{
  "id": 19835,
  "label": "cerulean cataract",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020374",
  "properties": {
    "xrefs": [
      "GARD:0009508",
      "ICD9:743.39",
      "MEDGEN:138007",
      "MESH:C537955",
      "Orphanet:98989",
      "SCTID:204138006",
      "UMLS:C0344523",
      "icd11.foundation:1188848969"
    ],
    "synonyms": [
      "blue-dot cataract",
      "cataract, congenital, blue dot type 1",
      "cataract, congenital, cerulean type 1"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "Cerulean cataract is a type of hereditary congenital cataract distinguished by bluish and white opacifications in the superficial layers of the fetal lens nucleus and adult lens nucleus and characterized by reduced visual acuity in childhood, eventually necessitating extraction of the lens."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 19837,
      "label": "early-onset partial cataract",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        12186
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016888",
          "MEDGEN:1842758",
          "Orphanet:98992",
          "UMLS:C5681643"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 5,
      "reference_id": "MONDO:0020377"
    }
  ],
  "children": [
    {
      "id": 8681,
      "label": "cataract 7",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19835
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110260",
          "GARD:0015046",
          "OMIM:115660"
        ],
        "synonyms": [
          "CTRCT7",
          "cataract 7",
          "cataract type 7",
          "cataract 7, cerulean type",
          "cataract, congenital, cerulean type, 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 17q24."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007279"
    },
    {
      "id": 14762,
      "label": "cataract 37",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19835
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110252",
          "GARD:0015800",
          "MEDGEN:482388",
          "OMIM:614422",
          "UMLS:C3280758"
        ],
        "synonyms": [
          "CTRCT37",
          "cataract 37",
          "cataract 37, autosomal dominant",
          "cataract type 37",
          "cataract, congenital, cerulean type, 5"
        ],
        "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 12q24.2-q24.3."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013744"
    }
  ],
  "roots": [
    {
      "id": 19837,
      "label": "early-onset partial cataract"
    }
  ]
}