{
  "id": 24620,
  "label": "hereditary gallbladder disorder",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0700225",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    },
    {
      "id": 6977,
      "label": "gallbladder disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4586
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060262",
          "EFO:0003832",
          "ICD10CM:K82",
          "ICD9:575.8",
          "ICD9:575.9",
          "MEDGEN:8947",
          "MESH:D005705",
          "NCIT:C34631",
          "SCTID:39621005",
          "UMLS:C0016977"
        ],
        "synonyms": [
          "Gall bladder disorder",
          "disease of gall bladder",
          "disease or disorder of gall bladder",
          "disorder of gall bladder",
          "gall bladder disease",
          "gall bladder disease or disorder",
          "gallbladder disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "A disease involving the gall bladder."
      },
      "child_count": 11,
      "reference_id": "MONDO:0005281"
    }
  ],
  "children": [
    {
      "id": 12070,
      "label": "gallbladder disease 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        13712,
        24620
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010939"
    },
    {
      "id": 13417,
      "label": "gallbladder disease 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        24620
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:372160",
          "MESH:C563687",
          "OMIM:609918",
          "UMLS:C1835925"
        ],
        "synonyms": [
          "GBD2",
          "gallbladder disease 2"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012365"
    },
    {
      "id": 13418,
      "label": "gallbladder disease 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        24620
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:332087",
          "MESH:C563686",
          "OMIM:609919",
          "UMLS:C1835924"
        ],
        "synonyms": [
          "GBD3",
          "gallbladder disease 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012366"
    }
  ],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 6977,
      "label": "gallbladder disorder"
    }
  ]
}