{
  "id": 14806,
  "label": "Usher syndrome type 3B",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013788",
  "properties": {
    "xrefs": [
      "DOID:0110842",
      "GARD:0015813",
      "MEDGEN:482696",
      "OMIM:614504",
      "UMLS:C3281066"
    ],
    "synonyms": [
      "HARS Usher syndrome",
      "USH3B",
      "Usher syndrome caused by mutation in HARS",
      "USHER syndrome, type IIIB",
      "Usher syndrome, type 3B"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Any Usher syndrome in which the cause of the disease is a mutation in the HARS gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16995,
      "label": "Usher syndrome type 3",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19319
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110828",
          "GARD:0005442",
          "MEDGEN:339336",
          "NANDO:1200944",
          "NCIT:C126329",
          "Orphanet:231183",
          "UMLS:C1568248",
          "icd11.foundation:1734357568"
        ],
        "synonyms": [
          "USH3",
          "Usher syndrome type 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A syndrome characterized by postlingual progressive hearing loss, abnormalities in the vestibular system, and onset of retinitis pigmentosa symptoms usually by the second decade of life."
      },
      "child_count": 2,
      "reference_id": "MONDO:0016485"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16995,
      "label": "Usher syndrome type 3"
    }
  ]
}