FHIR IG Statistics: ValueSet/2.16.840.1.113883.3.464.1003.105.12.1206
| Package | us.nlm.vsac |
| Resource Type | ValueSet |
| Id | 2.16.840.1.113883.3.464.1003.105.12.1206 |
| FHIR Version | R4 |
| Source | http://fhir.org/packages/us.nlm.vsac/https://vsac.nlm.nih.gov/valueset/2.16.840.1.113883.3.464.1003.105.12.1206/expansion |
| URL | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.464.1003.105.12.1206 |
| Version | 20210224 |
| Status | active |
| Date | 2022-03-07T11:14:02-05:00 |
| 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
No resources found
Resources that this resource uses
| CodeSystem |
| sct | SNOMED CT (all versions) |
| icd-10-cm | International Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM) |
Narrative
No narrative content found in resource
Source
{
"resourceType": "ValueSet",
"id": "2.16.840.1.113883.3.464.1003.105.12.1206",
"meta": {
"versionId": "9",
"lastUpdated": "2023-12-21T17:43:03.000-05:00",
"profile": [
"http://hl7.org/fhir/StructureDefinition/shareablevalueset",
"http://hl7.org/fhir/us/cqfmeasures/StructureDefinition/computable-valueset-cqfm",
"http://hl7.org/fhir/us/cqfmeasures/StructureDefinition/publishable-valueset-cqfm"
]
},
"extension": [
{
"url": "http://hl7.org/fhir/StructureDefinition/valueset-author",
"valueContactDetail": {
"name": "NCQA PHEMUR Author"
}
},
{
"url": "http://hl7.org/fhir/StructureDefinition/resource-lastReviewDate",
"valueDate": "2025-02-04"
},
{
"url": "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate",
"valueDate": "2021-02-24"
}
],
"url": "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.464.1003.105.12.1206",
"identifier": [
{
"system": "urn:ietf:rfc:3986",
"value": "urn:oid:2.16.840.1.113883.3.464.1003.105.12.1206"
}
],
"version": "20210224",
"name": "SeizureDisorder",
"title": "Seizure Disorder",
"status": "active",
"experimental": false,
"date": "2022-03-07T11:14:02-05:00",
"publisher": "NCQA PHEMUR",
"jurisdiction": [
{
"coding": [
{
"system": "urn:iso:std:iso:3166",
"code": "US"
}
]
}
],
"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": [
{
"valueSet": [
"http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.464.1003.105.11.1213"
]
},
{
"valueSet": [
"http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.464.1003.105.11.1212"
]
}
]
},
"expansion": {
"identifier": "urn:uuid:34d41dd3-88c2-42b7-bf62-5d852c792a1a",
"timestamp": "2025-05-23T22:13:25-04:00",
"total": 290,
"contains": [
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1163527006",
"display": "Epilepsy due to parasitic disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1163529009",
"display": "Epilepsy due to bacterial endocarditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1167371007",
"display": "Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1172593006",
"display": "Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1172630000",
"display": "Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1172844009",
"display": "Combined oxidative phosphorylation defect type 27 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1179282009",
"display": "Severe neurodevelopmental disorder with feeding difficulties, stereotypic hand movement, bilateral cataract (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1179359005",
"display": "Maternal epilepsy due to perinatal stroke (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1179360000",
"display": "Fetal epilepsy due to perinatal stroke (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1179547007",
"display": "Neonatal epilepsy due to perinatal stroke (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1187042007",
"display": "Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1187210007",
"display": "Intellectual disability, epilepsy, extrapyramidal syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1187250005",
"display": "Seizures, scoliosis, macrocephaly syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1187278006",
"display": "Spastic paraplegia, severe developmental delay, epilepsy syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1187304005",
"display": "Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1197587003",
"display": "Lethal neonatal spasticity, epileptic encephalopathy syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1208486005",
"display": "Multiple mitochondrial dysfunctions syndrome type 2 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1208939001",
"display": "Progressive myoclonic epilepsy type 7 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1217381009",
"display": "Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1222656005",
"display": "Synaptic Ras GTPase activating protein 1-related developmental and epileptic encephalopathy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1222659003",
"display": "Ring finger protein 13-related severe early-onset epileptic encephalopathy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1222662000",
"display": "Neonatal epileptic encephalopathy due to deficiency of glutaminase (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1228857005",
"display": "Progressive myoclonic epilepsy type 9 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1230376005",
"display": "Contactin associated protein 2-related developmental and epileptic encephalopathy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1231737000",
"display": "Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1237417007",
"display": "Carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1237619001",
"display": "Fatty acyl-coenzyme A reductase 1 deficiency (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1254960008",
"display": "Seizure co-occurrent and due to substance withdrawal (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1260117009",
"display": "Combined focal and generalized epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1260368003",
"display": "Epilepsy due to Rasmussen syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1260369006",
"display": "Epilepsy due to perinatal intraventricular hemorrhage (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1260370007",
"display": "Epilepsy due to perinatal periventricular hemorrhage (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1260371006",
"display": "Epilepsy due to perinatal cerebral ischemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1260374003",
"display": "Epilepsy due to congenital infectious disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1260375002",
"display": "Epilepsy due to glucose transporter protein type 1 deficiency syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1260377005",
"display": "Epilepsy due to congenital anomaly of brain (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1260407007",
"display": "Genetic generalized epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1269236003",
"display": "Primary hypomagnesemia, refractory seizures, intellectual disability syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1275631007",
"display": "Developmental and epileptic encephalopathy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "128613002",
