{
  "id": 18772,
  "label": "nodular regenerative hyperplasia of the liver",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018835",
  "properties": {
    "xrefs": [
      "GARD:0010929",
      "ICD9:573.8",
      "MEDGEN:1830387",
      "Orphanet:48372",
      "SCTID:715140008",
      "UMLS:C5779783",
      "icd11.foundation:1642018758"
    ],
    "synonyms": [
      "non-cirrhotic nodulation",
      "miliary hepatocellular adenomatosis",
      "nodular regenerative hyperplasia",
      "non-cirrhotic nodular transformation",
      "non-cirrhotic portal hypertension"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Nodular regenerative hyperplasia of the liver is a rare parenchymatous liver disease characterized by diffuse benign transformation of the hepatic parenchyma into multiple small nodules (composed of regenerating hepatocytes) and that is usually asymptomatic but can lead to the development of non-cirrhotic portal hypertension and its complications, including esophageal variceal bleeding, hypersplenism and ascites. It is often associated with rheumatologic, autoimmune, hematologic, and myeloproliferative disorders as well as various immune deficiency states and exposure certain drugs and toxins."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 6878,
      "label": "liver disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4586,
        6875
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:409",
          "EFO:0001421",
          "ICD10CM:K70-K77",
          "ICD9:573.8",
          "ICD9:573.9",
          "MEDGEN:893061",
          "MESH:D008107",
          "NCIT:C3196",
          "SCTID:235856003",
          "UMLS:C4021780",
          "icd11.foundation:1784240230"
        ],
        "synonyms": [
          "disease of liver",
          "disease or disorder of liver",
          "disorder of liver",
          "hepatic disease",
          "hepatic disorder",
          "liver and intrahepatic bile duct disorder",
          "liver disease",
          "liver disease or disorder",
          "liver disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A disease involving the liver."
      },
      "child_count": 64,
      "reference_id": "MONDO:0005154"
    },
    {
      "id": 23885,
      "label": "telomere syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19146
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026060",
          "MEDGEN:1668986",
          "NCIT:C152065",
          "UMLS:C4727832"
        ],
        "synonyms": [
          "STS",
          "short telomere syndrome"
        ],
        "definition": "Accelerated aging syndromes often caused by inheritable gene mutations resulting in decreased telomere lengths."
      },
      "child_count": 7,
      "reference_id": "MONDO:0100137"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 6878,
      "label": "liver disorder"
    },
    {
      "id": 23885,
      "label": "telomere syndrome"
    }
  ]
}