| Source | us.nlm.vsac#0.11.0:null (v4.0.1) |
| resourceType | ValueSet |
| id | 2.16.840.1.113883.3.464.1003.105.11.1213 |
| canonical | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.464.1003.105.11.1213 |
| version | 20230211 |
| status | active |
| publisher | NCQA PHEMUR |
| name | SeizureDisorder |
| title | Seizure Disorder |
| date | 2023-02-11T01:02:55-05:00 |
| Usages |
|
This value set contains 269 concepts
| Code | System | Display |
| 1163527006 | http://snomed.info/sct | Epilepsy due to disease caused by parasite (disorder) |
| 1163529009 | http://snomed.info/sct | Epilepsy due to bacterial endocarditis (disorder) |
| 1172593006 | http://snomed.info/sct | Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome (disorder) |
| 1172630000 | http://snomed.info/sct | Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability 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) |
| 1187210007 | http://snomed.info/sct | Intellectual disability, epilepsy, extrapyramidal syndrome (disorder) |
| 1187250005 | http://snomed.info/sct | Seizures, scoliosis, macrocephaly syndrome (disorder) |
| 1187278006 | http://snomed.info/sct | Spastic paraplegia, severe developmental delay, epilepsy syndrome (disorder) |
| 1187304005 | http://snomed.info/sct | Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome (disorder) |
| 1208939001 | http://snomed.info/sct | Progressive myoclonic epilepsy type 7 (disorder) |
| 1217381009 | http://snomed.info/sct | Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome (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) |
| 128613002 | http://snomed.info/sct | Seizure disorder (disorder) |
| 13973009 | http://snomed.info/sct | Grand mal status (disorder) |
| 14401000119109 | http://snomed.info/sct | Partial frontal lobe epilepsy (disorder) |
| 170706008 | http://snomed.info/sct | Epilepsy associated problems (finding) |
| 170709001 | http://snomed.info/sct | Epilepsy drug side effect (finding) |
| 191714002 | http://snomed.info/sct | Dissociative convulsions (disorder) |
| 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) |
| 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) |
| 230191005 | http://snomed.info/sct | Rasmussen syndrome (disorder) |
| 230381009 | http://snomed.info/sct | Localization-related epilepsy (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) |
| 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) |
| 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) |
| 230430000 | http://snomed.info/sct | Symptomatic myoclonic epilepsy (disorder) |
| 230432008 | http://snomed.info/sct | Familial febrile convulsions (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) |
| 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) |
| 230457003 | http://snomed.info/sct | Non-convulsive status epilepticus with three per second spike wave (disorder) |
| 230458008 | http://snomed.info/sct | Non-convulsive status epilepticus without three per second spike wave (disorder) |
| 23374007 | http://snomed.info/sct | Atypical absence seizure (finding) |
| 243857008 | http://snomed.info/sct | Epilepsy monitoring status (finding) |
| 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) |
| 290761000119103 | http://snomed.info/sct | Status epilepticus due to refractory simple partial epilepsy (disorder) |
| 307356008 | http://snomed.info/sct | Motor epilepsy (disorder) |
| 307357004 | http://snomed.info/sct | Jacksonian, focal or motor epilepsy (disorder) |
| 314827004 | http://snomed.info/sct | Epilepsy control good (finding) |
| 314828009 | http://snomed.info/sct | Epilepsy control poor (finding) |
| 322112361000132104 | http://snomed.info/sct | Epilepsy due to scarring of brain (disorder) |
| 329991000119104 | http://snomed.info/sct | Intractable atypical absence epilepsy (disorder) |
| 352818000 | http://snomed.info/sct | Tonic-clonic epilepsy (disorder) |
| 36803009 | http://snomed.info/sct | Idiopathic generalized epilepsy (disorder) |
| 39194005 | http://snomed.info/sct | Visual epilepsy (disorder) |
| 401178003 | http://snomed.info/sct | Epilepsy care arrangement (finding) |
| 407616001 | http://snomed.info/sct | Epilepsy severity (finding) |
| 407623000 | http://snomed.info/sct | Emergency epilepsy treatment since last appointment (finding) |
| 407675009 | http://snomed.info/sct | Complex partial epileptic seizure (disorder) |
| 413101007 | http://snomed.info/sct | Stress-induced epilepsy (disorder) |
| 422513000 | http://snomed.info/sct | Epilepsy, not 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) |
| 431141000124100 | http://snomed.info/sct | Myoclonic absence epilepsy, non-refractory (disorder) |
| 431991000124107 | http://snomed.info/sct | Petit mal status, non-refractory (finding) |
| 432151000124107 | http://snomed.info/sct | Myoclonic seizure, non-refractory (disorder) |
| 432161000124109 | http://snomed.info/sct | Severe myoclonic epilepsy in infancy, non-refractory (disorder) |
| 432271000124109 | http://snomed.info/sct | Tonic seizures, refractory (finding) |
| 432281000124107 | http://snomed.info/sct | Tonic seizures, non-refractory (finding) |
| 432291000124105 | http://snomed.info/sct | Temporal lobe epilepsy, non-refractory (disorder) |
| 432471000124108 | http://snomed.info/sct | Post-traumatic epilepsy, non-refractory (disorder) |
| 432501000124101 | http://snomed.info/sct | Atonic seizure, refractory (disorder) |
| 432511000124103 | http://snomed.info/sct | Atonic seizure, non-refractory (finding) |
| 432561000124100 | http://snomed.info/sct | Typical absence seizure, non-refractory (finding) |
| 432571000124107 | http://snomed.info/sct | Typical absence seizure, refractory (finding) |
