{
  "id": 18186,
  "label": "juvenile overlap myositis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018011",
  "properties": {
    "xrefs": [
      "GARD:0021497",
      "MEDGEN:1634026",
      "Orphanet:329894",
      "SCTID:766252004",
      "UMLS:C4707728"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "Juvenile overlap myositis is a rare juvenile idiopathic inflammatory myopathy characterized by the association of inflammatory myositis (manifesting with acral erythema, progressive weakness of the limbs, pain, general fatigue, moodiness or crankiness) with clinical and/or laboratory features of other autoimmune diseases (e.g. systemic lupus erythematosus, localized scleroderma, diabetes). Cardiac involvement has been reported in some patients."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18185,
      "label": "juvenile idiopathic inflammatory myopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19745
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021496",
          "MEDGEN:1842624",
          "Orphanet:329888",
          "UMLS:C5679857"
        ],
        "synonyms": [
          "JIIM"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 3,
      "reference_id": "MONDO:0018010"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18185,
      "label": "juvenile idiopathic inflammatory myopathy"
    }
  ]
}