Multimorbidity_epilepsy
Codelist metadata
-
Coding system
- SNOMED CT
-
Coding system release
- 39.5.0
-
Organisation
- University of Bristol
-
Codelist ID
- bristol/multimorbidity_epilepsy
-
Version ID
- 78ba0a45
Versions
About
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 |
|---|---|
| 100091000000100 | Epilepsy confirmed |
| 100941000119100 | Epilepsy in mother complicating pregnancy |
| 10750951000119106 | Epilepsy in mother complicating childbirth |
| 108211000000104 | Epilepsy impairs education |
| 109478007 | Kohlschutter's syndrome |
| 111498005 | Extratemporal epilepsy |
| 116401000119105 | Recurrent complex partial epilepsy |
| 119001000119108 | Intractable simple partial epilepsy |
| 138751003 | H/O: epilepsy |
| 13973009 | Tonic-clonic status epilepticus |
| 14401000119109 | Partial frontal lobe epilepsy |
| 147942004 | Epilepsy treatment changed |
| 147943009 | Epilepsy treatment started |
| 15523002 | Self-limited focal epilepsy |
| 161480008 | History of epilepsy |
| 164771000000107 | No epilepsy drug side effects |
| 165421000000100 | No epilepsy drug side effects |
| 170702005 | Epilepsy monitoring |
| 170703000 | Initial epilepsy assessment |
| 170704006 | Follow-up epilepsy assessment |
| 170706008 | Epilepsy associated problems |
| 170709001 | Epilepsy drug side effect |
| 170710006 | Epilepsy treatment changed |
| 170711005 | Epilepsy treatment started |
| 187931000119106 | Atypical absence epilepsy |
| 188951000000105 | Epilepsy monitoring verbal invite |
| 192451000000100 | Epilepsy monitoring verbal invite |
| 192845009 | Myoclonic encephalopathy |
| 192979009 | Generalized non-convulsive epilepsy |
| 192990004 | Myoclonic epilepsy in infancy |
| 192992007 | Epileptic seizures - myoclonic |
| 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 |
| 193011005 | Unilateral epilepsy |
| 193017009 | Kojevnikov's epilepsy |
| 193021002 | Cursive (running) epilepsy |
| 193022009 | Localization-related(focal)(partial)idiopathic epilepsy and epileptic syndromes with seizures of localized onset |
| 194499008 | [X]Status epilepticus, unspecified |
| 19598007 | Generalized epilepsy |
| 199451000000106 | Simple partial epileptic seizure |
| 20121000119105 | Partial occipital lobe epilepsy |
| 202061000000107 | Epilepsy monitoring call first letter |
| 202071000000100 | Epilepsy monitoring call second letter |
| 202081000000103 | Epilepsy monitoring call third letter |
| 21391000119102 | Partial parietal lobe epilepsy |
| 215071000000106 | Simple partial epileptic seizure |
| 2198002 | Visceral epilepsy |
| 230191005 | Rasmussen syndrome |
| 230290000 | Epileptic dementia |
| 230381009 | Focal epilepsy |
| 230382002 | Benign frontal epilepsy of childhood |
| 230383007 | Benign psychomotor epilepsy of childhood |
| 230384001 | Benign atypical partial epilepsy in childhood |
| 230385000 | Epilepsy with recurrent unilateral seizures in children |
| 230386004 | Childhood epilepsy with occipital paroxysms |
| 230387008 | Self-limited epilepsy with autonomic seizures |
| 230388003 | Childhood occipital visual epilepsy |
| 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 |
| 230410004 | Self-limited familial neonatal epilepsy |
| 230411000 | Benign non-familial neonatal convulsions |
| 230412007 | Myoclonic epilepsy of early childhood |
| 230413002 | Juvenile absence epilepsy |
| 230414008 | Epilepsy with generalized tonic-clonic seizures alone |
| 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 | Epilepsy with myoclonic-atonic seizures |
| 230422001 | Epilepsy with myoclonic absence |
| 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 |
| 230441003 | Drug-induced epilepsy |
| 230443000 | Narcotic withdrawal epilepsy |
| 230444006 | Menstrual epilepsy |
| 230445007 | Nocturnal epilepsy |
| 230447004 | Absence seizure with eyelid myoclonia |
| 230448009 | Writing epilepsy |
| 230449001 | Tactile epilepsy |
| 230450001 | Eating epilepsy |
| 230451002 | Tapping epilepsy |
| 230452009 | Toothbrushing epilepsy |
