{
  "id": 8689,
  "label": "cataract 41",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007287",
  "properties": {
    "xrefs": [
      "DOID:0110241",
      "GARD:0018234",
      "MEDGEN:811742",
      "OMIM:116400",
      "UMLS:C3805412"
    ],
    "synonyms": [
      "CTRCT41",
      "WFS1 early-onset non-syndromic cataract",
      "cataract 41",
      "cataract type 41",
      "early-onset non-syndromic cataract caused by mutation in WFS1",
      "cataract 41, congenital nuclear type"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "Any early-onset non-syndromic cataract in which the cause of the disease is a mutation in the WFS1 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19836,
      "label": "early-onset nuclear cataract",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19839
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016887",
          "MEDGEN:1842550",
          "MESH:C563333",
          "MedDRA:10007759",
          "MedDRA:10057735",
          "Orphanet:98991",
          "UMLS:C5681644"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 4,
      "reference_id": "MONDO:0020376"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19836,
      "label": "early-onset nuclear cataract"
    }
  ]
}