FHIR IG analytics
| Package | us.nlm.vsac |
| Resource Type | ValueSet |
| Id | ValueSet-2.16.840.1.113883.3.464.1003.105.11.1213.json |
| FHIR Version | R4 |
| Source | https://vsac.nlm.nih.gov/valueset/2.16.840.1.113883.3.464.1003.105.11.1213/expansion |
| URL | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.464.1003.105.11.1213 |
| Version | 20250110 |
| Status | active |
| Date | 2025-01-10T01:08:35-05:00 |
| Name | SeizureDisorder |
| Title | Seizure Disorder |
| Realm | us |
| Authority | hl7 |
| Purpose | (Clinical Focus: The purpose of this value set is to represent concepts for a diagnosis of a seizure disorder.),(Data Element Scope: This value set may use a model element related to Diagnosis.),(Inclusion Criteria: Includes concepts that represent a diagnosis of epilepsy or recurrent seizures.),(Exclusion Criteria: No exclusions.) |
Resources that use this resource
Resources that this resource uses
| CodeSystem |
| sct | SNOMED codes used in this IG |
Narrative
No narrative content found in resource
Source1
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"version": "20250110",
"name": "SeizureDisorder",
"title": "Seizure Disorder",
"status": "active",
"date": "2025-01-10T01:08:35-05:00",
"publisher": "NCQA PHEMUR",
"jurisdiction": [
{
"coding": [
{
"system": "urn:iso:std:iso:3166",
"code": "US"
}
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],
"purpose": "(Clinical Focus: The purpose of this value set is to represent concepts for a diagnosis of a seizure disorder.),(Data Element Scope: This value set may use a model element related to Diagnosis.),(Inclusion Criteria: Includes concepts that represent a diagnosis of epilepsy or recurrent seizures.),(Exclusion Criteria: No exclusions.)",
"compose": {
"include": [
{
"system": "http://snomed.info/sct",
"concept": [
{
"code": "111498005",
"display": "Extratemporal epilepsy (disorder)"
},
{
"code": "1163527006",
"display": "Epilepsy due to parasitic disease (disorder)"
},
{
"code": "1163529009",
"display": "Epilepsy due to bacterial endocarditis (disorder)"
},
{
"code": "116401000119105",
"display": "Recurrent complex partial epilepsy (disorder)"
},
{
"code": "1167371007",
"display": "Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome (disorder)"
},
{
"code": "1172593006",
"display": "Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome (disorder)"
},
{
"code": "1172630000",
"display": "Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome (disorder)"
},
{
"code": "1172844009",
"display": "Combined oxidative phosphorylation defect type 27 (disorder)"
},
{
"code": "1179282009",
"display": "Severe neurodevelopmental disorder with feeding difficulties, stereotypic hand movement, bilateral cataract (disorder)"
},
{
"code": "1179359005",
"display": "Maternal epilepsy due to perinatal stroke (disorder)"
},
{
"code": "1179360000",
"display": "Fetal epilepsy due to perinatal stroke (disorder)"
},
{
"code": "1179547007",
"display": "Neonatal epilepsy due to perinatal stroke (disorder)"
},
{
"code": "1187042007",
"display": "Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome (disorder)"
},
{
"code": "1187210007",
"display": "Intellectual disability, epilepsy, extrapyramidal syndrome (disorder)"
},
{
"code": "1187250005",
"display": "Seizures, scoliosis, macrocephaly syndrome (disorder)"
},
{
"code": "1187278006",
"display": "Spastic paraplegia, severe developmental delay, epilepsy syndrome (disorder)"
},
{
"code": "1187304005",
"display": "Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome (disorder)"
},
{
"code": "1197587003",
"display": "Lethal neonatal spasticity, epileptic encephalopathy syndrome (disorder)"
},
{
"code": "1208486005",
"display": "Multiple mitochondrial dysfunctions syndrome type 2 (disorder)"
},
{
"code": "1208939001",
"display": "Progressive myoclonic epilepsy type 7 (disorder)"
},
{
"code": "1217381009",
"display": "Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome (disorder)"
},
{
"code": "1222656005",
