{
  "id": 10612,
  "label": "Dubin-Johnson syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009380",
  "properties": {
    "xrefs": [
      "DOID:12308",
      "GARD:0002793",
      "MEDGEN:7181",
      "MESH:D007566",
      "MedDRA:10013800",
      "NCIT:C34741",
      "NORD:1063",
      "OMIM:237500",
      "Orphanet:234",
      "SCTID:44553005",
      "UMLS:C0022350",
      "icd11.foundation:1691610999"
    ],
    "synonyms": [
      "Dubin Johnson Syndrome",
      "Dubin-Johnson syndrome",
      "Dubin-Sprinz disease",
      "Sprinz-Nelson syndrome",
      "chronic idiopathic jaundice",
      "hyperbilirubinemia type 2",
      "DJS",
      "conjugated hyperbilirubinemia",
      "hyperbilirubinemia 2",
      "hyperbilirubinemia, Dubin-Johnson type"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Dubin-Johnson syndrome (DJS) is a benign, inherited liver disorder characterized clinically by chronic, predominantly conjugated, hyperbilirubinemia and histopathologically by black-brown pigment deposition in parenchymal liver cells."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    },
    {
      "id": 4498,
      "label": "hereditary hyperbilirubinemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17982,
        21324
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2741",
          "GARD:0023131",
          "MEDGEN:6963",
          "MESH:D006933",
          "NCIT:C84761",
          "OMIMPS:237450",
          "UMLS:C0020435"
        ],
        "synonyms": [
          "bilirubin metabolic disorder",
          "hyperbilirubinaemia",
          "hyperbilirubinemia",
          "hereditary hyperbilirubinemia"
        ],
        "definition": "An inherited disorder affecting the metabolism of bilirubin. It results in increased levels of bilirubin in the blood. Representative examples of this condition include Gilbert syndrome and Crigler-Najjar syndrome."
      },
      "child_count": 14,
      "reference_id": "MONDO:0002408"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 4498,
      "label": "hereditary hyperbilirubinemia"
    }
  ]
}