{
  "id": 25552,
  "label": "diffuse low-grade glioma, MAPK pathway–altered",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0859614",
  "properties": {
    "xrefs": [
      "DOID:0081260",
      "GARD:0026757",
      "NCIT:C185218"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A low grade glioma that is characterized by a gene alteration that results in a MAPK pathway abnormality, with morphological features of astrocytoma or oligodendroglioma."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 20693,
      "label": "low grade glioma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        20287
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060101",
          "DOID:0080829",
          "GARD:0025343",
          "MEDGEN:744283",
          "NCIT:C132067",
          "UMLS:C1997217"
        ],
        "synonyms": [
          "benign glioma",
          "glioma, benign",
          "low grade glioma",
          "low-grade glioma"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A grade I or grade II glioma arising from the central nervous system. This category includes pilocytic astrocytoma, diffuse astrocytoma, subependymal giant cell astrocytoma, ependymoma, oligodendroglioma, oligoastrocytoma, and angiocentric glioma."
      },
      "child_count": 6,
      "reference_id": "MONDO:0021637"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 20693,
      "label": "low grade glioma"
    }
  ]
}