{
  "concept_id": 4604,
  "concept_version_id": 12180,
  "coding_system": {
    "id": 5,
    "name": "Read codes v2",
    "description": "Read codes v2"
  },
  "name": "Epilepsy syndromes (Epilepsy aetiologies) Read codes",
  "description": null,
  "author": "",
  "entry_date": "2025-10-16",
  "validation_performed": false,
  "validation_description": null,
  "publication_doi": "",
  "publication_link": "",
  "secondary_publication_links": null,
  "paper_published": false,
  "source_reference": "",
  "citation_requirements": null,
  "owner_access": 3,
  "group_access": 1,
  "world_access": 1,
  "tags": null,
  "collections": null,
  "created_by": null,
  "modified_by": null,
  "owner": null,
  "group": null,
  "phenotype_owner": "PH1927",
  "phenotype_owner_history_id": 9241,
  "requested_entity_id": null,
  "components": [
    {
      "id": 10859,
      "name": "Inclusion 1",
      "logical_type": "INCLUDE",
      "source_type": "FILE_IMPORT",
      "source": "application/vnd.openxmlformats-officedocument.spreadsheetml.sheet",
      "codes": [
        {
          "id": 654118,
          "code": "Eu80300",
          "description": "[X]Acquired aphasia with epilepsy [Landau - Kleffner]"
        },
        {
          "id": 654119,
          "code": "Fyu50",
          "description": "[X]Other generalized epilepsy and epileptic syndromes"
        },
        {
          "id": 654120,
          "code": "Eu803",
          "description": "Acquired epileptic aphasia"
        },
        {
          "id": 654121,
          "code": "ZS82.",
          "description": "Acquired epileptic aphasia"
        },
        {
          "id": 654122,
          "code": "ZS82.00",
          "description": "Acquired epileptic aphasia"
        },
        {
          "id": 654123,
          "code": "ZS820",
          "description": "Acquired epileptic aphasia"
        },
        {
          "id": 654124,
          "code": "F10y0",
          "description": "Alper's disease"
        },
        {
          "id": 654125,
          "code": "^ESCTAT805326",
          "description": "Atypical absence epilepsy"
        },
        {
          "id": 654126,
          "code": "F1012",
          "description": "Batten's disease"
        },
        {
          "id": 654127,
          "code": "^ESCTBE500712",
          "description": "Benign atypical partial epilepsy in childhood"
        },
        {
          "id": 654128,
          "code": "^ESCT1368627",
          "description": "Benign childhood epilepsy with centrotemporal spikes, non-refractory"
        },
        {
          "id": 654129,
          "code": "^ESCT1368624",
          "description": "Benign childhood epilepsy with centrotemporal spikes, refractory"
        },
        {
          "id": 654130,
          "code": "^ESCT1349122",
          "description": "Benign familial mesial temporal lobe epilepsy"
        },
        {
          "id": 654131,
          "code": "^ESCTBE274612",
          "description": "Benign focal epilepsy of childhood"
        },
        {
          "id": 654132,
          "code": "^ESCTBE500710",
          "description": "Benign frontal epilepsy of childhood"
        },
        {
          "id": 654133,
          "code": "^ESCTBE476954",
          "description": "Benign myoclonic epilepsy in infancy"
        },
        {
          "id": 654134,
          "code": "^ESCTBE500717",
          "description": "Benign occipital epilepsy of childhood - early onset variant"
        },
        {
          "id": 654135,
          "code": "^ESCT1349309",
          "description": "Benign occipital lobe epilepsy"
        },
        {
          "id": 654136,
          "code": "^ESCT1349311",
          "description": "Benign partial epilepsy of infancy with complex partial seizures"
        },
        {
          "id": 654137,
          "code": "F25y4",
          "description": "Benign Rolandic epilepsy"
        },
        {
          "id": 654138,
          "code": "F25y400",
          "description": "Benign Rolandic epilepsy"
        },
        {
          "id": 654139,
          "code": "^ESCTCE321095",
          "description": "Centrotemporal epilepsy"
        },
        {
          "id": 654140,
          "code": "F1021",
          "description": "Cerebral degeneration in Niemann-Pick disease"
        },
        {
          "id": 654141,
          "code": "^ESCTCH332385",
