{
  "id": 22556,
  "label": "corneal dystrophy, Meesmann, 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0032904",
  "properties": {
    "xrefs": [
      "DOID:0080671",
      "GARD:0025769",
      "MEDGEN:1684798",
      "OMIM:618767",
      "UMLS:C5231495"
    ],
    "synonyms": [
      "CORNEAL DYSTROPHY, MEESMANN, 2",
      "MECD2"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "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"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 8772,
      "label": "Meesmann corneal dystrophy"
    }
  ]
}