{
  "id": 17679,
  "label": "idiopathic chronic eosinophilic pneumonia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017363",
  "properties": {
    "xrefs": [
      "GARD:0001130",
      "MEDGEN:443938",
      "MESH:C535590",
      "NORD:967",
      "Orphanet:2902",
      "UMLS:C2930941",
      "icd11.foundation:958353326"
    ],
    "synonyms": [
      "chronic eosinophilic pneumonia",
      "Chronic Eosinophilic Pneumonia",
      "Carrington syndrome",
      "Carrington's disease",
      "Carrington's pulmonary eosinophilia",
      "chronic eosinophilic pneumonia (CEP)",
      "chronic idiopathic eosinophilic pneumonia",
      "eosinophilic idiopathic chronic pneumopathy"
    ],
    "categories": [
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      },
      {
        "ref": "MONDO:0005087",
        "name": "respiratory system disorder"
      }
    ],
    "definition": "A very rare, severe, interstitial lung disease of insidious onset with subacute or chronic non-specific respiratory manifestations (dyspnea, cough, wheezing) often associated with systemic manifestations (fatigue, malaise, weight loss)."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16617,
      "label": "idiopathic eosinophilic pneumonia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7370,
        24405
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020246",
          "MEDGEN:836928",
          "Orphanet:182101",
          "SCTID:708031000",
          "UMLS:C3872845"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ]
      },
      "child_count": 4,
      "reference_id": "MONDO:0015927"
    },
    {
      "id": 18069,
      "label": "hypersensitivity pneumonitis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3133,
        16615,
        23261
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:841",
          "GARD:0000012",
          "ICD9:495",
          "ICD9:495.8",
          "ICD9:495.9",
          "MEDGEN:1446",
          "MESH:D000542",
          "MedDRA:10001890",
          "NCIT:C34369",
          "NORD:761",
          "Orphanet:31740",
          "SCTID:37471005",
          "UMLS:C0002390"
        ],
        "synonyms": [
          "HP",
          "allergic form of pneumonitis",
          "allergic pneumonitis",
          "exogen allergic alveolitis",
          "extrinsic allergic alveolitis",
          "hypersensitivity pneumonitis",
          "allergic interstitial pneumonitis",
          "alveolitis, extrinsic allergic",
          "extrinsic allergic pneumonia hypersensitivity pneumonitis"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ],
        "definition": "Hypersensitivity pneumonitis (HP) is a pulmonary disease with symptoms of dyspnea and cough resulting from the inhalation of an antigen to which the subject has been previously sensitized."
      },
      "child_count": 42,
      "reference_id": "MONDO:0017853"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16617,
      "label": "idiopathic eosinophilic pneumonia"
    },
    {
      "id": 18069,
      "label": "hypersensitivity pneumonitis"
    }
  ]
}