          "description": "Childhood absence epilepsy"
        },
        {
          "id": 654142,
          "code": "^ESCTCH500714",
          "description": "Childhood epilepsy with occipital paroxysms"
        },
        {
          "id": 654143,
          "code": "^ESCTCR500755",
          "description": "Cryptogenic generalised epilepsy"
        },
        {
          "id": 654144,
          "code": "^ESCTCR500777",
          "description": "Cryptogenic myoclonic epilepsy"
        },
        {
          "id": 654145,
          "code": "F25G.11",
          "description": "Dravet syndrome"
        },
        {
          "id": 654146,
          "code": "F25G1",
          "description": "Dravet syndrome"
        },
        {
          "id": 654147,
          "code": "^ESCT1177804",
          "description": "Dravet Syndrome"
        },
        {
          "id": 654148,
          "code": "F1422",
          "description": "Dyssynergia cerebellaris myoclonica"
        },
        {
          "id": 654149,
          "code": "F142200",
          "description": "Dyssynergia cerebellaris myoclonica"
        },
        {
          "id": 654150,
          "code": "F259.",
          "description": "Early infant epileptic encephalopathy wth suppression bursts"
        },
        {
          "id": 654151,
          "code": "F2590",
          "description": "Early infant epileptic encephalopathy wth suppression bursts"
        },
        {
          "id": 654152,
          "code": "F259.00",
          "description": "Early infant epileptic encephalopathy wth suppression bursts"
        },
        {
          "id": 654153,
          "code": "^ESCTEA321568",
          "description": "Early myoclonic encephalopathy"
        },
        {
          "id": 654154,
          "code": "^ESCTEP795518",
          "description": "Epilepsy of infancy with migrating focal seizures (EIMFS)"
        },
        {
          "id": 654155,
          "code": "^ESCTEP500794",
          "description": "Epilepsy with continuous spike wave during slow-wave sleep"
        },
        {
          "id": 654156,
          "code": "^ESCTEP784067",
          "description": "Epileptic encephalopathy"
        },
        {
          "id": 654157,
          "code": "^ESCT1363726",
          "description": "Familial infantile myoclonic epilepsy"
        },
        {
          "id": 654158,
          "code": "^ESCT1363784",
          "description": "Familial mesial temporal lobe epilepsy with febrile seizures"
        },
        {
          "id": 654159,
          "code": "^ESCT1363280",
          "description": "Familial temporal lobe epilepsy"
        },
        {
          "id": 654160,
          "code": "F28y4-1",
          "description": "Glucose transporter protein type 1 deficiency syndrome"
        },
        {
          "id": 654161,
          "code": "F28y411",
          "description": "Glucose transporter protein type 1 deficiency syndrome"
        },
        {
          "id": 654162,
          "code": "F28y400",
          "description": "GLUT1 deficiency syndrome"
        },
        {
          "id": 654163,
          "code": "EMISNQGL2",
          "description": "GLUT1 deficiency syndrome"
        },
        {
          "id": 654164,
          "code": "^ESCT1204977",
          "description": "Hypothalamic hamartoma with gelastic seizure"
        },
        {
          "id": 654165,
          "code": "F2560",
          "description": "Hypsarrhythmia"
        },
        {
          "id": 654166,
          "code": "F256000",
          "description": "Hypsarrhythmia"
        },
        {
          "id": 654167,
          "code": "^ESCTID309315",
          "description": "Idiopathic generalised epilepsy"
        },
        {
          "id": 654168,
          "code": "^ESCTID309316",
          "description": "Idiopathic generalized epilepsy"
        },
        {
          "id": 654169,
          "code": "^ESCTID500778",
          "description": "Idiopathic myoclonic epilepsy"
        },
        {
          "id": 654170,
          "code": "^ESCT1350026",
          "description": "Infantile epileptic dyskinetic encephalopathy"
        },
        {
          "id": 654171,
          "code": "F256.",
          "description": "Infantile spasms"
        },
        {
          "id": 654172,
          "code": "F256.00",
          "description": "Infantile spasms"
        },
        {
          "id": 654173,