| 230453004 | Decision-making epilepsy |
| 230454005 | Aquagenic epilepsy |
| 230456007 | Status epilepticus |
| 230457003 | Typical absence status epilepticus |
| 230458008 | Atypical absence status epilepticus |
| 230459000 | Non-convulsive simple partial status epilepticus |
| 230460005 | Complex partial status epilepticus |
| 237612000 | Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction |
| 241006 | Epilepsia partialis continua |
| 243857008 | Epilepsy monitoring status |
| 248371000000106 | Epilepsy monitoring telephone invitation |
| 251591000000109 | Epilepsy monitoring telephone invite |
| 267581004 | Progressive myoclonic epilepsy |
| 267592003 | Motor cortex epilepsy |
| 274571000000106 | Epilepsy monitoring telephone invite |
| 278510009 | Localization-related idiopathic epilepsy |
| 28055006 | West syndrome |
| 28602001 | Pyridoxine dependency syndrome |
| 290561000119105 | Aphasia co-occurrent with epilepsy |
| 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 |
| 290871000119101 | Infantile spasms co-occurrent with status epilepticus |
| 290881000119103 | Refractory infantile spasms co-occurrent with status epilepticus |
| 291311000119108 | Status epilepticus in benign Rolandic epilepsy |
| 307356008 | Motor epilepsy |
| 307357004 | Jacksonian, focal or motor epilepsy |
| 314827004 | Epilepsy control good |
| 314828009 | Epilepsy control poor |
| 322112361000132104 | Epilepsy due to scarring of brain |
| 3371000119106 | Refractory generalized convulsive epilepsy |
| 339861000000106 | Panayiotopoulos syndrome |
| 352818000 | Tonic-clonic epilepsy |
| 35796005 | Generalized nonconvulsive epilepsy |
| 361123003 | Psychomotor epilepsy |
| 361268000 | Alcohol-induced epilepsy |
| 36803009 | Idiopathic generalized epilepsy |
| 368831000000104 | Panayiotopoulos syndrome |
| 37356005 | Myoclonic seizure |
| 38281008 | Self-limited neonatal epilepsy |
| 38711000000108 | Epilepsy care arrangement |
| 39194005 | Visual epilepsy |
| 39745004 | Chronic progressive epilepsia partialis continua |
| 401062003 | Epilepsy medication review |
| 401178003 | Epilepsy care arrangement |
| 407616001 | Epilepsy severity |
| 407617005 | No seizures on treatment |
| 407618000 | 1 to 12 seizures a year |
| 407619008 | 2 to 4 seizures a month |
| 407620002 | 1 to 7 seizures a week |
| 407621003 | Daily seizures |
| 407622005 | Many seizures a day |
| 407623000 | Emergency epilepsy treatment since last appointment |
| 407627004 | Epilepsy confirmed |
| 40816002 | Retropulsion petit mal |
| 413101007 | Stress-induced epilepsy |
| 414851000000106 | [X]Status epilepticus, unspecified |
| 414860000 | No epilepsy drug side effects |
| 414921000000106 | [X]Status epilepticus, unspecified |
| 416090009 | Epilepsy monitoring verbal invite |
| 417568007 | Epilepsy monitoring call |
| 422513000 | Epilepsy, not refractory |
| 422724001 | Refractory localization-related epilepsy |
| 422873003 | Refractory epilepsia partialis continua |
| 425054007 | Refractory occipital lobe epilepsy |
| 425237009 | Refractory frontal lobe epilepsy |
| 425349008 | Refractory parietal lobe epilepsy |
| 431421000000105 | [X]Other status epilepticus |
| 434541000124109 | Benign childhood epilepsy with centrotemporal spikes, refractory |
| 434551000124106 | Benign childhood epilepsy with centrotemporal spikes, non-refractory |
| 44145005 | Self-limited epilepsy with centrotemporal spikes |
| 441678004 | Refractory generalized nonconvulsive epilepsy |
| 442481002 | Epilepsy characterized by intractable complex partial seizures |
| 442512002 | Status epilepticus without prominent motor symptoms |
| 445355009 | Refractory epilepsy |
| 45167004 | Moynahan's syndrome |
| 453081000000103 | [X]Other generalised epilepsy and epileptic syndromes |
| 455341000000105 | [X]Other epilepsy |
| 47161000000107 | Epilepsy medication review |
| 47391000119107 | Primary generalized absence epilepsy |
| 49776008 | Centrencephalic epilepsy |
| 50866000 | Childhood absence epilepsy |
| 509341000000107 | Petit-mal epilepsy |
