomed.info/sct | Myoclonic astatic epilepsy, refractory (disorder) |
| 438421000124109 | http://snomed.info/sct | Myoclonic astatic epilepsy, non-refractory (disorder) |
| 440211000124100 | http://snomed.info/sct | Generalized convulsive epilepsy, non-refractory (disorder) |
| 44145005 | http://snomed.info/sct | Benign Rolandic epilepsy (disorder) |
| 441678004 | http://snomed.info/sct | Refractory generalized nonconvulsive epilepsy (disorder) |
| 442151000124108 | http://snomed.info/sct | Autosomal dominant nocturnal frontal lobe epilepsy, refractory (disorder) |
| 442161000124105 | http://snomed.info/sct | Autosomal dominant nocturnal frontal lobe epilepsy, non-refractory (disorder) |
| 442481002 | http://snomed.info/sct | Epilepsy characterized by intractable complex partial seizures (disorder) |
| 442512002 | http://snomed.info/sct | Nonconvulsive status epilepticus (disorder) |
| 444441000124109 | http://snomed.info/sct | Generalized epilepsy with febrile seizures plus, refractory (disorder) |
| 444451000124106 | http://snomed.info/sct | Generalized epilepsy with febrile seizures plus, non-refractory (disorder) |
| 445355009 | http://snomed.info/sct | Refractory epilepsy (disorder) |
| 47391000119107 | http://snomed.info/sct | Primary generalized absence epilepsy (disorder) |
| 49776008 | http://snomed.info/sct | Centrencephalic epilepsy (disorder) |
| 50866000 | http://snomed.info/sct | Childhood absence epilepsy (disorder) |
| 5321000124109 | http://snomed.info/sct | Temporal lobe epilepsy with mesial temporal sclerosis (disorder) |
| 6204001 | http://snomed.info/sct | Juvenile myoclonic epilepsy (disorder) |
| 65120008 | http://snomed.info/sct | Generalized convulsive epilepsy (disorder) |
| 698021005 | http://snomed.info/sct | Autosomal dominant nocturnal frontal lobe epilepsy (disorder) |
| 698760002 | http://snomed.info/sct | Generalized non-convulsive absence epilepsy (disorder) |
| 698761003 | http://snomed.info/sct | Refractory juvenile myoclonic epilepsy (disorder) |
| 698762005 | http://snomed.info/sct | Refractory myoclonic epilepsy (disorder) |
| 698763000 | http://snomed.info/sct | Postoperative status epilepticus (disorder) |
| 698764006 | http://snomed.info/sct | Post infectious grand mal epilepsy (disorder) |
| 698767004 | http://snomed.info/sct | Post-cerebrovascular accident epilepsy (disorder) |
| 699688008 | http://snomed.info/sct | Generalized epilepsy with febrile seizures plus (disorder) |
| 702326000 | http://snomed.info/sct | Progressive myoclonus epilepsy with ataxia (disorder) |
| 703151001 | http://snomed.info/sct | History of single seizure (situation) |
| 703524005 | http://snomed.info/sct | Spinal muscular atrophy with progressive myoclonic epilepsy (disorder) |
| 710046001 | http://snomed.info/sct | Refractory idiopathic generalized epilepsy (disorder) |
| 715534008 | http://snomed.info/sct | Infantile convulsion and choreoathetosis syndrome (disorder) |
| 715629001 | http://snomed.info/sct | Generalized epilepsy and paroxysmal dyskinesia syndrome (disorder) |
| 716278005 | http://snomed.info/sct | Jeavons syndrome (disorder) |
| 716706009 | http://snomed.info/sct | Female restricted epilepsy with intellectual disability syndrome (disorder) |
| 717223008 | http://snomed.info/sct | X-linked epilepsy with learning disability and behavior disorder syndrome (disorder) |
| 717225001 | http://snomed.info/sct | Benign adult familial myoclonic epilepsy (disorder) |
| 71831005 | http://snomed.info/sct | Symptomatic generalized epilepsy (disorder) |
| 720519003 | http://snomed.info/sct | Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome (disorder) |
| 721088003 | http://snomed.info/sct | Developmental delay, epilepsy, neonatal diabetes syndrome (disorder) |
| 722386009 | http://snomed.info/sct | Celiac disease with epilepsy and cerebral calcification syndrome (disorder) |
