{
  "id": 15900,
  "label": "developmental and epileptic encephalopathy, 43",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014921",
  "properties": {
    "xrefs": [
      "DOID:0080447",
      "GARD:0016192",
      "MEDGEN:934679",
      "OMIM:617113",
      "UMLS:C4310712"
    ],
    "synonyms": [
      "DEE43",
      "EIEE43",
      "GABRB3 early infantile epileptic encephalopathy",
      "developmental and epileptic encephalopathy 43",
      "early infantile epileptic encephalopathy caused by mutation in GABRB3",
      "epileptic encephalopathy, early infantile, 43",
      "epileptic encephalopathy, early infantile, 43; EIEE43",
      "epileptic encephalopathy, early infantile, type 43"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the GABRB3 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17029,
      "label": "Lennox-Gastaut syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        23814,
        25084
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050561",
          "GARD:0009912",
          "ICD10CM:G40.81",
          "MEDGEN:116044",
          "MESH:D065768",
          "MedDRA:10048816",
          "NANDO:1200591",
          "NANDO:2200879",
          "NCIT:C84816",
          "NORD:1358",
          "OMIM:606369",
          "Orphanet:2382",
          "SCTID:230418006",
          "UMLS:C0238111",
          "icd11.foundation:651135242"
        ],
        "synonyms": [
          "LGS",
          "encephalopathy of childhood",
          "epileptic encephalopathy Lennox-Gastaut type",
          "macrocephaly and epileptic encephalopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Lennox-Gastaut syndrome (LGS) belongs to the group of severe childhood epileptic encephalopathies."
      },
      "child_count": 9,
      "reference_id": "MONDO:0016532"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17029,
      "label": "Lennox-Gastaut syndrome"
    }
  ]
}