"display": "Synaptic Ras GTPase activating protein 1-related developmental and epileptic encephalopathy (disorder)"
},
{
"code": "1222659003",
"display": "Ring finger protein 13-related severe early-onset epileptic encephalopathy (disorder)"
},
{
"code": "1222662000",
"display": "Neonatal epileptic encephalopathy due to deficiency of glutaminase (disorder)"
},
{
"code": "1228857005",
"display": "Progressive myoclonic epilepsy type 9 (disorder)"
},
{
"code": "1230376005",
"display": "Contactin associated protein 2-related developmental and epileptic encephalopathy (disorder)"
},
{
"code": "1231737000",
"display": "Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome (disorder)"
},
{
"code": "1237417007",
"display": "Carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation (disorder)"
},
{
"code": "1237619001",
"display": "Fatty acyl-coenzyme A reductase 1 deficiency (disorder)"
},
{
"code": "1254960008",
"display": "Seizure co-occurrent and due to substance withdrawal (disorder)"
},
{
"code": "1260117009",
"display": "Combined focal and generalized epilepsy (disorder)"
},
{
"code": "1260368003",
"display": "Epilepsy due to Rasmussen syndrome (disorder)"
},
{
"code": "1260369006",
"display": "Epilepsy due to perinatal intraventricular hemorrhage (disorder)"
},
{
"code": "1260370007",
"display": "Epilepsy due to perinatal periventricular hemorrhage (disorder)"
},
{
"code": "1260371006",
"display": "Epilepsy due to perinatal cerebral ischemia (disorder)"
},
{
"code": "1260374003",
"display": "Epilepsy due to congenital infectious disease (disorder)"
},
{
"code": "1260375002",
"display": "Epilepsy due to glucose transporter protein type 1 deficiency syndrome (disorder)"
},
{
"code": "1260377005",
"display": "Epilepsy due to congenital anomaly of brain (disorder)"
},
{
"code": "1260407007",
"display": "Genetic generalized epilepsy (disorder)"
},
{
"code": "1269236003",
"display": "Primary hypomagnesemia, refractory seizures, intellectual disability syndrome (disorder)"
},
{
"code": "1275631007",
"display": "Developmental and epileptic encephalopathy (disorder)"
},
{
"code": "128613002",
"display": "Seizure disorder (disorder)"
},
{
"code": "13973009",
"display": "Tonic-clonic status epilepticus (finding)"
},
{
"code": "14401000119109",
"display": "Partial frontal lobe epilepsy (disorder)"
},
{
"code": "170706008",
"display": "Epilepsy associated problems (finding)"
},
{
"code": "170709001",
"display": "Epilepsy drug side effect (finding)"
},
{
"code": "191714002",
"display": "Dissociative convulsions (disorder)"
},
{
"code": "192845009",
"display": "Myoclonic encephalopathy (disorder)"
},
{
"code": "192990004",
"display": "Myoclonic epilepsy in infancy (disorder)"
},
{
"code": "192999003",
"display": "Partial epilepsy with impairment of consciousness (disorder)"
},
{
"code": "193000002",
"display": "Temporal lobe epilepsy (disorder)"
},
{
"code": "193002005",
"display": "Psychosensory epilepsy (disorder)"
},
{
"code": "193003000",
"display": "Mesiobasal limbic epilepsy (disorder)"
},
{
"code": "193008009",
"display": "Somatosensory epilepsy (disorder)"
},
{
"code": "193009001",
"display": "Partial epilepsy with autonomic symptoms (disorder)"
},
{
"code": "193010006",
"display": "Visual reflex epilepsy (disorder)"
},
{
"code": "193021002",
"display": "Cursive (running) epilepsy (disorder)"
},
{
"code": "19598007",
"display": "Generalized epilepsy (disorder)"
},
{
"code": "20121000119105",
"display": "Partial occipital lobe epilepsy (disorder)"
},
{
"code": "21391000119102",
"display": "Partial parietal lobe epilepsy (disorder)"
},
{
"code": "2198002",
"display": "Visceral epilepsy (disorder)"
},
{
"code": "230191005",
"display": "Rasmussen syndrome (disorder)"
},
{
"code": "230381009",
"display": "Focal epilepsy (disorder)"
},
{
"code": "230389006",
"display": "Primary inherited reading epilepsy (disorder)"
},
{
"code": "230390002",
"display": "Localization-related symptomatic epilepsy (disorder)"
},
{
"code": "230391003",
"display": "Amygdalo-hippocampal epilepsy (disorder)"
},
{
"code": "230392005",
"display": "Rhinencephalic epilepsy (disorder)"