| 723125008 | http://snomed.info/sct | Epileptic encephalopathy (disorder) |
| 723676007 | http://snomed.info/sct | Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome (disorder) |
| 724274009 | http://snomed.info/sct | Infant epilepsy with migrant focal crisis (disorder) |
| 724549005 | http://snomed.info/sct | Epilepsy due to infectious disease of central nervous system (disorder) |
| 724576005 | http://snomed.info/sct | Pyridoxal 5-phosphate dependent epilepsy (disorder) |
| 724786008 | http://snomed.info/sct | Epilepsy due to perinatal anoxic-ischemic brain injury (disorder) |
| 724787004 | http://snomed.info/sct | Epilepsy due to cerebrovascular accident (disorder) |
| 724789001 | http://snomed.info/sct | Epilepsy due to intracranial tumor (disorder) |
| 724988000 | http://snomed.info/sct | Epilepsy co-occurrent and due to degenerative brain disorder (disorder) |
| 724989008 | http://snomed.info/sct | Epilepsy co-occurrent and due to mesial temporal sclerosis (disorder) |
| 724990004 | http://snomed.info/sct | Epilepsy due to immune disorder (disorder) |
| 724991000 | http://snomed.info/sct | Epilepsy co-occurrent and due to demyelinating disorder (disorder) |
| 724992007 | http://snomed.info/sct | Epilepsy co-occurrent and due to dementia (disorder) |
| 725163002 | http://snomed.info/sct | X-linked spasticity, intellectual disability, epilepsy syndrome (disorder) |
| 725413002 | http://snomed.info/sct | Febrile infection related epilepsy syndrome (disorder) |
| 726702005 | http://snomed.info/sct | Epileptic encephalopathy with global cerebral demyelination (disorder) |
| 733031004 | http://snomed.info/sct | Epilepsy, microcephaly, skeletal dysplasia syndrome (disorder) |
| 733032006 | http://snomed.info/sct | Epilepsy telangiectasia syndrome (disorder) |
| 733082001 | http://snomed.info/sct | Early-onset Lafora body disease (disorder) |
| 733195008 | http://snomed.info/sct | Epilepsy of infancy with migrating focal seizures (disorder) |
| 733623005 | http://snomed.info/sct | Autism spectrum disorder, epilepsy, arthrogryposis syndrome (disorder) |
| 734434007 | http://snomed.info/sct | Pyridoxine-dependent epilepsy (disorder) |
| 75023009 | http://snomed.info/sct | Post-traumatic epilepsy (disorder) |
| 763349002 | http://snomed.info/sct | Progressive myoclonic epilepsy with dystonia (disorder) |
| 763534009 | http://snomed.info/sct | Hot water reflex epilepsy (disorder) |
| 763622006 | http://snomed.info/sct | Thinking epilepsy (disorder) |
| 763632004 | http://snomed.info/sct | Startle epilepsy (disorder) |
| 763802009 | http://snomed.info/sct | Micturition induced epilepsy (disorder) |
| 763827002 | http://snomed.info/sct | Orgasm induced epilepsy (disorder) |
| 764453009 | http://snomed.info/sct | Action myoclonus renal failure syndrome (disorder) |
| 764522009 | http://snomed.info/sct | Familial focal epilepsy with variable foci (disorder) |
| 765093009 | http://snomed.info/sct | Rolandic epilepsy, speech dyspraxia syndrome (disorder) |
| 765170001 | http://snomed.info/sct | Sodium voltage-gated channel alpha subunit 8-related epilepsy with encephalopathy (disorder) |
| 765216006 | http://snomed.info/sct | Audiogenic epilepsy (disorder) |
| 766044005 | http://snomed.info/sct | Acute encephalopathy with biphasic seizures and late reduced diffusion (disorder) |
| 766815007 | http://snomed.info/sct | Perioral myoclonia with absences (disorder) |
| 767254005 | http://snomed.info/sct | Recurrent benign focal seizures of childhood (disorder) |
| 768666006 | http://snomed.info/sct | Syntaxin binding protein 1 encephalopathy with epilepsy (disorder) |
| 770405003 | http://snomed.info/sct | Benign familial mesial temporal lobe epilepsy (disorder) |
| 770431001 | http://snomed.info/sct | Early-onset epileptic encephalopathy and intellectual disability due to glutamate receptor, ionotropic, N-methyl-D-aspartate, subunit 2A mutation (disorder) |
