{
  "id": 9071,
  "label": "hepatic adenomas, familial",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007718",
  "properties": {
    "xrefs": [
      "DOID:0111366",
      "GARD:0024570",
      "MEDGEN:374515",
      "MESH:C564190",
      "OMIM:142330",
      "UMLS:C1840646"
    ],
    "synonyms": [
      "hepatic adenoma, somatic",
      "hepatic adenomas, familial",
      "liver cell adenomas, familial"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    },
    {
      "id": 18830,
      "label": "hepatocellular adenoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2884,
        3032,
        6714,
        21432,
        22952
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050868",
          "EFO:0000762",
          "GARD:0018847",
          "ICDO:8170/0",
          "MEDGEN:61655",
          "MESH:D018248",
          "MedDRA:10019827",
          "NCIT:C3758",
          "ONCOTREE:LIAD",
          "Orphanet:54272",
          "UMLS:C0206669",
          "icd11.foundation:1481070735"
        ],
        "synonyms": [
          "HCA",
          "adenoma of liver cells",
          "adenoma of the liver cells",
          "adenoma, hepatocellular, benign",
          "hepatocellular adenoma",
          "liver cell adenoma",
          "LIAD"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A benign epithelial neoplasm arising from the hepatocytes. Grossly, it appears as a soft, round mass which often contains areas of hemorrhage and necrosis. Morphologically, the neoplastic cells resemble normal hepatocytes and form plates separated by sinusoids. Most patients have a history of contraceptive or anabolic steroids use."
      },
      "child_count": 5,
      "reference_id": "MONDO:0018902"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 18830,
      "label": "hepatocellular adenoma"
    }
  ]
}