{
  "concept_id": 4691,
  "concept_version_id": 12183,
  "coding_system": {
    "id": 5,
    "name": "Read codes v2",
    "description": "Read codes v2"
  },
  "name": "Developmental and epileptic encephalopathies",
  "description": null,
  "author": "",
  "entry_date": "2025-11-19",
  "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": "PH1934",
  "phenotype_owner_history_id": 4534,
  "requested_entity_id": null,
  "components": [
    {
      "id": 10861,
      "name": "Inclusion 1",
      "logical_type": "INCLUDE",
      "source_type": "FILE_IMPORT",
      "source": "application/vnd.openxmlformats-officedocument.spreadsheetml.sheet",
      "codes": [
        {
          "id": 654493,
          "code": "F1011",
          "description": "Kufs Disease"
        },
        {
          "id": 654467,
          "code": "^ESCT1164424",
          "description": "Pyridoxine-dependent epilepsy"
        },
        {
          "id": 654468,
          "code": "^ESCT1177804",
          "description": "Dravet Syndrome"
        },
        {
          "id": 654469,
          "code": "^ESCT1207699",
          "description": "STXBP1 encephalopathy with epilepsy"
        },
        {
          "id": 654470,
          "code": "^ESCT1350026",
          "description": "Infantile epileptic dyskinetic encephalopathy"
        },
        {
          "id": 654471,
          "code": "^ESCT1357219",
          "description": "KCNQ2-related epileptic encephalopathy"
        },
        {
          "id": 654472,
          "code": "^ESCT1357293",
          "description": "Myoclonic epilepsy in non-progressive encephalopathy"
        },
        {
          "id": 654473,
          "code": "^ESCT1362418",
          "description": "Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome"
        },
        {
          "id": 654474,
          "code": "^ESCT1379158",
          "description": "Myoclonic epilepsy with ragged red fibres"
        },
        {
          "id": 654475,
          "code": "^ESCTAT805326",
          "description": "Atypical absence epilepsy"
        },
        {
          "id": 654476,
          "code": "^ESCTBE500712",
          "description": "Benign atypical partial epilepsy in childhood"
        },
        {
          "id": 654477,
          "code": "^ESCTEA321568",
          "description": "Early myoclonic encephalopathy"
        },
        {
          "id": 654478,
          "code": "^ESCTEP500794",
          "description": "Epilepsy with continuous spike wave during slow-wave sleep"
        },
        {
          "id": 654479,
          "code": "^ESCTEP784067",
          "description": "Epileptic encephalopathy"
        },
        {
          "id": 654480,
          "code": "^ESCTEP795518",
          "description": "Epilepsy of infancy with migrating focal seizures (EIMFS)"
        },
        {
          "id": 654481,
          "code": "^ESCTIN808972",
          "description": "Infantile spasms co-occurrent with status epilepticus"
        },
        {
          "id": 654482,
          "code": "^ESCTIN808973",
          "description": "Infantile spasms with status epilepticus"
        },
        {
          "id": 654483,
          "code": "^ESCTKU350778",
          "description": "Kufs type neuronal ceroid lipofuscinosis"
        },
        {
          "id": 654484,
          "code": "^ESCTLA500792",
          "description": "Landau-Kleffner syndrome"
        },
        {
          "id": 654485,
          "code": "^ESCTMY500762",
          "description": "Myoclonic astatic epilepsy"
        },
        {
          "id": 654486,
          "code": "^ESCTUN500768",
          "description": "Unverricht-Lundborg syndrome"
        },
        {
          "id": 654487,
          "code": "C3151",
          "description": "MELAS"
        },
        {
          "id": 654488,
          "code": "C3272",
          "description": "Niemann-Pick disease"
        },
        {
          "id": 654489,
          "code": "EMISNQGL2",
          "description": "GLUT1 deficiency syndrome"
        },
        {
          "id": 654490,
          "code": "Eu803",
          "description": "Acquired epileptic aphasia"
        },
        {
          "id": 654491,
          "code": "Eu80300",
          "description": "[X]Acquired aphasia with epilepsy [Landau - Kleffner]"
        },
        {
          "id": 654492,
          "code": "F1010",
          "description": "Janksy-Bielschowsky disease (CLN2)"
        },
        {
          "id": 654494,
          "code": "F1012",
          "description": "Batten's disease"
        },
        {
          "id": 654495,
          "code": "F1021",
          "description": "Cerebral degeneration in Niemann-Pick disease"
        },
        {
          "id": 654496,
          "code": "F10y0",
          "description": "Alper's disease"
        },
        {
          "id": 654497,
