{
    "disease_id": "DOID:0060252", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008417", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008417", 
            "name": "sclerocornea, autosomal dominant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060252", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060252", 
            "name": "isolated congenital sclerocornea"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060252", 
        "description": "A corneal disease in which the cornea blends with sclera, resulting in clouding of the cornea.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060252", 
        "name": "sclerocornea"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060252#disease-associations", 
            "id": "0060252", 
            "database": "Alliance of Genome Resources"
        }
    ]
}