          "code": "^ESCTIN808972",
          "description": "Infantile spasms co-occurrent with status epilepticus"
        },
        {
          "id": 654174,
          "code": "F256z.",
          "description": "Infantile spasms NOS"
        },
        {
          "id": 654175,
          "code": "F256z00",
          "description": "Infantile spasms NOS"
        },
        {
          "id": 654176,
          "code": "F256z",
          "description": "Infantile spasms NOS"
        },
        {
          "id": 654177,
          "code": "^ESCTIN808973",
          "description": "Infantile spasms with status epilepticus"
        },
        {
          "id": 654178,
          "code": "^ESCT1362418",
          "description": "Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome"
        },
        {
          "id": 654179,
          "code": "^ESCT1183138",
          "description": "Infantile-onset symptomatic epilepsy syndrome"
        },
        {
          "id": 654180,
          "code": "^ESCT1170675",
          "description": "Intractable idiopathic partial epilepsy"
        },
        {
          "id": 654181,
          "code": "F1010",
          "description": "Janksy-Bielschowsky disease (CLN2)"
        },
        {
          "id": 654182,
          "code": "^ESCTJE774510",
          "description": "Jeavons syndrome"
        },
        {
          "id": 654183,
          "code": "^ESCTJM259887",
          "description": "JME - Juvenile myoclonic epilepsy"
        },
        {
          "id": 654184,
          "code": "F2504",
          "description": "Juvenile absence epilepsy"
        },
        {
          "id": 654185,
          "code": "F250400",
          "description": "Juvenile absence epilepsy"
        },
        {
          "id": 654186,
          "code": "F25A.",
          "description": "Juvenile myoclonic epilepsy"
        },
        {
          "id": 654187,
          "code": "F25A0",
          "description": "Juvenile myoclonic epilepsy"
        },
        {
          "id": 654188,
          "code": "F25A.00",
          "description": "Juvenile myoclonic epilepsy"
        },
        {
          "id": 654189,
          "code": "^ESCT1357219",
          "description": "KCNQ2-related epileptic encephalopathy"
        },
        {
          "id": 654190,
          "code": "F1011",
          "description": "Kufs Disease"
        },
        {
          "id": 654191,
          "code": "^ESCTKU350778",
          "description": "Kufs type neuronal ceroid lipofuscinosis"
        },
        {
          "id": 654192,
          "code": "ZS82.11",
          "description": "Landau-Kleffner syndrome"
        },
        {
          "id": 654193,
          "code": "ZS821",
          "description": "Landau-Kleffner syndrome"
        },
        {
          "id": 654194,
          "code": "^ESCTLA500792",
          "description": "Landau-Kleffner syndrome"
        },
        {
          "id": 654195,
          "code": "F2505",
          "description": "Lennox-Gastaut syndrome"
        },
        {
          "id": 654196,
          "code": "F250500",
          "description": "Lennox-Gastaut syndrome"
        },
        {
          "id": 654197,
          "code": "F25y2",
          "description": "Locl-rlt(foc)(part)idiop epilep&epilptic syn seiz locl onset"
        },
        {
          "id": 654198,
          "code": "F25y200",
          "description": "Locl-rlt(foc)(part)idiop epilep&epilptic syn seiz locl onset"
        },
        {
          "id": 654199,
          "code": "C3151",
          "description": "MELAS"
        },
        {
          "id": 654200,
          "code": "^ESCT1349343",
          "description": "Mesial temporal lobe epilepsy with hippocampal sclerosis (MTLE-HS)"
        },
        {
          "id": 654201,
          "code": "^ESCTMY500766",
          "description": "Myoclonic absence epilepsy"
        },
        {
          "id": 654202,
          "code": "^ESCTMY500762",
          "description": "Myoclonic astatic epilepsy"
        },
        {
          "id": 654203,
          "code": "^ESCT1357293",
          "description": "Myoclonic epilepsy in non-progressive encephalopathy"
        },
        {
          "id": 654204,
          "code": "^ESCT1379158",
          "description": "Myoclonic epilepsy with ragged red fibres"
        },
        {
          "id": 654205,
          "code": "F2511",
