{
  "id": 12070,
  "label": "gallbladder disease 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010939",
  "properties": {
    "xrefs": [
      "GARD:0016683",
      "MEDGEN:760527",
      "MedDRA:10068936",
      "OMIM:600803",
      "Orphanet:69663",
      "SCTID:715577009",
      "UMLS:C2609268",
      "icd11.foundation:1261516421"
    ],
    "synonyms": [
      "ABCB4 gene mutation-associated cholelithiasis",
      "GBD1",
      "LPAC",
      "cholelithiasis with ABCB4 gene mutation",
      "cholelithiasis, low phospholipid-associated",
      "gallbladder disease 1",
      "gallbladder disease type 1",
      "low phospholipid associated cholelithiasis"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ],
    "definition": "A rare genetic hepatic disease characterized by low biliary phospholipid concentration with symptomatic and recurring cholelithiasis which develops before the age of 40 years."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 13712,
      "label": "cholelithiasis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6624
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:10211",
          "EFO:0004799",
          "ICD10CM:K80",
          "ICD10WHO:K80",
          "ICD9:574",
          "ICD9:574.20",
          "ICD9:574.5",
          "MEDGEN:3039",
          "MESH:D002769",
          "NCIT:C122822",
          "SCTID:266474003",
          "UMLS:C0008350",
          "icd11.foundation:1268183934"
        ],
        "synonyms": [
          "gallstones"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "The presence of crystallized deposits forming in the gallbladder or biliary tree, primarily composed of cholesterol, bilirubin, and bile."
      },
      "child_count": 4,
      "reference_id": "MONDO:0012672"
    },
    {
      "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": 13712,
      "label": "cholelithiasis"
    },
    {
      "id": 24620,
      "label": "hereditary gallbladder disorder"
    }
  ]
}