{
  "id": 24828,
  "label": "cellular interstitial pneumonitis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0800121",
  "properties": {
    "xrefs": [
      "GARD:0026441"
    ],
    "categories": [
      {
        "ref": "MONDO:0005087",
        "name": "respiratory system disorder"
      }
    ],
    "definition": "An interstitial lung disease specific to infancy that is characterized by tachypnea at birth and persistent disease, diffuse interstitial thickening due to pale oval and spindle-shaped histiocytes without scarring."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17419,
      "label": "interstitial lung disease specific to infancy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17417
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1842984",
          "Orphanet:264694",
          "UMLS:C5679737"
        ],
        "synonyms": [
          "ILD specific to infancy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ]
      },
      "child_count": 5,
      "reference_id": "MONDO:0017019"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17419,
      "label": "interstitial lung disease specific to infancy"
    }
  ]
}