},
{
"code": "230393000",
"display": "Lateral temporal epilepsy (disorder)"
},
{
"code": "230394006",
"display": "Frontal lobe epilepsy (disorder)"
},
{
"code": "230395007",
"display": "Supplementary motor epilepsy (disorder)"
},
{
"code": "230396008",
"display": "Cingulate epilepsy (disorder)"
},
{
"code": "230397004",
"display": "Anterior frontopolar epilepsy (disorder)"
},
{
"code": "230398009",
"display": "Orbitofrontal epilepsy (disorder)"
},
{
"code": "230399001",
"display": "Dorsolateral epilepsy (disorder)"
},
{
"code": "230400008",
"display": "Opercular epilepsy (disorder)"
},
{
"code": "230401007",
"display": "Non-progressive Kozhevnikow syndrome (disorder)"
},
{
"code": "230403005",
"display": "Parietal lobe epilepsy (disorder)"
},
{
"code": "230404004",
"display": "Occipital lobe epilepsy (disorder)"
},
{
"code": "230406002",
"display": "Localization-related symptomatic epilepsy with specific precipitant (disorder)"
},
{
"code": "230407006",
"display": "Hemiplegia-hemiconvulsion-epilepsy syndrome (disorder)"
},
{
"code": "230408001",
"display": "Localization-related cryptogenic epilepsy (disorder)"
},
{
"code": "230414008",
"display": "Epilepsy with generalized tonic-clonic seizures alone (disorder)"
},
{
"code": "230416005",
"display": "Cryptogenic West syndrome (disorder)"
},
{
"code": "230417001",
"display": "Symptomatic West syndrome (disorder)"
},
{
"code": "230418006",
"display": "Lennox-Gastaut syndrome (disorder)"
},
{
"code": "230419003",
"display": "Cryptogenic Lennox-Gastaut syndrome (disorder)"
},
{
"code": "230420009",
"display": "Symptomatic Lennox-Gastaut syndrome (disorder)"
},
{
"code": "230421008",
"display": "Epilepsy with myoclonic-atonic seizures (disorder)"
},
{
"code": "230422001",
"display": "Epilepsy with myoclonic absence (disorder)"
},
{
"code": "230423006",
"display": "Unverricht-Lundborg syndrome (disorder)"
},
{
"code": "230425004",
"display": "Lafora disease (disorder)"
},
{
"code": "230426003",
"display": "Myoclonic epilepsy with ragged red fibers (disorder)"
},
{
"code": "230432008",
"display": "Familial febrile convulsions (disorder)"
},
{
"code": "230437002",
"display": "Severe myoclonic epilepsy in infancy (disorder)"
},
{
"code": "230438007",
"display": "Acquired epileptic aphasia (disorder)"
},
{
"code": "230439004",
"display": "Epilepsy with continuous spike wave during slow-wave sleep (disorder)"
},
{
"code": "230440002",
"display": "Secondary reading epilepsy (disorder)"
},
{
"code": "230443000",
"display": "Narcotic withdrawal epilepsy (disorder)"
},
{
"code": "230444006",
"display": "Menstrual epilepsy (disorder)"
},
{
"code": "230445007",
"display": "Nocturnal epilepsy (disorder)"
},
{
"code": "230448009",
"display": "Writing epilepsy (disorder)"
},
{
"code": "230450001",
"display": "Eating epilepsy (disorder)"
},
{
"code": "230452009",
"display": "Toothbrushing epilepsy (disorder)"
},
{
"code": "230453004",
"display": "Decision-making epilepsy (disorder)"
},
{
"code": "230454005",
"display": "Aquagenic epilepsy (disorder)"
},
{
"code": "230456007",
"display": "Status epilepticus (finding)"
},
{
"code": "230457003",
"display": "Typical absence status epilepticus (finding)"
},
{
"code": "230458008",
"display": "Atypical absence status epilepticus (finding)"
},
{
"code": "23374007",
"display": "Atypical absence seizure (finding)"
},
{
"code": "243857008",
"display": "Epilepsy monitoring status (finding)"
},
{
"code": "267581004",
"display": "Progressive myoclonic epilepsy (disorder)"
},
{
"code": "267592003",
"display": "Motor cortex epilepsy (disorder)"
},
{
"code": "278510009",
"display": "Localization-related idiopathic epilepsy (disorder)"
},
{
"code": "28055006",
"display": "West syndrome (disorder)"
},
{
"code": "290731000119106",
"display": "Idiopathic partial status epilepticus (finding)"
},
{
"code": "290741000119102",
"display": "Intractable idiopathic partial epilepsy (disorder)"
},
{
"code": "307356008",
"display": "Motor epilepsy (disorder)"
},
{
"code": "307357004",
