{
    "disease_id": "DOID:0111409",
    "recommended_name": {
        "id": "DOID:0111409",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111409",
        "name": "exudative vitreoretinopathy 3",
        "description": "An exudative vitreoretinopathy that has_material_basis_in heterozygous mutation in a region on chromosome 11p13-p12."
    },
    "synonyms": [
        {
            "id": "DOID:0111409",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111409",
            "name": "EVR3",
            "description": ""
        },
        {
            "id": "MONDO:0011592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011592",
            "name": "exudative vitreoretinopathy 3",
            "description": ""
        },
        {
            "id": "MONDO:0011592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011592",
            "name": "EVR3",
            "description": ""
        },
        {
            "id": "MONDO:0011592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011592",
            "name": "exudative vitreoretinopathy 3",
            "description": ""
        }
    ]
}