{
    "disease_id": "DOID:0060673", 
    "synonyms": [], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060673", 
        "description": "A corneal disease characterized by a central corneal leukoma and absence of the posterior corneal stroma and Descemet membrane that has_material_basis_in mutation in the PAX6 gene on chromosome 11p13, the PITX2 gene on chromosome 4q25, the CYP1B1 gene on chromosome 2p22.2, or the FOXC1 gene on chromosome 6p25.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060673", 
        "name": "Peters anomaly"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060673#disease-associations", 
            "id": "0060673", 
            "database": "Alliance of Genome Resources"
        }
    ]
}