{
  "id": 25557,
  "label": "grade I lymphomatoid granulomatosis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0859747",
  "properties": {
    "xrefs": [
      "DOID:0081308",
      "GARD:0026759",
      "MEDGEN:83443",
      "NCIT:C7931",
      "UMLS:C0279065"
    ],
    "categories": [
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      },
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "A lymphomatoid granulomatosis that is characterized by the presence of a polymorphous lymphoid infiltrate without cytologic atypia. Large lymphocytes are absent or rare. By in situ hybridization, EBV-positive cells are infrequently seen."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19291,
      "label": "lymphomatoid granulomatosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17660,
        18833
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081307",
          "GARD:0006943",
          "ICDO:9766/1",
          "MEDGEN:6161",
          "MESH:D008230",
          "MedDRA:10025325",
          "NCIT:C7930",
          "NORD:1385",
          "ONCOTREE:LYG",
          "Orphanet:86869",
          "SCTID:239940004",
          "UMLS:C0024307",
          "icd11.foundation:1890408959"
        ],
        "synonyms": [
          "LYG"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "A very rare Epstein-Barr virus (EBV)-driven lymphoproliferative disease most commonly occurring in adults (in the fourth to sixth decade of life) and commonly affecting the lungs (with presentations varying from small bilateral pulmonary nodules to large necrotic and sometimes cavitating lesions), skin, central nervous system, and kidneys, but only very rarely affecting the lymph nodes and spleen. The symptoms associated with LYG depend on the site of disease involvement but mainly include cough, dyspnea or chest pain (in those with pulmonary involvement) and constitutional symptoms such as weight loss and fever."
      },
      "child_count": 6,
      "reference_id": "MONDO:0019466"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19291,
      "label": "lymphomatoid granulomatosis"
    }
  ]
}