{
    "disease_id": "DOID:0080264",
    "recommended_name": {
        "id": "DOID:0080264",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080264",
        "name": "exudative vitreoretinopathy 7",
        "description": "An exudative vitreoretinopathy that has_material_basis_in heterozygous mutation in the CTNNB1 gene on chromosome 3p22.1."
    },
    "synonyms": [
        {
            "id": "DOID:0080264",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0080264",
            "name": "EVR7",
            "description": ""
        },
        {
            "id": "MONDO:0033123",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033123",
            "name": "exudative vitreoretinopathy 7",
            "description": ""
        },
        {
            "id": "MONDO:0033123",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033123",
            "name": "exudative vitreoretinopathy 7",
            "description": ""
        },
        {
            "id": "MONDO:0033123",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033123",
            "name": "EVR7",
            "description": ""
        },
        {
            "id": "MIM:617572",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617572",
            "name": "Vitreoretinopathy, exudative 7",
            "description": "Vitreoretinopathy, exudative 7"
        }
    ]
}