Epilepsy diagnosis codes
Codelist metadata
-
Coding system
- SNOMED CT
-
Coding system release
- 39.2.0
-
Organisation
- NHSD Primary Care Domain Refsets
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Codelist ID
- nhsd-primary-care-domain-refsets/epil_cod
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Version Tag
- 20241205
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Version ID
- 28ffb643
Versions
About
Description
Taken from the EPIL_COD refset published by NHSD.
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 |
|---|---|
| 1156803005 | Neonatal glycine encephalopathy |
| 1156826003 | Infantile glycine encephalopathy |
| 1163527006 | Epilepsy due to parasitic disease |
| 1163529009 | Epilepsy due to bacterial endocarditis |
| 116401000119105 | Recurrent complex partial epilepsy |
| 1167371007 | Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome |
| 1172627007 | Early-onset epilepsy, intellectual disability, brain anomalies syndrome |
| 1172630000 | Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome |
| 1179360000 | Fetal epilepsy due to perinatal stroke |
| 1179547007 | Neonatal epilepsy due to perinatal stroke |
| 1187042007 | Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome |
| 1187278006 | Spastic paraplegia, severe developmental delay, epilepsy syndrome |
| 1197587003 | Lethal neonatal spasticity, epileptic encephalopathy syndrome |
| 1208939001 | Progressive myoclonic epilepsy type 7 |
| 1220594007 | Pierpont syndrome |
| 122601000000109 | Juvenile myoclonic epilepsy |
| 1228857005 | Progressive myoclonic epilepsy type 9 |
| 1230376005 | Contactin associated protein 2-related developmental and epileptic encephalopathy |
| 1236807002 | Encephalopathy due to mitochondrial and peroxisomal fission defect |
| 1260117009 | Combined focal and generalized epilepsy |
| 1260368003 | Epilepsy due to Rasmussen syndrome |
| 1260369006 | Epilepsy due to perinatal intraventricular hemorrhage |
| 1260370007 | Epilepsy due to perinatal periventricular hemorrhage |
| 1260371006 | Epilepsy due to perinatal cerebral ischemia |
| 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 |
| 1260407007 | Genetic generalized epilepsy |
| 127324008 | Myoclonic disorder |
| 1275631007 | Developmental and epileptic encephalopathy |
| 13973009 | Tonic-clonic status epilepticus |
| 189198006 | Epileptic drop attack |
| 192845009 | Myoclonic encephalopathy |
| 192979009 | Generalized non-convulsive epilepsy |
| 192983009 | Juvenile absence 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 |
| 193004006 | Epileptic automatism |
| 193008009 | Somatosensory epilepsy |
| 193009001 | Partial epilepsy with autonomic symptoms |
| 193010006 | Visual reflex epilepsy |
| 193011005 | Unilateral epilepsy |
| 193021002 | Cursive (running) epilepsy |
| 193022009 | Localization-related(focal)(partial)idiopathic epilepsy and epileptic syndromes with seizures of localized onset |
| 19598007 | Generalized epilepsy |
| 199451000000106 | Simple partial epileptic seizure |
| 230191005 | Rasmussen syndrome |
| 230381009 | Focal epilepsy |
| 230387008 | Self-limited epilepsy with autonomic seizures |
| 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 |
| 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 |
| 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 |
| 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 | Typical absence status epilepticus |
| 230458008 | Atypical absence status epilepticus |
| 230459000 | Non-convulsive simple partial status epilepticus |
| 230460005 | Complex partial status epilepticus |
| 241006 | Epilepsia partialis continua |
| 267581004 | Progressive myoclonic epilepsy |
| 267592003 | Motor cortex epilepsy |
| 278510009 | Localization-related idiopathic epilepsy |
| 28055006 | West syndrome |
| 290741000119102 | Intractable idiopathic partial epilepsy |
| 290871000119101 | Infantile spasms co-occurrent with status epilepticus |
| 291311000119108 | Status epilepticus in benign Rolandic epilepsy |
| 307356008 | Motor epilepsy |
| 307357004 | Jacksonian, focal or motor epilepsy |
| 322112361000132104 | Epilepsy due to scarring of brain |
| 352818000 | Tonic-clonic epilepsy |
