{
  "id": 18878,
  "label": "idiopathic bronchiectasis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018956",
  "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)."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 6582,
      "label": "bronchiectasis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3582,
        5714,
        6740
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:9563",
          "ICD10CM:J47",
          "ICD10WHO:J47",
          "ICD9:494",
          "MEDGEN:14234",
          "MESH:D001987",
          "NANDO:2100036",
          "NANDO:2200206",
          "NCIT:C84475",
          "OMIMPS:211400",
          "SCTID:12295008",
          "UMLS:C0006267",
          "icd11.foundation:1935524933"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ],
        "definition": "Segmental, irreversible dilation of the bronchial tree resulting in the accumulation of secretions which leads to obstruction. The most common cause is bacterial infection."
      },
      "child_count": 3,
      "reference_id": "MONDO:0004822"
    },
    {
      "id": 24405,
      "label": "idiopathic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29381
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:548250",
          "UMLS:C0277553"
        ],
        "synonyms": [
          "idiopathic disorder"
        ],
        "definition": "A disease or disorder for which the cause is of uncertain or unknown."
      },
      "child_count": 79,
      "reference_id": "MONDO:0700007"
    }
  ],
  "children": [
    {
      "id": 10152,
      "label": "bronchiectasis with or without elevated sweat chloride 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18878
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080526",
          "GARD:0018054",
          "MEDGEN:440868",
          "MESH:C567618",
          "OMIM:211400",
          "UMLS:C2749757"
        ],
        "synonyms": [
          "bronchiectasis with or without elevated sweat chloride 1",
          "bronchiectasis with or without elevated sweat chloride 1, modifier of",
          "bronchiectasis with or without elevated sweat chloride type 1",
          "BESC1",
          "cystic fibrosis-like syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0008887"
    },
    {
      "id": 14125,
      "label": "bronchiectasis with or without elevated sweat chloride 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18878
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080527",
          "GARD:0018055",
          "MEDGEN:414437",
          "MESH:C567813",
          "OMIM:613021",
          "UMLS:C2751666"
        ],
        "synonyms": [
          "SCNN1A bronchiectasis",
          "bronchiectasis caused by mutation in SCNN1A",
          "bronchiectasis with or without elevated sweat chloride 2",
          "bronchiectasis with or without elevated sweat chloride type 2",
          "BESC2",
          "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 SCNN1A gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013087"
    },
    {
      "id": 14150,
      "label": "bronchiectasis with or without elevated sweat chloride 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18878
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013112"
    }
  ],
  "roots": [
    {
      "id": 6582,
      "label": "bronchiectasis"
    },
    {
      "id": 24405,
      "label": "idiopathic disease"
    }
  ]
}