{
  "id": 15577,
  "label": "Senior-Loken syndrome 8",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014579",
  "properties": {
    "xrefs": [
      "GARD:0016081",
      "MEDGEN:905171",
      "OMIM:616307",
      "UMLS:C4225376"
    ],
    "synonyms": [
      "Senior-Loken syndrome 8",
      "Senior-Loken syndrome caused by mutation in WDR19",
      "Senior-Loken syndrome type 8",
      "WDR19 Senior-Loken syndrome",
      "SENIOR-Loken syndrome 8",
      "SLSN8"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ],
    "definition": "Any Senior-Loken syndrome in which the cause of the disease is a mutation in the WDR19 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18059,
      "label": "Senior-Loken syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7000,
        7611,
        16626
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050576",
          "GARD:0000322",
          "MEDGEN:96045",
          "MESH:C537580",
          "NANDO:1201049",
          "NCIT:C168588",
          "OMIMPS:266900",
          "Orphanet:3156",
          "UMLS:C0403553",
          "icd11.foundation:1975732692"
        ],
        "synonyms": [
          "SLSN",
          "nephronophthisis with retinal dystrophy",
          "renal dysplasia-retinal aplasia syndrome",
          "Senior Loken syndrome",
          "renal dysplasia retinal aplasia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "Senior-Loken syndrome (SLSN) is a very rare autosomal recessive oculo-renal disease characterized by the association of nephronophthisis (NPHP), a chronic kidney disease, with retinal dystrophy."
      },
      "child_count": 27,
      "reference_id": "MONDO:0017842"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18059,
      "label": "Senior-Loken syndrome"
    }
  ]
}