{
  "id": 2982,
  "label": "small intestinal neuroendocrine tumor G1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0000540",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 4994,
      "label": "small intestine neuroendocrine tumor, well differentiated, low or intermediate grade",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2885,
        18542
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0023316",
          "MEDGEN:474161",
          "NCIT:C96061",
          "UMLS:C3272528"
        ],
        "synonyms": [
          "small intestinal NET",
          "small intestinal neuroendocrine tumor",
          "small intestinal neuroendocrine tumour",
          "small intestinal well differentiated endocrine tumor",
          "small intestinal well differentiated endocrine tumour",
          "small intestine neuroendocrine tumor",
          "small intestine neuroendocrine tumour",
          "small intestinal well differentiated endocrine tumor/carcinoma",
          "carcinoid tumor of small intestine",
          "carcinoid tumour of small intestine"
        ],
        "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 small intestine."
      },
      "child_count": 12,
      "reference_id": "MONDO:0002995"
    },
    {
      "id": 20650,
      "label": "intestinal neuroendocrine tumor G1",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2885,
        4896,
        7051
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025331",
          "MEDGEN:138099",
          "MESH:C562842",
          "NCIT:C4637",
          "OMIM:114900",
          "SCTID:276816003",
          "UMLS:C0349535"
        ],
        "synonyms": [
          "carcinoid tumor of intestine",
          "carcinoid tumor of the intestine",
          "carcinoid tumour of intestine",
          "carcinoid tumour of the intestine",
          "grade 1 neuroendocrine neoplasm of intestine",
          "intestinal NET G1",
          "intestinal carcinoid tumor",
          "intestinal carcinoid tumour",
          "intestinal neuroendocrine tumor G1",
          "intestine NET G1",
          "intestine carcinoid tumor",
          "intestine carcinoid tumor (disease)",
          "intestine carcinoid tumour",
          "intestine carcinoid tumour (disease)",
          "intestine neuroendocrine neoplasm G1",
          "intestine 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 small or large 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": 6,
      "reference_id": "MONDO:0021533"
    }
  ],
  "children": [
    {
      "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": 4994,
      "label": "small intestine neuroendocrine tumor, well differentiated, low or intermediate grade"
    },
    {
      "id": 20650,
      "label": "intestinal neuroendocrine tumor G1"
    }
  ]
}