"display": "Seizure disorder (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "13973009",
"display": "Tonic-clonic status epilepticus (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "170709001",
"display": "Epilepsy drug side effect (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "192845009",
"display": "Myoclonic encephalopathy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "192990004",
"display": "Myoclonic epilepsy in infancy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "193000002",
"display": "Temporal lobe epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "193003000",
"display": "Mesiobasal limbic temporal lobe epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "193010006",
"display": "Visual reflex epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "193021002",
"display": "Cursive (running) epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "19598007",
"display": "Generalized epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230191005",
"display": "Rasmussen syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230381009",
"display": "Focal epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230389006",
"display": "Primary inherited reading epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230391003",
"display": "Amygdalo-hippocampal temporal lobe epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230393000",
"display": "Lateral temporal lobe epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230394006",
"display": "Frontal lobe epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230395007",
"display": "Supplementary motor cortex frontal lobe epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230396008",
"display": "Cingulate frontal lobe epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230397004",
"display": "Anterior frontopolar frontal lobe epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230398009",
"display": "Orbitofrontal frontal lobe epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230399001",
"display": "Dorsolateral frontal lobe epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230400008",
"display": "Opercular frontal lobe epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230403005",
"display": "Parietal lobe epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230404004",
"display": "Occipital lobe epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230407006",
"display": "Hemiplegia-hemiconvulsion-epilepsy syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230414008",
"display": "Epilepsy with generalized tonic-clonic seizures alone (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230416005",
"display": "Cryptogenic West syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230417001",
"display": "Symptomatic West syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230418006",
"display": "Lennox-Gastaut syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230419003",
"display": "Cryptogenic Lennox-Gastaut syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230420009",
"display": "Symptomatic Lennox-Gastaut syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230421008",
"display": "Epilepsy with myoclonic-atonic seizures (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230422001",
"display": "Epilepsy with myoclonic absence (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230423006",
"display": "Unverricht-Lundborg syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230425004",
"display": "Lafora disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230426003",
"display": "Myoclonic epilepsy with ragged red fibers (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230432008",
"display": "Familial febrile convulsions (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230437002",
"display": "Severe myoclonic epilepsy in infancy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230438007",
"display": "Acquired epileptic aphasia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230439004",
"display": "Epilepsy with continuous spike wave during slow-wave sleep (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230440002",
"display": "Secondary reading epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230443000",
"display": "Narcotic withdrawal epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230444006",
"display": "Menstrual epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230448009",
"display": "Writing epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230450001",
"display": "Eating epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230452009",
"display": "Toothbrushing epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230453004",
"display": "Decision-making epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230454005",
"display": "Aquagenic epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230456007",
"display": "Status epilepticus (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230457003",
"display": "Typical absence status epilepticus (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230458008",
"display": "Atypical absence status epilepticus (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "23374007",
"display": "Atypical absence seizure (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "243857008",
"display": "Epilepsy monitoring status (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "267581004",
"display": "Progressive myoclonic epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "267592003",
"display": "Primary motor cortex frontal lobe epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "28055006",
"display": "West syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "290731000119106",
"display": "Idiopathic partial status epilepticus (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "314827004",
"display": "Epilepsy control good (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "314828009",
"display": "Epilepsy control poor (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "322112361000132104",
"display": "Epilepsy due to scarring of brain (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "36803009",
"display": "Idiopathic generalized epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "39194005",
"display": "Visual epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "407623000",
"display": "Emergency epilepsy treatment since last appointment (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "407675009",
"display": "Focal onset impaired awareness epileptic seizure (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "413101007",
"display": "Stress-induced epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "431111000124104",
"display": "Lennox-Gastaut syndrome, refractory (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "431121000124107",
"display": "Lennox-Gastaut syndrome, non-refractory (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "435331000124109",
"display": "Acquired epileptic aphasia, refractory (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "435341000124104",
"display": "Rasmussen syndrome, refractory (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "438113009",
