{
  "id": 18185,
  "label": "juvenile idiopathic inflammatory myopathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018010",
  "properties": {
    "xrefs": [
      "GARD:0021496",
      "MEDGEN:1842624",
      "Orphanet:329888",
      "UMLS:C5679857"
    ],
    "synonyms": [
      "JIIM"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "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": [
    {
      "id": 9377,
      "label": "juvenile dermatomyositis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16899,
        18185
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:14203",
          "EFO:0000557",
          "GARD:0006805",
          "ICD10CM:M33.0",
          "MEDGEN:120486",
          "MESH:C000598745",
          "MedDRA:10008521",
          "NANDO:2200418",
          "NCIT:C27576",
          "Orphanet:93672",
          "SCTID:1212005",
          "UMLS:C0263666",
          "icd11.foundation:1428089375"
        ],
        "synonyms": [
          "childhood dermatomyositis",
          "inflammation of myoseptum",
          "juvenile DM",
          "juvenile dermatomyositis",
          "myoseptum inflammation",
          "myoseptumitis",
          "JDM",
          "JPM",
          "childhood type dermatomyositis",
          "juvenile myositis",
          "myopathy, familial idiopathic inflammatory",
          "myositis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "Juvenile dermatomyositis (JDM) is the early-onset form of dermatomyositis (DM), a systemic, autoimmune inflammatory muscle disorder, characterized by proximal muscle weakness, evocative skin lesion, and systemic manifestations."
      },
      "child_count": 0,
      "reference_id": "MONDO:0008054"
    },
    {
      "id": 18186,
      "label": "juvenile overlap myositis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18185
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0018011"
    },
    {
      "id": 19492,
      "label": "juvenile polymyositis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18185,
        19007
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:1001988",
          "GARD:0012742",
          "MEDGEN:819736",
          "NANDO:2200419",
          "NCIT:C114358",
          "Orphanet:93568",
          "SCTID:738526005",
          "UMLS:C3826988",
          "icd11.foundation:633330307"
        ],
        "synonyms": [
          "JPM",
          "juvenile PM"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "An idiopathic inflammatory myopathy of childhood resulting in muscle weakness."
      },
      "child_count": 0,
      "reference_id": "MONDO:0019734"
    }
  ],
  "roots": [
    {
      "id": 19745,
      "label": "acquired idiopathic inflammatory myopathy"
    }
  ]
}