{
  "id": 13114,
  "label": "congenital corneal opacities, cornea guttata, and corectopia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012046",
  "properties": {
    "xrefs": [
      "GARD:0024838",
      "MEDGEN:324911",
      "MESH:C563921",
      "OMIM:608484",
      "UMLS:C1837970"
    ],
    "synonyms": [
      "congenital corneal opacities, cornea guttata, and corectopia",
      "corneal opacities, congenital, with cornea guttata and corectopia"
    ],
    "categories": [
      {
        "ref": "MONDO:0002409",
        "name": "auditory system disorder"
      },
      {
        "ref": "MONDO:0024623",
        "name": "otorhinolaryngologic disease"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 7034,
      "label": "otosclerosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4547,
        18718,
        22991
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12185",
          "EFO:0004213",
          "GARD:0027719",
          "HP:0000362",
          "ICD10CM:H80",
          "ICD10WHO:H80",
          "ICD9:387",
          "ICD9:387.8",
          "ICD9:387.9",
          "MEDGEN:10508",
          "MESH:D010040",
          "NCIT:C185242",
          "OMIMPS:166800",
          "Orphanet:2794",
          "SCTID:11543004",
          "UMLS:C0029899",
          "icd11.foundation:1242649410"
        ],
        "synonyms": [
          "otosclerosis",
          "otosclerosis (disease)"
        ],
        "categories": [
          {
            "ref": "MONDO:0002409",
            "name": "auditory system disorder"
          },
          {
            "ref": "MONDO:0024623",
            "name": "otorhinolaryngologic disease"
          }
        ],
        "definition": "Formation of spongy bone in the labyrinth capsule which can progress toward the stapes (stapedial fixation) or anteriorly toward the cochlea leading to conductive, sensorineural, or mixed hearing loss. Several genes are associated with familial otosclerosis with varied clinical signs."
      },
      "child_count": 33,
      "reference_id": "MONDO:0005349"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 7034,
      "label": "otosclerosis"
    }
  ]
}