{
  "id": 10667,
  "label": "hypouricemia, hypercalcinuria, and decreased bone density",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009438",
  "properties": {
    "xrefs": [
      "GARD:0015186",
      "MEDGEN:343419",
      "MESH:C565475",
      "OMIM:242050",
      "UMLS:C1855793"
    ],
    "synonyms": [
      "hypouricemia, hypercalcinuria, and decreased bone density"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 10320,
      "label": "hereditary renal hypouricemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16626
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0009496",
          "ICD9:790.6",
          "MEDGEN:1643078",
          "MESH:C537757",
          "Orphanet:94088",
          "SCTID:236478009",
          "UMLS:C4551590",
          "icd11.foundation:479364233"
        ],
        "synonyms": [
          "Dalmatian hypouricemia",
          "hypouricemia, renal",
          "renal hypouricemia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "Hereditary renal hypouricemia (HRH) is a rare autosomal recessively inherited renal membrane transport disorder affecting urate reabsorption in the proximal tubules leading to usually asymptomatic hypouricemia and predisposing to urolithiasis and exercise induced acute renal failure (EIARF)."
      },
      "child_count": 3,
      "reference_id": "MONDO:0009071"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 10320,
      "label": "hereditary renal hypouricemia"
    }
  ]
}