{
  "id": 16726,
  "label": "overlap myositis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016099",
  "properties": {
    "xrefs": [
      "GARD:0020352",
      "MEDGEN:1814440",
      "Orphanet:206572",
      "UMLS:C5679784"
    ],
    "synonyms": [
      "adult-onset overlap myositis",
      "non-specific myositis"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "Overlap myositis (OM) is a form of idiopathic inflammatory myopathy (IIM) characterized by myositis with at least one clinical and/or autoantibody overlap feature."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19745,
      "label": "acquired idiopathic inflammatory myopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16731,
        24391,
        24405
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0009128",
          "ICD9:359.79",
          "Orphanet:98482",
          "icd11.foundation:464294586"
        ],
        "synonyms": [
          "IIm",
          "IMM",
          "idiopathic inflammatory myopathies",
          "idiopathic inflammatory myositis",
          "idiopathic inflammatory myopathy, familial"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "An umbrella term for diseases which have chronic muscle inflammation and weakness of unknown etiology. The types of idiopathic inflammatory myopathy are further defined by either clinicopathologic criteria or by the presence of certain autoantibodies."
      },
      "child_count": 27,
      "reference_id": "MONDO:0020122"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19745,
      "label": "acquired idiopathic inflammatory myopathy"
    }
  ]
}