          "description": "Neonatal myoclonic epilepsy"
        },
        {
          "id": 654206,
          "code": "F251100",
          "description": "Neonatal myoclonic epilepsy"
        },
        {
          "id": 654207,
          "code": "C3272",
          "description": "Niemann-Pick disease"
        },
        {
          "id": 654208,
          "code": "F259.11",
          "description": "Ohtahara syndrome"
        },
        {
          "id": 654209,
          "code": "F2591",
          "description": "Ohtahara syndrome"
        },
        {
          "id": 654210,
          "code": "F251111",
          "description": "Otohara syndrome"
        },
        {
          "id": 654211,
          "code": "F25y5",
          "description": "Panayiotopoulos syndrome"
        },
        {
          "id": 654212,
          "code": "F25y500",
          "description": "Panayiotopoulos syndrome"
        },
        {
          "id": 654213,
          "code": "^ESCTPR309317",
          "description": "Primary generalised epilepsy"
        },
        {
          "id": 654214,
          "code": "^ESCTPR500720",
          "description": "Primary inherited reading epilepsy"
        },
        {
          "id": 654215,
          "code": "F1321",
          "description": "Progressive myoclonic epilepsy"
        },
        {
          "id": 654216,
          "code": "F132100",
          "description": "Progressive myoclonic epilepsy"
        },
        {
          "id": 654217,
          "code": "^ESCT1164424",
          "description": "Pyridoxine-dependent epilepsy"
        },
        {
          "id": 654218,
          "code": "^ESCTRA500472",
          "description": "Rasmussen encephalitis"
        },
        {
          "id": 654219,
          "code": "F0352",
          "description": "Rasmussen syndrome"
        },
        {
          "id": 654220,
          "code": "F035200",
          "description": "Rasmussen syndrome"
        },
        {
          "id": 654221,
          "code": "^ESCT1205388",
          "description": "Recurrent benign focal seizures of childhood"
        },
        {
          "id": 654222,
          "code": "^ESCTRE751247",
          "description": "Refractory juvenile myoclonic epilepsy"
        },
        {
          "id": 654223,
          "code": "F2561",
          "description": "Salaam attacks"
        },
        {
          "id": 654224,
          "code": "F256100",
          "description": "Salaam attacks"
        },
        {
          "id": 654225,
          "code": "F25G.",
          "description": "Severe myoclonic epilepsy in infancy"
        },
        {
          "id": 654226,
          "code": "F25G.00",
          "description": "Severe myoclonic epilepsy in infancy"
        },
        {
          "id": 654227,
          "code": "F25G0",
          "description": "Severe myoclonic epilepsy in infancy"
        },
        {
          "id": 654228,
          "code": "^ESCTST281552",
          "description": "Sturge-Weber disease"
        },
        {
          "id": 654229,
          "code": "PK61.",
          "description": "Sturge-Weber syndrome"
        },
        {
          "id": 654230,
          "code": "PK610",
          "description": "Sturge-Weber syndrome"
        },
        {
          "id": 654231,
          "code": "PK61.00",
          "description": "Sturge-Weber syndrome"
        },
        {
          "id": 654232,
          "code": "^ESCT1207699",
          "description": "STXBP1 encephalopathy with epilepsy"
        },
        {
          "id": 654233,
          "code": "F132111",
          "description": "Unverricht - Lundborg disease"
        },
        {
          "id": 654234,
          "code": "^ESCTUN500768",
          "description": "Unverricht-Lundborg syndrome"
        },
        {
          "id": 654235,
          "code": "F256.12",
          "description": "West syndrome"
        }
      ]
    }
  ],
  "version_history": [
    {
      "version_id": 12180,
      "version_name": "Epilepsy syndromes (Epilepsy aetiologies) Read codes",
      "version_date": "2025-11-27T11:31:30.104673Z",
      "is_published": true,
      "is_latest": true
    },
    {
      "version_id": 12040,
      "version_name": "Epilepsy syndromes (Epilepsy aetiologies) Read codes",
      "version_date": "2025-10-16T10:42:55.749014Z",
      "is_published": true,
      "is_latest": false
    }
  ]
}