"display": "Jacksonian, focal or motor epilepsy (disorder)"
},
{
"code": "314827004",
"display": "Epilepsy control good (finding)"
},
{
"code": "314828009",
"display": "Epilepsy control poor (finding)"
},
{
"code": "322112361000132104",
"display": "Epilepsy due to scarring of brain (disorder)"
},
{
"code": "361123003",
"display": "Psychomotor epilepsy (disorder)"
},
{
"code": "36803009",
"display": "Idiopathic generalized epilepsy (disorder)"
},
{
"code": "39194005",
"display": "Visual epilepsy (disorder)"
},
{
"code": "401178003",
"display": "Epilepsy care arrangement (finding)"
},
{
"code": "407616001",
"display": "Epilepsy severity (finding)"
},
{
"code": "407623000",
"display": "Emergency epilepsy treatment since last appointment (finding)"
},
{
"code": "407675009",
"display": "Focal onset impaired awareness epileptic seizure (finding)"
},
{
"code": "413101007",
"display": "Stress-induced epilepsy (disorder)"
},
{
"code": "430061000124109",
"display": "Early myoclonic encephalopathy, refractory (disorder)"
},
{
"code": "430071000124102",
"display": "Early myoclonic encephalopathy, non-refractory (disorder)"
},
{
"code": "431111000124104",
"display": "Lennox-Gastaut syndrome, refractory (disorder)"
},
{
"code": "431121000124107",
"display": "Lennox-Gastaut syndrome, non-refractory (disorder)"
},
{
"code": "431141000124100",
"display": "Myoclonic absence epilepsy, non-refractory (disorder)"
},
{
"code": "431991000124107",
"display": "Petit mal status, non-refractory (finding)"
},
{
"code": "432171000124102",
"display": "Severe myoclonic epilepsy in infancy, refractory (disorder)"
},
{
"code": "432271000124109",
"display": "Tonic seizures, refractory (finding)"
},
{
"code": "432281000124107",
"display": "Tonic seizures, non-refractory (finding)"
},
{
"code": "432511000124103",
"display": "Atonic seizure, non-refractory (finding)"
},
{
"code": "432561000124100",
"display": "Typical absence seizure, non-refractory (finding)"
},
{
"code": "432571000124107",
"display": "Typical absence seizure, refractory (finding)"
},
{
"code": "434521000124102",
"display": "Atypical absence seizure, refractory (finding)"
},
{
"code": "434531000124104",
"display": "Atypical absence seizure, non-refractory (finding)"
},
{
"code": "435321000124106",
"display": "Acquired epileptic aphasia, non-refractory (disorder)"
},
{
"code": "435331000124109",
"display": "Acquired epileptic aphasia, refractory (disorder)"
},
{
"code": "435341000124104",
"display": "Rasmussen syndrome, refractory (disorder)"
},
{
"code": "436011000124108",
"display": "Petit mal status, refractory (finding)"
},
{
"code": "438113009",
"display": "Convulsive syncope (finding)"
},
{
"code": "438421000124109",
"display": "Myoclonic astatic epilepsy, non-refractory (disorder)"
},
{
"code": "44145005",
"display": "Benign Rolandic epilepsy (disorder)"
},
{
"code": "442151000124108",
"display": "Autosomal dominant nocturnal frontal lobe epilepsy, refractory (disorder)"
},
{
"code": "442161000124105",
"display": "Autosomal dominant nocturnal frontal lobe epilepsy, non-refractory (disorder)"
},
{
"code": "442511009",
"display": "Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome (disorder)"
},
{
"code": "442512002",
"display": "Status epilepticus without prominent motor symptoms (finding)"
},
{
"code": "44423001",
"display": "Early myoclonic encephalopathy (disorder)"
},
{
"code": "444441000124109",
"display": "Generalized epilepsy with febrile seizures plus, refractory (disorder)"
},
{
"code": "444451000124106",
"display": "Generalized epilepsy with febrile seizures plus, non-refractory (disorder)"
},
{
"code": "460731000124105",
"display": "Recurrent seizure (disorder)"
},
{
"code": "5321000124109",
"display": "Temporal lobe epilepsy with mesial temporal sclerosis (disorder)"
},
{
"code": "68761002",
"display": "Epileptic vertigo (disorder)"
},
{
"code": "698021005",
"display": "Autosomal dominant nocturnal frontal lobe epilepsy (disorder)"
},
{
"code": "698763000",
"display": "Postoperative status epilepticus (disorder)"
},
{
"code": "698764006",
