{
  "id": 13004,
  "label": "epilepsy, familial adult myoclonic, 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011930",
  "properties": {
    "xrefs": [
      "DOID:0111692",
      "GARD:0018083",
      "MEDGEN:375031",
      "MESH:C564313",
      "OMIM:607876",
      "UMLS:C1842852"
    ],
    "synonyms": [
      "ADRA2B epilepsy, familial adult myoclonic",
      "epilepsy, familial adult myoclonic caused by mutation in ADRA2B",
      "epilepsy, familial adult myoclonic, 2",
      "epilepsy, familial adult myoclonic, type 2",
      "FAME2",
      "benign adult familial myoclonic epilepsy 2",
      "cortical myoclonic tremor with epilepsy, familial, 2",
      "cortical myoclonus and epilepsy, autosomal dominant",
      "epilepsy, familial ADULT myoclonic, 2"
    ],
    "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 ADRA2B 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"
    }
  ]
}