{
  "id": 14707,
  "label": "pancreatic cancer, susceptibility to, 4",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013685",
  "properties": {
    "xrefs": [
      "GARD:0027851",
      "MEDGEN:482072",
      "OMIM:614320",
      "UMLS:C3280442"
    ],
    "synonyms": [
      "BRCA1 familial pancreatic carcinoma",
      "familial pancreatic carcinoma caused by mutation in BRCA1",
      "pancreatic cancer, susceptibility to, 4",
      "pancreatic cancer, susceptibility to, type 4",
      "PNCA4",
      "susceptibility to pancreatic cancer 4"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Any familial pancreatic carcinoma in which the cause of the disease is a mutation in the BRCA1 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 24663,
      "label": "BRCA1-related cancer predisposition",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16218
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026408"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "Hereditary cancer predisposition due to variation(s) in the BRCA1 gene. Germline pathogenic or likely pathogenic variants in the BRCA1 gene confer an autosomal dominant predisposition to hereditary breast and ovarian cancer. Tumor formation at other sites, including pancreatic cancer have been described."
      },
      "child_count": 2,
      "reference_id": "MONDO:0700268"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 24663,
      "label": "BRCA1-related cancer predisposition"
    }
  ]
}