{
  "id": 8773,
  "label": "lattice corneal dystrophy type I",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007380",
  "properties": {
    "xrefs": [
      "GARD:0009678",
      "MEDGEN:305533",
      "MESH:C537881",
      "OMIM:122200",
      "Orphanet:98964",
      "SCTID:419197009",
      "UMLS:C1690006"
    ],
    "synonyms": [
      "Biber-Haab-Dimmer dystrophy",
      "LCD1",
      "LCDI",
      "Lcd1",
      "classic lattice corneal dystrophy",
      "lattice corneal dystrophy type 1",
      "CDL1",
      "LCD",
      "corneal dystrophy, lattice type 1",
      "corneal dystrophy, lattice type I",
      "lattice corneal dystrophy, type 1"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "Type I lattice corneal dystrophy (LCDI) is a frequent form of stromal corneal dystrophy characterized by a network of delicate interdigitating branching filamentous opacities within the cornea with progressive visual impairment and no systemic manifestations."
  },
  "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": 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"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3131,
      "label": "epithelial-stromal TGFBI dystrophy"
    },
    {
      "id": 6468,
      "label": "lattice corneal dystrophy"
    }
  ]
}