Epilepsy diagnosis codes
Metadata
- Coding system
- SNOMED CT (UK Clinical Edition)
- Coding system release
- 40.2.0
- Organisation
- NHSD Primary Care Domain Refsets
- Codelist ID
- nhsd-primary-care-domain-refsets/epil_cod
- Version Tag
- 20250627
- Version ID
- 0aa78980
- Number of codes included
- 476
About
Description
Taken from the `EPIL_COD` refset published by NHSD. Contains public sector information licensed under the UK Open Government Licence v3.0 (https://www.nationalarchives.gov.uk/doc/open-government-licence/version/3/).
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 |
---|---|
104101000000101 | Complex partial epileptic seizure |
104111000000104 | Early infantile epileptic encephalopathy with suppression bursts |
109478007 | Kohlschutter's syndrome |
111498005 | Extratemporal epilepsy |
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 |
117891000119100 | Focal onset aware epileptic seizure |
1179282009 | Severe neurodevelopmental disorder with feeding difficulties, stereotypic hand movement, bilateral cataract |
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 |
1187250005 | Seizures, scoliosis, macrocephaly syndrome |
1187278006 | Spastic paraplegia, severe developmental delay, epilepsy syndrome |
1187304005 | Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome |
119001000119108 | Intractable simple partial epilepsy |
1197587003 | Lethal neonatal spasticity, epileptic encephalopathy syndrome |
1208486005 | Multiple mitochondrial dysfunctions syndrome type 2 |
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 |
1208991001 | Myoclonic epileptic seizure |
1217136003 | Tonic-clonic epileptic seizure |
1217209006 | Generalized onset tonic-clonic epileptic seizure |
1220594007 | Pierpont syndrome |
1222656005 | Synaptic Ras GTPase activating protein 1-related developmental and epileptic encephalopathy |
1222659003 | Ring finger protein 13-related severe early-onset epileptic encephalopathy |
1222662000 | Neonatal epileptic encephalopathy due to deficiency of glutaminase |
122601000000109 | Juvenile myoclonic epilepsy |
122621000000100 | Drug-induced epilepsy |
122631000000103 | Menstrual epilepsy |
122641000000107 | Stress-induced epilepsy |
122651000000105 | Photosensitive epilepsy |
1228857005 | Progressive myoclonic epilepsy type 9 |
1230376005 | Contactin associated protein 2-related developmental and epileptic encephalopathy |
1231282002 | Self-limited familial neonatal-infantile epilepsy |
1231737000 | Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome |
1236807002 | Encephalopathy due to mitochondrial and peroxisomal fission defect |
1236975007 | Behavioral arrest epileptic seizure |
1237571004 | Self-limited familial infantile epilepsy |
1259196009 | Focal onset nonmotor onset epileptic seizure |
1259197000 | Focal onset myoclonic epileptic seizure |
1259198005 | Impaired awareness epileptic seizure |
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 |
1264275009 | Focal onset automatism epileptic seizure |
1269236003 | Primary hypomagnesemia, refractory seizures, intellectual disability syndrome |
1269356000 | Focal onset aware automatism epileptic seizure |
1269358004 | Focal onset impaired awareness motor onset epileptic seizure |
1269359007 | Focal onset epileptic spasms |
1269360002 | Focal onset tonic epileptic seizure |
1269361003 | Focal onset aware tonic epileptic seizure |
1269362005 | Focal onset impaired awareness tonic epileptic seizure |
1269363000 | Focal onset clonic epileptic seizure |
1269364006 | Focal onset aware clonic epileptic seizure |
1269365007 | Focal onset impaired awareness clonic epileptic seizure |
1269366008 | Focal onset atonic epileptic seizure |
1269367004 | Focal onset aware atonic epileptic seizure |
1269368009 | Focal onset impaired awareness atonic epileptic seizure |
1269369001 | Focal onset aware myoclonic epileptic seizure |
1269370000 | Focal onset impaired awareness myoclonic epileptic seizure |
1269371001 | Focal onset hyperkinetic epileptic seizure |
1269372008 | Focal onset aware hyperkinetic epileptic seizure |
1269373003 | Focal onset impaired awareness hyperkinetic epileptic seizure |
1269374009 | Focal onset impaired awareness automatism epileptic seizure |
