{
  "id": 23807,
  "label": "intraosseous spindle cell rhabdomyosarcoma with TFCP2/NCOA2 rearrangements",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0100055",
  "properties": {
    "xrefs": [
      "GARD:0026027",
      "MEDGEN:1791329",
      "NCIT:C178236",
      "UMLS:C5554888"
    ],
    "synonyms": [
      "intraosseous rhabdomyosarcoma with FUS-TFCP2 fusion",
      "intraosseous rhabdomyosarcoma defined by FUS-TFCP2 fusion"
    ],
    "definition": "Intraosseous spindle cell rhabdomyosarcoma characterized by the fusion of the EWSR1 or FUS gene with the TFCP2 gene, or the MEIS1 gene with the NCOA2 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4642,
      "label": "spindle cell rhabdomyosarcoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4933,
        6928
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3260",
          "GARD:0023175",
          "ICD9:171.9",
          "ICDO:8912/3",
          "MEDGEN:224766",
          "NCIT:C6519",
          "ONCOTREE:SCRMS",
          "SCTID:404055006",
          "UMLS:C1266134"
        ],
        "synonyms": [
          "spindle cell rhabdomyosarcoma (morphologic abnormality)",
          "SCRMS"
        ],
        "definition": "An uncommon variant of rhabdomyosarcoma characterized by the presence of whorls of spindle cells forming a storiform pattern. In children it usually arises in the paratesticular region. In adults it usually arises from the deep soft tissues in the head and neck."
      },
      "child_count": 6,
      "reference_id": "MONDO:0002581"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4642,
      "label": "spindle cell rhabdomyosarcoma"
    }
  ]
}