{
  "id": 3211,
  "label": "corneal disorder",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0000942",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 24,
  "parents": [
    {
      "id": 7019,
      "label": "eye disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4171,
        21415
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1242",
          "DOID:5614",
          "EFO:0003966",
          "ICD9:360",
          "ICD9:360.29",
          "ICD9:360.89",
          "ICD9:360.9",
          "ICD9:379.8",
          "ICD9:379.90",
          "MEDGEN:5092",
          "MESH:D005128",
          "NCIT:C26767",
          "SCTID:371405004",
          "UMLS:C0015397"
        ],
        "synonyms": [
          "disease of eye",
          "disease of eyeball of camera-type eye",
          "disease or disorder of eyeball of camera-type eye",
          "disorder of eye",
          "disorder of eyeball of camera-type eye",
          "eye disease",
          "eye disorder",
          "eyeball of camera-type eye disease",
          "eyeball of camera-type eye disease or disorder",
          "globe disease",
          "disease of eyeball",
          "disorder of eye proper",
          "disorder of eyeball",
          "disorder of globe"
        ],
        "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 eye. Representative examples include conjunctivitis, glaucoma, cataract, conjunctival squamous cell carcinoma, uveal melanoma, and retinoblastoma."
      },
      "child_count": 240,
      "reference_id": "MONDO:0005328"
    }
  ],
  "children": [
    {
      "id": 3110,
      "label": "cornea plana",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3211,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060287",
          "GARD:0016657",
          "HP:0007720",
          "ICD10CM:Q13.4",
          "MEDGEN:576329",
          "OMIMPS:121400",
          "Orphanet:53691",
          "SCTID:204145006",
          "UMLS:C0344529",
          "icd11.foundation:262157734"
        ],
        "synonyms": [
          "congenital cornea plana",
          "flat cornea"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A rare developmental defect of the eye characterized by usually bilateral absence of the normal protrusion of the cornea from the sclera, the corneal curvature being the same as that of the adjacent sclera. Most patients develop hyperopia, hazy corneal limbus, and arcus lipoides at an early age. The condition may present as an autosomal dominant or an autosomal recessive form, with the latter showing more severe signs and symptoms (such as a round and opaque thickening located centrally in the cornea) and more frequent association with other ocular anomalies."
      },
      "child_count": 4,
      "reference_id": "MONDO:0000733"
    },
    {
      "id": 3422,
      "label": "pseudopterygium",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3211,
        3218
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11028",
          "ICD9:372.52",
          "MEDGEN:509821",
          "SCTID:66139007",
          "UMLS:C0155161",
          "icd11.foundation:1195759310"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0001178"
    },
    {
      "id": 3540,
      "label": "corneal deposit",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3211
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11547",
          "ICD10CM:H18.0",
          "ICD9:371.10",
          "MEDGEN:511537",
          "SCTID:74460005",
          "UMLS:C0162281",
          "icd11.foundation:1760427912"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 3,
      "reference_id": "MONDO:0001308"
    },
    {
      "id": 3542,
      "label": "Bowman's membrane folds or rupture",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3211
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11552",
          "ICD9:371.31",
          "MEDGEN:509796",
          "SCTID:45382000",
          "UMLS:C0155115"
        ],
        "synonyms": [
          "folds and/or rupture of bowman's membrane"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0001310"
    },
    {
      "id": 3723,
      "label": "corneal degeneration",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3211
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1237",
          "ICD10CM:H18.4",
          "ICD9:371.4",
          "ICD9:371.40",
          "ICD9:371.49",
          "MEDGEN:56352",
          "SCTID:111521006",
          "UMLS:C0155118",
          "icd11.foundation:699504167"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 5,
      "reference_id": "MONDO:0001515"
    },
    {
      "id": 3781,
      "label": "corneal staphyloma",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3211
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12753",
          "ICD10CM:H18.72",
          "ICD9:371.73",
          "MEDGEN:509034",
          "SCTID:52476003",
          "UMLS:C0152440",
          "icd11.foundation:212928655"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0001579"
    },
    {
      "id": 3904,
      "label": "corneal argyrosis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3211
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13447",
          "ICD10CM:H18.02",
          "ICD9:371.16",
          "MEDGEN:509793",
          "SCTID:21328003",
          "UMLS:C0155108"
        ],
        "synonyms": [
          "argentous corneal deposits"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0001716"
    },
    {
      "id": 4117,
      "label": "corneal ectasia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3211
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1436",
          "ICD10CM:H18.71",
          "ICD9:371.71",
          "MEDGEN:509803",
          "SCTID:14748007",
          "UMLS:C0155135",
          "icd11.foundation:1703179358"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0001950"
    },
    {
      "id": 4377,
      "label": "keratopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3211
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2283",
          "MEDGEN:68615",
          "NCIT:C27012",
          "UMLS:C0235270"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Any disorder of the cornea."
