{
    "disease_id": "DOID:0080671",
    "recommended_name": {
        "id": "DOID:0080671",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080671",
        "name": "Meesmann corneal dystrophy 2",
        "description": "A Messmann corneal dystrophy that is characterized by fragility of the anterior corneal epithelium and the presence of intraepithelial microcysts and that has_material_basis_in  heterozygous mutation in the KRT3 gene on chromosome 12q13."
    },
    "synonyms": [
        {
            "id": "MIM:618767",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618767",
            "name": "Corneal dystrophy, Meesmann 2",
            "description": "Corneal dystrophy, Meesmann 2"
        }
    ]
}