{
  "id": 8770,
  "label": "granular corneal dystrophy type I",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007377",
  "properties": {
    "xrefs": [
      "DOID:0080530",
      "GARD:0009677",
      "MEDGEN:351521",
      "MESH:C537304",
      "OMIM:121900",
      "Orphanet:98962",
      "SCTID:419039007",
      "UMLS:C1641846"
    ],
    "synonyms": [
      "GCD1",
      "GCDI",
      "classic GCD",
      "classic granular corneal dystrophy",
      "corneal dystrophy Groenouw type I",
      "granular corneal dystrophy type 1",
      "CDGG1",
      "Groenouw type I corneal dystrophy",
      "corneal dystrophy granular type",
      "corneal dystrophy punctate or nodular",
      "corneal dystrophy, Groenouw type 1",
      "corneal dystrophy, Groenouw type I",
      "corneal dystrophy, punctate or nodular",
      "granular corneal dystrophy, type 1"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "Type I granular corneal dystrophy (GCDI) is a rare form of stromal corneal dystrophy characterized by multiple small deposits in the superficial central corneal stroma, and progressive visual impairment, which may sometimes be severe."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3131,
      "label": "epithelial-stromal TGFBI dystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        18261
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060441",
          "GARD:0022827"
        ],
        "synonyms": [
          "TGFBI corneal dystrophy (disease)",
          "corneal dystrophy (disease) caused by mutation in TGFBI"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Any corneal dystrophy (disease) in which the cause of the disease is a mutation in the TGFBI gene."
      },
      "child_count": 16,
      "reference_id": "MONDO:0000764"
    },
    {
      "id": 19763,
      "label": "stromal corneal dystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18261
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060442",
          "GARD:0019519",
          "ICD9:371.56",
          "MEDGEN:20973",
          "Orphanet:98626",
          "SCTID:231931001",
          "UMLS:C0038457",
          "icd11.foundation:1392780216"
        ],
        "synonyms": [
          "corneal dystrophy (disease) of substantia propria of cornea",
          "corneal stromal dystrophy",
          "substantia propria of cornea corneal dystrophy (disease)",
          "stromal dystrophy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "The stromal corneal dystrophies refer to a group of rare genetically determined corneal dystrophies (CDs) characterized by lesions affecting the corneal stroma, and variable effects on vision depending on the type of dystrophy."
      },
      "child_count": 10,
      "reference_id": "MONDO:0020213"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3131,
      "label": "epithelial-stromal TGFBI dystrophy"
    },
    {
      "id": 19763,
      "label": "stromal corneal dystrophy"
    }
  ]
}