{
  "id": 7692,
  "label": "cecum neuroendocrine tumor G1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0006126",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 7325,
      "label": "cecal neoplasm",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4178,
        7078
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1517",
          "EFO:0009255",
          "MEDGEN:2922",
          "MESH:D002430",
          "NCIT:C4433",
          "SCTID:126839008",
          "UMLS:C0007528"
        ],
        "synonyms": [
          "caecum neoplasm",
          "caecum neoplasm (disease)",
          "caecum tumor",
          "caecum tumour",
          "cecum neoplasm",
          "cecum tumor",
          "cecum tumour",
          "neoplasm of caecum",
          "neoplasm of cecum",
          "neoplasm of the cecum",
          "tumor of caecum",
          "tumor of cecum",
          "tumor of the cecum",
          "tumour of caecum",
          "tumour of cecum",
          "tumour of the cecum",
          "cecal benign neoplasm"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "A benign or malignant neoplasm that affects the cecum. Representative examples of benign neoplasms include lipoma and leiomyoma. Representative examples of malignant neoplasms include carcinoma, lymphoma, and sarcoma. Cecal adenomas always exhibit epithelial dysplasia and are considered premalignant neoplasms."
      },
      "child_count": 10,
      "reference_id": "MONDO:0005694"
    },
    {
      "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"
    }
  ],
  "children": [
    {
      "id": 7665,
      "label": "appendix neuroendocrine tumor G1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        7692,
        16040
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050911",
          "EFO:1000092",
          "GARD:0024288",
          "ICD9:209.11",
          "ICDO:8240/1",
          "MEDGEN:90758",
          "NCIT:C4138",
          "SCTID:253002004",
          "UMLS:C0334298"
        ],
        "synonyms": [
          "appendiceal carcinoid tumor",
          "appendiceal carcinoid tumour",
          "appendix NET G1",
          "appendix NET G1 (carcinoid)",
          "appendix carcinoid tumor",
          "appendix carcinoid tumour",
          "appendix neuroendocrine tumor G1 (carcinoid)",
          "appendix neuroendocrine tumour G1 (carcinoid)",
          "carcinoid tumor of appendix",
          "carcinoid tumor of the appendix",
          "carcinoid tumour of appendix",
          "carcinoid tumour of the appendix",
          "grade 1 neuroendocrine neoplasm of vermiform appendix",
          "vermiform appendix NET G1",
          "vermiform appendix carcinoid tumor",
          "vermiform appendix carcinoid tumor (disease)",
          "vermiform appendix carcinoid tumour",
          "vermiform appendix carcinoid tumour (disease)",
          "vermiform appendix neuroendocrine neoplasm G1",
          "vermiform appendix neuroendocrine tumor, well differentiated, low grade",
          "appendix carcinoid endocrine tumor",
          "appendix carcinoid endocrine tumour"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A well differentiated, low grade tumor with neuroendocrine differentiation that arises from the appendix. 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:0006091"
    }
  ],
  "roots": [
    {
      "id": 7325,
      "label": "cecal neoplasm"
    },
    {
      "id": 7716,
      "label": "colon neuroendocrine tumor G1"
    }
  ]
}