| 509631000000107 | Epilepsy monitoring call first letter |
| 509641000000103 | Epilepsy monitoring call second letter |
| 509741000000106 | Epilepsy monitoring call first letter |
| 509751000000109 | Epilepsy monitoring call second letter |
| 509761000000107 | Epilepsy monitoring call third letter |
| 509771000000100 | Epilepsy monitoring call third letter |
| 525931000000107 | [D]Nocturnal seizure |
| 527611000000103 | Childhood absence epilepsy |
| 528361000000108 | Partial epilepsy without mention of impairment of consciousness |
| 565791000000100 | Epilepsy monitoring NOS |
| 57254004 | Fukuhara syndrome |
| 603681000000103 | Partial epilepsy without mention of impairment of consciousness NOS |
| 6204001 | Juvenile myoclonic epilepsy |
| 624141000000106 | Generalized non-convulsive epilepsy NOS |
| 626021000000108 | Other specified generalized convulsive epilepsy |
| 626031000000105 | Generalized convulsive epilepsy NOS |
| 643961000000106 | Other specified partial epilepsy without mention of impairment of consciousness |
| 643971000000104 | Infantile spasms NOS |
| 646461000000108 | Partial epilepsy with impairment of consciousness NOS |
| 65120008 | Generalized convulsive epilepsy |
| 654351000000107 | Other specified generalized non-convulsive epilepsy |
| 68448003 | Myoclonus epilepsy AND ragged red fibers |
| 698021005 | Familial sleep-related hypermotor epilepsy |
| 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 |
| 699688008 | Genetic epilepsy with febrile seizures plus |
| 702326000 | Progressive myoclonus epilepsy with ataxia |
| 7033004 | Absence status epilepticus |
| 703524005 | Spinal muscular atrophy with progressive myoclonic epilepsy |
| 706841000000105 | [D]Nocturnal seizure |
| 710046001 | Refractory idiopathic generalized epilepsy |
| 71427006 | Cursive seizure |
| 715534008 | Infantile convulsion and choreoathetosis syndrome |
| 715629001 | Generalized epilepsy and paroxysmal dyskinesia syndrome |
| 716278005 | Epilepsy with eyelid myoclonia |
| 716706009 | Female restricted epilepsy with intellectual disability syndrome |
| 717223008 | X-linked epilepsy with learning disability and behavior disorder syndrome |
| 717225001 | Benign adult familial myoclonic epilepsy |
| 71831005 | Symptomatic generalized epilepsy |
| 720519003 | Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome |
| 721088003 | Developmental delay, epilepsy, neonatal diabetes syndrome |
| 722386009 | Celiac disease with epilepsy and cerebral calcification syndrome |
| 723125008 | Epileptic encephalopathy |
| 723625009 | Simpson Golabi Behmel syndrome type 2 |
| 723676007 | Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome |
| 724274009 | Infant epilepsy with migrant focal crisis |
| 724549005 | Epilepsy due to infectious disease of central nervous system |
| 724576005 | Pyridoxal 5-phosphate dependent epilepsy |
| 724785007 | Epilepsy due to perinatal stroke |
| 724786008 | Epilepsy due to perinatal anoxic-ischemic brain injury |
| 724787004 | Epilepsy due to cerebrovascular accident |
| 724788009 | Epilepsy due to and following traumatic brain injury |
| 724789001 | Epilepsy due to intracranial tumor |
| 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 |
| 725163002 | X-linked spasticity, intellectual disability, epilepsy syndrome |
| 725413002 | Febrile infection related epilepsy syndrome |
| 726702005 | Epileptic encephalopathy with global cerebral demyelination |
| 733031004 | Epilepsy, microcephaly, skeletal dysplasia syndrome |
| 733032006 | Epilepsy telangiectasia syndrome |
| 733082001 | Early-onset Lafora body disease |
| 733195008 | Epilepsy of infancy with migrating focal seizures |
| 733623005 | Autism spectrum disorder, epilepsy, arthrogryposis syndrome |
| 734434007 | Pyridoxine-dependent epilepsy |
| 75023009 | Post-traumatic epilepsy |
| 763349002 | Progressive myoclonic epilepsy with dystonia |
| 763534009 | Hot water reflex epilepsy |
| 763622006 | Thinking epilepsy |
| 763632004 | Startle epilepsy |