"display": "Post infectious grand mal epilepsy (disorder)"
},
{
"code": "698767004",
"display": "Post-cerebrovascular accident epilepsy (disorder)"
},
{
"code": "699688008",
"display": "Genetic epilepsy with febrile seizures plus (disorder)"
},
{
"code": "702326000",
"display": "Progressive myoclonus epilepsy with ataxia (disorder)"
},
{
"code": "702344008",
"display": "Pitt-Hopkins syndrome (disorder)"
},
{
"code": "7033004",
"display": "Absence status epilepticus (finding)"
},
{
"code": "703524005",
"display": "Spinal muscular atrophy with progressive myoclonic epilepsy (disorder)"
},
{
"code": "715425000",
"display": "Benign focal seizure of adolescence (disorder)"
},
{
"code": "715629001",
"display": "Generalized epilepsy and paroxysmal dyskinesia syndrome (disorder)"
},
{
"code": "716278005",
"display": "Epilepsy with eyelid myoclonia (disorder)"
},
{
"code": "716706009",
"display": "Female restricted epilepsy with intellectual disability syndrome (disorder)"
},
{
"code": "717223008",
"display": "X-linked epilepsy with learning disability and behavior disorder syndrome (disorder)"
},
{
"code": "717225001",
"display": "Benign adult familial myoclonic epilepsy (disorder)"
},
{
"code": "717276003",
"display": "Folinic acid responsive seizure syndrome (disorder)"
},
{
"code": "719810000",
"display": "X-linked intellectual disability with seizure and psoriasis syndrome (disorder)"
},
{
"code": "720519003",
"display": "Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome (disorder)"
},
{
"code": "721088003",
"display": "Developmental delay, epilepsy, neonatal diabetes syndrome (disorder)"
},
{
"code": "721207002",
"display": "Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome (disorder)"
},
{
"code": "722110003",
"display": "Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome (disorder)"
},
{
"code": "722386009",
"display": "Celiac disease with epilepsy and cerebral calcification syndrome (disorder)"
},
{
"code": "722762005",
"display": "Ganglioside GM3 synthase deficiency (disorder)"
},
{
"code": "723125008",
"display": "Epileptic encephalopathy (disorder)"
},
{
"code": "723304001",
"display": "Microcephaly, seizure, intellectual disability, heart disease syndrome (disorder)"
},
{
"code": "723676007",
"display": "Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome (disorder)"
},
{
"code": "723926008",
"display": "Perceptual disturbances and seizures co-occurrent and due to alcohol withdrawal (disorder)"
},
{
"code": "724274009",
"display": "Infant epilepsy with migrant focal crisis (disorder)"
},
{
"code": "724549005",
"display": "Epilepsy due to infectious disease of central nervous system (disorder)"
},
{
"code": "724576005",
"display": "Pyridoxal 5-phosphate dependent epilepsy (disorder)"
},
{
"code": "724668002",
"display": "Seizure co-occurrent and due to sedative withdrawal (disorder)"
},
{
"code": "724669005",
"display": "Seizure co-occurrent and due to hypnotic withdrawal (disorder)"
},
{
"code": "724670006",
"display": "Seizure co-occurrent and due to anxiolytic withdrawal (disorder)"
},
{
"code": "724671005",
"display": "Perceptual disturbances and seizures co-occurrent and due to sedative withdrawal (disorder)"
},
{
"code": "724672003",
"display": "Perceptual disturbances and seizures co-occurrent and due to hypnotic withdrawal (disorder)"
},
{
"code": "724727001",
"display": "Seizure co-occurrent and due to psychoactive substance withdrawal (disorder)"
},
{
"code": "724728006",
"display": "Perceptual disturbances and seizures co-occurrent and due to psychoactive substance withdrawal (disorder)"
},
{
"code": "724786008",
"display": "Epilepsy due to perinatal anoxic-ischemic brain injury (disorder)"
},
{
"code": "724787004",
"display": "Epilepsy due to cerebrovascular accident (disorder)"
},
{
"code": "724789001",
"display": "Epilepsy due to intracranial tumor (disorder)"
},
{
"code": "724988000",
"display": "Epilepsy co-occurrent and due to degenerative brain disorder (disorder)"
},
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FHIR
FHIRsmith