{
  "id": 15370,
  "label": "tumor predisposition syndrome 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014368",
  "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."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 21418,
      "label": "susceptibility to familial cutaneous melanoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16218
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027916",
          "MEDGEN:1388845",
          "OMIMPS:155600",
          "UMLS:C4511622"
        ],
        "synonyms": [
          "hereditary cutaneous melanoma (disease)",
          "melanoma, cutaneous malignant"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A susceptibility or predisposition to cutaneous melanoma (disease) that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 10,
      "reference_id": "MONDO:0024462"
    },
    {
      "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": 21418,
      "label": "susceptibility to familial cutaneous melanoma"
    },
    {
      "id": 23982,
      "label": "glioma susceptibility"
    }
  ]
}