{
  "id": 5262,
  "label": "epithelial predominant Wilms' tumor",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0003322",
  "properties": {
    "xrefs": [
      "DOID:5189",
      "GARD:0023448",
      "MEDGEN:76000",
      "NCIT:C9146",
      "UMLS:C0279608"
    ],
    "synonyms": [
      "epithelial predominant Wilms tumor",
      "epithelial predominant Wilms tumour",
      "epithelial predominant kidney Wilms tumor",
      "epithelial predominant kidney Wilms tumour",
      "epithelial predominant kidney adenosarcoma",
      "epithelial predominant nephroblastoma",
      "epithelial predominant renal Wilm's tumor",
      "epithelial predominant renal Wilm's tumour",
      "epithelial predominant renal Wilms tumor",
      "epithelial predominant renal Wilms' tumor",
      "epithelial predominant renal Wilms' tumour",
      "epithelial predominant renal adenosarcoma"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ],
    "definition": "Wilms tumor of the kidney characterized by the predominance of the epithelial component. The epithelial cells may form papillary and tubular patterns and pseudorosettes."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18919,
      "label": "kidney Wilms tumor",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4465,
        7641
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2154",
          "DOID:5176",
          "GARD:0007892",
          "ICDO:8960/3",
          "MedDRA:10029145",
          "NANDO:2200043",
          "NCIT:C40407",
          "NORD:1855",
          "ONCOTREE:WT",
          "Orphanet:654",
          "SCTID:302849000"
        ],
        "synonyms": [
          "Wilms tumor",
          "Wilms tumour",
          "Wilms' tumor",
          "Wilms' tumour",
          "Wilms tumor of the kidney",
          "Wilms tumour of the kidney",
          "Wilms' Tumor",
          "Wilms' tumor of the kidney",
          "Wilms' tumour of the kidney",
          "kidney Wilms tumor",
          "nephroblastoma",
          "nephroblastoma, malignant",
          "renal Wilms tumor",
          "renal Wilms tumour",
          "renal Wilms' tumor",
          "renal embryonic tumor",
          "renal embryonic tumour",
          "adult nephroblastoma",
          "adult renal Wilms' tumour",
          "childhood renal Wilms tumor",
          "childhood renal Wilms tumour",
          "childhood renal Wilms' cancer",
          "embryonal nephroma",
          "nonanaplastic renal Wilm's tumor",
          "nonanaplastic renal Wilm's tumour"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "An embryonal pediatric tumor of the kidney which may also be seen rarely in adults. The peak incidence of Wilms tumor is between the second and fifth year of life. Microscopically, it is composed of a mixture of cellular elements (blastemal, stromal, and epithelial). The most common sites of metastasis include the regional lymph nodes, lungs, and liver."
      },
      "child_count": 16,
      "reference_id": "MONDO:0019004"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18919,
      "label": "kidney Wilms tumor"
    }
  ]
}