{
  "id": 25033,
  "label": "Birt-Hogg-Dube syndrome 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0800445",
  "properties": {
    "xrefs": [
      "DOID:0050676",
      "GARD:0002322",
      "ICD9:704.8",
      "MESH:D058249",
      "MedDRA:10067736",
      "NCIT:C28244",
      "OMIM:135150",
      "Orphanet:122",
      "SCTID:110985001"
    ],
    "synonyms": [
      "Hornstein-Knickenberg syndrome",
      "fibrofolliculomas with trichodiscomas and acrochordons"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Any Birt-Hogg-Dube (BHD) syndrome in which the cause of the disease is a variation in the FLCN gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 25032,
      "label": "Birt-Hogg-Dube syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        4370
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0028061",
          "MEDGEN:91070",
          "OMIMPS:135150",
          "UMLS:C0346010"
        ],
        "synonyms": [
          "BHD"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 4,
      "reference_id": "MONDO:0800444"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 25032,
      "label": "Birt-Hogg-Dube syndrome"
    }
  ]
}