{
    "disease_id": "DOID:0060305", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010649", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010649", 
            "name": "isolated congenital megalocornea"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010649", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010649", 
            "name": "MGC1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010649", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010649", 
            "name": "congenital anterior megalophthalmia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010649", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010649", 
            "name": "megalocornea; MGC1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010649", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010649", 
            "name": "Mgcn"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060305", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060305", 
            "name": "anterior megalophthalmos"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060305", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060305", 
            "name": "congenital anterior megalophthalmia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060305", 
        "description": "A corneal disease that is characterized by a bilaterally enlarged corneal diameter without an increase in intraocular pressure and that has_material_basis_in mutation in the CHRDL1 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060305", 
        "name": "megalocornea"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060305#disease-associations", 
            "id": "0060305", 
            "database": "Alliance of Genome Resources"
        }
    ]
}