{
  "id": 13712,
  "label": "cholelithiasis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012672",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 4,
  "parents": [
    {
      "id": 6624,
      "label": "biliary tract disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4586
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:9741",
          "EFO:0009534",
          "ICD9:576.9",
          "MEDGEN:108201",
          "MESH:D001660",
          "SCTID:105997008",
          "UMLS:C0549613"
        ],
        "synonyms": [
          "biliary tree disease",
          "biliary tree disease or disorder",
          "disease of biliary tree",
          "disease or disorder of biliary tree",
          "disorder of biliary tree"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "A disease involving the biliary tree."
      },
      "child_count": 15,
      "reference_id": "MONDO:0004868"
    }
  ],
  "children": [
    {
      "id": 8161,
      "label": "cholecystolithiasis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6977,
        13712
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11151",
          "EFO:1000864",
          "MEDGEN:215268",
          "MESH:D041761",
          "MedDRA:10049890",
          "UMLS:C0947622"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "Single or multiple, ovoid or irregular, solid particles that are formed from bile, cholesterol, and calcium in the gallbladder cavity."
      },
      "child_count": 0,
      "reference_id": "MONDO:0006698"
    },
    {
      "id": 8162,
      "label": "choledocholithiasis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4899,
        7031,
        13712
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11755",
          "EFO:1000865",
          "MEDGEN:148784",
          "MESH:D042883",
          "MedDRA:10049891",
          "UMLS:C0701818"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "Presence or formation of gallstones in the common bile duct."
      },
      "child_count": 0,
      "reference_id": "MONDO:0006699"
    },
    {
      "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": 18751,
      "label": "primary intrahepatic lithiasis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        13712
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021974",
          "MEDGEN:1814175",
          "Orphanet:480506",
          "UMLS:C5576557"
        ],
        "synonyms": [
          "PIHL",
          "primary hepatolithiasis"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "A rare biliary tract disease characterized by stone formation within the intrahepatic bile ducts without any known cause, leading to bile stasis and repeated cholangitic episodes."
      },
      "child_count": 0,
      "reference_id": "MONDO:0018806"
    }
  ],
  "roots": [
    {
      "id": 6624,
      "label": "biliary tract disorder"
    }
  ]
}