{
  "id": 17695,
  "label": "pleomorphic rhabdomyosarcoma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017386",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 6928,
      "label": "rhabdomyosarcoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18239
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3247",
          "EFO:0002918",
          "GARD:0011951",
          "HP:0002859",
          "ICD9:171.9",
          "ICDO:8900/3",
          "MEDGEN:20561",
          "MESH:D012208",
          "MedDRA:10039022",
          "NANDO:2200056",
          "NCIT:C3359",
          "ONCOTREE:RMS",
          "Orphanet:780",
          "SCTID:302847003",
          "UMLS:C0035412"
        ],
        "synonyms": [
          "rhabdomyosarcoma",
          "rhabdomyosarcoma (disease)",
          "rhabdomyosarcoma, malignant"
        ],
        "definition": "A rare aggressive malignant mesenchymal neoplasm arising from skeletal muscle. It usually occurs in children and young adults. Only a small percentage of tumors arise in the skeletal muscle of the extremities. The majority arise in other anatomical sites."
      },
      "child_count": 20,
      "reference_id": "MONDO:0005212"
    }
  ],
  "children": [
    {
      "id": 6054,
      "label": "childhood pleomorphic rhabdomyosarcoma",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        8005,
        17695
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:7463",
          "GARD:0023891",
          "MEDGEN:76002",
          "NCIT:C7959",
          "UMLS:C0279614"
        ],
        "synonyms": [
          "Pleomorphic rhabdomyosarcoma",
          "childhood anaplastic rhabdomyosarcoma",
          "paediatric pleomorphic rhabdomyosarcoma",
          "pediatric pleomorphic rhabdomyosarcoma",
          "pleomorphic childhood rhabdomyosarcoma",
          "pleomorphic rhabdomyosarcoma of childhood"
        ],
        "definition": "A rare aggressive rhabdomyosarcoma occurring in children. The neoplasm is characterized by the presence of bizarre round, spindle, and polygonal cells."
      },
      "child_count": 0,
      "reference_id": "MONDO:0004233"
    },
    {
      "id": 6315,
      "label": "adult pleomorphic rhabdomyosarcoma",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17695
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0004513"
    }
  ],
  "roots": [
    {
      "id": 6928,
      "label": "rhabdomyosarcoma"
    }
  ]
}