{
  "id": 19818,
  "label": "coloboma of iris",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020356",
  "properties": {
    "xrefs": [
      "GARD:0001434",
      "HP:0000612",
      "ICD10CM:Q13.0",
      "MEDGEN:116097",
      "MedDRA:10052642",
      "NCIT:C98879",
      "Orphanet:98944",
      "SCTID:9446007",
      "UMLS:C0240063",
      "icd11.foundation:1552972259"
    ],
    "synonyms": [
      "coloboma of iris",
      "coloboma of iris (disease)",
      "coloboma of the iris"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "A congenital or acquired defect characterized by the presence of a hole in or adjacent to the iris."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 8743,
      "label": "coloboma, ocular, autosomal dominant",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3690,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1859952",
          "OMIM:120200",
          "UMLS:C5886785"
        ],
        "synonyms": [
          "coloboma, ocular",
          "coloboma, ocular, autosomal dominant",
          "coloboma of iris, choroid, and retina",
          "coloboma, Uveoretinal"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 4,
      "reference_id": "MONDO:0007350"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 8743,
      "label": "coloboma, ocular, autosomal dominant"
    }
  ]
}