"display": "Convulsive syncope (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "44145005",
"display": "Self-limited epilepsy with centrotemporal spikes (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "442151000124108",
"display": "Autosomal dominant nocturnal frontal lobe epilepsy, refractory (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "442511009",
"display": "Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "442512002",
"display": "Status epilepticus without prominent motor symptoms (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "44423001",
"display": "Early myoclonic encephalopathy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "460731000124105",
"display": "Recurrent seizure (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "5321000124109",
"display": "Temporal lobe epilepsy with mesial temporal sclerosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "68761002",
"display": "Epileptic vertigo (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "698021005",
"display": "Familial sleep-related hypermotor epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "698764006",
"display": "Post infectious grand mal epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "698767004",
"display": "Post-cerebrovascular accident epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "699688008",
"display": "Genetic epilepsy with febrile seizures plus (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "702326000",
"display": "Progressive myoclonus epilepsy with ataxia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "702344008",
"display": "Pitt-Hopkins syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "7033004",
"display": "Absence status epilepticus (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "703524005",
"display": "Spinal muscular atrophy with progressive myoclonic epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "715425000",
"display": "Benign focal seizure of adolescence (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "715629001",
"display": "Generalized epilepsy and paroxysmal dyskinesia syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "716278005",
"display": "Epilepsy with eyelid myoclonia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "716706009",
"display": "Female restricted epilepsy with intellectual disability syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "717223008",
"display": "X-linked epilepsy with learning disability and behavior disorder syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "717225001",
"display": "Benign adult familial myoclonic epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "717276003",
"display": "Folinic acid responsive seizure syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "719810000",
"display": "X-linked intellectual disability with seizure and psoriasis syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "720519003",
"display": "Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "721088003",
"display": "Developmental delay, epilepsy, neonatal diabetes syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "721207002",
"display": "Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "722110003",
"display": "Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "722386009",
"display": "Celiac disease with epilepsy and cerebral calcification syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "722762005",
"display": "Ganglioside GM3 synthase deficiency (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "723125008",
"display": "Epileptic encephalopathy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "723304001",
"display": "Microcephaly, seizure, intellectual disability, heart disease syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "723676007",
"display": "Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "723926008",
"display": "Perceptual disturbances and seizures co-occurrent and due to alcohol withdrawal (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "724274009",
"display": "Infant epilepsy with migrant focal crisis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "724549005",
"display": "Epilepsy due to infectious disease of central nervous system (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "724576005",
"display": "Pyridoxal 5-phosphate dependent epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "724668002",
"display": "Seizure co-occurrent and due to sedative withdrawal (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "724669005",
"display": "Seizure co-occurrent and due to hypnotic withdrawal (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "724670006",
"display": "Seizure co-occurrent and due to anxiolytic withdrawal (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "724671005",
"display": "Perceptual disturbances and seizures co-occurrent and due to sedative withdrawal (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "724672003",
"display": "Perceptual disturbances and seizures co-occurrent and due to hypnotic withdrawal (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "724727001",
"display": "Seizure co-occurrent and due to psychoactive substance withdrawal (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "724728006",
"display": "Perceptual disturbances and seizures co-occurrent and due to psychoactive substance withdrawal (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "724786008",
"display": "Epilepsy due to perinatal anoxic-ischemic brain injury (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "724787004",
"display": "Epilepsy due to cerebrovascular accident (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "724789001",
"display": "Epilepsy due to intracranial tumor (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "724988000",
"display": "Epilepsy co-occurrent and due to degenerative brain disorder (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "724989008",
"display": "Epilepsy co-occurrent and due to mesial temporal sclerosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "724990004",
"display": "Epilepsy due to immune disorder (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "724991000",
"display": "Epilepsy co-occurrent and due to demyelinating disorder (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "724992007",
"display": "Epilepsy co-occurrent and due to dementia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "725163002",
"display": "X-linked spasticity, intellectual disability, epilepsy syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "725413002",
"display": "Febrile infection related epilepsy syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "726702005",
"display": "Epileptic encephalopathy with global cerebral demyelination (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "733031004",
"display": "Epilepsy, microcephaly, skeletal dysplasia syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "733032006",
"display": "Epilepsy telangiectasia syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "733082001",
"display": "Early-onset Lafora body disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "733195008",