127324008 | Myoclonic disorder |
1275631007 | Developmental and epileptic encephalopathy |
1279990000 | Focal onset aware nonmotor onset epileptic seizure |
1279991001 | Focal onset impaired awareness nonmotor onset epileptic seizure |
1281831009 | Focal onset behavior arrest epileptic seizure |
1281832002 | Focal onset aware behavior arrest epileptic seizure |
1281833007 | Focal onset impaired awareness behavior arrest epileptic seizure |
1281834001 | Focal onset impaired awareness cognitive epileptic seizure |
1281835000 | Focal onset autonomic epileptic seizure |
1281836004 | Focal onset impaired awareness autonomic epileptic seizure |
1281837008 | Focal onset aware emotional epileptic seizure |
1281838003 | Focal onset impaired awareness emotional epileptic seizure |
1281839006 | Focal onset sensory epileptic seizure |
1281840008 | Impaired awareness nonmotor onset epileptic seizure |
1284864005 | Focal onset impaired awareness sensory epileptic seizure |
1284865006 | Focal onset cognitive epileptic seizure with memory impairment |
1285078002 | Focal onset emotional epileptic seizure |
128612007 | Focal onset motor onset epileptic seizure |
1299164006 | Status epilepticus with prominent motor symptoms |
1299165007 | Myoclonic status epilepticus |
1299166008 | Generalized tonic-clonic status epilepticus |
1299167004 | Focal to bilateral tonic-clonic status epilepticus |
1300128003 | Methenyltetrahydrofolate synthetase-related developmental delay, microcephaly, short stature, epilepsy syndrome |
1303273003 | Interferon regulatory factor 2 binding protein like-related regressive neurodevelopmental disorder, dystonia, seizures syndrome |
13973009 | Tonic-clonic status epilepticus |
14401000119109 | Partial frontal lobe epilepsy |
14521008 | Focal onset sensory epileptic seizure with visual symptoms |
147945002 | Nocturnal epilepsy |
155036009 | (Epilepsy) or (epileptic attack) |
155037000 | Childhood absence epilepsy |
155038005 | Generalised epilepsy |
155040000 | Temporal lobe epilepsy |
155042008 | West syndrome |
155043003 | Generalised epilepsy |
155044009 | Localisation-related epilepsy |
155045005 | Epilepsy NOS |
15523002 | Self-limited focal epilepsy |
157437008 | Traumatic epilepsy |
170714002 | Nocturnal epilepsy |
187931000119106 | Atypical absence epilepsy |
189198006 | Epileptic drop attack |
192567003 | Acquired epileptic aphasia |
192728006 | Rasmussen syndrome |
192845009 | Myoclonic encephalopathy |
192979009 | Generalized non-convulsive epilepsy |
192980007 | Childhood absence epilepsy |
192981006 | Atonic epileptic seizure |
192982004 | Epileptic seizures - akinetic |
192983009 | Juvenile absence epilepsy |
192984003 | Lennox-Gastaut syndrome |
192985002 | Other specified generalized non-convulsive epilepsy |
192987005 | Generalized non-convulsive epilepsy NOS |
192989008 | Generalised epilepsy |
192990004 | Myoclonic epilepsy in infancy |
192991000 | Clonic epileptic seizure |
192992007 | Epileptic seizures - myoclonic |
192993002 | Tonic epileptic seizure |
192994008 | Generalised epilepsy |
192996005 | Other specified generalized convulsive epilepsy |
192997001 | Generalized convulsive epilepsy NOS |
192999003 | Partial epilepsy with impairment of consciousness |
193000002 | Temporal lobe epilepsy |
193001003 | Psychomotor epilepsy |
193002005 | Psychosensory epilepsy |
193003000 | Mesiobasal limbic temporal lobe epilepsy |
193004006 | Epileptic automatism |
193005007 | Partial epilepsy with impairment of consciousness NOS |
193006008 | Partial epilepsy without mention of impairment of consciousness |
193008009 | Somatosensory epilepsy |
193009001 | Partial epilepsy with autonomic symptoms |
193010006 | Visual reflex epilepsy |
193011005 | Unilateral epilepsy |
193012003 | Other specified partial epilepsy without mention of impairment of consciousness |
193013008 | Partial epilepsy without mention of impairment of consciousness NOS |
193014002 | West syndrome |
193015001 | West syndrome |
193017009 | Kojevnikov's epilepsy |
193020001 | Other forms of epilepsy |
193021002 | Cursive (running) epilepsy |
193022009 | Localization-related(focal)(partial)idiopathic epilepsy and epileptic syndromes with seizures of localized onset |
