{
  "id": 10049,
  "label": "gelatinous drop-like corneal dystrophy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008777",
  "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."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3130,
      "label": "epithelial and subepithelial corneal dystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18261
      ],
      "type_id": 0,
      "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"
          }
        ]
      },
      "child_count": 5,
      "reference_id": "MONDO:0000763"
    },
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    },
    {
      "id": 6468,
      "label": "lattice corneal dystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19763
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:8943",
          "GARD:0024087",
          "HP:0001149",
          "ICD10CM:H18.54",
          "ICD9:277.39",
          "ICD9:357.4",
          "MEDGEN:56355",
          "SCTID:1192004",
          "UMLS:C0155127",
          "icd11.foundation:1247885635"
        ],
        "synonyms": [
          "lattice corneal dystrophy",
          "lattice corneal dystrophy (disease)"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 3,
      "reference_id": "MONDO:0004686"
    },
    {
      "id": 19762,
      "label": "superficial corneal dystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18261
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD9:371.52",
          "MEDGEN:746687",
          "Orphanet:98625",
          "SCTID:430888006",
          "UMLS:C2315777"
        ],
        "synonyms": [
          "anterior corneal dystrophy",
          "corneal epithelium corneal dystrophy (disease)",
          "dystrophy of anterior cornea"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "The superficial corneal dystrophies refer to a group of rare genetically determined corneal dystrophies (CDs) characterized by lesions affecting the corneal epithelium and its basement membrane and the superficial corneal stroma, and variable effects on vision depending on the type of dystrophy."
      },
      "child_count": 12,
      "reference_id": "MONDO:0020212"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3130,
      "label": "epithelial and subepithelial corneal dystrophy"
    },
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 6468,
      "label": "lattice corneal dystrophy"
    },
    {
      "id": 19762,
      "label": "superficial corneal dystrophy"
    }
  ]
}