{
  "id": 18776,
  "label": "isolated congenital hepatic fibrosis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018840",
  "properties": {
    "xrefs": [
      "GARD:0021995",
      "ICD9:777.8",
      "MEDGEN:40449",
      "MESH:C562378",
      "NANDO:2100267",
      "NANDO:2200936",
      "NCIT:C97071",
      "NORD:1225",
      "Orphanet:485426",
      "SCTID:79607001",
      "UMLS:C0009714"
    ],
    "synonyms": [
      "isolated CHF",
      "Congenital Hepatic Fibrosis",
      "congenital hepatic fibrosis",
      "nonsyndromic congenital hepatic fibrosis",
      "congenital fibrose liver"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "A congenital disorder usually inherited in an autosomal recessive pattern. It affects the hepatobiliary system and the kidneys. It is characterized by liver fibrosis, portal hypertension, and renal cysts."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "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"
    },
    {
      "id": 8725,
      "label": "cirrhosis, familial",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6879,
        23885
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0024551",
          "MEDGEN:350049",
          "MESH:C566123",
          "NCIT:C84411",
          "OMIM:215600",
          "SCTID:6183001",
          "UMLS:C1861556"
        ],
        "synonyms": [
          "cirrhosis, familial",
          "cryptogenic cirrhosis",
          "hereditary cirrhosis of liver",
          "Indian childhood cirrhosis",
          "Sen syndrome",
          "cirrhosis, Noncryptogenic, susceptibility to",
          "cirrhosis, cryptogenic",
          "cirrhosis, familial, with pulmonary hypertension",
          "copper toxicosis, idiopathic",
          "copper-overload cirrhosis",
          "endemic Tyrolean infantile cirrhosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Cirrhosis in which no causative agent can be identified."
      },
      "child_count": 9,
      "reference_id": "MONDO:0007329"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 6624,
      "label": "biliary tract disorder"
    },
    {
      "id": 8725,
      "label": "cirrhosis, familial"
    }
  ]
}