{
  "id": 6315,
  "label": "adult pleomorphic rhabdomyosarcoma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0004513",
  "properties": {
    "xrefs": [
      "DOID:8251",
      "GARD:0024045",
      "ICDO:8901/3",
      "MEDGEN:233966",
      "NCIT:C27369",
      "UMLS:C1332211"
    ],
    "synonyms": [
      "adult pleomorphic rhabdomyosarcoma",
      "pleomorphic rhabdomyosarcoma of adults"
    ],
    "definition": "An aggressive rhabdomyosarcoma occurring in adults. The neoplasm is characterized by the presence of bizarre round, spindle, and polygonal cells. Clinical presentation includes a rapidly enlarging painful mass usually in the lower extremities."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17695,
      "label": "pleomorphic rhabdomyosarcoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6928
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3250",
          "GARD:0021165",
          "ICD9:171.9",
          "MEDGEN:137770",
          "NCIT:C4258",
          "ONCOTREE:PLRMS",
          "Orphanet:293199",
          "SCTID:404054005",
          "UMLS:C0334480"
        ],
        "synonyms": [
          "pleomorphic rhabdomyosarcoma"
        ],
        "definition": "An aggressive malignant mesenchymal neoplasm with skeletal muscle differentiation, occurring in adults and rarely in children. The tumor is characterized by the presence of bizarre round, spindle, and polygonal cells. Clinical presentation includes a rapidly enlarging painful mass usually of the lower extremities."
      },
      "child_count": 2,
      "reference_id": "MONDO:0017386"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17695,
      "label": "pleomorphic rhabdomyosarcoma"
    }
  ]
}