{
  "id": 25823,
  "label": "digenic Alport syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0958104",
  "properties": {
    "xrefs": [
      "GARD:0026932",
      "MEDGEN:1863937",
      "Orphanet:653722",
      "UMLS:C5925113"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18887,
      "label": "Alport syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        7021
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:10983",
          "GARD:0005785",
          "ICD10CM:Q87.81",
          "MEDGEN:339209",
          "MedDRA:10001843",
          "NANDO:1200712",
          "NANDO:2200126",
          "NCIT:C34842",
          "NORD:756",
          "OMIMPS:301050",
          "Orphanet:63",
          "UMLS:C1567741",
          "icd11.foundation:1170919425"
        ],
        "synonyms": [
          "hereditary nephritis",
          "Alport deafness-nephropathy",
          "Alport syndrome",
          "Alport's syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A rare renal disease characterized by glomerular nephropathy with hematuria progressing to end-stage renal disease (ESRD), frequently associated with sensorineural deafness, and occasionally with ocular anomalies."
      },
      "child_count": 10,
      "reference_id": "MONDO:0018965"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18887,
      "label": "Alport syndrome"
    }
  ]
}