{
  "id": 11403,
  "label": "Dent disease type 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010225",
  "properties": {
    "xrefs": [
      "DOID:0081453",
      "GARD:0001804",
      "MEDGEN:336322",
      "OMIM:300009",
      "Orphanet:93622",
      "SCTID:717789008",
      "UMLS:C1848336",
      "icd11.foundation:1984074789"
    ],
    "synonyms": [
      "CLCN5 Dent disease",
      "Dent disease caused by mutation in CLCN5",
      "Dent disease type 1",
      "dent disease 1, X-linked recessive",
      "nephrolithiasis type 1",
      "DENT disease 1",
      "nephrolithiasis 2",
      "nephrolithiasis, hypercalciuric, X-linked",
      "urolithiasis, hypercalciuric, X-linked"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ],
    "definition": "Dent disease type 1 is a type of Dent disease with predominantly renal manifestations."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16406,
      "label": "Dent disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        8001,
        16626
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050699",
          "GARD:0013105",
          "MEDGEN:168056",
          "MESH:D057973",
          "MedDRA:10069199",
          "NCIT:C123260",
          "NORD:1040",
          "OMIMPS:300009",
          "Orphanet:1652",
          "SCTID:444645005",
          "UMLS:C0878681",
          "icd11.foundation:1762998355"
        ],
        "synonyms": [
          "Dent syndrome",
          "X-linked recessive hypercalciuric hypophosphatemic rickets",
          "X-linked recessive hypophosphatemic rickets",
          "X-linked recessive nephrolithiasis",
          "low-molecular-weight proteinuria with hypercalciuria and nephrocalcinosis",
          "renal Fanconi syndrome with nephrocalcinosis and renal stones",
          "Dent disease 1",
          "Dent disease 2",
          "Dents disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "Dent disease is a rare genetic renal tubular disease characterized by manifestations of proximal tubule dysfunction."
      },
      "child_count": 4,
      "reference_id": "MONDO:0015612"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16406,
      "label": "Dent disease"
    }
  ]
}