{
  "id": 9365,
  "label": "myoclonic epilepsy, Hartung type",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008041",
  "properties": {
    "xrefs": [
      "GARD:0024596",
      "MEDGEN:371857",
      "MESH:C563550",
      "OMIM:159600",
      "UMLS:C1834581"
    ],
    "synonyms": [
      "myoclonic epilepsy, Hartung type"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 24301,
      "label": "myoclonic epilepsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16436
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027276",
          "MEDGEN:4988",
          "UMLS:C0014550"
        ],
        "synonyms": [
          "myoclonic epilepsy syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A group of epilepsy syndromes in which myoclonic seizures are a prominent feature."
      },
      "child_count": 7,
      "reference_id": "MONDO:0100577"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 24301,
      "label": "myoclonic epilepsy"
    }
  ]
}