{
  "id": 18687,
  "label": "hereditary neuroendocrine tumor of small intestine",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018698",
  "properties": {
    "xrefs": [
      "GARD:0021899",
      "MEDGEN:1826066",
      "Orphanet:456333",
      "UMLS:C5679993"
    ],
    "synonyms": [
      "hereditary neuroendocrine tumor of small bowel",
      "hereditary neuroendocrine tumor of the small intestine",
      "hereditary neuroendocrine tumour of small bowel",
      "hereditary neuroendocrine tumour of the small intestine",
      "hereditary small intestine neuroendocrine neoplasm"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "An instance of neuroendocrine tumor of the small intestine that is caused by an inherited modification of the individual's genome."
  },
  "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": 18542,
      "label": "small intestine neuroendocrine neoplasm",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4896,
        6071
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:4434",
          "EFO:1001928",
          "GARD:0021765",
          "MEDGEN:233453",
          "NCIT:C5803",
          "Orphanet:423975",
          "UMLS:C1336005"
        ],
        "synonyms": [
          "NET of the small intestine",
          "neuroendocrine neoplasm of small intestine",
          "neuroendocrine neoplasm of the small intestine",
          "neuroendocrine tumor of small bowel",
          "neuroendocrine tumour of small bowel",
          "small intestinal neuroendocrine neoplasm",
          "small intestine NET",
          "small intestine neuroendocrine neoplasm",
          "small intestine neuroendocrine tumor",
          "small intestine neuroendocrine tumour",
          "neuroendocrine tumor of the small intestine",
          "neuroendocrine tumour of the small intestine",
          "small intestine neuroendocrine tumor, well differentiated, low or intermediate grade"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A neoplasm with neuroendocrine differentiation that arises from the small intestine. It includes well differentiated neuroendocrine tumors (low and intermediate grade) and poorly differentiated neuroendocrine carcinomas (high grade)."
      },
      "child_count": 6,
      "reference_id": "MONDO:0018510"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 18542,
      "label": "small intestine neuroendocrine neoplasm"
    }
  ]
}