{
  "id": 25088,
  "label": "idiopathic pulmonary fibrosis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0800504",
  "properties": {
    "xrefs": [
      "DOID:0050156",
      "GARD:0028067",
      "ICD10CM:J84.112",
      "MEDGEN:321462",
      "MESH:D054990",
      "NCIT:C35716",
      "Orphanet:2032",
      "UMLS:C1800706",
      "icd11.foundation:1074069640"
    ],
    "synonyms": [
      "IPF"
    ],
    "categories": [
      {
        "ref": "MONDO:0005087",
        "name": "respiratory system disorder"
      }
    ],
    "definition": "An interstitial lung disease with a poor prognosis, that is characterized by the progressive formation of scar tissue within the lungs in the absence of any known cause."
  },
  "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"
    },
    {
      "id": 16615,
      "label": "interstitial lung disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6971
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3082",
          "EFO:0004244",
          "ICD10CM:J80-J84",
          "MEDGEN:1788738",
          "MESH:D017563",
          "MedDRA:10022611",
          "NCIT:C164315",
          "Orphanet:182095",
          "SCTID:233703007",
          "UMLS:C5441745"
        ],
        "synonyms": [
          "ILD",
          "interstitial lung disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ],
        "definition": "A diverse group of lung diseases that affect the lung parenchyma. They are characterized by an initial inflammation of pulmonary alveoli that extends to the interstitium and beyond leading to diffuse pulmonary fibrosis. Interstitial lung diseases are classified by their etiology (known or unknown causes), and radiological-pathological features."
      },
      "child_count": 14,
      "reference_id": "MONDO:0015925"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4517,
      "label": "idiopathic interstitial pneumonia"
    },
    {
      "id": 16615,
      "label": "interstitial lung disease"
    }
  ]
}