{
  "id": 9029,
  "label": "fibronectin glomerulopathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007671",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 19482,
      "label": "glomerular disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6948
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:1002049",
          "GTR:AN0966176",
          "ICD10CM:N00-N08",
          "MEDGEN:451033",
          "NCIT:C120887",
          "Orphanet:93548",
          "SCTID:197679002",
          "UMLS:C0268731"
        ],
        "synonyms": [
          "disease of renal glomerulus",
          "disease or disorder of renal glomerulus",
          "disorder of renal glomerulus",
          "glomerulopathy",
          "renal glomerulus disease",
          "renal glomerulus disease or disorder",
          "glomerulopathies"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "A disease involving the renal glomerulus."
      },
      "child_count": 6,
      "reference_id": "MONDO:0019722"
    },
    {
      "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": 12287,
      "label": "glomerulopathy with fibronectin deposits 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9029
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011165"
    },
    {
      "id": 21473,
      "label": "glomerulopathy with fibronectin deposits 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9029
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0009268",
          "MEDGEN:98017",
          "OMIM:137950",
          "UMLS:C0403557"
        ],
        "synonyms": [
          "GFND1",
          "glomerulopathy with fibronectin deposits 1",
          "glomerulopathy with giant fibrillar deposits",
          "lobular glomerulopathy, familial"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0024527"
    }
  ],
  "roots": [
    {
      "id": 19482,
      "label": "glomerular disorder"
    },
    {
      "id": 23932,
      "label": "inherited kidney disorder"
    }
  ]
}