{
    "disease_id": "DOID:0060673",
    "recommended_name": {
        "id": "DOID:0060673",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060673",
        "name": "Peters anomaly",
        "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."
    },
    "synonyms": []
}