{
  "id": 7716,
  "label": "colon neuroendocrine tumor G1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0006155",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 4,
  "parents": [
    {
      "id": 7723,
      "label": "colorectal neuroendocrine tumor G1",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7022,
        20650
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:1000195",
          "GARD:0024315",
          "MEDGEN:474244",
          "NCIT:C96160",
          "UMLS:C3272611"
        ],
        "synonyms": [
          "colorectal NET G1",
          "colorectal carcinoid tumor",
          "colorectal carcinoid tumour",
          "colorectal neuroendocrine tumor G1",
          "colorectum NET G1",
          "colorectum carcinoid tumor",
          "colorectum carcinoid tumour",
          "colorectum neuroendocrine neoplasm G1",
          "colorectum neuroendocrine tumor, well differentiated, low grade",
          "grade 1 neuroendocrine neoplasm of colorectum",
          "large intestinal neuroendocrine tumor G1",
          "large intestinal neuroendocrine tumour G1"
        ],
        "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 or rectum. 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:0006162"
    },
    {
      "id": 16041,
      "label": "neuroendocrine tumor of the colon, well differentiated, low or intermediate grade tumor",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2885,
        4895,
        21434
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025057",
          "MEDGEN:1617490",
          "NCIT:C135212",
          "UMLS:C4525742"
        ],
        "synonyms": [
          "carcinoid tumor of colon",
          "carcinoid tumour of colon",
          "colon neuroendocrine tumor",
          "colon neuroendocrine tumour",
          "neuroendocrine neoplasm of the colon",
          "NET of the colon",
          "colonic NET"
        ],
        "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 colon."
      },
      "child_count": 9,
      "reference_id": "MONDO:0015067"
    }
  ],
  "children": [
    {
      "id": 7667,
      "label": "ascending colon neuroendocrine tumor G1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        7716
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0024290",
          "MEDGEN:231386",
          "NCIT:C6427",
          "UMLS:C1332340"
        ],
        "synonyms": [
          "ascending colon NET G1",
          "ascending colon carcinoid tumor",
          "ascending colon carcinoid tumor (disease)",
          "ascending colon carcinoid tumour",
          "ascending colon carcinoid tumour (disease)",
          "ascending colon neuroendocrine neoplasm G1",
          "ascending colon neuroendocrine tumor G1",
          "ascending colon neuroendocrine tumor, well differentiated, low grade",
          "carcinoid tumor of ascending colon",
          "carcinoid tumor of the ascending colon",
          "carcinoid tumour of ascending colon",
          "carcinoid tumour of the ascending colon",
          "grade 1 neuroendocrine neoplasm of ascending 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 ascending 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": 0,
      "reference_id": "MONDO:0006093"
    },
    {
      "id": 7692,
      "label": "cecum neuroendocrine tumor G1",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7325,
        7716
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0024301",
          "MEDGEN:167703",
          "NCIT:C5501",
          "UMLS:C0854488"
        ],
        "synonyms": [
          "caecal carcinoid tumor",
          "caecal carcinoid tumour",
          "caecum NET G1",
          "caecum carcinoid tumor",
          "caecum carcinoid tumor (disease)",
          "caecum carcinoid tumour",
          "caecum carcinoid tumour (disease)",
          "caecum neuroendocrine neoplasm G1",
          "caecum neuroendocrine tumor, well differentiated, low grade",
          "carcinoid tumor of cecum",
          "carcinoid tumor of the cecum",
          "carcinoid tumour of cecum",
          "carcinoid tumour of the cecum",
          "cecal carcinoid tumor",
          "cecal carcinoid tumour",
          "cecum NET G1",
          "cecum carcinoid tumor",
          "cecum carcinoid tumour",
          "cecum neuroendocrine tumor G1",
          "grade 1 neuroendocrine neoplasm of caecum"
        ],
        "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 cecum. 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": 2,
      "reference_id": "MONDO:0006126"
    },
    {
      "id": 7800,
      "label": "ileal neuroendocrine tumor G1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2982,
        7716,
        16039
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0006250"
    },
    {
      "id": 7804,
      "label": "jejunal neuroendocrine tumor G1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2982,
        7716,
        16038
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:1000308",
          "GARD:0024349",
          "MEDGEN:235235",
          "NCIT:C6429",
          "UMLS:C1334296"
        ],
        "synonyms": [
          "carcinoid tumor of jejunum",
          "carcinoid tumor of the jejunum",
          "carcinoid tumour of jejunum",
          "carcinoid tumour of the jejunum",
          "grade 1 neuroendocrine neoplasm of jejunum",
          "jejunal NET G1",
          "jejunal carcinoid tumor",
          "jejunal carcinoid tumour",
          "jejunum NET G1",
          "jejunum carcinoid tumor",
          "jejunum carcinoid tumor (disease)",
          "jejunum carcinoid tumour",
          "jejunum carcinoid tumour (disease)",
          "jejunum neuroendocrine neoplasm G1",
          "jejunum 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 jejunum. 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": 0,
      "reference_id": "MONDO:0006257"
    }
  ],
  "roots": [
    {
      "id": 7723,
      "label": "colorectal neuroendocrine tumor G1"
    },
    {
      "id": 16041,
      "label": "neuroendocrine tumor of the colon, well differentiated, low or intermediate grade tumor"
    }
  ]
}