"display": "Epilepsy of infancy with migrating focal seizures (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "733623005",
"display": "Autism spectrum disorder, epilepsy, arthrogryposis syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "734434007",
"display": "Pyridoxine-dependent epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "75023009",
"display": "Post-traumatic epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "763349002",
"display": "Progressive myoclonic epilepsy with dystonia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "763534009",
"display": "Hot water reflex epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "763622006",
"display": "Thinking epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "763632004",
"display": "Startle epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "763802009",
"display": "Micturition induced epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "763827002",
"display": "Orgasm induced epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "763861000",
"display": "Pachygyria, intellectual disability, epilepsy syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "764453009",
"display": "Action myoclonus renal failure syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "764522009",
"display": "Familial focal epilepsy with variable foci (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "765089003",
"display": "Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "765093009",
"display": "Rolandic epilepsy, speech dyspraxia syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "765170001",
"display": "Sodium voltage-gated channel alpha subunit 8-related epilepsy with encephalopathy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "765216006",
"display": "Audiogenic epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "766044005",
"display": "Acute encephalopathy with biphasic seizures and late reduced diffusion (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "766815007",
"display": "Perioral myoclonia with absences (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "766932005",
"display": "Hypothalamic hamartoma with gelastic seizure (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "768473009",
"display": "Purine rich element binding protein A syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "768555009",
"display": "5q31.3 microdeletion syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "770405003",
"display": "Familial mesial temporal lobe epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "770431001",
"display": "Early-onset epileptic encephalopathy and intellectual disability due to glutamate receptor, ionotropic, N-methyl-D-aspartate, subunit 2A mutation (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "770623004",
"display": "Benign occipital lobe epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "770624005",
"display": "Benign partial epilepsy of infancy with complex partial seizures (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "770643005",
"display": "Mesial temporal lobe epilepsy with hippocampal sclerosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "770678005",
"display": "Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "770755007",
"display": "Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "770758009",
"display": "New-onset refractory status epilepticus (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "770898002",
"display": "Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "771141002",
"display": "Benign partial epilepsy with secondarily generalized seizures in infancy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "771303004",
"display": "Severe neonatal onset encephalopathy with microcephaly (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "771448004",
"display": "Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "771469002",
"display": "Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "771516000",
"display": "Solute carrier family 35 member A2 congenital disorder of glycosylation (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "773230003",
"display": "Cyclin-dependent kinase-like 5 deficiency (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "773497001",
"display": "Partial corpus callosum agenesis, cerebellar vermis hypoplasia with posterior fossa cysts syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "773498006",
"display": "Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "773548008",
"display": "Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "773643006",
"display": "Multiple congenital anomalies, hypotonia, seizures syndrome type 2 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "778001003",
"display": "Potassium voltage-gated channel subfamily Q member 2 related epileptic encephalopathy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "778047006",
"display": "Myoclonic epilepsy in non-progressive encephalopathy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "778063003",
"display": "Cryptogenic late-onset epileptic spasms (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "780827006",
"display": "Synaptic Ras GTPase activating protein 1- related intellectual disability (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "782737003",
"display": "Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "782772000",
"display": "Congenital muscular dystrophy with intellectual disability and severe epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "782825008",
"display": "Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "783055005",
"display": "Progressive myoclonic epilepsy type 5 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "783062001",
"display": "Progressive myoclonic epilepsy type 6 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "783064000",
"display": "Progressive myoclonic epilepsy type 3 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "783139000",
"display": "Progressive myoclonic epilepsy type 8 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "783739005",
"display": "Familial temporal lobe epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "784345005",
"display": "Malignant migrating partial seizures of infancy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "784372002",
"display": "Familial mesial temporal lobe epilepsy with febrile seizures (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "784377008",
"display": "Familial epilepsy with auditory features (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "785303004",
"display": "Multiple congenital anomalies, hypotonia, seizures syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "785726009",
"display": "Hyperekplexia epilepsy syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "788417006",
"display": "Alopecia, epilepsy, intellectual disability syndrome Moynahan type (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "789063000",
"display": "Primary hyperaldosteronism, seizures, neurological abnormalities syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "79631006",
"display": "Absence seizure (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "79745005",
