{
  "id": 25255,
  "label": "myxoid glioneuronal tumor",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0858944",
  "properties": {
    "xrefs": [
      "DOID:0081285",
      "MEDGEN:1791986",
      "NCIT:C179229",
      "UMLS:C5555545"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A central nervous system benign neoplasm that is characterized by a dinucleotide mutation at codon 385 of the PDGFR gene. It usually occurs in the septum pellucidum but has also been described in the corpus callosum and periventricular white matter of the lateral ventricle. It is composed of oligodendrocyte-like cells in a prominent myxoid stroma."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3033,
      "label": "central nervous system organ benign neoplasm",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3049,
        7694
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060090",
          "MEDGEN:488882",
          "NCIT:C188049",
          "UMLS:C0347509"
        ],
        "synonyms": [
          "central nervous system benign neoplasm"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A benign neoplasm that involves the central nervous system."
      },
      "child_count": 26,
      "reference_id": "MONDO:0000628"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3033,
      "label": "central nervous system organ benign neoplasm"
    }
  ]
}