{
  "id": 10937,
  "label": "nail-patella-like renal disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009724",
  "properties": {
    "xrefs": [
      "GARD:0000321",
      "ICD9:756.89",
      "MEDGEN:140789",
      "MESH:C537228",
      "OMIM:256020",
      "Orphanet:2613",
      "SCTID:236527004",
      "UMLS:C0403548"
    ],
    "synonyms": [
      "Salcedo syndrome",
      "focal segmental glomerulosclerosis 10",
      "nail-patella-like renal disease",
      "glomerular basement Membrane disease, nail-patella syndrome type",
      "nail patella like renal disease"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ],
    "definition": "A severe nephropathy characterized by renal dysfunction, proteinuria, edema and microscopic haematuria. It has been described in three brothers, two of which died from end-stage renal insufficiency."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "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": [],
  "roots": [
    {
      "id": 23932,
      "label": "inherited kidney disorder"
    }
  ]
}