{
  "id": 25642,
  "label": "auditory neuropathy, autosomal dominant 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0957279",
  "properties": {
    "xrefs": [
      "GARD:0026809",
      "MEDGEN:1841178",
      "OMIM:620384",
      "UMLS:C5830542"
    ],
    "categories": [
      {
        "ref": "MONDO:0002409",
        "name": "auditory system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "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": 20787,
      "label": "auditory neuropathy"
    }
  ]
}