{
  "id": 5693,
  "label": "hereditary kidney oncocytoma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0003824",
  "properties": {
    "xrefs": [
      "DOID:6244",
      "MEDGEN:209307",
      "NCIT:C8960",
      "UMLS:C0879606"
    ],
    "synonyms": [
      "familial renal oncocytoma",
      "hereditary kidney oncocytoma",
      "hereditary renal oncocytoma"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ],
    "definition": "An inherited condition characterized by the development of kidney oncocytomas which are often bilateral and multifocal. This condition may be connected to Birt-Hogg-Dube syndrome."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 5694,
      "label": "kidney oncocytoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4584,
        11932,
        22952
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:6245",
          "MEDGEN:91094",
          "MESH:C537750",
          "NCIT:C4526",
          "ONCOTREE:ROCY",
          "SCTID:254922006",
          "UMLS:C0346255"
        ],
        "synonyms": [
          "kidney oncocytic neoplasm",
          "kidney oncocytoma",
          "oncocytoma of kidney",
          "oncocytoma of the kidney",
          "renal epithelial oncocytic neoplasm",
          "renal epithelial oncocytic tumor",
          "renal epithelial oncocytic tumour",
          "renal oncocytoma",
          "ROCY",
          "oncocytoma kidney",
          "oncocytoma renal"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "A benign tumor of the kidney, characterized by the presence of large cells with abundant eosinophilic granular cytoplasm. The majority of these tumors are discovered incidentally, during work-up of other conditions."
      },
      "child_count": 3,
      "reference_id": "MONDO:0003825"
    },
    {
      "id": 23932,
      "label": "inherited kidney disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6948
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "genetic renal disease",
          "inherited kidney disease",
          "inherited renal disorder",
          "nephrogenetic disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions, with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology that are characterized by abnormalities in the kidney or urinary system."
      },
      "child_count": 52,
      "reference_id": "MONDO:0100191"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5694,
      "label": "kidney oncocytoma"
    },
    {
      "id": 23932,
      "label": "inherited kidney disorder"
    }
  ]
}