{
  "id": 21459,
  "label": "aniridia 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0024507",
  "properties": {
    "xrefs": [
      "DOID:0070532",
      "GARD:0025407",
      "MEDGEN:576337",
      "OMIM:106210",
      "SCTID:253231007",
      "UMLS:C0344542"
    ],
    "synonyms": [
      "aniridia",
      "AN1",
      "aniridia 1",
      "cataract with late-onset corneal dystrophy",
      "aniridia II",
      "aniridia II, formerly",
      "cataract, congenital, with late-onset corneal dystrophy"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 8531,
      "label": "isolated aniridia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        19047
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0005816",
          "OMIMPS:106210",
          "Orphanet:250923"
        ],
        "synonyms": [
          "nonsyndromic aniridia",
          "aniridia without systemic involvement"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Isolated aniridia is a congenital bilateral ocular malformation characterized by the complete or partial absence of the iris."
      },
      "child_count": 6,
      "reference_id": "MONDO:0007119"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 8531,
      "label": "isolated aniridia"
    }
  ]
}