{
  "id": 12460,
  "label": "autosomal dominant nonsyndromic hearing loss 17",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011350",
  "properties": {
    "xrefs": [
      "DOID:0110548",
      "GARD:0009726",
      "MEDGEN:350942",
      "OMIM:603622",
      "UMLS:C1863659"
    ],
    "synonyms": [
      "DFNA17",
      "MYH9 autosomal dominant nonsyndromic deafness",
      "autosomal dominant deafness 17",
      "autosomal dominant nonsyndromic deafness 17",
      "autosomal dominant nonsyndromic deafness caused by mutation in MYH9",
      "autosomal dominant nonsyndromic deafness type 17",
      "deafness, autosomal dominant 17",
      "deafness, autosomal dominant nonsyndromic sensorineural 17",
      "deafness, autosomal dominant type 17",
      "nonsyndromic hereditary deafness DFNA17",
      "cochleosaccular degeneration",
      "late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration"
    ],
    "categories": [
      {
        "ref": "MONDO:0002409",
        "name": "auditory system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MYH9 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19392,
      "label": "autosomal dominant nonsyndromic hearing loss",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        19315
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050564",
          "GARD:0016791",
          "MEDGEN:1843285",
          "OMIMPS:124900",
          "Orphanet:90635",
          "UMLS:C5779548"
        ],
        "synonyms": [
          "autosomal dominant deafness",
          "autosomal dominant isolated neurosensory hearing loss type DFNA",
          "autosomal dominant isolated sensorineural hearing loss type DFNA",
          "autosomal dominant non-syndromic neurosensory hearing loss type DFNA",
          "autosomal dominant non-syndromic sensorineural hearing loss type DFNA",
          "autosomal dominant nonsyndromic hearing impairment",
          "autosomal dominant nonsyndromic hearing loss",
          "autosomal dominant isolated deafness",
          "autosomal dominant isolated neurosensory deafness type DFNA",
          "autosomal dominant isolated sensorineural deafness type DFNA",
          "autosomal dominant non-syndromic neurosensory deafness type DFNA",
          "autosomal dominant non-syndromic sensorineural deafness type DFNA",
          "autosomal dominant nonsyndromic deafness",
          "autosomal dominant nonsyndromic genetic deafness",
          "autosomal dominant nonsyndromic hearing loss and deafness",
          "deafness, autosomal dominant",
          "nonsyndromic deafness, autosomal dominant",
          "nonsyndromic genetic deafness, autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0002409",
            "name": "auditory system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Autosomal dominant form of nonsyndromic deafness."
      },
      "child_count": 150,
      "reference_id": "MONDO:0019587"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19392,
      "label": "autosomal dominant nonsyndromic hearing loss"
    }
  ]
}