{
  "id": 25254,
  "label": "infant-type hemispheric glioma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0858940",
  "properties": {
    "xrefs": [
      "DOID:0081278",
      "GARD:0026636",
      "MEDGEN:1806401",
      "NCIT:C185471",
      "Orphanet:695136",
      "UMLS:C5669919"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A malignant astrocytoma that is characterized by receptor tyrosine kinase fusions in the NTRK family, ROS1, ALK, or MET genes, that arises in the cerebral hemisphere and occurs in early childhood."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 20692,
      "label": "astrocytic tumor",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        20287
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3069",
          "GARD:0012928",
          "MedDRA:10003571",
          "NCIT:C6958",
          "Orphanet:94"
        ],
        "synonyms": [
          "astrocytic neoplasm",
          "astrocytic tumor",
          "astrocytoma, no ICD-O subtype",
          "astroglioma",
          "astrocytoma",
          "astrocytoma of cerebrum"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A glial tumor of the brain or spinal cord showing astrocytic differentiation. It includes the following clinicopathological entities: pilocytic astrocytoma, diffuse astrocytoma, anaplastic astrocytoma, pleomorphic xanthoastrocytoma, subependymal giant cell astrocytoma, and glioblastoma."
      },
      "child_count": 8,
      "reference_id": "MONDO:0021636"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 20692,
      "label": "astrocytic tumor"
    }
  ]
}