{
  "id": 10320,
  "label": "hereditary renal hypouricemia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009071",
  "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)."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 16626,
      "label": "inherited renal tubular disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        20667,
        23932
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020306",
          "MEDGEN:1826140",
          "Orphanet:183592",
          "UMLS:C5680544"
        ],
        "synonyms": [
          "genetic renal tubular disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ]
      },
      "child_count": 56,
      "reference_id": "MONDO:0015962"
    }
  ],
  "children": [
    {
      "id": 10667,
      "label": "hypouricemia, hypercalcinuria, and decreased bone density",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10320
      ],
      "type_id": 0,
      "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"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0009438"
    },
    {
      "id": 11767,
      "label": "hypouricemia, familial renal, due to tubular hypersecretion",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0015296",
          "MEDGEN:334869",
          "MESH:C564405",
          "OMIM:307830",
          "UMLS:C1843972"
        ],
        "synonyms": [
          "hypouricemia, familial renal, due to tubular hypersecretion"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010620"
    },
    {
      "id": 25960,
      "label": "hypouricemia, renal",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        10320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027035",
          "OMIMPS:220150"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0968951"
    }
  ],
  "roots": [
    {
      "id": 16626,
      "label": "inherited renal tubular disease"
    }
  ]
}