{
  "id": 25083,
  "label": "childhood-onset idiopathic generalized epilepsy syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0800499",
  "properties": {
    "xrefs": [
      "GARD:0027302"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "An idiopathic generalized epilepsy that has an onset during childhood."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 7224,
      "label": "idiopathic generalized epilepsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24300
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 2,
      "reference_id": "MONDO:0005579"
    },
    {
      "id": 19725,
      "label": "childhood-onset epilepsy syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16436
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019437",
          "MEDGEN:1843031",
          "Orphanet:98259",
          "UMLS:C5681526"
        ],
        "synonyms": [
          "childhood epilepsy syndrome",
          "childhood-onset epilepsy syndrome",
          "epilepsy syndrome of childhood",
          "paediatric epilepsy syndrome",
          "pediatric epilepsy syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A epilepsy syndrome that occurs during childhood."
      },
      "child_count": 16,
      "reference_id": "MONDO:0020072"
    }
  ],
  "children": [
    {
      "id": 11962,
      "label": "childhood absence epilepsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        25083
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050708",
          "DOID:1825",
          "GARD:0016667",
          "MEDGEN:924120",
          "OMIMPS:600131",
          "Orphanet:64280",
          "SCTID:50866000",
          "UMLS:C4281785",
          "icd11.foundation:726403046"
        ],
        "synonyms": [
          "pyknolepsy",
          "petit mal seizure"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A familial generalized pediatric epilepsy, characterized by very frequent (multiple per day) absence seizures, usually occurring in children between the ages of 4 and 10 years, with, in most cases, a good prognosis."
      },
      "child_count": 1,
      "reference_id": "MONDO:0010826"
    }
  ],
  "roots": [
    {
      "id": 7224,
      "label": "idiopathic generalized epilepsy"
    },
    {
      "id": 19725,
      "label": "childhood-onset epilepsy syndrome"
    }
  ]
}