"display": "Reflex epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "80651009",
"display": "Aicardi's syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "82381000119103",
"display": "Epileptic dementia with behavioral disturbance (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "84757009",
"display": "Epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "860804005",
"display": "Epilepsy due to infectious encephalitis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "860806007",
"display": "Epilepsy due to infectious meningitis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "860815000",
"display": "Epilepsy due to neonatal central nervous system infection (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "95208000",
"display": "Photogenic epilepsy (disorder)"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.001",
"display": "Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.009",
"display": "Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, without status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.011",
"display": "Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.019",
"display": "Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, without status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.101",
"display": "Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.109",
"display": "Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, without status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.111",
"display": "Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.119",
"display": "Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, without status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.201",
"display": "Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.209",
"display": "Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, without status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.211",
"display": "Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.219",
"display": "Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, without status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.301",
"display": "Generalized idiopathic epilepsy and epileptic syndromes, not intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.309",
"display": "Generalized idiopathic epilepsy and epileptic syndromes, not intractable, without status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.311",
"display": "Generalized idiopathic epilepsy and epileptic syndromes, intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.319",
"display": "Generalized idiopathic epilepsy and epileptic syndromes, intractable, without status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.401",
"display": "Other generalized epilepsy and epileptic syndromes, not intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.409",
"display": "Other generalized epilepsy and epileptic syndromes, not intractable, without status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.411",
"display": "Other generalized epilepsy and epileptic syndromes, intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.419",
"display": "Other generalized epilepsy and epileptic syndromes, intractable, without status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.42",
"display": "Cyclin-Dependent Kinase-Like 5 Deficiency Disorder"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.501",
"display": "Epileptic seizures related to external causes, not intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.509",
"display": "Epileptic seizures related to external causes, not intractable, without status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.801",
"display": "Other epilepsy, not intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.802",
"display": "Other epilepsy, not intractable, without status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.803",
"display": "Other epilepsy, intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.804",
"display": "Other epilepsy, intractable, without status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.811",
"display": "Lennox-Gastaut syndrome, not intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.812",
"display": "Lennox-Gastaut syndrome, not intractable, without status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.813",
"display": "Lennox-Gastaut syndrome, intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.814",
"display": "Lennox-Gastaut syndrome, intractable, without status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.821",
"display": "Epileptic spasms, not intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.822",
"display": "Epileptic spasms, not intractable, without status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.823",
"display": "Epileptic spasms, intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.824",
"display": "Epileptic spasms, intractable, without status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.833",
"display": "Dravet syndrome, intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.834",
"display": "Dravet syndrome, intractable, without status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.89",
"display": "Other seizures"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.901",
"display": "Epilepsy, unspecified, not intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.909",
"display": "Epilepsy, unspecified, not intractable, without status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.911",
"display": "Epilepsy, unspecified, intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.919",
"display": "Epilepsy, unspecified, intractable, without status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.A01",
"display": "Absence epileptic syndrome, not intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.A09",
"display": "Absence epileptic syndrome, not intractable, without status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.A11",
"display": "Absence epileptic syndrome, intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.A19",
"display": "Absence epileptic syndrome, intractable, without status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.B01",
"display": "Juvenile myoclonic epilepsy, not intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.B09",
"display": "Juvenile myoclonic epilepsy, not intractable, without status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.B11",
"display": "Juvenile myoclonic epilepsy, intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.B19",
"display": "Juvenile myoclonic epilepsy, intractable, without status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.C01",
"display": "Lafora progressive myoclonus epilepsy, not intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.C09",
"display": "Lafora progressive myoclonus epilepsy, not intractable, without status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.C11",
"display": "Lafora progressive myoclonus epilepsy, intractable, with status epilepticus"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G40.C19",
"display": "Lafora progressive myoclonus epilepsy, intractable, without status epilepticus"
}
]
}
}
FHIR