{
  "id": 25041,
  "label": "juvenile absence epilepsy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0800453",
  "properties": {
    "xrefs": [
      "DOID:0060172",
      "GARD:0002162",
      "MEDGEN:1388059",
      "NCIT:C129868",
      "Orphanet:1941",
      "SCTID:230413002",
      "UMLS:C4317339",
      "icd11.foundation:519416529"
    ],
    "synonyms": [
      "JAE",
      "epilepsy juvenile absence"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A genetic epilepsy with onset occurring around puberty. Juvenile absence epilepsy is characterized by sporadic occurrence of absence seizures, frequently associated with a long-life prevalence of generalized tonic-clonic seizures (GTCS) and sporadic myoclonic jerks."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "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"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 25071,
      "label": "variable-age onset idiopathic generalized epilepsy syndrome"
    }
  ]
}