{
  "id": 20936,
  "label": "autosomal dominant non-nuclear cataract",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0022673",
  "properties": {
    "xrefs": [
      "MEDGEN:318648",
      "MESH:C538284",
      "OMIM:601286",
      "UMLS:C1832526"
    ],
    "synonyms": [
      "CCP",
      "PCC",
      "autosomal dominant nonnuclear polymorphic congenital cataract",
      "cataract congenital dominant non nuclear",
      "cataract, Nonnuclear polymorphic congenital, autosomal dominant",
      "cataract, polymorphic congenital"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 20935,
      "label": "autosomal dominant cataract",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        4370,
        6853
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "cataract congenital autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A syndromic cataract that has autosomal dominant inheritance."
      },
      "child_count": 3,
      "reference_id": "MONDO:0022672"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 20935,
      "label": "autosomal dominant cataract"
    }
  ]
}