      },
      "child_count": 2,
      "reference_id": "MONDO:0002261"
    },
    {
      "id": 5071,
      "label": "keratitis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3211,
        20399
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:4677",
          "EFO:0009449",
          "ICD10CM:H16",
          "ICD10WHO:H16",
          "ICD9:370",
          "ICD9:370.8",
          "ICD9:370.9",
          "MEDGEN:44013",
          "MESH:D007634",
          "NCIT:C26805",
          "SCTID:5888003",
          "UMLS:C0022568"
        ],
        "synonyms": [
          "cornea inflammation",
          "inflammation of cornea"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A corneal disease that is characterized by inflammation of the cornea."
      },
      "child_count": 22,
      "reference_id": "MONDO:0003085"
    },
    {
      "id": 8173,
      "label": "corneal edema",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3211
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11030",
          "EFO:1000879",
          "ICD9:371.2",
          "ICD9:371.20",
          "MEDGEN:3242",
          "MESH:D015715",
          "MedDRA:10011007",
          "SCTID:27194006",
          "UMLS:C0010037"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Hazy, swollen cornea."
      },
      "child_count": 4,
      "reference_id": "MONDO:0006712"
    },
    {
      "id": 10485,
      "label": "brittle cornea syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3211,
        7611,
        19720,
        21247
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:14775",
          "GARD:0001019",
          "OMIMPS:229200",
          "Orphanet:90354",
          "SCTID:719096006"
        ],
        "synonyms": [
          "brittle cornea syndrome",
          "brittle cornea syndrome type 1",
          "kyphoscoliosis type",
          "brittle cornea syndrome 2",
          "BCS1",
          "EDS VIB (formerly)",
          "Ehlers-Danlos syndrome type 6B (formerly)",
          "Ehlers-Danlos syndrome type 6b",
          "brittle cornea syndrome 1"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Brittle cornea syndrome is a form of Ehlers-Danlos syndrome characterized by a severe ocular manifestations due to extreme corneal thinning and fragility with rupture in the absence of significant trauma, and progression to blindness. Extraocular manifestations comprise deafness, developmental hip dysplasia, and joint hypermobility."
      },
      "child_count": 8,
      "reference_id": "MONDO:0009242"
    },
    {
      "id": 10797,
      "label": "megalocornea",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3211,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060305",
          "HP:0000485",
          "HP:0007660",
          "MEDGEN:1807965",
          "MESH:C562829",
          "OMIM:249300",
          "SCTID:268158009",
          "UMLS:C5574682",
          "icd11.foundation:58849242"
        ],
        "synonyms": [
          "megalocornea",
          "megalocornea (disease)"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0009576"
    },
    {
      "id": 11733,
      "label": "X-linked corneal dermoid",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3211,
        4370
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0002580",
          "MEDGEN:375481",
          "MESH:C535376",
          "OMIM:304730",
          "Orphanet:1661",
          "SCTID:715426004",
          "UMLS:C1844671",
          "icd11.foundation:118076382"
        ],
        "synonyms": [
          "Guízar Vázquez-Luengas-muñoz syndrome",
          "corneal dystrophy epithelial-short stature syndrome",
          "CND",
          "Guizar-Vazquez Luengas-Munoz syndrome",
          "bilateral corneal dermoids",
          "corneal dermoids and short stature",
          "dermoids of cornea"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "X-linked corneal dermoid (X-CND) is an exceedingly rare, benign, congenital, corneal tumor characterized by bilateral opacification of the cornea with superficial grayish layers and irregular raised whitish plaques, as well as fine blood vessels covering the central cornea, and intact peripheral corneal borders.No other ocular or systemic abnormality is noted. The pattern of inheritance described in the affected family is consistent with X-linked transmission."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010579"
    },
    {
      "id": 12519,
      "label": "Peters anomaly",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3211,
        19321
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060673",
          "DOID:0080610",
          "GARD:0007377",
          "HP:0000659",
          "ICD9:743.44",
          "MEDGEN:91031",
          "MESH:C537884",
          "MedDRA:10059202",
          "OMIM:604229",
          "Orphanet:708",
          "SCTID:204153003",
          "UMLS:C0344559",
          "icd11.foundation:1902926622"
        ],
        "synonyms": [
          "Peters anomaly",
          "Peters anomaly (disease)",
          "Peters congenital glaucoma",
          "anterior segment dysgenesis 5, multiple subtypes",
          "ASGD5",
          "anterior segment dysgenesis 5"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Peters anomaly (PA) is a congenital corneal opacity disorder characterized by a central corneal leukoma that obstructs the pupil leading to visual loss as well as absence of the posterior corneal stroma and Descemet membrane."
