{
  "id": 19007,
  "label": "polymyositis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0019127",
  "properties": {
    "xrefs": [
      "DOID:0080745",
      "EFO:0003063",
      "GARD:0007425",
      "ICD10CM:M33.2",
      "ICD9:710.4",
      "MEDGEN:39086",
      "MESH:D017285",
      "MedDRA:10036102",
      "NANDO:1200276",
      "NCIT:C26925",
      "Orphanet:732",
      "SCTID:31384009",
      "UMLS:C0085655",
      "Wikipedia:Polymyositis",
      "icd11.foundation:1157134196"
    ],
    "synonyms": [
      "PM",
      "polymyositis"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "A rare idiopathic inflammatory myopathy characterized by symmetric proximal muscle weakness and elevated muscle enzymes."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "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": 16899,
      "label": "dermatomyositis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4496,
        7203,
        19007
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:10223",
          "EFO:0000398",
          "GARD:0006263",
          "ICD10CM:M33",
          "ICD9:710.3",
          "MEDGEN:8331",
          "MESH:D003882",
          "MedDRA:10012503",
          "NANDO:1200274",
          "NCIT:C26744",
          "NORD:1048",
          "Orphanet:221",
          "SCTID:396230008",
          "UMLS:C0011633",
          "icd11.foundation:739030149"
        ],
        "synonyms": [
          "DM",
          "dermatomyositis",
          "dermatopolymyositis",
          "adult dermatomyositis",
          "Amyopathic dermatomyositis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "Dermatomyositis (DM) is a type of idiopathic inflammatory myopathy characterized by evocative skin lesions and symmetrical proximal muscle weakness."
      },
      "child_count": 33,
      "reference_id": "MONDO:0016367"
    },
    {
      "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"
    }
  ]
}