{
  "id": 7800,
  "label": "ileal neuroendocrine tumor G1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0006250",
  "properties": {
    "xrefs": [
      "EFO:1000300",
      "GARD:0024347",
      "ICD9:209.03",
      "MEDGEN:155426",
      "NCIT:C4935",
      "SCTID:425318003",
      "UMLS:C0745216"
    ],
    "synonyms": [
      "carcinoid tumor of ileum",
      "carcinoid tumor of the ileum",
      "carcinoid tumour of ileum",
      "carcinoid tumour of the ileum",
      "grade 1 neuroendocrine neoplasm of ileum",
      "ileal NET G1",
      "ileal carcinoid tumor",
      "ileal carcinoid tumour",
      "ileal neuroendocrine tumor G1",
      "ileum NET G1",
      "ileum carcinoid tumor",
      "ileum carcinoid tumor (disease)",
      "ileum carcinoid tumour",
      "ileum carcinoid tumour (disease)",
      "ileum neuroendocrine neoplasm G1",
      "ileum neuroendocrine tumor, well differentiated, low grade"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "A well differentiated, low grade neuroendocrine tumor (carcinoid tumor) that arises from the ileum. The mitotic count is less than 2 per 10 HPF and/or the Ki67 index is equal to or less than 2 percent."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2982,
      "label": "small intestinal neuroendocrine tumor G1",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4994,
        20650
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050925",
          "GARD:0022796",
          "MEDGEN:91150",
          "NCIT:C4638",
          "SCTID:276818002",
          "UMLS:C0349536"
        ],
        "synonyms": [
          "carcinoid tumor of small bowel",
          "carcinoid tumor of small intestine",
          "carcinoid tumor of the small bowel",
          "carcinoid tumor of the small intestine",
          "carcinoid tumour of small bowel",
          "carcinoid tumour of small intestine",
          "carcinoid tumour of the small bowel",
          "carcinoid tumour of the small intestine",
          "grade 1 neuroendocrine neoplasm of small intestine",
          "small bowel carcinoid tumor",
          "small bowel carcinoid tumour",
          "small intestinal NET G1",
          "small intestinal carcinoid tumor",
          "small intestinal carcinoid tumour",
          "small intestinal neuroendocrine tumor G1",
          "small intestine NET G1",
          "small intestine carcinoid tumor",
          "small intestine carcinoid tumor (disease)",
          "small intestine carcinoid tumour",
          "small intestine carcinoid tumour (disease)",
          "small intestine neuroendocrine neoplasm G1",
          "small intestine neuroendocrine tumor, well differentiated, low grade",
          "small intestine carcinoid neuroendocrine tumor",
          "small intestine carcinoid neuroendocrine tumour"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A well differentiated, low grade neuroendocrine tumor (carcinoid tumor) that arises from the small intestine. The mitotic count is less than 2 per 10 HPF and/or the Ki67 index is equal to or less than 2 percent."
      },
      "child_count": 4,
      "reference_id": "MONDO:0000540"
    },
    {
      "id": 7716,
      "label": "colon neuroendocrine tumor G1",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7723,
        16041
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:1000188",
          "GARD:0024313",
          "MEDGEN:234158",
          "NCIT:C5497",
          "UMLS:C1333084"
        ],
        "synonyms": [
          "carcinoid tumor of colon",
          "carcinoid tumor of the colon",
          "carcinoid tumour of colon",
          "carcinoid tumour of the colon",
          "colon NET G1",
          "colon carcinoid tumor",
          "colon carcinoid tumor (disease)",
          "colon carcinoid tumour",
          "colon carcinoid tumour (disease)",
          "colon neuroendocrine neoplasm G1",
          "colon neuroendocrine tumor G1",
          "colon neuroendocrine tumor, well differentiated, low grade",
          "colonic carcinoid tumor",
          "colonic carcinoid tumour",
          "grade 1 neuroendocrine neoplasm of colon"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A well differentiated, low grade neuroendocrine tumor (carcinoid tumor) that arises from the colon. The mitotic count is less than 2 per 10 HPF and/or the Ki67 index is equal to or less than 2 percent."
      },
      "child_count": 8,
      "reference_id": "MONDO:0006155"
    },
    {
      "id": 16039,
      "label": "ileal neuroendocrine tumor, well differentiated, low or intermediate grade",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4994,
        8249
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019753",
          "MEDGEN:1611292",
          "NCIT:C135092",
          "Orphanet:100078",
          "UMLS:C4525628"
        ],
        "synonyms": [
          "ileal neuroendocrine neoplasm",
          "ileal neuroendocrine tumor",
          "ileal neuroendocrine tumour"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A well differentiated, low or intermediate grade tumor with neuroendocrine differentiation that arises from the ileum."
      },
      "child_count": 2,
      "reference_id": "MONDO:0015065"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2982,
      "label": "small intestinal neuroendocrine tumor G1"
    },
    {
      "id": 7716,
      "label": "colon neuroendocrine tumor G1"
    },
    {
      "id": 16039,
      "label": "ileal neuroendocrine tumor, well differentiated, low or intermediate grade"
    }
  ]
}