{
  "id": 13258,
  "label": "autosomal dominant auditory neuropathy 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012196",
  "properties": {
    "xrefs": [
      "DOID:0060690",
      "GARD:0018127",
      "MEDGEN:322984",
      "MESH:C563790",
      "OMIM:609129",
      "UMLS:C1836743"
    ],
    "synonyms": [
      "AUNA1",
      "DIAPH3 auditory neuropathy",
      "NSDAN",
      "auditory neuropathy caused by mutation in DIAPH3",
      "auditory neuropathy, autosomal dominant, type 1",
      "autosomal dominant auditory neuropathy type 1",
      "auditory neuropathy, autosomal dominant, 1",
      "auditory neuropathy, nonsyndromic dominant"
    ],
    "categories": [
      {
        "ref": "MONDO:0002409",
        "name": "auditory system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any auditory neuropathy in which the cause of the disease is a mutation in the DIAPH3 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"
    },
    {
      "id": 20787,
      "label": "auditory neuropathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7048,
        22991,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0009274",
          "MEDGEN:338895",
          "MESH:C538268",
          "NCIT:C116364",
          "OMIMPS:609129",
          "SCTID:443805006",
          "UMLS:C1852271"
        ],
        "synonyms": [
          "ANSD",
          "auditory dys-synchrony",
          "auditory neuropathy",
          "auditory neuropathy spectrum disorder",
          "familial auditory neuropathy",
          "progressive auditory neuropathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002409",
            "name": "auditory system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A hearing disorder characterized by impaired transmission of signals through the auditory nerve, resulting in mild to severe hearing loss and poor speech perception."
      },
      "child_count": 15,
      "reference_id": "MONDO:0021944"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19392,
      "label": "autosomal dominant nonsyndromic hearing loss"
    },
    {
      "id": 20787,
      "label": "auditory neuropathy"
    }
  ]
}