{
  "id": 10759,
  "label": "lymphoid interstitial pneumonia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009537",
  "properties": {
    "xrefs": [
      "DOID:0050159",
      "GARD:0016700",
      "ICD10CM:J84.2",
      "ICD9:516.8",
      "MEDGEN:82682",
      "MESH:C562489",
      "MedDRA:10062997",
      "NANDO:1200424",
      "NCIT:C27558",
      "OMIM:247610",
      "Orphanet:79128",
      "SCTID:44274007",
      "UMLS:C0264511",
      "icd11.foundation:1140418798"
    ],
    "synonyms": [
      "diffuse hyperplasia of bronchus-associated lymphoid tissue",
      "lymphocytic interst. pneumonitis",
      "lymphocytic interstitial pneumonia",
      "lymphocytic interstitial pneumonitis",
      "lymphoid interstitial pneumonia",
      "LIP"
    ],
    "categories": [
      {
        "ref": "MONDO:0005087",
        "name": "respiratory system disorder"
      }
    ],
    "definition": "Interstitial pneumonia characterized by the presence of bibasilar pulmonary interstitial infiltrates composed of lymphocytes and plasma cells. It may be associated with autoimmune and lymphoproliferative disorders. Signs and symptoms include fever, cough, and dyspnea. Symptomatic patients may require immunosuppressive treatment."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4517,
      "label": "idiopathic interstitial pneumonia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6953,
        24405
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2797",
          "GARD:0013337",
          "ICD10CM:J84.11",
          "MEDGEN:389939",
          "MESH:D054988",
          "NANDO:1200416",
          "NANDO:2200199",
          "NCIT:C35714",
          "Orphanet:98300",
          "SCTID:700249006",
          "UMLS:C2350236"
        ],
        "synonyms": [
          "IIP",
          "IIp",
          "idiopathic fibrosing alveolitis",
          "idiopathic interstitial pneumonitis",
          "noninfectious pneumonia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ],
        "definition": "A class of diffuse lung diseases that typically affect the pulmonary interstitium, although some also have a component affecting the airways (for instance, Cryptogenic organizing pneumonitis)."
      },
      "child_count": 20,
      "reference_id": "MONDO:0002429"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4517,
      "label": "idiopathic interstitial pneumonia"
    }
  ]
}