{
  "id": 12282,
  "label": "autosomal recessive nonsyndromic hearing loss 15",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011160",
  "properties": {
    "xrefs": [
      "DOID:0110470",
      "GARD:0022591",
      "MEDGEN:355626",
      "MESH:C566611",
      "OMIM:601869",
      "UMLS:C1866094"
    ],
    "synonyms": [
      "autosomal recessive nonsyndromic hearing loss 15",
      "DFNB15",
      "DFNB72",
      "DFNB95",
      "GIPC3 autosomal recessive nonsyndromic deafness",
      "autosomal recessive deafness 15",
      "autosomal recessive deafness 72",
      "autosomal recessive deafness 95",
      "autosomal recessive nonsyndromic deafness 15",
      "autosomal recessive nonsyndromic deafness caused by mutation in GIPC3",
      "autosomal recessive nonsyndromic deafness type 15",
      "deafness, autosomal recessive 15",
      "deafness, autosomal recessive 72",
      "deafness, autosomal recessive 95",
      "deafness, autosomal recessive type 15"
    ],
    "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 GIPC3 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"
    }
  ]
}