{
  "id": 12917,
  "label": "thyroid Hurthle cell carcinoma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011836",
  "properties": {
    "xrefs": [
      "DOID:8161",
      "GARD:0009428",
      "MEDGEN:196672",
      "MESH:C536913",
      "NCIT:C4946",
      "OMIM:607464",
      "ONCOTREE:THHC",
      "SCTID:423158009",
      "UMLS:C0749424"
    ],
    "synonyms": [
      "Hurthle cell carcinoma of the thyroid",
      "Hurthle cell carcinoma of the thyroid gland",
      "Hurthle cell carcinoma of thyroid",
      "Hurthle cell carcinoma of thyroid gland",
      "Hurthle cell thyroid gland carcinoma",
      "oncocytic carcinoma of the thyroid",
      "oncocytic carcinoma of thyroid",
      "thyroid Hurthle cell carcinoma",
      "thyroid carcinoma, Hurthle cell",
      "thyroid gland Hurthle cell carcinoma",
      "thyroid gland oncocytic follicular carcinoma",
      "thyroid oncocytic carcinoma",
      "Hurthle cell thyroid cancer",
      "Hurthle cell thyroid neoplasia",
      "follicular thyroid cancer, Hurthle cell type",
      "thyroid cancer, Hurthle cell",
      "thyroid cancer, follicular, Hurthle cell type"
    ],
    "categories": [
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    },
    {
      "id": 6768,
      "label": "thyroid gland follicular carcinoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16290,
        21537
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3962",
          "EFO:0000501",
          "GARD:0024144",
          "HP:0006731",
          "ICDO:8330/3",
          "ICDO:8331/3",
          "MEDGEN:64630",
          "MESH:D018263",
          "NCIT:C8054",
          "ONCOTREE:THFO",
          "SCTID:255028004",
          "UMLS:C0206682"
        ],
        "synonyms": [
          "follicular cancer of the thyroid",
          "follicular cancer of the thyroid gland",
          "follicular cancer of thyroid",
          "follicular cancer of thyroid gland",
          "thyroid gland follicular cancer",
          "well-differentiated follicular carcinoma",
          "carcinoma of thyroid follicle",
          "carcinoma, follicular cell, malignant",
          "follicular carcinoma",
          "follicular carcinoma of the thyroid",
          "follicular carcinoma of the thyroid gland",
          "follicular carcinoma of thyroid",
          "follicular carcinoma of thyroid gland",
          "follicular thyroid cancer",
          "follicular thyroid carcinoma",
          "follicular thyroid gland carcinoma",
          "thyroid follicle carcinoma",
          "thyroid follicular carcinoma",
          "thyroid gland follicular carcinoma",
          "well-differentiated follicular adenocarcinoma",
          "follicular adenocarcinoma",
          "follicular adenocarcinoma (morphologic abnormality)",
          "follicular adenocarcinoma, well differentiated",
          "follicular adenocarcinoma, well differentiated (morphologic abnormality)",
          "thyroid gland adenocarcinoma"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A differentiated adenocarcinoma arising from the follicular cells of the thyroid gland. The nuclear features which characterize the thyroid gland papillary carcinoma are absent. Radiation exposure is a risk factor and it comprises approximately 10% to 15% of thyroid cancers. Clinically, it usually presents as a solitary mass in the thyroid gland. It is generally unifocal and thickly encapsulated and shows invasion of the capsule or the vessels. Diagnostic procedures include thyroid ultrasound and fine needle biopsy."
      },
      "child_count": 14,
      "reference_id": "MONDO:0005034"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 6768,
      "label": "thyroid gland follicular carcinoma"
    }
  ]
}