{
  "id": 13972,
  "label": "myopia 16, autosomal dominant",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012932",
  "properties": {
    "xrefs": [
      "MEDGEN:390819",
      "MESH:C567259",
      "OMIM:612554",
      "UMLS:C2675523"
    ],
    "synonyms": [
      "MYP16",
      "myopia 16",
      "myopia 16, autosomal dominant"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3606,
      "label": "myopia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6646,
        24305
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11830",
          "HP:0000545",
          "ICD10CM:H52.1",
          "ICD9:367.1",
          "MEDGEN:44558",
          "MESH:D009216",
          "OMIMPS:160700",
          "SCTID:57190000",
          "UMLS:C0027092",
          "icd11.foundation:1666440799"
        ],
        "synonyms": [
          "myopia",
          "myopia (disease)",
          "near-sightedness"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "The condition in which the individual does not see far distances clearly."
      },
      "child_count": 90,
      "reference_id": "MONDO:0001384"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3606,
      "label": "myopia"
    }
  ]
}