| 434211000124108 | http://snomed.info/sct | Grand mal status epilepticus, non-refractory (disorder) |
| 434491000124104 | http://snomed.info/sct | Idiopathic generalized epilepsy, non-refractory (disorder) |
| 434521000124102 | http://snomed.info/sct | Atypical absence seizure, refractory (finding) |
| 434531000124104 | http://snomed.info/sct | Atypical absence seizure, non-refractory (finding) |
| 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) |
| 436011000124108 | http://snomed.info/sct | Petit mal status, refractory (finding) |
| 438113009 | http://snomed.info/sct | Convulsive syncope (finding) |
| 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) |
| 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) |
| 442511009 | http://snomed.info/sct | Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome (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) |
| 460731000124105 | http://snomed.info/sct | Recurrent seizure (disorder) |
| 47391000119107 | http://snomed.info/sct | Primary generalized absence epilepsy (disorder) |
| 5321000124109 | http://snomed.info/sct | Temporal lobe epilepsy with mesial temporal sclerosis (disorder) |
| 65120008 | http://snomed.info/sct | Generalized convulsive epilepsy (disorder) |
| 68761002 | http://snomed.info/sct | Epileptic vertigo (disorder) |
| 698021005 | http://snomed.info/sct | Autosomal dominant nocturnal frontal lobe epilepsy (disorder) |
| 698760002 | http://snomed.info/sct | Generalized non-convulsive absence 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) |
| 702344008 | http://snomed.info/sct | Pitt-Hopkins syndrome (disorder) |
| 7033004 | http://snomed.info/sct | Absence status epilepticus (finding) |
| 703524005 | http://snomed.info/sct | Spinal muscular atrophy with progressive myoclonic epilepsy (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) |
| 719810000 | http://snomed.info/sct | X-linked intellectual disability with seizure and psoriasis syndrome (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) |
| 721207002 | http://snomed.info/sct | Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome (disorder) |
| 722110003 | http://snomed.info/sct | Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome (disorder) |
| 722386009 | http://snomed.info/sct | Celiac disease with epilepsy and cerebral calcification syndrome (disorder) |
| 722762005 | http://snomed.info/sct | Ganglioside GM3 synthase deficiency (disorder) |
| 723125008 | http://snomed.info/sct | Epileptic encephalopathy (disorder) |
| 723304001 | http://snomed.info/sct | Microcephaly, seizure, intellectual disability, heart disease syndrome (disorder) |
| 723676007 | http://snomed.info/sct | Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome (disorder) |
| 723926008 | http://snomed.info/sct | Perceptual disturbances and seizures co-occurrent and due to alcohol withdrawal (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) |
| 724668002 | http://snomed.info/sct | Seizure co-occurrent and due to sedative withdrawal (disorder) |
| 724669005 | http://snomed.info/sct | Seizure co-occurrent and due to hypnotic withdrawal (disorder) |
| 724670006 | http://snomed.info/sct | Seizure co-occurrent and due to anxiolytic withdrawal (disorder) |
| 724671005 | http://snomed.info/sct | Perceptual disturbances and seizures co-occurrent and due to sedative withdrawal (disorder) |
| 724672003 | http://snomed.info/sct | Perceptual disturbances and seizures co-occurrent and due to hypnotic withdrawal (disorder) |
| 724727001 | http://snomed.info/sct | Seizure co-occurrent and due to psychoactive substance withdrawal (disorder) |
| 724728006 | http://snomed.info/sct | Perceptual disturbances and seizures co-occurrent and due to psychoactive substance withdrawal (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) |
| 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) |
| 763861000 | http://snomed.info/sct | Pachygyria, intellectual disability, epilepsy syndrome (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) |
| 768473009 | http://snomed.info/sct | Purine rich element binding protein A syndrome (disorder) |
| 768555009 | http://snomed.info/sct | 5q31.3 microdeletion syndrome (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) |
| 770623004 | http://snomed.info/sct | Benign occipital lobe epilepsy (disorder) |
| 770643005 | http://snomed.info/sct | Mesial temporal lobe epilepsy with hippocampal sclerosis (disorder) |
| 770678005 | http://snomed.info/sct | Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome (disorder) |
| 770755007 | http://snomed.info/sct | Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome (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) |
| 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) |
| 773230003 | http://snomed.info/sct | Cyclin-dependent kinase-like 5 deficiency (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) |
| 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) |
| 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) |
| 785303004 | http://snomed.info/sct | Multiple congenital anomalies, hypotonia, seizures syndrome (disorder) |
| 785726009 | http://snomed.info/sct | Hyperekplexia epilepsy syndrome (disorder) |
| 788417006 | http://snomed.info/sct | Alopecia, epilepsy, intellectual disability syndrome Moynahan type (disorder) |
| 789063000 | http://snomed.info/sct | Primary hyperaldosteronism, seizures, neurological abnormalities syndrome (disorder) |
| 79631006 | http://snomed.info/sct | Absence seizure (finding) |
| 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) |
| 84191000119107 | http://snomed.info/sct | Partial epileptic seizure of temporal lobe 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) |
Produced 08 Sep 2023