{
  "id": 17585,
  "label": "congenital pulmonary airway malformation type 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017249",
  "properties": {
    "xrefs": [
      "GARD:0021094",
      "MEDGEN:1760964",
      "Orphanet:280832",
      "UMLS:C5437763",
      "icd11.foundation:1455719613"
    ],
    "synonyms": [
      "CCAM type 1",
      "CPAM type 1",
      "congenital cystic adenomatoid malformation of the lung type 1",
      "congenital cystic adenomatous malformation of the lung type 1",
      "congenital cystic disease of the lung type 1"
    ],
    "categories": [
      {
        "ref": "MONDO:0005087",
        "name": "respiratory system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17071,
      "label": "congenital pulmonary airway malformation",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6815,
        20383
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018772",
          "MEDGEN:8225",
          "MESH:D015615",
          "NCIT:C98892",
          "Orphanet:2444",
          "SCTID:111318005",
          "UMLS:C0010668",
          "icd11.foundation:2091138945"
        ],
        "synonyms": [
          "CCAM",
          "CPAM",
          "congenital cystic adenomatoid malformation of lung",
          "congenital cystic adenomatoid malformation of the lung",
          "congenital cystic adenomatous malformation of the lung",
          "congenital cystic disease of the lung",
          "congenital cystic adenomatoid malformation",
          "cystic adenomatoid malformation of lung"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ],
        "definition": "An abnormality in lung development that is characterized by a multicystic mass resulting from an adenomatous overgrowth of the terminal bronchioles with a consequent reduction of pulmonary alveoli. This anomaly is classified into three types by the cyst size."
      },
      "child_count": 10,
      "reference_id": "MONDO:0016580"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17071,
      "label": "congenital pulmonary airway malformation"
    }
  ]
}