{
  "id": 8772,
  "label": "Meesmann corneal dystrophy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007379",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "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": 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": [
    {
      "id": 20190,
      "label": "corneal dystrophy, Meesmann, 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        8772
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080670",
          "GARD:0025252",
          "MEDGEN:1684668",
          "OMIM:122100",
          "UMLS:C5231499"
        ],
        "synonyms": [
          "CORNEAL DYSTROPHY, MEESMANN, 1",
          "Corneal Dystrophy, Juvenile Epithelial, of Meesmann",
          "Corneal Dystrophy, Meesmann Epithelial",
          "MECD1",
          "Meesmann Corneal Dystrophy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0020791"
    },
    {
      "id": 22556,
      "label": "corneal dystrophy, Meesmann, 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        8772
      ],
      "type_id": 0,
      "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"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032904"
    }
  ],
  "roots": [
    {
      "id": 3130,
      "label": "epithelial and subepithelial corneal dystrophy"
    },
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 19762,
      "label": "superficial corneal dystrophy"
    }
  ]
}