{
  "id": 21986,
  "label": "interstitial lung disease 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0030608",
  "properties": {
    "xrefs": [
      "DOID:0060941",
      "GARD:0027931",
      "MEDGEN:1794231",
      "OMIM:619611",
      "UMLS:C5562021"
    ],
    "synonyms": [
      "ILD1",
      "interstitial lung disease 1"
    ],
    "categories": [
      {
        "ref": "MONDO:0005087",
        "name": "respiratory system disorder"
      }
    ],
    "definition": "An interstitial lung disease in which the cause of the disease is a variation in the SFTPA1 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 22225,
      "label": "inherited interstitial lung disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        16615
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027936",
          "OMIMPS:619611"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ],
        "definition": "An instance of interstitial lung disease that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 26,
      "reference_id": "MONDO:0031199"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 22225,
      "label": "inherited interstitial lung disease"
    }
  ]
}