{
  "id": 16617,
  "label": "idiopathic eosinophilic pneumonia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015927",
  "properties": {
    "xrefs": [
      "GARD:0020246",
      "MEDGEN:836928",
      "Orphanet:182101",
      "SCTID:708031000",
      "UMLS:C3872845"
    ],
    "categories": [
      {
        "ref": "MONDO:0005087",
        "name": "respiratory system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 7370,
      "label": "eosinophilic pneumonia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6953
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:5870",
          "EFO:0007257",
          "GARD:0027348",
          "MEDGEN:282904",
          "NCIT:C35150",
          "UMLS:C1527407"
        ],
        "synonyms": [
          "eosinophilic pneumonia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ],
        "definition": "An inflammatory lung disorder characterized by an increased number of eosinophils in the lungs. The majority of cases are idiopathic, without identifiable cause. In a minority of cases, medications, fungal infections, and environmental triggers have been implicated. It manifests as acute or chronic. Acute eosinophilic pneumonia is a severe and rapidly progressing pneumonia that may lead to respiratory failure requiring mechanical ventilation. Chronic eosinophilic pneumonia follows a slower course and manifests as fever, dyspnea, cough, and weight loss."
      },
      "child_count": 2,
      "reference_id": "MONDO:0005749"
    },
    {
      "id": 24405,
      "label": "idiopathic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29381
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:548250",
          "UMLS:C0277553"
        ],
        "synonyms": [
          "idiopathic disorder"
        ],
        "definition": "A disease or disorder for which the cause is of uncertain or unknown."
      },
      "child_count": 79,
      "reference_id": "MONDO:0700007"
    }
  ],
  "children": [
    {
      "id": 17679,
      "label": "idiopathic chronic eosinophilic pneumonia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16617,
        18069
      ],
      "type_id": 0,
      "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)."
      },
      "child_count": 0,
      "reference_id": "MONDO:0017363"
    },
    {
      "id": 19004,
      "label": "idiopathic acute eosinophilic pneumonia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6566,
        12971,
        16617,
        20092
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:9503",
          "GARD:0000519",
          "MEDGEN:1371970",
          "NCIT:C35301",
          "NORD:728",
          "Orphanet:724",
          "SCTID:64936001",
          "UMLS:C4518469",
          "icd11.foundation:1455309767"
        ],
        "synonyms": [
          "Acute Eosinophilic Pneumonia",
          "IAEP",
          "Loeffler syndrome",
          "Loffler syndrome",
          "Loffler's syndrome",
          "Löffler syndrome",
          "pulmonary infiltrates with eosinophilia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Idiopathic acute eosinophilic pneumonia (IAEP) is an eosinophilic pneumonia of undetermined etiology that is characterized by acute febrile hypoxic respiratory failure associated with diffuse radiographic infiltrates and pulmonary eosinophilia, but without concurring allergy or infection."
      },
      "child_count": 0,
      "reference_id": "MONDO:0019122"
    }
  ],
  "roots": [
    {
      "id": 7370,
      "label": "eosinophilic pneumonia"
    },
    {
      "id": 24405,
      "label": "idiopathic disease"
    }
  ]
}