{
  "id": 14357,
  "label": "epilepsy, familial adult myoclonic, 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013322",
  "properties": {
    "xrefs": [
      "DOID:0111695",
      "GARD:0018084",
      "MEDGEN:462210",
      "MESH:C567098",
      "OMIM:613608",
      "UMLS:C3150860"
    ],
    "synonyms": [
      "FAME3",
      "cortical myoclonic tremor with epilepsy, familial, 3",
      "epilepsy, familial ADULT myoclonic, 3"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2751,
      "label": "epilepsy, familial adult myoclonic",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24270,
        24301
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111689",
          "GARD:0022720",
          "OMIMPS:601068"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An epilepsy syndrome characterized by adult-onset cortical myoclonus typically first seen as tremulous finger movements and myoclonus of the extremities."
      },
      "child_count": 16,
      "reference_id": "MONDO:0000160"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2751,
      "label": "epilepsy, familial adult myoclonic"
    }
  ]
}