{
  "id": 7665,
  "label": "appendix neuroendocrine tumor G1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0006091",
  "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."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "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": 16040,
      "label": "neuroendocrine tumor of the appendix, well differentiated, low or intermediate grade",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16041,
        18543,
        21454
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019754",
          "MEDGEN:474400",
          "NCIT:C96422",
          "ONCOTREE:AWDNET",
          "Orphanet:100079",
          "SCTID:725167001",
          "UMLS:C3272767",
          "icd11.foundation:1590340268"
        ],
        "synonyms": [
          "NEN of appendix",
          "appendiceal NEN",
          "appendiceal neuroendocrine neoplasm",
          "appendiceal neuroendocrine tumor",
          "appendiceal neuroendocrine tumour",
          "appendix NET",
          "appendix neuroendocrine tumor",
          "appendix neuroendocrine tumour",
          "appendix well differentiated endocrine tumor",
          "appendix well differentiated endocrine tumor/carcinoma",
          "appendix well differentiated endocrine tumour",
          "neuroendocrine neoplasm of appendix",
          "well-differentiated neuroendocrine tumor of the appendix",
          "well-differentiated neuroendocrine tumour of the appendix"
        ],
        "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 appendix."
      },
      "child_count": 12,
      "reference_id": "MONDO:0015066"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 7692,
      "label": "cecum neuroendocrine tumor G1"
    },
    {
      "id": 16040,
      "label": "neuroendocrine tumor of the appendix, well differentiated, low or intermediate grade"
    }
  ]
}