{
  "id": 22762,
  "label": "RELA fusion-positive ependymoma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0033980",
  "properties": {
    "xrefs": [
      "DOID:0080892",
      "GARD:0022210",
      "MEDGEN:927113",
      "NCIT:C129351",
      "Orphanet:530792",
      "UMLS:C4289581"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 5210,
      "label": "ependymal tumor",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        20287
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:1000027",
          "GARD:0016527",
          "MEDGEN:232459",
          "NCIT:C6770",
          "ONCOTREE:EPMT",
          "Orphanet:301",
          "UMLS:C1333407"
        ],
        "synonyms": [
          "ependymal neoplasm",
          "ependymal tumor",
          "ependymal tumors",
          "ependymal tumours",
          "ependymomal tumor",
          "ependymomal tumour"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A group of neoplasms which arise from the ependymal lining of the cerebral ventricles and from the remnants of the central canal of the spinal cord. Ependymal tumors occur predominantly in children and young adults with varied morphological features and biological behavior. There are 4 types: ependymoma, anaplastic ependymoma, myxopapillary ependymoma and subependymoma. (WHO)"
      },
      "child_count": 6,
      "reference_id": "MONDO:0003266"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5210,
      "label": "ependymal tumor"
    }
  ]
}