{
  "concept_id": 4693,
  "concept_version_id": 12184,
  "coding_system": {
    "id": 5,
    "name": "Read codes v2",
    "description": "Read codes v2"
  },
  "name": "Aetiology specific epilepsies",
  "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,
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  "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": 10862,
      "name": "Inclusion 1",
      "logical_type": "INCLUDE",
      "source_type": "FILE_IMPORT",
      "source": "application/vnd.openxmlformats-officedocument.spreadsheetml.sheet",
      "codes": [
        {
          "id": 654533,
          "code": "^ESCT1204977",
          "description": "Hypothalamic hamartoma with gelastic seizure"
        },
        {
          "id": 654534,
          "code": "^ESCT1349343",
          "description": "Mesial temporal lobe epilepsy with hippocampal sclerosis (MTLE-HS)"
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        {
          "id": 654535,
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          "description": "Rasmussen encephalitis"
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        {
          "id": 654536,
          "code": "^ESCTST281552",
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        {
          "id": 654537,
          "code": "EMISNQGL2",
          "description": "GLUT1 deficiency syndrome"
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        {
          "id": 654538,
          "code": "F0352",
          "description": "Rasmussen syndrome"
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        {
          "id": 654539,
          "code": "F035200",
          "description": "Rasmussen syndrome"
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        {
          "id": 654540,
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        {
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        {
          "id": 654542,
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        },
        {
          "id": 654543,
          "code": "PK61.",
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        {
          "id": 654544,
          "code": "PK61.00",
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        {
          "id": 654545,
          "code": "PK610",
          "description": "Sturge-Weber syndrome"
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      ]
    }
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  "version_history": [
    {
      "version_id": 12184,
      "version_name": "Aetiology specific epilepsies",
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      "version_id": 12146,
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}