{
  "id": 14150,
  "label": "bronchiectasis with or without elevated sweat chloride 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013112",
  "properties": {
    "xrefs": [
      "DOID:0080528",
      "GARD:0018056",
      "MEDGEN:414351",
      "MESH:C567772",
      "OMIM:613071",
      "UMLS:C2751324"
    ],
    "synonyms": [
      "SCNN1G bronchiectasis",
      "bronchiectasis caused by mutation in SCNN1G",
      "bronchiectasis with or without elevated sweat chloride 3",
      "bronchiectasis with or without elevated sweat chloride type 3",
      "BESC3",
      "cystic fibrosis-like syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0005087",
        "name": "respiratory system disorder"
      }
    ],
    "definition": "Any bronchiectasis in which the cause of the disease is a mutation in the SCNN1G gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18878,
      "label": "idiopathic bronchiectasis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6582,
        24405
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016664",
          "MEDGEN:573462",
          "Orphanet:60033",
          "SCTID:233629001",
          "UMLS:C0339985"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ],
        "definition": "Idiopathic bronchiectasis (IB) is a progressive lung disease characterized by chronic dilation of the bronchi and destruction of the bronchial walls in the absence of any underlying cause (such as post infectious disease, aspiration, immunodeficiency, congenital abnormalities and ciliary anomalies)."
      },
      "child_count": 6,
      "reference_id": "MONDO:0018956"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18878,
      "label": "idiopathic bronchiectasis"
    }
  ]
}