{
  "id": 6484,
  "label": "liver solitary fibrous tumor",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0004705",
  "properties": {
    "xrefs": [
      "DOID:907",
      "GARD:0024092",
      "MEDGEN:232273",
      "NCIT:C5752",
      "UMLS:C1333965"
    ],
    "synonyms": [
      "fibroma of liver",
      "fibroma of the liver",
      "hepatic fibroma",
      "liver fibroma",
      "liver localised fibrous mesothelioma",
      "liver localised fibrous tumour",
      "liver localized fibrous mesothelioma",
      "liver localized fibrous tumor",
      "liver solitary fibrous tumor"
    ],
    "categories": [
      {
        "ref": "MONDO:0003900",
        "name": "connective tissue disorder"
      },
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "A solitary fibrous tumor that arises from the liver. It affects females more frequently than males. Signs and symptoms include the presence of an abdominal mass and abdominal discomfort."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 6889,
      "label": "fibroma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7762
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050871",
          "EFO:0002424",
          "ICD9:215.9",
          "ICDO:8810/0",
          "MEDGEN:42016",
          "MESH:D005350",
          "NCIT:C3041",
          "SCTID:424568000",
          "UMLS:C0016045"
        ],
        "synonyms": [
          "fibroma",
          "fibroma, benign"
        ],
        "categories": [
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "A non-metastasizing neoplasm arising from the fibrous tissue. It is characterized by the presence of spindle-shaped fibroblasts."
      },
      "child_count": 11,
      "reference_id": "MONDO:0005167"
    },
    {
      "id": 16812,
      "label": "solitary fibrous tumor",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7762
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0015014",
          "ICD9:238.1",
          "ICDO:8815/0",
          "ICDO:8815/1",
          "ICDO:9051/0",
          "MEDGEN:224764",
          "MESH:D054364",
          "MedDRA:10018825",
          "NCIT:C7634",
          "ONCOTREE:SFT",
          "Orphanet:2126",
          "UMLS:C1266119"
        ],
        "synonyms": [
          "SFT",
          "localised fibrous mesothelioma",
          "localised fibrous tumour",
          "localized fibrous mesothelioma",
          "localized fibrous tumor",
          "solitary fibrous tumor",
          "submesothelial fibroma",
          "hemangiopericytoma",
          "solitary fibrous tumor/hemangiopericytoma"
        ],
        "categories": [
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "Solitary fibrous tumor (SFT) represents a diverse group of ubiquitous rare spindle cell neoplasms that may be benign or malignant and that most frequently arises from the pleura and peritoneum and rarely from other sites such as head and neck, liver and skeletal muscle. SFT may be clinically asymptomatic or may present with enlarging mass, compressive effects depending on the site involved and rarely with paraneoplastic manifestations (osteoarthropathy or hypoglycemia)."
      },
      "child_count": 5,
      "reference_id": "MONDO:0016238"
    },
    {
      "id": 21432,
      "label": "liver and intrahepatic bile duct neoplasm",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4223,
        4585,
        6878
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:916",
          "MEDGEN:232599",
          "NCIT:C7103",
          "NCIT:C7106",
          "ONCOTREE:LIVER",
          "SCTID:126851005",
          "UMLS:C1333976"
        ],
        "synonyms": [
          "epithelial hepatic and intrahepatic bile duct neoplasm",
          "hepatic and intrahepatic bile duct neoplasm",
          "liver and intrahepatic bile duct epithelial neoplasm",
          "liver and intrahepatic bile duct neoplasm",
          "liver neoplasm",
          "liver neoplasm (disease)",
          "liver tumor",
          "liver tumour",
          "neoplasm of liver",
          "tumor of liver",
          "tumour of liver"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A benign or malignant neoplasm that affects the liver parenchyma or intrahepatic bile ducts. Representative examples of benign neoplasms include hepatocellular adenoma, and bile duct adenoma. Representative examples of malignant neoplasms include hepatocellular carcinoma, intrahepatic cholangiocarcinoma, and lymphoma."
      },
      "child_count": 51,
      "reference_id": "MONDO:0024477"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 6889,
      "label": "fibroma"
    },
    {
      "id": 16812,
      "label": "solitary fibrous tumor"
    },
    {
      "id": 21432,
      "label": "liver and intrahepatic bile duct neoplasm"
    }
  ]
}