{
  "id": 3130,
  "label": "epithelial and subepithelial corneal dystrophy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0000763",
  "properties": {
    "xrefs": [
      "DOID:0060440",
      "GARD:0022826"
    ],
    "synonyms": [
      "epithelial and subepithelial dystrophy"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 5,
  "parents": [
    {
      "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"
    }
  ],
  "children": [
    {
      "id": 8768,
      "label": "epithelial basement membrane dystrophy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3130,
        3131,
        19762
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060447",
          "GARD:0009732",
          "MEDGEN:99275",
          "MESH:C535477",
          "OMIM:121820",
          "Orphanet:98956",
          "SCTID:373426005",
          "UMLS:C0521723"
        ],
        "synonyms": [
          "Cogan corneal dystrophy",
          "Cogan microcystic epithelial dystrophy",
          "EBMD",
          "Map-dot-fingerprint dystrophy",
          "anterior basement membrane dystrophy",
          "Map-dot-fingerprint dystrophy of cornea",
          "corneal dystrophy, Map-Dot-Fingerprint type",
          "corneal dystrophy, anterior basement Membrane",
          "corneal dystrophy, epithelial basement MEMBRANE",
          "corneal dystrophy, microcystic",
          "epithelial basement membrane corneal dystrophy",
          "microcystic dystrophy of the cornea"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0007375"
    },
    {
      "id": 8772,
      "label": "Meesmann corneal dystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3130,
        5714,
        19762
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060451",
          "GARD:0009688",
          "ICD9:371.51",
          "MEDGEN:83283",
          "MESH:D053559",
          "NCIT:C84795",
          "OMIMPS:122100",
          "Orphanet:98954",
          "SCTID:1674008",
          "UMLS:C0339277"
        ],
        "synonyms": [
          "MECD",
          "Meesmann corneal dystrophy",
          "juvenile epithelial of Meesmann corneal dystrophy",
          "juvenile hereditary epithelial dystrophy of Meesmann",
          "Meesman dystrophy",
          "Meesmann corneal epithelial dystrophy",
          "corneal dystrophy, Meesmann",
          "corneal dystrophy, Meesmann epithelial",
          "corneal dystrophy, juvenile epithelial of Meesmann",
          "corneal dystrophy, juvenile epithelial, of Meesmann"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Meesmann corneal dystrophy (MECD) is a rare form of superficial corneal dystrophy characterized by distinct tiny bubble-like, round-to-oval punctate bilateral opacities in the central corneal epithelium, and to a lesser extent in the peripheral cornea, with little impact on vision."
      },
      "child_count": 6,
      "reference_id": "MONDO:0007379"
    },
    {
      "id": 10049,
      "label": "gelatinous drop-like corneal dystrophy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3130,
        5714,
        6468,
        19762
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060449",
          "GARD:0009647",
          "MEDGEN:90939",
          "MESH:C535480",
          "NANDO:1201006",
          "NCIT:C142805",
          "OMIM:204870",
          "Orphanet:98957",
          "UMLS:C0339273",
          "icd11.foundation:1062815669"
        ],
        "synonyms": [
          "GDCD",
          "corneal amyloidosis",
          "gelatinous drop-like corneal dystrophy",
          "primary familial amyloidosis of the cornea",
          "subepithelial amyloidosis of the cornea",
          "CDGDL",
          "Cdgdl",
          "GDLD",
          "amyloid corneal dystrophy, Japanese type",
          "amyloidosis corneal",
          "amyloidosis, corneal",
          "corneal dystrophy, gelatinous drop-like",
          "corneal dystrophy, lattice type 3",
          "lattice corneal dystrophy type 3",
          "lattice corneal dystrophy, type 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Gelatinous drop-like corneal dystrophy (GDCD) is a form of superficial corneal dystrophy characterized by multiple prominent milky-white gelatinous nodules beneath the corneal epithelium, and marked visual impairment."
      },
      "child_count": 0,
      "reference_id": "MONDO:0008777"
    },
    {
      "id": 11585,
      "label": "Lisch epithelial corneal dystrophy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3130,
        5714,
        19762
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060450",
          "GARD:0016877",
          "MEDGEN:411737",
          "MESH:C567588",
          "OMIM:300778",
          "OMIM:620763",
          "Orphanet:98955",
          "SCTID:724175002",
          "UMLS:C2749050",
          "icd11.foundation:1571503165"
        ],
        "synonyms": [
          "LECD",
          "Lisch epithelial corneal dystrophy",
          "band-shaped and whorled microcystic dystrophy of the corneal epithelium",
          "corneal dystrophy, Lisch epithelial, X-linked dominant",
          "band-Shaped and whorled microcystic corneal epithelial dystrophy",
          "corneal dystrophy, Lisch epithelial"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Lisch epithelial corneal dystrophy (LECD) is a very rare form of superficial corneal dystrophy characterized by feather-shaped opacities and microcysts in the corneal epithelium arranged in a band-shaped and sometimes whorled pattern, occasionally with impaired vision."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010425"
    },
    {
      "id": 14064,
      "label": "subepithelial mucinous corneal dystrophy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3130,
        19762
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060454",
          "GARD:0016878",
          "MEDGEN:411595",
          "MESH:C567547",
          "OMIM:612867",
          "Orphanet:98959",
          "SCTID:723582004",
          "UMLS:C2748503",
          "icd11.foundation:943706174"
        ],
        "synonyms": [
          "SMCD",
          "subepithelial mucinous corneal dystrophy",
          "corneal dystrophy, subepithelial mucinous"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Subepithelial mucinous corneal dystrophy (SMCD) is a very rare form of superficial corneal dystrophy characterized by frequent recurrent corneal erosions in the first decade of life, with progressive loss of vision."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013026"
    }
  ],
  "roots": [
    {
      "id": 18261,
      "label": "corneal dystrophy"
    }
  ]
}