{
  "id": 14515,
  "label": "cataract 36",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013484",
  "properties": {
    "xrefs": [
      "DOID:0110247",
      "MEDGEN:462654",
      "OMIM:613887",
      "UMLS:C3151304"
    ],
    "synonyms": [
      "CATC4",
      "CTRCT36",
      "TDRD7 cataract (disease)",
      "cataract (disease) caused by mutation in TDRD7",
      "cataract 36",
      "cataract type 36",
      "cataract, autosomal recessive congenital 4"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "Any cataract in which the cause of the disease is a mutation in the TDRD7 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 6853,
      "label": "cataract",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3420,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:83",
          "HP:0000518",
          "ICD9:366",
          "ICD9:366.44",
          "ICD9:366.8",
          "ICD9:366.9",
          "MEDGEN:39462",
          "MESH:D002386",
          "NCIT:C26713",
          "OMIMPS:116200",
          "SCTID:193570009",
          "UMLS:C0086543",
          "icd11.foundation:109841337"
        ],
        "synonyms": [
          "cataract",
          "cataract (disease)",
          "opacity of the lens"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Partial or complete opacity of the crystalline lens of one or both eyes that decreases visual acuity and eventually results in blindness. Some cataracts appear in infancy or in childhood, but most develop in older individuals. (Sternberg Diagnostic Surgical Pathology, 3rd ed.)"
      },
      "child_count": 58,
      "reference_id": "MONDO:0005129"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 6853,
      "label": "cataract"
    }
  ]
}