{
  "id": 13417,
  "label": "gallbladder disease 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012365",
  "properties": {
    "xrefs": [
      "MEDGEN:372160",
      "MESH:C563687",
      "OMIM:609918",
      "UMLS:C1835925"
    ],
    "synonyms": [
      "GBD2",
      "gallbladder disease 2"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 24620,
      "label": "hereditary gallbladder disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6977
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "OMIMPS:600803"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "An instance of gallbladder disorder that is caused by an inherited genomic modification in an individual."
      },
      "child_count": 6,
      "reference_id": "MONDO:0700225"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 24620,
      "label": "hereditary gallbladder disorder"
    }
  ]
}