| 770438007 | http://snomed.info/sct | Infantile spasm and broad thumb syndrome (disorder) |
| 770622009 | http://snomed.info/sct | Benign infantile focal epilepsy with midline spikes and waves during sleep (disorder) |
| 770623004 | http://snomed.info/sct | Benign occipital lobe epilepsy (disorder) |
| 770624005 | http://snomed.info/sct | Benign partial epilepsy of infancy with complex partial seizures (disorder) |
| 770643005 | http://snomed.info/sct | Mesial temporal lobe epilepsy with hippocampal sclerosis (disorder) |
| 770758009 | http://snomed.info/sct | New-onset refractory status epilepticus (disorder) |
| 770898002 | http://snomed.info/sct | Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency (disorder) |
| 771141002 | http://snomed.info/sct | Benign partial epilepsy with secondarily generalized seizures in infancy (disorder) |
| 771142009 | http://snomed.info/sct | Cortical dysplasia with focal epilepsy syndrome (disorder) |
| 771223000 | http://snomed.info/sct | Infantile epileptic dyskinetic encephalopathy (disorder) |
| 771448004 | http://snomed.info/sct | Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency (disorder) |
| 771469002 | http://snomed.info/sct | Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) |
| 773421009 | http://snomed.info/sct | Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression (disorder) |
| 773497001 | http://snomed.info/sct | Partial corpus callosum agenesis, cerebellar vermis hypoplasia with posterior fossa cysts syndrome (disorder) |
| 773498006 | http://snomed.info/sct | Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency (disorder) |
| 773548008 | http://snomed.info/sct | Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome (disorder) |
| 773643006 | http://snomed.info/sct | Multiple congenital anomalies, hypotonia, seizures syndrome type 2 (disorder) |
| 778001003 | http://snomed.info/sct | Potassium voltage-gated channel subfamily Q member 2 related epileptic encephalopathy (disorder) |
| 778047006 | http://snomed.info/sct | Myoclonic epilepsy in non-progressive encephalopathy (disorder) |
| 778063003 | http://snomed.info/sct | Cryptogenic late-onset epileptic spasms (disorder) |
| 780827006 | http://snomed.info/sct | Synaptic Ras GTPase activating protein 1- related intellectual disability (disorder) |
| 782737003 | http://snomed.info/sct | Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome (disorder) |
| 782772000 | http://snomed.info/sct | Congenital muscular dystrophy with intellectual disability and severe epilepsy (disorder) |
| 782825008 | http://snomed.info/sct | Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome (disorder) |
| 783055005 | http://snomed.info/sct | Progressive myoclonic epilepsy type 5 (disorder) |
| 783062001 | http://snomed.info/sct | Progressive myoclonic epilepsy type 6 (disorder) |
| 783064000 | http://snomed.info/sct | Progressive myoclonic epilepsy type 3 (disorder) |
| 783139000 | http://snomed.info/sct | Progressive myoclonic epilepsy type 8 (disorder) |
| 783739005 | http://snomed.info/sct | Familial temporal lobe epilepsy (disorder) |
| 784342008 | http://snomed.info/sct | Familial infantile myoclonic epilepsy (disorder) |
| 784372002 | http://snomed.info/sct | Familial mesial temporal lobe epilepsy with febrile seizures (disorder) |
| 784377008 | http://snomed.info/sct | Autosomal dominant epilepsy with auditory features (disorder) |
| 785726009 | http://snomed.info/sct | Hyperekplexia epilepsy syndrome (disorder) |
| 788417006 | http://snomed.info/sct | Alopecia, epilepsy, intellectual disability syndrome Moynahan type (disorder) |
| 79745005 | http://snomed.info/sct | Reflex epilepsy (disorder) |
| 82381000119103 | http://snomed.info/sct | Epileptic dementia with behavioral disturbance (disorder) |