193024005 | Benign childhood epilepsy with centrotemporal spike |
193025006 | Other forms of epilepsy NOS |
193026007 | (Epilepsy NOS) or (fit in known epileptic NOS) |
194490007 | [X]Other generalized epilepsy and epileptic syndromes |
194491006 | [X]Other epilepsy |
19598007 | Generalized epilepsy |
199451000000106 | Simple partial epileptic seizure |
20121000119105 | Partial occipital lobe epilepsy |
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 temporal lobe epilepsy |
230392005 | Rhinencephalic epilepsy |
230393000 | Lateral temporal lobe epilepsy |
230394006 | Frontal lobe epilepsy |
230395007 | Supplementary motor cortex frontal lobe epilepsy |
230396008 | Cingulate frontal lobe epilepsy |
230397004 | Anterior frontopolar frontal lobe epilepsy |
230398009 | Orbitofrontal frontal lobe epilepsy |
230399001 | Dorsolateral frontal lobe epilepsy |
230400008 | Opercular frontal lobe 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 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 |
230424000 | 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 |
230446008 | Epilepsy only in relation to photic stimulation |
230448009 | Writing epilepsy |
230449001 | Tactile epilepsy |
230450001 | Eating epilepsy |
230451002 | Tapping 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 |
230459000 | Non-convulsive simple partial status epilepticus |
230460005 | Complex partial status epilepticus |
241006 | Epilepsia partialis continua |
246529004 | Focal onset aware motor onset Jacksonian epileptic seizure |
246530009 | Focal onset motor onset versive epileptic seizure |
246533006 | Focal onset aware sensory epileptic seizure |
246535004 | Focal onset cognitive epileptic seizure with dysphasia |
246536003 | Focal onset aware cognitive epileptic seizure |
246538002 | Focal onset cognitive epileptic seizure with illusions |
246539005 | Focal onset cognitive epileptic seizure with hallucinations |
246544003 | Focal to bilateral tonic-clonic epileptic seizure |
246545002 | Generalized onset epileptic seizure |
267581004 | Progressive myoclonic epilepsy |
267592003 | Primary motor cortex frontal lobe epilepsy |
267593008 | Epilepsy NOS |
267698007 | (Epilepsy) or (epileptic attack) |
278510009 | Localization-related idiopathic epilepsy |
28055006 | West syndrome |
28602001 | Pyridoxine dependency syndrome |
288197007 | West syndrome |
290561000119105 | Aphasia co-occurrent with epilepsy |
290671000119100 | Status epilepticus due to complex partial epileptic seizure |
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 |
29753000 | Focal onset epileptic seizure |
307356008 | Motor epilepsy |
307357004 | Jacksonian, focal or motor epilepsy |
307358009 | Psychomotor epilepsy |
309847002 | Fit (in known epileptic) NOS |
313307000 | Epileptic seizure |
322112361000132104 | Epilepsy due to scarring of brain |
3371000119106 | Refractory generalized convulsive epilepsy |
33941008 | Focal onset cognitive epileptic seizure |
339861000000106 | Panayiotopoulos syndrome |
34601006 | Focal onset somatosensory epileptic seizure |
352818000 | Tonic-clonic epilepsy |
35691006 | Combined deficiency of sialidase AND beta galactosidase |
35796005 | Generalized nonconvulsive epilepsy |
361123003 | Psychomotor epilepsy |
361268000 | Alcohol-induced epilepsy |
36803009 | Idiopathic generalized epilepsy |
368831000000104 | Panayiotopoulos syndrome |
37356005 | Myoclonic seizure |
380941000000104 | Progressive encephalopathy with oedema, hypsarrhythmia and optic atrophy syndrome |
39194005 | Visual epilepsy |
39745004 | Chronic progressive epilepsia partialis continua |
407675009 | Focal onset impaired awareness epileptic seizure |
40816002 | Retropulsion petit mal |
413101007 | Stress-induced epilepsy |
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 |
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 |
442511009 | Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome |
442512002 | Status epilepticus without prominent motor symptoms |
44423001 | Early myoclonic encephalopathy |
445355009 | Refractory epilepsy |
45167004 | Moynahan's syndrome |
453081000000103 | [X]Other generalised epilepsy and epileptic syndromes |
455341000000105 | [X]Other epilepsy |
