{
  "id": 13233,
  "label": "autosomal recessive nonsyndromic hearing loss 36",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012170",
  "properties": {
    "xrefs": [
      "DOID:0110494",
      "GARD:0022611",
      "MEDGEN:324662",
      "MESH:C563815",
      "OMIM:609006",
      "UMLS:C1837007"
    ],
    "synonyms": [
      "autosomal recessive nonsyndromic hearing loss 36",
      "deafness, neurosensory, without vestibular involvement, autosomal dominant",
      "DFNB36",
      "ESPN autosomal recessive nonsyndromic deafness",
      "autosomal recessive deafness 36",
      "autosomal recessive nonsyndromic deafness 36",
      "autosomal recessive nonsyndromic deafness caused by mutation in ESPN",
      "autosomal recessive nonsyndromic deafness type 36",
      "deafness, autosomal dominant, without vestibular involvement",
      "deafness, autosomal recessive 36",
      "deafness, autosomal recessive 36, with or without vestibular involvement"
    ],
    "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 ESPN 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"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19393,
      "label": "hearing loss, autosomal recessive"
    }
  ]
}