{
    "disease_id": "DOID:0050535",
    "recommended_name": {
        "id": "DOID:0050535",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0050535",
        "name": "exudative vitreoretinopathy",
        "description": "A retinal vascular disease characterized by the prevention of blood vessel formation at the edges of the retina and the hemorrhage of the blood vessels in the retina."
    },
    "synonyms": [
        {
            "id": "DOID:0050535",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050535",
            "name": "FEVR",
            "description": ""
        },
        {
            "id": "DOID:0050535",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050535",
            "name": "familial exudative vitreoretinopathy",
            "description": ""
        },
        {
            "id": "MONDO:0007589",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007589",
            "name": "exudative vitreoretinopathy 1",
            "description": ""
        },
        {
            "id": "MONDO:0007589",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007589",
            "name": "exudative vitreoretinopathy 1",
            "description": ""
        },
        {
            "id": "MONDO:0007589",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007589",
            "name": "Fevr, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0007589",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007589",
            "name": "retinopathy of prematurity",
            "description": ""
        },
        {
            "id": "MONDO:0007589",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007589",
            "name": "Criswick-Schepens syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007589",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007589",
            "name": "exudative vitreoretinopathy type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007589",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007589",
            "name": "exudative vitreoretinopathy, familial, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0007589",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007589",
            "name": "EVR1",
            "description": ""
        },
        {
            "id": "MONDO:0007589",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007589",
            "name": "exudative vitreoretinopathy 1; EVR1",
            "description": ""
        },
        {
            "id": "MIM:133780",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/133780",
            "name": "Vitreoretinopathy, exudative 1",
            "description": "Vitreoretinopathy, exudative 1"
        }
    ]
}