{
  "id": 15616,
  "label": "myoclonic dystonia 26",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014620",
  "properties": {
    "xrefs": [
      "DOID:0090036",
      "GARD:0016103",
      "MEDGEN:904244",
      "OMIM:616398",
      "UMLS:C4225341"
    ],
    "synonyms": [
      "KCTD17 myoclonus-dystonia syndrome",
      "myoclonic dystonia type 26",
      "myoclonus-dystonia syndrome caused by mutation in KCTD17",
      "DYT26",
      "dystonia 26, myoclonic"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any myoclonus-dystonia syndrome in which the cause of the disease is a mutation in the KCTD17 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3179,
      "label": "myoclonus-dystonia syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19719
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0090033",
          "GARD:0007139",
          "ICD9:333.99",
          "MESH:C536096",
          "NANDO:1200522",
          "Orphanet:36899",
          "SCTID:439732004"
        ],
        "synonyms": [
          "DYT-SGCE",
          "dystonia with myoclonus",
          "hereditary essential myoclonus",
          "myoclonic dystonia",
          "myoclonus-dystonia syndrome",
          "DYT11",
          "Hereditary essential myoclonus",
          "alcohol-responsive dystonia",
          "dystonia 11",
          "dystonia 11, myoclonic",
          "dystonia, alcohol responsive",
          "dystonia, alcohol-responsive",
          "dystonia-11, myoclonic",
          "myoclonus, hereditary essential",
          "myoclonus-Dystonia",
          "myoclonus-dystonia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Myoclonus-dystonia syndrome (MDS) is a rare movement disorder characterized by mild to moderate dystonia along with 'lightning-like' myoclonic jerks."
      },
      "child_count": 3,
      "reference_id": "MONDO:0000903"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3179,
      "label": "myoclonus-dystonia syndrome"
    }
  ]
}