{
  "id": 19419,
  "label": "sclerocornea",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0019629",
  "properties": {
    "xrefs": [
      "DOID:0060252",
      "GARD:0016800",
      "HP:0000647",
      "MEDGEN:344000",
      "MESH:C565209",
      "Orphanet:91490",
      "UMLS:C1853235",
      "icd11.foundation:995798428"
    ],
    "synonyms": [
      "isolated congenital sclerocornea",
      "sclerocornea",
      "sclerocornea (disease)"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "A corneal disease in which the cornea blends with sclera, resulting in clouding of the cornea."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 3211,
      "label": "corneal disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7019
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:10124",
          "EFO:0009464",
          "ICD9:371.30",
          "ICD9:371.89",
          "ICD9:371.9",
          "MEDGEN:3617",
          "MESH:D003316",
          "NCIT:C26731",
          "SCTID:15250008",
          "UMLS:C0010034",
          "icd11.foundation:980864631"
        ],
        "synonyms": [
          "cornea disease",
          "cornea disease or disorder",
          "corneal disease",
          "corneal disorder",
          "disease of cornea",
          "disease or disorder of cornea",
          "disorder of cornea"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A non-neoplastic or neoplastic disorder that affects the cornea. Representative examples include keratitis, bullous keratopathy, and squamous cell carcinoma."
      },
      "child_count": 24,
      "reference_id": "MONDO:0000942"
    }
  ],
  "children": [
    {
      "id": 9712,
      "label": "sclerocornea, autosomal dominant",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19419
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0024619",
          "MEDGEN:356662",
          "MESH:C566692",
          "OMIM:181700",
          "UMLS:C1866984"
        ],
        "synonyms": [
          "sclerocornea, autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0008417"
    },
    {
      "id": 11209,
      "label": "anterior segment dysgenesis 7",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19321,
        19419
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080612",
          "GARD:0017327",
          "MEDGEN:462967",
          "OMIM:269400",
          "Orphanet:289499",
          "UMLS:C3151617"
        ],
        "synonyms": [
          "CCMCO",
          "PXDN anterior segment dysgenesis",
          "PXDN-related ocular dysgenesis",
          "anterior segment dysgenesis 7",
          "anterior segment dysgenesis 7, with sclerocornea",
          "anterior segment dysgenesis caused by mutation in PXDN",
          "sclerocornea with other ocular anomalies",
          "ASGD7",
          "COPOA",
          "congenital cataract microcornea with corneal opacity",
          "corneal opacification and other ocular anomalies",
          "corneal opacification with Other ocular anomalies",
          "corneal opacification with other ocular anomalies",
          "sclerocornea with Other ocular anomalies"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Any anterior segment dysgenesis in which the cause of the disease is a mutation in the PXDN gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010015"
    }
  ],
  "roots": [
    {
      "id": 3211,
      "label": "corneal disorder"
    }
  ]
}