{
  "id": 20935,
  "label": "autosomal dominant cataract",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0022672",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 2903,
      "label": "autosomal dominant disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2905
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050736",
          "ICD9:758.5",
          "MEDGEN:539206",
          "SCTID:11164009",
          "UMLS:C0265385"
        ],
        "synonyms": [
          "autosomal dominant disease or disorder",
          "autosomal dominant hereditary disorder",
          "autosomal dominant inherited disorder",
          "disease or disorder, autosomal dominant",
          "disease, autosomal dominant"
        ],
        "definition": "Autosomal dominant form of disease."
      },
      "child_count": 192,
      "reference_id": "MONDO:0000426"
    },
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    },
    {
      "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": [
    {
      "id": 20936,
      "label": "autosomal dominant non-nuclear cataract",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20935
      ],
      "type_id": 0,
      "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"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0022673"
    }
  ],
  "roots": [
    {
      "id": 2903,
      "label": "autosomal dominant disease"
    },
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 6853,
      "label": "cataract"
    }
  ]
}