{
  "id": 12936,
  "label": "granular corneal dystrophy type II",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011855",
  "properties": {
    "xrefs": [
      "DOID:0060444",
      "GARD:0009278",
      "ICD9:371.56",
      "MEDGEN:220900",
      "MESH:C535474",
      "OMIM:607541",
      "Orphanet:98963",
      "SCTID:397568004",
      "UMLS:C1275685"
    ],
    "synonyms": [
      "Avellino corneal dystrophy",
      "CGD2",
      "GCD2",
      "GCDII",
      "avellino corneal dystrophy",
      "combined granular-lattice corneal dystrophy",
      "granular corneal dystrophy type 2",
      "granular-lattice corneal dystrophy",
      "ACD",
      "CDA",
      "combined granular-lattice corneal dystrophies",
      "corneal dystrophy Avellino type",
      "corneal dystrophy, AVELLINO type",
      "granular and lattice corneal dystrophies",
      "granular corneal dystrophy, type 2",
      "granular-lattice (Avellino) corneal dystrophy"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "Type II granular corneal dystrophy (GCDII) is a rare form of stromal corneal dystrophy characterized by irregular-shaped well-demarcated granular deposits in the superficial central corneal stroma, and progressive visual impairment."
  },
  "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"
    }
  ]
}