          "code": "F1321",
          "description": "Progressive myoclonic epilepsy"
        },
        {
          "id": 654498,
          "code": "F132100",
          "description": "Progressive myoclonic epilepsy"
        },
        {
          "id": 654499,
          "code": "F132111",
          "description": "Unverricht - Lundborg disease"
        },
        {
          "id": 654500,
          "code": "F1422",
          "description": "Dyssynergia cerebellaris myoclonica"
        },
        {
          "id": 654501,
          "code": "F142200",
          "description": "Dyssynergia cerebellaris myoclonica"
        },
        {
          "id": 654502,
          "code": "F2505",
          "description": "Lennox-Gastaut syndrome"
        },
        {
          "id": 654503,
          "code": "F250500",
          "description": "Lennox-Gastaut syndrome"
        },
        {
          "id": 654504,
          "code": "F251111",
          "description": "Otohara syndrome"
        },
        {
          "id": 654505,
          "code": "F256.",
          "description": "Infantile spasms"
        },
        {
          "id": 654506,
          "code": "F256.00",
          "description": "Infantile spasms"
        },
        {
          "id": 654507,
          "code": "F256.12",
          "description": "West syndrome"
        },
        {
          "id": 654508,
          "code": "F2560",
          "description": "Hypsarrhythmia"
        },
        {
          "id": 654509,
          "code": "F256000",
          "description": "Hypsarrhythmia"
        },
        {
          "id": 654510,
          "code": "F2561",
          "description": "Salaam attacks"
        },
        {
          "id": 654511,
          "code": "F256100",
          "description": "Salaam attacks"
        },
        {
          "id": 654512,
          "code": "F256z",
          "description": "Infantile spasms NOS"
        },
        {
          "id": 654513,
          "code": "F256z.",
          "description": "Infantile spasms NOS"
        },
        {
          "id": 654514,
          "code": "F256z00",
          "description": "Infantile spasms NOS"
        },
        {
          "id": 654515,
          "code": "F259.",
          "description": "Early infant epileptic encephalopathy wth suppression bursts"
        },
        {
          "id": 654516,
          "code": "F259.00",
          "description": "Early infant epileptic encephalopathy wth suppression bursts"
        },
        {
          "id": 654517,
          "code": "F259.11",
          "description": "Ohtahara syndrome"
        },
        {
          "id": 654518,
          "code": "F2590",
          "description": "Early infant epileptic encephalopathy wth suppression bursts"
        },
        {
          "id": 654519,
          "code": "F2591",
          "description": "Ohtahara syndrome"
        },
        {
          "id": 654520,
          "code": "F25G.",
          "description": "Severe myoclonic epilepsy in infancy"
        },
        {
          "id": 654521,
          "code": "F25G.00",
          "description": "Severe myoclonic epilepsy in infancy"
        },
        {
          "id": 654522,
          "code": "F25G.11",
          "description": "Dravet syndrome"
        },
        {
          "id": 654523,
          "code": "F25G0",
          "description": "Severe myoclonic epilepsy in infancy"
        },
        {
          "id": 654524,
          "code": "F25G1",
          "description": "Dravet syndrome"
        },
        {
          "id": 654525,
          "code": "F28y400",
          "description": "GLUT1 deficiency syndrome"
        },
        {
          "id": 654526,
          "code": "F28y4-1",
          "description": "Glucose transporter protein type 1 deficiency syndrome"
        },
        {
          "id": 654527,
          "code": "F28y411",
          "description": "Glucose transporter protein type 1 deficiency syndrome"
        },
        {
          "id": 654528,
          "code": "ZS82.",
          "description": "Acquired epileptic aphasia"
        },
        {
          "id": 654529,
          "code": "ZS82.00",
          "description": "Acquired epileptic aphasia"
        },
        {
          "id": 654530,
          "code": "ZS82.11",
          "description": "Landau-Kleffner syndrome"
        },
        {
          "id": 654531,
          "code": "ZS820",
          "description": "Acquired epileptic aphasia"
        },
        {
          "id": 654532,
          "code": "ZS821",
          "description": "Landau-Kleffner syndrome"
        }
      ]
    }
  ],
  "version_history": [
    {
      "version_id": 12183,
      "version_name": "Developmental and epileptic encephalopathies",
      "version_date": "2025-11-27T13:00:23.739999Z",
      "is_published": true,
      "is_latest": true
    }
  ]
}