{
  "id": 23982,
  "label": "glioma susceptibility",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0100242",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 10,
  "parents": [
    {
      "id": 16218,
      "label": "hereditary neoplastic syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        20011,
        20301
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019921",
          "MEDGEN:14326",
          "MESH:D009386",
          "NCIT:C3266",
          "Orphanet:140162",
          "SCTID:699346009",
          "UMLS:C0027672"
        ],
        "synonyms": [
          "cancer syndrome, hereditary",
          "cancer syndromes, hereditary",
          "familial neoplastic syndrome",
          "familial tumor syndrome",
          "familial tumour syndrome",
          "hereditary cancer syndrome",
          "hereditary cancer syndromes",
          "hereditary neoplastic syndrome",
          "hereditary neoplastic syndromes",
          "hereditary tumor syndrome",
          "hereditary tumour syndrome",
          "inherited cancer syndrome",
          "inherited cancer-predisposing syndrome",
          "neoplastic syndrome, hereditary",
          "syndrome, hereditary cancer",
          "syndrome, hereditary neoplastic",
          "syndromes, hereditary cancer",
          "syndromes, hereditary neoplastic"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "The inherited predisposition toward getting a tumor."
      },
      "child_count": 351,
      "reference_id": "MONDO:0015356"
    }
  ],
  "children": [
    {
      "id": 12882,
      "label": "glioma susceptibility 4",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        23982
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027807",
          "MEDGEN:416425",
          "OMIM:607248",
          "UMLS:C2750944"
        ],
        "synonyms": [
          "GLM4",
          "glioma susceptibility 4"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0011800"
    },
    {
      "id": 14130,
      "label": "glioma susceptibility 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        23982
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013092"
    },
    {
      "id": 14131,
      "label": "glioma susceptibility 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        23982,
        24664
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027837",
          "MEDGEN:442777",
          "OMIM:613029",
          "UMLS:C2751641"
        ],
        "synonyms": [
          "BRCA2 malignant glioma",
          "glioblastoma 3",
          "glioma susceptibility 3",
          "glioma susceptibility type 3",
          "malignant glioma caused by mutation in BRCA2",
          "GLM3"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "Any malignant glioma in which the cause of the disease is a mutation in the BRCA2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013093"
    },
    {
      "id": 14132,
      "label": "glioma susceptibility 5",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        23982
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027838",
          "MEDGEN:414430",
          "OMIM:613030",
          "UMLS:C2751640"
        ],
        "synonyms": [
          "GLM5",
          "glioma susceptibility 5"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0013094"
    },
    {
      "id": 14133,
      "label": "glioma susceptibility 6",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        23982
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027839",
          "MEDGEN:414429",
          "OMIM:613031",
          "UMLS:C2751639"
        ],
        "synonyms": [
          "GLM6",
          "glioma susceptibility 6"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0013095"
    },
    {
      "id": 14134,
      "label": "glioma susceptibility 7",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        23982
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027840",
          "MEDGEN:416602",
          "OMIM:613032",
          "UMLS:C2751638"
        ],
        "synonyms": [
          "GLM7",
          "glioma susceptibility 7"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0013096"
    },
    {
      "id": 14135,
      "label": "glioma susceptibility 8",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        23982
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027841",
          "MEDGEN:416601",
          "OMIM:613033",
          "UMLS:C2751637"
        ],
        "synonyms": [
          "GLM8",
          "glioma susceptibility 8"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0013097"
    },
    {
      "id": 15065,
      "label": "melanoma, cutaneous malignant, susceptibility to, 9",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21418,
        23982
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027856",
          "MEDGEN:767488",
          "OMIM:615134",
          "UMLS:C3554574"
        ],
        "synonyms": [
          "melanoma, cutaneous malignant, 9",
          "melanoma, cutaneous malignant, susceptibility to, 9",
          "melanoma, cutaneous malignant, susceptibility to, type 9",
          "CMM9",
          "susceptibility to cutaneous malignant melanoma 9"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0014056"
    },
    {
      "id": 15370,
      "label": "tumor predisposition syndrome 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21418,
        23982
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018582",
          "MEDGEN:862913",
          "OMIM:615848",
          "OMIM:616568",
          "UMLS:C4014476"
        ],
        "synonyms": [
          "CMM10",
          "GLM9",
          "POT1 tumor predisposition",
          "POT1-TPD",
          "POT1-related tumor predisposition syndrome",
          "glioma susceptibility 9",
          "glioma susceptibility type 9",
          "malignant glioma caused by mutation in POT1",
          "melanoma, cutaneous malignant, susceptibility to, 10",
          "melanoma, cutaneous malignant, susceptibility to, type 10"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "Any hereditary cancer predisposition due to variation(s) in the POT1 gene, which confers a predisposition to development of various types of benign and malignant neoplasms."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014368"
    },
    {
      "id": 21451,
      "label": "glioma susceptibility 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        23982
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027917",
          "MEDGEN:413414",
          "OMIM:137800",
          "UMLS:C2750850"
        ],
        "synonyms": [
          "GLM1",
          "glioblastoma, somatic",
          "glioma susceptibility 1",
          "glioma susceptibility 1, autosomal dominant, somatic mutation",
          "glioma, susceptibility to, somatic",
          "astrocytoma",
          "ependymoma",
          "glioblastoma multiforme",
          "glioma of brain, familial",
          "oligodendroglioma",
          "subependymoma"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0024498"
    }
  ],
  "roots": [
    {
      "id": 16218,
      "label": "hereditary neoplastic syndrome"
    }
  ]
}