{
  "id": 12114,
  "label": "autosomal recessive nonsyndromic hearing loss 9",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010986",
  "properties": {
    "xrefs": [
      "DOID:0110535",
      "GARD:0022588",
      "MEDGEN:331376",
      "OMIM:601071",
      "UMLS:C1832828"
    ],
    "synonyms": [
      "autosomal recessive nonsyndromic hearing loss 9",
      "DFNB9",
      "NRSD9",
      "OTOF autosomal recessive nonsyndromic deafness",
      "auditory neuropathy, autosomal recessive, 1",
      "auditory neuropathy, nonsyndromic recessive",
      "autosomal recessive deafness 9",
      "autosomal recessive nonsyndromic deafness 9",
      "autosomal recessive nonsyndromic deafness caused by mutation in OTOF",
      "autosomal recessive nonsyndromic deafness type 9",
      "deafness, autosomal recessive 9",
      "deafness, autosomal recessive type 9",
      "neurosensory nonsyndromic recessive deafness 9"
    ],
    "categories": [
      {
        "ref": "MONDO:0002409",
        "name": "auditory system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the OTOF gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19393,
      "label": "hearing loss, autosomal recessive",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7611,
        19315
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050565",
          "GARD:0018117",
          "MEDGEN:337623",
          "MESH:C564609",
          "OMIM:607197",
          "OMIMPS:220290",
          "Orphanet:90636",
          "UMLS:C1846647"
        ],
        "synonyms": [
          "hearing loss, autosomal recessive",
          "autosomal recessive isolated neurosensory deafness type DFNB",
          "autosomal recessive isolated sensorineural deafness type DFNB",
          "autosomal recessive non-syndromic neurosensory deafness type DFNB",
          "autosomal recessive non-syndromic sensorineural deafness type DFNB",
          "autosomal recessive nonsyndromic deafness",
          "autosomal recessive nonsyndromic genetic deafness",
          "deafness, autosomal recessive",
          "deafness, neurosensory nonsyndromic recessive, DFN",
          "nonsyndromic deafness, autosomal recessive",
          "nonsyndromic genetic deafness, autosomal recessive"
        ],
        "categories": [
          {
            "ref": "MONDO:0002409",
            "name": "auditory system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Autosomal recessive form of nonsyndromic deafness."
      },
      "child_count": 204,
      "reference_id": "MONDO:0019588"
    },
    {
      "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": 19393,
      "label": "hearing loss, autosomal recessive"
    },
    {
      "id": 20787,
      "label": "auditory neuropathy"
    }
  ]
}