{
  "id": 9112,
  "label": "nonpapillary renal cell carcinoma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007763",
  "properties": {
    "xrefs": [
      "DOID:0050387",
      "GARD:0024575",
      "OMIM:144700"
    ],
    "synonyms": [
      "renal cell carcinoma",
      "renal carcinoma, chromophobe, somatic",
      "renal cell carcinoma, clear cell",
      "renal cell carcinoma, clear cell, somatic",
      "renal cell carcinoma, somatic",
      "CCRCC",
      "clear cell renal cell adenocarcinoma",
      "clear cell renal cell carcinoma",
      "RCC",
      "adenocarcinoma of kidney",
      "hypernephroma",
      "nonpapillary renal carcinoma 1 locus",
      "renal cell carcinoma, nonpapillary"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 6814,
      "label": "renal cell carcinoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6712,
        6923
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:4450",
          "EFO:0000681",
          "GARD:0013215",
          "HP:0005584",
          "ICD9:189.0",
          "MEDGEN:766",
          "MESH:D002292",
          "MedDRA:10067946",
          "NANDO:2200045",
          "NORD:1657",
          "ONCOTREE:RCC",
          "Orphanet:217071",
          "SCTID:702391001",
          "UMLS:C0007134"
        ],
        "synonyms": [
          "RCC",
          "renal cell carcinoma",
          "renal cell carcinoma (disease)",
          "kidney adenocarcinoma",
          "renal cell adenocarcinoma"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "A carcinoma that arises from glandular epithelial cells of the kidney"
      },
      "child_count": 22,
      "reference_id": "MONDO:0005086"
    }
  ],
  "children": [
    {
      "id": 6743,
      "label": "clear cell renal carcinoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6742,
        7199,
        9112
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:4467",
          "EFO:0000349",
          "GARD:0009574",
          "ICD9:189.0",
          "MEDGEN:76018",
          "NCIT:C4033",
          "ONCOTREE:CCRCC",
          "Orphanet:319276",
          "SCTID:254915003",
          "UMLS:C0279702"
        ],
        "synonyms": [
          "Grawitz tumor",
          "Grawitz tumour",
          "RCC, clear cell adenocarcinoma",
          "clear cell adenocarcinoma of kidney",
          "clear cell adenocarcinoma of the kidney",
          "clear cell adenocarcinoma, kidney",
          "clear cell carcinoma of kidney",
          "clear cell carcinoma of the kidney",
          "clear cell renal cell cancer",
          "clear cell renal cell carcinoma",
          "conventional (clear cell) renal cell adenocarcinoma",
          "conventional (clear cell) renal cell carcinoma",
          "conventional renal cell carcinoma",
          "kidney clear cell adenocarcinoma",
          "kidney clear cell carcinoma",
          "renal cell carcinoma, clear cell adenocarcinoma",
          "renal clear cell adenocarcinoma",
          "renal clear cell carcinoma",
          "clear-cell metastatic renal cell carcinoma",
          "hypernephroma"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "A malignant epithelial neoplasm of the kidney characterized by the presence of lipid-containing clear cells within a vascular network. The tumor may metastasize to unusual sites and late metastasis is common."
      },
      "child_count": 6,
      "reference_id": "MONDO:0005005"
    },
    {
      "id": 18494,
      "label": "clear cell papillary renal cell carcinoma",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9112
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021721",
          "MEDGEN:1388623",
          "NCIT:C121955",
          "ONCOTREE:CCPRC",
          "Orphanet:404511",
          "SCTID:734015000",
          "UMLS:C4518333"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "Clear cell papillary renal cell carcinoma is a rare, indolent subtype of clear cell renal carcinoma, arising from epithelial cells in the renal cortex. It most frequently manifests with a well-circumscribed, well-encapsulated, unicentric, unilateral, small tumor that typically does not metastasize. Clinically it can present with flank or abdominal pain or hematuria, although most patients are usually asymptomatic at the time of diagnosis. Bilateral and/or multifocal presentation should raise the suspicion of von Hippel-Lindau syndrome."
      },
      "child_count": 0,
      "reference_id": "MONDO:0018448"
    }
  ],
  "roots": [
    {
      "id": 6814,
      "label": "renal cell carcinoma"
    }
  ]
}