{
  "id": 16160,
  "label": "familial pancreatic carcinoma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015278",
  "properties": {
    "xrefs": [
      "GARD:0004206",
      "MEDGEN:419700",
      "MESH:C535837",
      "NCIT:C43298",
      "OMIM:260350",
      "Orphanet:1333",
      "SCTID:715414009",
      "UMLS:C2931038",
      "icd11.foundation:1385362916"
    ],
    "synonyms": [
      "familial pancreatic cancer",
      "familial pancreatic carcinoma",
      "hereditary exocrine pancreatic carcinoma",
      "hereditary pancreatic cancer",
      "hereditary pancreatic carcinoma",
      "pancreatic cancer, somatic",
      "pancreatic carcinoma, somatic",
      "pancreatic acinar carcinoma"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Familial pancreatic carcinoma is defined by the presence of pancreatic cancer (PC) in two or more first-degree relatives."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    },
    {
      "id": 6912,
      "label": "exocrine pancreatic carcinoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4251,
        7738
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:4905",
          "EFO:0002618",
          "GARD:0027717",
          "MEDGEN:65917",
          "NCIT:C3850",
          "SCTID:372142002",
          "UMLS:C0235974"
        ],
        "synonyms": [
          "cancer of pancreas",
          "cancer of the pancreas",
          "exocrine cancer",
          "pancreas cancer",
          "pancreatic cancer",
          "carcinoma of exocrine pancreas",
          "carcinoma of the pancreas",
          "exocrine pancreas carcinoma",
          "pancreas carcinoma",
          "pancreatic cancer (not islets)",
          "pancreatic carcinoma, familial"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A carcinoma that arises from epithelial cells of the exocrine pancreas"
      },
      "child_count": 16,
      "reference_id": "MONDO:0005192"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 6912,
      "label": "exocrine pancreatic carcinoma"
    }
  ]
}