{
  "id": 18314,
  "label": "idiopathic nephrotic syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018170",
  "properties": {
    "xrefs": [
      "GARD:0021539",
      "MEDGEN:501252",
      "NANDO:1200719",
      "NCIT:C122796",
      "Orphanet:357502",
      "UMLS:C3496337"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Nephrotic syndrome for which no cause has been identified."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 5,
  "parents": [
    {
      "id": 7058,
      "label": "nephrotic syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        4437
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1184",
          "EFO:0004255",
          "GARD:0027721",
          "ICD10CM:N04",
          "ICD10WHO:N04",
          "ICD9:581",
          "ICD9:581.9",
          "MEDGEN:10308",
          "MESH:D009404",
          "NANDO:2100009",
          "NCIT:C34845",
          "SCTID:52254009",
          "UMLS:C0027726",
          "icd11.foundation:1184209951"
        ],
        "synonyms": [
          "nephrotic syndrome",
          "nephrotic syndromes",
          "syndrome, nephrotic",
          "syndromes, nephrotic",
          "nephrosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A collection of symptoms that include severe edema, proteinuria, and hypoalbuminemia; it is indicative of renal dysfunction."
      },
      "child_count": 8,
      "reference_id": "MONDO:0005377"
    },
    {
      "id": 24405,
      "label": "idiopathic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29381
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:548250",
          "UMLS:C0277553"
        ],
        "synonyms": [
          "idiopathic disorder"
        ],
        "definition": "A disease or disorder for which the cause is of uncertain or unknown."
      },
      "child_count": 79,
      "reference_id": "MONDO:0700007"
    }
  ],
  "children": [
    {
      "id": 18921,
      "label": "familial idiopathic steroid-resistant nephrotic syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4449,
        18314,
        23429
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0003946",
          "MEDGEN:902527",
          "Orphanet:656",
          "SCTID:718141008",
          "UMLS:C4273714",
          "icd11.foundation:1385860879"
        ],
        "synonyms": [
          "familial idiopathic nephrotic syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "Familial idiopathic steroid-resistant nephrotic syndrome is characterized by a nephrotic syndrome with often early onset."
      },
      "child_count": 42,
      "reference_id": "MONDO:0019006"
    },
    {
      "id": 18961,
      "label": "idiopathic steroid-sensitive nephrotic syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18314
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016678",
          "Orphanet:69061"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "Steroid-sensitive nephrotic syndrome (SSNS) is a kidney disease defined by selective proteinuria, hypoalbuminaemia and, on renal biopsy, minimal changes without immunoglobulin deposits."
      },
      "child_count": 4,
      "reference_id": "MONDO:0019067"
    },
    {
      "id": 19230,
      "label": "sporadic idiopathic steroid-resistant nephrotic syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18314,
        23429
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025136",
          "MEDGEN:897207",
          "Orphanet:84271",
          "SCTID:717191005",
          "UMLS:C4274017"
        ],
        "synonyms": [
          "sporadic idiopathic nephrosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "Steroid-resistant, sporadic idiopathic nephrotic syndrome, is a heterogeneous entity. Nephrotic syndrome is characterized by marked proteinuria, with reduced plasmatic levels of albumin, and potentially with edema."
      },
      "child_count": 6,
      "reference_id": "MONDO:0019401"
    },
    {
      "id": 22853,
      "label": "idiopathic multidrug-resistant nephrotic syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4449,
        18314
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022287",
          "ICD10CM:N04.8",
          "MEDGEN:1842472",
          "Orphanet:567550",
          "UMLS:C5681293"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0035459"
    },
    {
      "id": 22854,
      "label": "idiopathic steroid-resistant nephrotic syndrome with sensitivity to second-line immunosuppressive therapy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18314
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022288",
          "ICD10CM:N04.8",
          "MEDGEN:1842217",
          "Orphanet:567552",
          "UMLS:C5680133"
        ],
        "synonyms": [
          "idiopathic steroid-resistant nephrotic syndrome with sensitivity to intensified immunosuppression"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0035460"
    }
  ],
  "roots": [
    {
      "id": 7058,
      "label": "nephrotic syndrome"
    },
    {
      "id": 24405,
      "label": "idiopathic disease"
    }
  ]
}