{
  "id": 4660,
  "label": "hepatic angiomyolipoma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0002605",
  "properties": {
    "xrefs": [
      "DOID:3317",
      "GARD:0023185",
      "MEDGEN:272705",
      "NCIT:C27485",
      "UMLS:C1333962"
    ],
    "synonyms": [
      "liver PEComa",
      "liver angiomyolipoma"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "An angiomyolipoma arising from the liver."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4658,
      "label": "angiomyolipoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7885
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3314",
          "ICDO:8860/0",
          "MEDGEN:64622",
          "MESH:D018207",
          "NCIT:C3734",
          "UMLS:C0206633"
        ],
        "synonyms": [
          "angiomyolipoma (morphologic abnormality)"
        ],
        "definition": "A neoplasm with perivascular epithelioid cell differentiation often associated with tuberous sclerosis. It is characterized by a mixture of epithelioid cells, smooth muscle, vessels, and mature adipose tissue. The kidney is the most common site of involvement. Other sites of involvement include the liver, lung, lymph nodes, and retroperitoneum. The vast majority of cases follow a benign clinical course. However, cases of metastatic angiomyolipomas with sarcomatoid features have been described."
      },
      "child_count": 3,
      "reference_id": "MONDO:0002603"
    },
    {
      "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": 4658,
      "label": "angiomyolipoma"
    },
    {
      "id": 21432,
      "label": "liver and intrahepatic bile duct neoplasm"
    }
  ]
}