{
  "id": 17421,
  "label": "interstitial lung disease specific to adulthood",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017026",
  "properties": {
    "xrefs": [
      "MEDGEN:1842399",
      "Orphanet:264735",
      "UMLS:C5679743"
    ],
    "synonyms": [
      "ILD specific to adulthood"
    ],
    "categories": [
      {
        "ref": "MONDO:0005087",
        "name": "respiratory system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "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": [
    {
      "id": 3896,
      "label": "pulmonary sarcoidosis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17421,
        19178
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13406",
          "GARD:0022993",
          "ICD10CM:D86.0",
          "ICD9:517.8",
          "MEDGEN:19873",
          "MESH:D017565",
          "NCIT:C34997",
          "SCTID:24369008",
          "UMLS:C0036205"
        ],
        "synonyms": [
          "lung sarcoidosis",
          "sarcoidosis of lung"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ],
        "definition": "Sarcoidosis affecting the lung parenchyma. It is characterized by the presence of non-necrotizing granulomas in the lung tissues. It is manifested with dyspnea, cough, fever, night sweats, fatigue, and weight loss."
      },
      "child_count": 0,
      "reference_id": "MONDO:0001708"
    },
    {
      "id": 17422,
      "label": "Langerhans cell histiocytosis specific to adulthood",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17421,
        18407,
        20356
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025086",
          "MEDGEN:859694",
          "NANDO:2200031",
          "NCIT:C114929",
          "Orphanet:264750",
          "UMLS:C3900100"
        ],
        "synonyms": [
          "Langerhans cell histiocytosis",
          "Langerhans cell granulomatosis specific to adulthood",
          "adult Langerhans cell histiocytosis",
          "histiocytosis X specific to adulthood"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Langerhans cell histiocytosis that occurs during adulthood."
      },
      "child_count": 3,
      "reference_id": "MONDO:0017029"
    }
  ],
  "roots": [
    {
      "id": 16615,
      "label": "interstitial lung disease"
    }
  ]
}