{
  "id": 19402,
  "label": "Zollinger-Ellison syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0019610",
  "properties": {
    "xrefs": [
      "DOID:0050782",
      "EFO:0007549",
      "GARD:0007918",
      "HP:0002044",
      "MEDGEN:53129",
      "MESH:D015043",
      "MedDRA:10017852",
      "NCIT:C3453",
      "NORD:1877",
      "Orphanet:913",
      "SCTID:302824004",
      "SCTID:53132006",
      "UMLS:C0043515",
      "icd11.foundation:375645550"
    ],
    "synonyms": [
      "Zollinger Ellison syndrome",
      "Zollinger-Ellison syndrome",
      "Zollinger-Ellison syndrome (disease)",
      "Z E syndrome",
      "Z-E syndrome",
      "ZES",
      "gastrinoma",
      "pancreatic ulcerogenic tumor syndrome",
      "pancreatic ulcerogenic tumour syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Zollinger-Ellison syndrome (ZES) is characterized by severe peptic disease (ulcers/esophageal disease) caused by hypergastrinemia secondary to a gastrinoma resulting in increased gastric acid secretion."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3954,
      "label": "gastrin secretion abnormality",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4104
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13656",
          "ICD9:251.5",
          "MEDGEN:507382",
          "SCTID:47344007",
          "UMLS:C0000774"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ]
      },
      "child_count": 1,
      "reference_id": "MONDO:0001770"
    },
    {
      "id": 20301,
      "label": "neoplastic syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        21214
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:362147",
          "NCIT:C54705",
          "UMLS:C1882062"
        ],
        "synonyms": [
          "cancer-related syndrome",
          "neoplastic syndrome",
          "tumor syndrome",
          "tumour syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A broad classification for disorders in which the development of neoplasms typically occur in association with a characteristic set of signs or symptoms. These disorders may be inherited or acquired."
      },
      "child_count": 22,
      "reference_id": "MONDO:0021058"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3954,
      "label": "gastrin secretion abnormality"
    },
    {
      "id": 20301,
      "label": "neoplastic syndrome"
    }
  ]
}