{
  "id": 16148,
  "label": "cryptogenic organizing pneumonia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015264",
  "properties": {
    "xrefs": [
      "DOID:0050157",
      "EFO:1001300",
      "GARD:0001620",
      "ICD10CM:J84.116",
      "ICD9:516.36",
      "MEDGEN:116663",
      "MESH:D018549",
      "NANDO:1200421",
      "NCIT:C62586",
      "NORD:873",
      "Orphanet:1302",
      "SCTID:68409003",
      "SCTID:719218000",
      "UMLS:C0242770",
      "icd11.foundation:1937662238"
    ],
    "synonyms": [
      "COP",
      "Organizing Pneumonia",
      "bronchiolitis obliterans organizing pneumonia",
      "cryptogenic organizing pneumonitis",
      "organising pneumonia",
      "organizing pneumonia",
      "constrictive bronchiolitis",
      "idiopathic BOOP",
      "idiopathic bronchiolitis obliterans organising pneumonia",
      "idiopathic bronchiolitis obliterans organizing pneumonia"
    ],
    "categories": [
      {
        "ref": "MONDO:0005087",
        "name": "respiratory system disorder"
      }
    ],
    "definition": "Cryptogenic organizing pneumonia (COP) is a form of idiopathic interstitial pneumonia characterized pathologically by organizing pneumonia (OP) that presents with non-specific flu-like symptoms, as well as cough and dyspnea and where no etiological agent is found."
  },
  "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"
    }
  ]
}