{
  "id": 15174,
  "label": "epilepsy, familial adult myoclonic, 5",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014167",
  "properties": {
    "xrefs": [
      "DOID:0111691",
      "GARD:0018086",
      "MEDGEN:815704",
      "OMIM:615400",
      "UMLS:C3809374"
    ],
    "synonyms": [
      "CNTN2 epilepsy, familial adult myoclonic",
      "epilepsy, familial adult myoclonic caused by mutation in CNTN2",
      "epilepsy, familial adult myoclonic, 5",
      "epilepsy, familial adult myoclonic, type 5",
      "epilepsy, myoclonic, familial adult, 5",
      "FAME5",
      "cortical myoclonic tremor with epilepsy, familial, 5",
      "epilepsy, familial ADULT myoclonic, 5"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any epilepsy, familial adult myoclonic in which the cause of the disease is a mutation in the CNTN2 gene."
  },
  "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"
    }
  ]
}