{
  "id": 12115,
  "label": "autosomal recessive nonsyndromic hearing loss 8",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010987",
  "properties": {
    "xrefs": [
      "DOID:0110527",
      "GARD:0022589",
      "MEDGEN:322046",
      "OMIM:601072",
      "UMLS:C1832827"
    ],
    "synonyms": [
      "autosomal recessive nonsyndromic hearing loss 8",
      "DFNB10",
      "DFNB8",
      "NRSD8",
      "autosomal recessive deafness 10",
      "autosomal recessive deafness 8",
      "autosomal recessive nonsyndromic deafness 8",
      "autosomal recessive nonsyndromic deafness type 8",
      "childhood-onset neurosensory autosomal recessive deafness 8",
      "deafness, autosomal recessive 10",
      "deafness, autosomal recessive 8",
      "deafness, autosomal recessive 8/10",
      "deafness, autosomal recessive type 8",
      "deafness, childhood-onset neurosensory, autosomal recessive 8",
      "neurosensory nonsyndromic recessive deafness 8"
    ],
    "categories": [
      {
        "ref": "MONDO:0002409",
        "name": "auditory system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "An autosomal recessive nonsyndromic deafness that has material basis in mutation in the TMPRSS3 gene on chromosome 21q22."
  },
  "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"
    }
  ]
}