{
  "id": 13157,
  "label": "autosomal recessive nonsyndromic hearing loss 32",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012091",
  "properties": {
    "xrefs": [
      "DOID:0110466",
      "DOID:0110491",
      "GARD:0022610",
      "MEDGEN:373370",
      "MESH:C563884",
      "OMIM:608653",
      "UMLS:C1837608"
    ],
    "synonyms": [
      "CDC14A autosomal recessive nonsyndromic deafness",
      "DFNB105",
      "DFNB32",
      "autosomal recessive deafness 105",
      "autosomal recessive deafness 32",
      "autosomal recessive nonsyndromic deafness 105",
      "autosomal recessive nonsyndromic deafness 32",
      "autosomal recessive nonsyndromic deafness caused by mutation in CDC14A",
      "autosomal recessive nonsyndromic deafness type 105",
      "autosomal recessive nonsyndromic deafness type 32",
      "deafness, autosomal recessive 105",
      "deafness, autosomal recessive 32",
      "deafness, autosomal recessive 32, with or without immotile sperm",
      "deafness, autosomal recessive type 105"
    ],
    "categories": [
      {
        "ref": "MONDO:0002409",
        "name": "auditory system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in variation in the chromosome region 1p22.1-p13.3."
  },
  "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"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19393,
      "label": "hearing loss, autosomal recessive"
    }
  ]
}