{
  "id": 13319,
  "label": "cataract 35",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012260",
  "properties": {
    "xrefs": [
      "DOID:0110261",
      "GARD:0009492",
      "MEDGEN:373050",
      "MESH:C563728",
      "OMIM:609376",
      "UMLS:C1836272"
    ],
    "synonyms": [
      "CATCN1",
      "CTRCT35",
      "cataract 35",
      "cataract type 35",
      "cataract, congenital nuclear, autosomal recessive 1"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "A cataract that has material basis in variation in the region 19q13."
  },
  "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"
    }
  ]
}