{
  "id": 14272,
  "label": "pancreatic cancer, susceptibility to, 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013236",
  "properties": {
    "xrefs": [
      "GARD:0027846",
      "MEDGEN:461897",
      "OMIM:613348",
      "UMLS:C3150547"
    ],
    "synonyms": [
      "PALB2 familial pancreatic carcinoma",
      "familial pancreatic carcinoma caused by mutation in PALB2",
      "pancreatic cancer, susceptibility to, 3",
      "pancreatic cancer, susceptibility to, type 3",
      "Pnca3",
      "susceptibility to pancreatic cancer 3"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Any familial pancreatic carcinoma in which the cause of the disease is a mutation in the PALB2 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 24667,
      "label": "PALB2-related cancer predisposition",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16218
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026412"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "Hereditary cancer predisposition due to variation(s) in the PALB2 gene. Pathogenic germline variation in PALB2 confers an autosomal dominant predisposition to tumor formation at multiple primary sites, including breast cancer, ovarian cancer, and pancreatic cancer."
      },
      "child_count": 1,
      "reference_id": "MONDO:0700272"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 24667,
      "label": "PALB2-related cancer predisposition"
    }
  ]
}