{
  "id": 11310,
  "label": "thymoma, familial",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010127",
  "properties": {
    "xrefs": [
      "GARD:0024710",
      "MEDGEN:376447",
      "MESH:C564767",
      "OMIM:274230",
      "UMLS:C1848814"
    ],
    "synonyms": [
      "hereditary thymoma (disease)",
      "thymoma, familial",
      "thymic neoplasia"
    ],
    "categories": [
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      },
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "An instance of thymoma (disease) that is caused by an inherited modification of the individual's genome."
  },
  "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": 7959,
      "label": "thymoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18240
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3275",
          "EFO:1000581",
          "GARD:0016922",
          "HP:0100522",
          "ICD9:239.89",
          "ICDO:8580/1",
          "MEDGEN:52743",
          "MESH:D013945",
          "MedDRA:10043670",
          "NCIT:C3411",
          "ONCOTREE:THYM",
          "Orphanet:99867",
          "SCTID:444231005",
          "UMLS:C0040100",
          "icd11.foundation:33869057"
        ],
        "synonyms": [
          "primary thymic epithelial neoplasm",
          "primary thymic epithelial tumor",
          "primary thymic epithelial tumour",
          "thymoma",
          "thymoma (disease)",
          "THYM"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "A neoplasm arising from the epithelial cells of the thymus. Although thymomas are usually encapsulated tumors, they may invade the capsule and infiltrate the surrounding tissues or even metastasize to distant anatomic sites. The following morphologic subtypes are currently recognized: type A, type B, type AB, metaplastic, micronodular, microscopic, and sclerosing thymoma. Thymomas type B are further subdivided into types B1, B2, and B3. Thymoma type B3 usually has the most aggressive clinical course."
      },
      "child_count": 8,
      "reference_id": "MONDO:0006456"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 7959,
      "label": "thymoma"
    }
  ]
}