{
  "id": 4745,
  "label": "appendix mucinous cystadenocarcinoma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0002703",
  "properties": {
    "xrefs": [
      "DOID:3607",
      "GARD:0023218",
      "MEDGEN:204256",
      "NCIT:C5511",
      "UMLS:C1096639"
    ],
    "synonyms": [
      "appendiceal colloid cystadenocarcinoma",
      "appendiceal colloidal cystadenocarcinoma",
      "appendiceal mucinous cystadenocarcinoma",
      "appendix colloid cystadenocarcinoma",
      "appendix colloidal cystadenocarcinoma",
      "appendix mucinous cystadenocarcinoma",
      "colloid cystadenocarcinoma of appendix",
      "colloid cystadenocarcinoma of the appendix",
      "colloidal cystadenocarcinoma of appendix",
      "colloidal cystadenocarcinoma of the appendix",
      "mucinous cystadenocarcinoma of appendix",
      "mucinous cystadenocarcinoma of the appendix",
      "vermiform appendix mucinous cystadenocarcinoma"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ],
    "definition": "An adenocarcinoma arising from the appendix, characterized by the presence of mucinous stroma formation and cystic structures."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 7469,
      "label": "mucinous cystadenocarcinoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6700,
        7240
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3603",
          "EFO:0007378",
          "ICDO:8470/3",
          "MEDGEN:60211",
          "MESH:D018282",
          "NCIT:C3776",
          "UMLS:C0206699"
        ],
        "synonyms": [
          "Pseudomucinous adenocarcinoma",
          "Pseudomucinous cystadenocarcinoma",
          "mucinous cystadenocarcinoma",
          "mucinous cystadenocarcinoma (morphologic abnormality)",
          "mucinous cystadenocarcinoma NOS (morphologic abnormality)"
        ],
        "definition": "An invasive adenocarcinoma characterized by cystic changes and the presence of malignant glandular cells which contain intracytoplasmic mucin. It may arise from the ovary, pancreas, appendix, and lung."
      },
      "child_count": 8,
      "reference_id": "MONDO:0005858"
    },
    {
      "id": 18424,
      "label": "mucinous adenocarcinoma of the appendix",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6745,
        7662
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021629",
          "MEDGEN:317382",
          "NCIT:C43558",
          "ONCOTREE:MAAP",
          "Orphanet:391723",
          "UMLS:C1706832",
          "icd11.foundation:425095558"
        ],
        "synonyms": [
          "appendiceal mucinous adenocarcinoma",
          "appendix mucinous adenocarcinoma",
          "vermiform appendix mucinous adenocarcinoma"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "Mucinous adenocarcinoma of the appendix is a very rare, slow growing, well-differentiated epithelial neoplasm of the appendix characterized by abundant mucin production. Clinically, it presents as acute appendicitis (with abdominal pain, fever, leukocytosis) or as pseudomyxoma peritonei (wide-spread presence of mucin within the peritoneal cavity), however some patients may be completely asymptomatic at the time of diagnosis. In many cases, a second gastrointestinal malignancy is present."
      },
      "child_count": 4,
      "reference_id": "MONDO:0018330"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 7469,
      "label": "mucinous cystadenocarcinoma"
    },
    {
      "id": 18424,
      "label": "mucinous adenocarcinoma of the appendix"
    }
  ]
}