{
  "id": 6170,
  "label": "childhood multilocular cystic kidney neoplasm",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0004356",
  "properties": {
    "xrefs": [
      "DOID:7762",
      "MEDGEN:232064",
      "NCIT:C6566",
      "UMLS:C1332983"
    ],
    "synonyms": [
      "childhood multilocular cystic kidney neoplasm",
      "childhood multilocular cystic kidney tumor",
      "childhood multilocular cystic kidney tumour",
      "childhood multilocular cystic renal neoplasm",
      "childhood multilocular cystic renal tumor",
      "childhood multilocular cystic renal tumour",
      "paediatric multilocular cystic kidney neoplasm",
      "paediatric multilocular cystic kidney tumour",
      "paediatric multilocular cystic renal neoplasm",
      "paediatric multilocular cystic renal tumour",
      "pediatric multilocular cystic kidney neoplasm",
      "pediatric multilocular cystic kidney tumor",
      "pediatric multilocular cystic renal neoplasm",
      "pediatric multilocular cystic renal tumor",
      "benign multilocular cystic renal tumour"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ],
    "definition": "A cystic neoplasm which arises from the kidney and occurs in children. It includes the cystic partially differentiated nephroblastoma and cases in which nephroblastomatous elements are not present."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 4767,
      "label": "childhood kidney neoplasm",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        20320,
        20396
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3675",
          "MEDGEN:232356",
          "NCIT:C6563",
          "UMLS:C1333003"
        ],
        "synonyms": [
          "kidney neoplasm",
          "childhood kidney neoplasm",
          "childhood kidney tumor",
          "childhood kidney tumour",
          "childhood renal neoplasm",
          "childhood renal tumor",
          "childhood renal tumour",
          "kidney neoplasm of childhood",
          "paediatric kidney neoplasm",
          "paediatric kidney tumour",
          "paediatric renal neoplasm",
          "paediatric renal tumour",
          "pediatric kidney neoplasm",
          "pediatric kidney tumor",
          "pediatric renal neoplasm",
          "pediatric renal tumor"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "A kidney neoplasm that occurs during childhood."
      },
      "child_count": 6,
      "reference_id": "MONDO:0002730"
    }
  ],
  "children": [
    {
      "id": 21983,
      "label": "cystic partially differentiated nephroblastoma",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6170,
        21577
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:7571",
          "GARD:0025603",
          "ICDO:8959/1",
          "ICDO:8959/3",
          "MEDGEN:220423",
          "NCIT:C6897",
          "UMLS:C1266139"
        ],
        "synonyms": [
          "cystic partially differentiated nephroblastoma",
          "malignant cystic nephroma",
          "malignant multilocular cystic nephroma"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "A variant of Wilms tumor of the kidney characterized by the presence of cystic spaces separated by septa. The septa contain immature epithelial cells, immature stromal cells, and blastema cells. Surgical resection is usually curative."
      },
      "child_count": 0,
      "reference_id": "MONDO:0030604"
    }
  ],
  "roots": [
    {
      "id": 4767,
      "label": "childhood kidney neoplasm"
    }
  ]
}