{
  "id": 12496,
  "label": "focal segmental glomerulosclerosis 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011390",
  "properties": {
    "xrefs": [
      "DOID:0111129",
      "GARD:0015362",
      "MEDGEN:349053",
      "MESH:C565831",
      "OMIM:603965",
      "UMLS:C1858915"
    ],
    "synonyms": [
      "FSGS2",
      "TRPC6 focal segmental glomerulosclerosis",
      "focal segmental glomerulosclerosis 2",
      "focal segmental glomerulosclerosis caused by mutation in TRPC6",
      "focal segmental glomerulosclerosis type 2",
      "glomerulosclerosis, focal segmental, 2"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ],
    "definition": "Any focal segmental glomerulosclerosis in which the cause of the disease is a mutation in the TRPC6 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 7046,
      "label": "inherited focal segmental glomerulosclerosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        23932,
        24049
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0024175",
          "NANDO:1200722",
          "NANDO:2200113",
          "OMIMPS:603278"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "An instance of focal segmental glomerulosclerosis that is caused by an inherited genomic modification in an individual."
      },
      "child_count": 16,
      "reference_id": "MONDO:0005363"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 7046,
      "label": "inherited focal segmental glomerulosclerosis"
    }
  ]
}