{
  "id": 19922,
  "label": "isolated congenital ectropion",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020463",
  "properties": {
    "xrefs": [
      "GARD:0019673",
      "MEDGEN:1842688",
      "Orphanet:99171",
      "UMLS:C5681630"
    ],
    "synonyms": [
      "nonsyndromic congenital ectropion"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "A congenital ectropion that is not part of a larger syndrome."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19756,
      "label": "congenital ectropion",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4190
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019502",
          "ICD10CM:Q10.1",
          "MEDGEN:540010",
          "Orphanet:98570",
          "SCTID:26590002",
          "UMLS:C0266578",
          "icd11.foundation:945558601"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 3,
      "reference_id": "MONDO:0020161"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19756,
      "label": "congenital ectropion"
    }
  ]
}