      },
      "child_count": 4,
      "reference_id": "MONDO:0011414"
    },
    {
      "id": 16178,
      "label": "pellucid marginal degeneration",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3211
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0011895",
          "MEDGEN:573069",
          "Orphanet:137672",
          "UMLS:C0339288",
          "icd11.foundation:1662005062"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0015298"
    },
    {
      "id": 16321,
      "label": "keratoconus",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3211,
        5714,
        24305
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:10126",
          "HP:0000563",
          "ICD10CM:H18.6",
          "ICD9:371.6",
          "ICD9:371.60",
          "MEDGEN:44015",
          "MESH:D007640",
          "MedDRA:10023353",
          "NCIT:C26806",
          "OMIMPS:148300",
          "Orphanet:156071",
          "Orphanet:2335",
          "SCTID:65636009",
          "UMLS:C0022578",
          "icd11.foundation:945228622"
        ],
        "synonyms": [
          "keratoconus",
          "keratoconus (disease)",
          "isolated keratoconus",
          "KC",
          "noninflammatory corneal thining"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A degenerative, structural disorder of the eye, characterized by a cone-shaped protrusion of the cornea. It may lead to visual disturbances."
      },
      "child_count": 33,
      "reference_id": "MONDO:0015486"
    },
    {
      "id": 18261,
      "label": "corneal dystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3211
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2566",
          "GARD:0027867",
          "HP:0001131",
          "ICD9:371.5",
          "ICD9:371.50",
          "MEDGEN:3619",
          "MESH:D003317",
          "MedDRA:10011005",
          "NCIT:C34513",
          "Orphanet:34533",
          "SCTID:5587004",
          "UMLS:C0010036",
          "icd11.foundation:1291475891"
        ],
        "synonyms": [
          "corneal dystrophy",
          "corneal dystrophy (disease)"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "The term corneal dystrophy embraces a heterogeneous group of bilateral genetically determined non-inflammatory corneal diseases that are usually restricted to the cornea. The designation is imprecise but remains in vogue because of its clinical value."
      },
      "child_count": 13,
      "reference_id": "MONDO:0018102"
    },
    {
      "id": 19419,
      "label": "sclerocornea",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3211
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 2,
      "reference_id": "MONDO:0019629"
    },
    {
      "id": 20447,
      "label": "cornea neoplasm",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3211,
        20431
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:90940",
          "NCIT:C4361",
          "UMLS:C0339304"
        ],
        "synonyms": [
          "cornea neoplasm (disease)",
          "cornea tumor",
          "cornea tumour",
          "corneal neoplasm",
          "corneal tumor",
          "corneal tumour",
          "neoplasm of cornea",
          "neoplasm of the cornea",
          "tumor of cornea",
          "tumor of the cornea",
          "tumour of cornea",
          "tumour of the cornea"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A neoplasm (disease) that involves the cornea."
      },
      "child_count": 6,
      "reference_id": "MONDO:0021238"
    },
    {
      "id": 20779,
      "label": "Arnold stickler bourne syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3211,
        4370,
        6139,
        6948
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0000366",
          "MEDGEN:419426",
          "MESH:C537431",
          "UMLS:C2931492"
        ],
        "synonyms": [
          "corneal crystals myopathy and nephropathy",
          "corneal crystals myopathy and neuropathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0021921"
    },
    {
      "id": 21714,
      "label": "limbal stem cell deficiency",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3211
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020123",
          "MEDGEN:295775",
          "Orphanet:171673",
          "UMLS:C1561989"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0025667"
    },
    {
      "id": 22743,
      "label": "thygeson superficial punctate keratopathy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3211
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022131",
          "MEDGEN:1638070",
          "Orphanet:519406",
          "UMLS:C4551636"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "An insidious, chronic and recurrent disorder, characterized by small and elevated oval corneal intraepithelial, whitish-gray opacities, extending to the entire anterior surface of the cornea of both eyes. Corneal lesions show a tendency for the central pupillary area distribution with mild or absent conjunctival inflammation and no association to systemic disease."
      },
      "child_count": 0,
      "reference_id": "MONDO:0033816"
    },
    {
      "id": 22744,
      "label": "Terrien marginal degeneration",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3211
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022133",
          "MEDGEN:543256",
          "Orphanet:519410",
          "UMLS:C0271283"
        ],
        "synonyms": [
          "Terrien's marginal degeneration"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A distinct marginal thinning of the cornea which causes high degree of against-the-rule astigmatism"
      },
      "child_count": 0,
      "reference_id": "MONDO:0033818"
    }
  ],
  "roots": [
    {
      "id": 7019,
      "label": "eye disorder"
    }
  ]
}