{
  "id": 12287,
  "label": "glomerulopathy with fibronectin deposits 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011165",
  "properties": {
    "xrefs": [
      "GARD:0009914",
      "MEDGEN:356149",
      "OMIM:601894",
      "SCTID:722759007",
      "UMLS:C1866075"
    ],
    "synonyms": [
      "FN1 fibronectin glomerulopathy",
      "fibronectin glomerulopathy caused by mutation in FN1",
      "glomerulopathy with fibronectin deposits 2",
      "glomerulopathy with fibronectin deposits type 2",
      "GFND2",
      "fibronectin glomerulopathy",
      "glomerular nephritis familial with fibronectin deposits",
      "glomerular nephritis, familial, with fibronectin deposits"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ],
    "definition": "Any fibronectin glomerulopathy in which the cause of the disease is a mutation in the FN1 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 9029,
      "label": "fibronectin glomerulopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19482,
        23932
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0015019",
          "MEDGEN:854773",
          "MESH:C536826",
          "MESH:C562900",
          "NANDO:2200133",
          "OMIMPS:137950",
          "Orphanet:84090",
          "SCTID:236535001",
          "UMLS:C3888104",
          "icd11.foundation:1877494378"
        ],
        "synonyms": [
          "GFND",
          "fibronectin glomerulopathy",
          "glomerulopathy with fibronectin deposits",
          "GFND1",
          "GFND2",
          "glomerular nephritis, familial, with fibronectin deposits",
          "glomerulopathy with fibronectin deposits 1",
          "glomerulopathy with fibronectin deposits 2",
          "glomerulopathy with giant fibrillar deposits",
          "lobular glomerulopathy, familial"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "A hereditary kidney disease characterized by proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life."
      },
      "child_count": 4,
      "reference_id": "MONDO:0007671"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 9029,
      "label": "fibronectin glomerulopathy"
    }
  ]
}