{
    "disease_id": "DOID:0080264", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0033123", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0033123", 
            "name": "EVR7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0033123", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0033123", 
            "name": "exudative vitreoretinopathy 7; EVR7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080264", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080264", 
            "name": "EVR7"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080264", 
        "description": "An exudative vitreoretinopathy that has_material_basis_in heterozygous mutation in CTNNB1 on chromosome 3p22.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080264", 
        "name": "exudative vitreoretinopathy 7"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080264#disease-associations", 
            "id": "0080264", 
            "database": "Alliance of Genome Resources"
        }
    ]
}