| 35691006 | Combined deficiency of sialidase AND beta galactosidase |
| 361123003 | Psychomotor epilepsy |
| 361268000 | Alcohol-induced epilepsy |
| 37356005 | Myoclonic seizure |
| 380941000000104 | Progressive encephalopathy with oedema, hypsarrhythmia and optic atrophy syndrome |
| 407675009 | Focal onset impaired awareness epileptic seizure |
| 40816002 | Retropulsion petit mal |
| 413101007 | Stress-induced epilepsy |
| 434541000124109 | Benign childhood epilepsy with centrotemporal spikes, refractory |
| 434551000124106 | Benign childhood epilepsy with centrotemporal spikes, non-refractory |
| 44145005 | Self-limited epilepsy with centrotemporal spikes |
| 442511009 | Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome |
| 44423001 | Early myoclonic encephalopathy |
| 491261000000105 | PEHO (progressive encephalopathy with oedema, hypsarrhythmia and optic atrophy) syndrome |
| 50866000 | Childhood absence epilepsy |
| 509341000000107 | Petit-mal epilepsy |
| 527611000000103 | Childhood absence epilepsy |
| 6204001 | Juvenile myoclonic epilepsy |
| 65120008 | Generalized convulsive epilepsy |
| 698761003 | Refractory juvenile myoclonic epilepsy |
| 698762005 | Refractory myoclonic epilepsy |
| 698767004 | Post-cerebrovascular accident epilepsy |
| 702326000 | Progressive myoclonus epilepsy with ataxia |
| 716278005 | Epilepsy with eyelid myoclonia |
| 71831005 | Symptomatic generalized epilepsy |
| 725163002 | X-linked spasticity, intellectual disability, epilepsy syndrome |
| 733082001 | Early-onset Lafora body disease |
| 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 |
| 765089003 | Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome |
| 765093009 | Rolandic epilepsy, speech dyspraxia syndrome |
| 765170001 | Sodium voltage-gated channel alpha subunit 8-related epilepsy with encephalopathy |
| 765216006 | Audiogenic epilepsy |
| 766815007 | Perioral myoclonia with absences |
| 766932005 | Hypothalamic hamartoma with gelastic seizure |
| 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 |
| 770560008 | Lissencephaly due to LIS1 mutation |
| 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 |
| 770678005 | Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome |
| 770758009 | New-onset refractory status epilepticus |
| 771141002 | Benign partial epilepsy with secondarily generalized seizures in infancy |
| 771142009 | Cortical dysplasia with focal epilepsy syndrome |
| 771223000 | Infantile epileptic dyskinetic encephalopathy |
| 771303004 | Severe neonatal onset encephalopathy with microcephaly |
| 771448004 | Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency |
| 771469002 | Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome |
| 773230003 | Cyclin-dependent kinase-like 5 deficiency |
| 773421009 | Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression |
| 773497001 | Partial corpus callosum agenesis, cerebellar vermis hypoplasia with posterior fossa cysts syndrome |
| 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 |
| 782737003 | Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome |
| 782744007 | Lipoic acid synthetase deficiency |
| 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 |
| 784345005 | Malignant migrating partial seizures of infancy |
| 784372002 | Familial mesial temporal lobe epilepsy with febrile seizures |
| 784377008 | Familial epilepsy with auditory features |
| 785303004 | Multiple congenital anomalies, hypotonia, seizures syndrome |
| 788417006 | Alopecia, epilepsy, intellectual disability syndrome Moynahan type |
| 789063000 | Primary hyperaldosteronism, seizures, neurological abnormalities syndrome |
| 79745005 | Reflex epilepsy |
| 80651009 | Aicardi's syndrome |
| 84201000119105 | Intractable partial temporal lobe epilepsy with impairment of consciousness |
| 84757009 | Epilepsy |
| 860804005 | Epilepsy due to infectious encephalitis |
| 860806007 | Epilepsy due to infectious meningitis |
| 860815000 | Epilepsy due to neonatal central nervous system infection |
| 89525009 | Focal onset emotional epileptic seizure with laughing |
| 95208000 | Photogenic epilepsy |
Codes not in the full codelist are in faint grey.