{
    "disease_id": "DOID:0080671", 
    "synonyms": [
        {
            "url": "https://www.omim.org/entry/618767", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:618767", 
            "name": "Corneal dystrophy, Meesmann 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080671", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080671", 
        "name": "Meesmann corneal dystrophy 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/618767", 
            "id": "618767", 
            "database": "MIM"
        }
    ]
}