{
  "id": 12674,
  "label": "familial papillary thyroid carcinoma with renal papillary neoplasia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011578",
  "properties": {
    "xrefs": [
      "GARD:0016853",
      "MEDGEN:381339",
      "MESH:C565310",
      "OMIM:605642",
      "Orphanet:97290",
      "SCTID:717734005",
      "UMLS:C1854104"
    ],
    "synonyms": [
      "PTC-RCC",
      "ptc-RCC",
      "Prn1",
      "Ptcprn",
      "thyroid carcinoma, papillary, with papillary renal neoplasia"
    ],
    "categories": [
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Familial papillary thyroid carcinoma with renal papillary neoplasia (fPTC/PRN) is an extremely rare inherited tumor syndrome within the familial nonmedullary thyroid cancer group (fNMTC)."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18106,
      "label": "familial nonmedullary thyroid carcinoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        16049
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021421",
          "MEDGEN:502247",
          "OMIMPS:188550",
          "Orphanet:319494",
          "UMLS:C3501843"
        ],
        "synonyms": [
          "thyroid cancer, nonmedullary"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Familial nonmedullary thyroid carcinoma (fNMTC) is a rare non-syndromic form of thyroid cancer characterized by occurrence of thyroid carcinoma (TC) as the primary feature in a familial setting."
      },
      "child_count": 6,
      "reference_id": "MONDO:0017896"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18106,
      "label": "familial nonmedullary thyroid carcinoma"
    }
  ]
}