{
  "id": 15462,
  "label": "focal segmental glomerulosclerosis 8",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014462",
  "properties": {
    "xrefs": [
      "DOID:0111133",
      "GARD:0016051",
      "MEDGEN:863430",
      "OMIM:616032",
      "UMLS:C4014993"
    ],
    "synonyms": [
      "ANLN focal segmental glomerulosclerosis",
      "FSGS8",
      "focal segmental glomerulosclerosis 8",
      "focal segmental glomerulosclerosis caused by mutation in ANLN",
      "focal segmental glomerulosclerosis type 8",
      "glomerulosclerosis, focal segmental, 8"
    ],
    "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 ANLN 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"
    }
  ]
}