| 763802009 | Micturition induced epilepsy |
| 763827002 | Orgasm induced epilepsy |
| 764453009 | Action myoclonus renal failure syndrome |
| 764522009 | Familial focal epilepsy with variable foci |
| 765093009 | Rolandic epilepsy, speech dyspraxia syndrome |
| 765170001 | Sodium voltage-gated channel alpha subunit 8-related epilepsy with encephalopathy |
| 765216006 | Audiogenic epilepsy |
| 766044005 | Acute encephalopathy with biphasic seizures and late reduced diffusion |
| 766815007 | Perioral myoclonia with absences |
| 767254005 | Recurrent benign focal seizures of childhood |
| 768666006 | Syntaxin binding protein 1 encephalopathy with epilepsy |
| 770405003 | Familial mesial temporal lobe epilepsy |
| 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 |
| 770622009 | Benign infantile focal epilepsy with midline spikes and waves during sleep |
| 770623004 | Benign occipital lobe epilepsy |
| 770624005 | Benign partial epilepsy of infancy with complex partial seizures |
| 770643005 | Mesial temporal lobe epilepsy with hippocampal sclerosis |
| 770758009 | New-onset refractory status epilepticus |
| 770898002 | Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency |
| 771141002 | Benign partial epilepsy with secondarily generalized seizures in infancy |
| 771142009 | Cortical dysplasia with focal epilepsy syndrome |
| 771223000 | Infantile epileptic dyskinetic encephalopathy |
| 771448004 | Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency |
| 771469002 | Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome |
| 773421009 | Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression |
| 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 |
| 773643006 | Multiple congenital anomalies, hypotonia, seizures syndrome type 2 |
| 778001003 | Potassium voltage-gated channel subfamily Q member 2 related epileptic encephalopathy |
| 778047006 | Myoclonic epilepsy in non-progressive encephalopathy |
| 778063003 | Cryptogenic late-onset epileptic spasms |
| 780827006 | Synaptic Ras GTPase activating protein 1- related intellectual disability |
| 782737003 | Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome |
| 782772000 | Congenital muscular dystrophy with intellectual disability and severe epilepsy |
| 782825008 | Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome |
| 783055005 | Progressive myoclonic epilepsy type 5 |
| 783062001 | Progressive myoclonic epilepsy type 6 |
| 783064000 | Progressive myoclonic epilepsy type 3 |
| 783139000 | Progressive myoclonic epilepsy type 8 |
| 783739005 | Familial temporal lobe epilepsy |
| 784342008 | Familial infantile myoclonic epilepsy |
| 784372002 | Familial mesial temporal lobe epilepsy with febrile seizures |
| 784377008 | Familial epilepsy with auditory features |
| 785726009 | Hyperekplexia epilepsy syndrome |
| 788417006 | Alopecia, epilepsy, intellectual disability syndrome Moynahan type |
| 79745005 | Reflex epilepsy |
| 810161000000101 | Epilepsy monitoring in secondary care |
| 81371000000101 | Epilepsy medication review |
| 82381000119103 | Epileptic dementia with behavioral disturbance |
| 8291000119107 | Atonic epilepsy |
| 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 |
| 84757009 | Epilepsy |
| 850201000000104 | Epilepsy annual review |
| 850311000000107 | Epilepsy care management |
| 850321000000101 | Self management of epilepsy |
| 850361000000109 | Epilepsy self-management plan review |
| 855761000000102 | Severe myoclonic epilepsy in infancy |
| 860804005 | Epilepsy due to infectious encephalitis |
| 860806007 | Epilepsy due to infectious meningitis |
| 860815000 | Epilepsy due to neonatal central nervous system infection |
| 88491000000102 | Epilepsy limits activities |
| 93141000000105 | Epilepsy restricts employment |
| 93151000000108 | Epilepsy prevents employment |
| 93211000000101 | Epilepsy does not limit activities |
| 95208000 | Photogenic epilepsy |
| 95211000000102 | Epilepsy confirmed |
Codes not in the full codelist are in faint grey.