{
  "id": 25654,
  "label": "nephrolithiasis, calcium oxalate",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0957318",
  "properties": {
    "xrefs": [
      "MEDGEN:318935",
      "OMIMPS:167030",
      "UMLS:C1833683"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 9482,
      "label": "nephrolithiasis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6948,
        21555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:585",
          "EFO:0004253",
          "ICD9:592",
          "MEDGEN:98227",
          "MESH:D053040",
          "NCIT:C114667",
          "SCTID:266556005",
          "UMLS:C0392525"
        ],
        "synonyms": [
          "calculus of kidney and ureter",
          "kidney stone",
          "renal calculi",
          "CAON",
          "nephrolithiasis, calcium oxalate",
          "urolithiasis, calcium oxalate"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "The presence of a calculus in the pelvis of the kidney; this is most often composed of mineral salts and proteins."
      },
      "child_count": 6,
      "reference_id": "MONDO:0008171"
    },
    {
      "id": 23932,
      "label": "inherited kidney disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6948
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "genetic renal disease",
          "inherited kidney disease",
          "inherited renal disorder",
          "nephrogenetic disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions, with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology that are characterized by abnormalities in the kidney or urinary system."
      },
      "child_count": 52,
      "reference_id": "MONDO:0100191"
    }
  ],
  "children": [
    {
      "id": 20128,
      "label": "nephrolithiasis susceptibility caused by SLC26A1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20011,
        25654
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080652",
          "MEDGEN:1830325",
          "OMIM:167030",
          "UMLS:C5779632"
        ],
        "synonyms": [
          "CAON",
          "nephrolithiasis, calcium oxalate",
          "urolithiasis, calcium oxalate"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0020722"
    },
    {
      "id": 25865,
      "label": "nephrolithiasis, calcium oxalate, 2, with or without nephrocalcinosis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        25654
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1841152",
          "OMIM:620374",
          "UMLS:C5830516"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0958191"
    }
  ],
  "roots": [
    {
      "id": 9482,
      "label": "nephrolithiasis"
    },
    {
      "id": 23932,
      "label": "inherited kidney disorder"
    }
  ]
}