{
  "id": 14130,
  "label": "glioma susceptibility 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013092",
  "properties": {
    "xrefs": [
      "GARD:0027836",
      "MEDGEN:414431",
      "OMIM:613028",
      "UMLS:C2751642"
    ],
    "synonyms": [
      "PTEN malignant glioma",
      "glioma susceptibility 2",
      "glioma susceptibility type 2",
      "malignant glioma caused by mutation in PTEN",
      "GLM2"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Any malignant glioma in which the cause of the disease is a mutation in the PTEN gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 23982,
      "label": "glioma susceptibility",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16218
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027996",
          "OMIMPS:137800"
        ],
        "synonyms": [
          "glioma, susceptibility",
          "glioma, susceptibility to"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "An inherited susceptibility or predisposition to developing glioma."
      },
      "child_count": 10,
      "reference_id": "MONDO:0100242"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 23982,
      "label": "glioma susceptibility"
    }
  ]
}