| 8291000119107 | http://snomed.info/sct | Atonic epilepsy (disorder) |
| 84161000119100 | http://snomed.info/sct | Partial epileptic seizure of parietal lobe with impairment of consciousness (disorder) |
| 84171000119106 | http://snomed.info/sct | Partial epileptic seizure of frontal lobe with impairment of consciousness (disorder) |
| 84181000119109 | http://snomed.info/sct | Partial epileptic seizure of occipital lobe with impairment of consciousness (disorder) |
| 84191000119107 | http://snomed.info/sct | Partial epileptic seizure of temporal lobe with impairment of consciousness (disorder) |
| 84201000119105 | http://snomed.info/sct | Intractable partial temporal lobe epilepsy with impairment of consciousness (disorder) |
| 84211000119108 | http://snomed.info/sct | Intractable partial parietal lobe epilepsy with impairment of consciousness (disorder) |
| 84221000119101 | http://snomed.info/sct | Intractable partial frontal lobe epilepsy with impairment of consciousness (disorder) |
| 84231000119103 | http://snomed.info/sct | Intractable partial occipital lobe epilepsy with impairment of consciousness (disorder) |
| 84757009 | http://snomed.info/sct | Epilepsy (disorder) |
| 860804005 | http://snomed.info/sct | Epilepsy due to infectious encephalitis (disorder) |
| 860806007 | http://snomed.info/sct | Epilepsy due to infectious meningitis (disorder) |
| 860815000 | http://snomed.info/sct | Epilepsy due to neonatal central nervous system infection (disorder) |
| 95208000 | http://snomed.info/sct | Photogenic epilepsy (disorder) |
| G40.001 | http://hl7.org/fhir/sid/icd-10-cm | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, with status epilepticus |
| G40.009 | http://hl7.org/fhir/sid/icd-10-cm | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, without status epilepticus |
| G40.011 | http://hl7.org/fhir/sid/icd-10-cm | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, with status epilepticus |
| G40.019 | http://hl7.org/fhir/sid/icd-10-cm | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, without status epilepticus |
| G40.101 | http://hl7.org/fhir/sid/icd-10-cm | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, with status epilepticus |
| G40.109 | http://hl7.org/fhir/sid/icd-10-cm | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, without status epilepticus |
| G40.111 | http://hl7.org/fhir/sid/icd-10-cm | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, with status epilepticus |
| G40.119 | http://hl7.org/fhir/sid/icd-10-cm | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, without status epilepticus |
| G40.201 | http://hl7.org/fhir/sid/icd-10-cm | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, with status epilepticus |
| G40.209 | http://hl7.org/fhir/sid/icd-10-cm | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, without status epilepticus |
| G40.211 | http://hl7.org/fhir/sid/icd-10-cm | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, with status epilepticus |
| G40.219 | http://hl7.org/fhir/sid/icd-10-cm | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, without status epilepticus |
| G40.301 | http://hl7.org/fhir/sid/icd-10-cm | Generalized idiopathic epilepsy and epileptic syndromes, not intractable, with status epilepticus |
| G40.309 | http://hl7.org/fhir/sid/icd-10-cm | Generalized idiopathic epilepsy and epileptic syndromes, not intractable, without status epilepticus |
| G40.311 | http://hl7.org/fhir/sid/icd-10-cm | Generalized idiopathic epilepsy and epileptic syndromes, intractable, with status epilepticus |
| G40.319 | http://hl7.org/fhir/sid/icd-10-cm | Generalized idiopathic epilepsy and epileptic syndromes, intractable, without status epilepticus |
| G40.401 | http://hl7.org/fhir/sid/icd-10-cm | Other generalized epilepsy and epileptic syndromes, not intractable, with status epilepticus |
