Resource ValueSet/FHIR Server from package us.nlm.vsac#0.22.0 (188 ms)
| Package | us.nlm.vsac |
| Type | ValueSet |
| Id | Id |
| FHIR Version | R4 |
| Source | http://fhir.org/packages/us.nlm.vsac/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 |
| Experimental | False |
| 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
Source
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"version" : "20250110",
"name" : "SeizureDisorder",
"title" : "Seizure Disorder",
"status" : "active",
"date" : "2025-01-10T01:08:35-05:00",
"publisher" : "NCQA PHEMUR",
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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" : {
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{
"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)"
},
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XIG built as of ??metadata-date??. Found ??metadata-resources?? resources in ??metadata-packages?? packages.
FHIR