{
  "id": 16725,
  "label": "immune-mediated necrotizing myopathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016098",
  "properties": {
    "xrefs": [
      "GARD:0020351",
      "MEDGEN:899492",
      "Orphanet:206569",
      "SCTID:715863001",
      "UMLS:C3267047"
    ],
    "synonyms": [
      "IMNM",
      "NAM",
      "anti-HMG-CoA myopathy",
      "anti-SRP myopathy",
      "autoimmune necrotizing myositis",
      "immune myopathy with myocyte necrosis",
      "necrotizing autoimmune myopathy"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "Necrotizing autoimmune myopathy (NAM) is a rare form of idiopathic inflammatory myopathy characterized clinically by acute or subacute proximal muscle weakness, and histopathologically by myocyte necrosis and regeneration without significant inflammation."
  },
  "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"
    }
  ]
}