| G40.409 | http://hl7.org/fhir/sid/icd-10-cm | Other generalized epilepsy and epileptic syndromes, not intractable, without status epilepticus |
| G40.411 | http://hl7.org/fhir/sid/icd-10-cm | Other generalized epilepsy and epileptic syndromes, intractable, with status epilepticus |
| G40.419 | http://hl7.org/fhir/sid/icd-10-cm | Other generalized epilepsy and epileptic syndromes, intractable, without status epilepticus |
| G40.42 | http://hl7.org/fhir/sid/icd-10-cm | Cyclin-Dependent Kinase-Like 5 Deficiency Disorder |
| G40.501 | http://hl7.org/fhir/sid/icd-10-cm | Epileptic seizures related to external causes, not intractable, with status epilepticus |
| G40.509 | http://hl7.org/fhir/sid/icd-10-cm | Epileptic seizures related to external causes, not intractable, without status epilepticus |
| G40.801 | http://hl7.org/fhir/sid/icd-10-cm | Other epilepsy, not intractable, with status epilepticus |
| G40.802 | http://hl7.org/fhir/sid/icd-10-cm | Other epilepsy, not intractable, without status epilepticus |
| G40.803 | http://hl7.org/fhir/sid/icd-10-cm | Other epilepsy, intractable, with status epilepticus |
| G40.804 | http://hl7.org/fhir/sid/icd-10-cm | Other epilepsy, intractable, without status epilepticus |
| G40.811 | http://hl7.org/fhir/sid/icd-10-cm | Lennox-Gastaut syndrome, not intractable, with status epilepticus |
| G40.812 | http://hl7.org/fhir/sid/icd-10-cm | Lennox-Gastaut syndrome, not intractable, without status epilepticus |
| G40.813 | http://hl7.org/fhir/sid/icd-10-cm | Lennox-Gastaut syndrome, intractable, with status epilepticus |
| G40.814 | http://hl7.org/fhir/sid/icd-10-cm | Lennox-Gastaut syndrome, intractable, without status epilepticus |
| G40.821 | http://hl7.org/fhir/sid/icd-10-cm | Epileptic spasms, not intractable, with status epilepticus |
| G40.822 | http://hl7.org/fhir/sid/icd-10-cm | Epileptic spasms, not intractable, without status epilepticus |
| G40.823 | http://hl7.org/fhir/sid/icd-10-cm | Epileptic spasms, intractable, with status epilepticus |
| G40.824 | http://hl7.org/fhir/sid/icd-10-cm | Epileptic spasms, intractable, without status epilepticus |
| G40.833 | http://hl7.org/fhir/sid/icd-10-cm | Dravet syndrome, intractable, with status epilepticus |
| G40.834 | http://hl7.org/fhir/sid/icd-10-cm | Dravet syndrome, intractable, without status epilepticus |
| G40.89 | http://hl7.org/fhir/sid/icd-10-cm | Other seizures |
| G40.901 | http://hl7.org/fhir/sid/icd-10-cm | Epilepsy, unspecified, not intractable, with status epilepticus |
| G40.909 | http://hl7.org/fhir/sid/icd-10-cm | Epilepsy, unspecified, not intractable, without status epilepticus |
| G40.911 | http://hl7.org/fhir/sid/icd-10-cm | Epilepsy, unspecified, intractable, with status epilepticus |
| G40.919 | http://hl7.org/fhir/sid/icd-10-cm | Epilepsy, unspecified, intractable, without status epilepticus |
| G40.A01 | http://hl7.org/fhir/sid/icd-10-cm | Absence epileptic syndrome, not intractable, with status epilepticus |
| G40.A09 | http://hl7.org/fhir/sid/icd-10-cm | Absence epileptic syndrome, not intractable, without status epilepticus |
| G40.A11 | http://hl7.org/fhir/sid/icd-10-cm | Absence epileptic syndrome, intractable, with status epilepticus |
| G40.A19 | http://hl7.org/fhir/sid/icd-10-cm | Absence epileptic syndrome, intractable, without status epilepticus |
| G40.B01 | http://hl7.org/fhir/sid/icd-10-cm | Juvenile myoclonic epilepsy, not intractable, with status epilepticus |
| G40.B09 | http://hl7.org/fhir/sid/icd-10-cm | Juvenile myoclonic epilepsy, not intractable, without status epilepticus |
| G40.B11 | http://hl7.org/fhir/sid/icd-10-cm | Juvenile myoclonic epilepsy, intractable, with status epilepticus |
| G40.B19 | http://hl7.org/fhir/sid/icd-10-cm | Juvenile myoclonic epilepsy, intractable, without status epilepticus |
Produced 08 Sep 2023