{
  "id": 7224,
  "label": "idiopathic generalized epilepsy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0005579",
  "properties": {
    "xrefs": [
      "DOID:1827",
      "EFO:0005917",
      "MEDGEN:75725",
      "MESH:C562694",
      "OMIM:600669",
      "OMIMPS:600669",
      "SCTID:19598007",
      "UMLS:C0270850"
    ],
    "synonyms": [
      "generalized epilepsy",
      "EIG",
      "IGE",
      "epilepsy, idiopathic generalized",
      "hereditary idiopathic generalized epilepsy",
      "idiopathic generalised epilepsy",
      "idiopathic generalized epilepsy"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A generalised epilepsy that encompasses several common seizure phenotypes including childhood absence epilepsy, juvenile absence epilepsy, juvenile myoclonic epilepsy and epilepsy with generalized tonic-clonic seizures alone. These epilepsy syndromes have polygenic inheritance with or without environmental factors contributing to seizure susceptibility. Seizure types include one or a combination of absence seizures, myoclonic seizures and/or generalized tonic-clonic seizures."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 24300,
      "label": "hereditary generalized epilepsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24270,
        24299
      ],
      "type_id": 0,
      "properties": {
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An instance of generalized epilepsy that is caused by an inherited genomic modification in an individual."
      },
      "child_count": 4,
      "reference_id": "MONDO:0100576"
    }
  ],
  "children": [
    {
      "id": 25071,
      "label": "variable-age onset idiopathic generalized epilepsy syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7224,
        24339
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027390"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any idiopathic generalized epilepsy syndrome that has a variable-age onset."
      },
      "child_count": 8,
      "reference_id": "MONDO:0800487"
    },
    {
      "id": 25083,
      "label": "childhood-onset idiopathic generalized epilepsy syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7224,
        19725
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027302"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An idiopathic generalized epilepsy that has an onset during childhood."
      },
      "child_count": 2,
      "reference_id": "MONDO:0800499"
    }
  ],
  "roots": [
    {
      "id": 24300,
      "label": "hereditary generalized epilepsy"
    }
  ]
}