47391000119107 | Primary generalized absence epilepsy |
491261000000105 | PEHO (progressive encephalopathy with oedema, hypsarrhythmia and optic atrophy) syndrome |
49776008 | Centrencephalic epilepsy |
50866000 | Childhood absence epilepsy |
509341000000107 | Petit-mal epilepsy |
52125007 | Focal onset sensory epileptic seizure with gustatory symptoms |
527611000000103 | Childhood absence epilepsy |
528361000000108 | Partial epilepsy without mention of impairment of consciousness |
57254004 | Fukuhara syndrome |
603681000000103 | Partial epilepsy without mention of impairment of consciousness NOS |
61927004 | Focal onset sensory epileptic seizure with auditory symptoms |
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 |
643981000000102 | Other forms of epilepsy |
643991000000100 | Other forms of epilepsy NOS |
646461000000108 | Partial epilepsy with impairment of consciousness NOS |
65120008 | Generalized convulsive epilepsy |
654351000000107 | Other specified generalized non-convulsive epilepsy |
67139004 | Localization-related epilepsy |
68448003 | Myoclonus epilepsy AND ragged red fibers |
689141000000102 | Fit (in known epileptic) NOS |
698021005 | Familial sleep-related hypermotor epilepsy |
698760002 | Generalized non-convulsive absence epilepsy |
698761003 | Refractory juvenile myoclonic epilepsy |
698762005 | Refractory myoclonic epilepsy |
698764006 | Post infectious grand mal epilepsy |
698767004 | Post-cerebrovascular accident epilepsy |
699688008 | Genetic epilepsy with febrile seizures plus |
700448000 | Epilepsy, ataxia, sensorineural deafness, and tubulopathy syndrome |
702326000 | Progressive myoclonus epilepsy with ataxia |
703524005 | Spinal muscular atrophy with progressive myoclonic epilepsy |
703951000000109 | Epilepsy NOS |
710046001 | Refractory idiopathic generalized epilepsy |
715425000 | Benign focal seizure of adolescence |
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 |
717276003 | Folinic acid responsive seizure syndrome |
71831005 | Symptomatic generalized epilepsy |
719810000 | X-linked intellectual disability with seizure and psoriasis syndrome |
720519003 | Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome |
721207002 | Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome |
722110003 | Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome |
722762005 | Ganglioside GM3 synthase deficiency |
723125008 | Epileptic encephalopathy |
723304001 | Microcephaly, seizure, intellectual disability, heart disease syndrome |
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 |
734434007 | Pyridoxine-dependent epilepsy |
7454002 | Focal onset aware autonomic epileptic seizure |
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 |
768473009 | Purine rich element binding protein A syndrome |
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 |
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 |
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 |
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 |
771516000 | Solute carrier family 35 member A2 congenital disorder of glycosylation |
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 |
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 |
77450009 | Unclassified epileptic seizures |
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 |
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 |
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 |
785726009 | Hyperekplexia epilepsy syndrome |
788417006 | Alopecia, epilepsy, intellectual disability syndrome Moynahan type |
789063000 | Primary hyperaldosteronism, seizures, neurological abnormalities syndrome |
79745005 | Reflex epilepsy |
80651009 | Aicardi's syndrome |
82381000119103 | Epileptic dementia with behavioral disturbance |
82401000 | Focal onset aware motor onset epileptic seizure |
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 |
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 |
87095001 | Focal onset sensory epileptic seizure with olfactory symptoms |
887101000000101 | Epilepsy, ataxia, sensorineural deafness and tubulopathy syndrome |
89525009 | Focal onset emotional epileptic seizure with laughing |
95208000 | Photogenic epilepsy |
981000119108 | Single epileptic seizure |