{
    "disease_id": "DOID:0111569",
    "recommended_name": {
        "id": "DOID:0111569",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111569",
        "name": "autosomal dominant vitreoretinochoroidopathy",
        "description": "A hereditary retinal dystrophy characterized by abnormal chorioretinal hypopigmentation and hyperpigmentation typically lying between the vortex veins and the ora serrata for 360 degrees and other ocular developmental anomalies that has_material_basis_in heterozygous mutation in BEST1 on chromosome 11q12.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111569",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111569",
            "name": "ADVIRC",
            "description": ""
        },
        {
            "id": "DOID:0111569",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111569",
            "name": "VRCP autosomal dominant",
            "description": ""
        },
        {
            "id": "DOID:0111569",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111569",
            "name": "vitreoretinochoroidopathy dominant",
            "description": ""
        },
        {
            "id": "DOID:0111569",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111569",
            "name": "vitreoretinochoroidopathy, autosomal dominant, with nanophthalmos",
            "description": ""
        },
        {
            "id": "DOID:0111569",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111569",
            "name": "vitreoretinochoroidopathy with microcornea, glaucoma, and cataract",
            "description": ""
        },
        {
            "id": "MONDO:0008662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008662",
            "name": "autosomal dominant vitreoretinochoroidopathy",
            "description": "Autosomal dominant vitreoretinochoroidopathy (ADVIRC) is a genetic vitreous-retinal disease characterized by ocular developmental anomalies such as microcornea, a shallow anterior chamber, glaucoma and cataract. Abnormal chorioretinal pigmentation is present, usually lying between the vortex veins and the ora serrata for 360 degrees."
        },
        {
            "id": "MONDO:0008662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008662",
            "name": "vitreoretinochoroidopathy, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008662",
            "name": "vitreoretinochoroidopathy, autosomal dominant, with nanophthalmos",
            "description": ""
        },
        {
            "id": "MONDO:0008662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008662",
            "name": "microcornea, Rod-cone dystrophy, cataract, and posterior staphyloma",
            "description": ""
        },
        {
            "id": "MONDO:0008662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008662",
            "name": "VRCP",
            "description": ""
        },
        {
            "id": "MONDO:0008662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008662",
            "name": "vitreoretinochoroidopathy dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008662",
            "name": "vitreoretinochoroidopathy; VRCP",
            "description": ""
        },
        {
            "id": "MONDO:0008662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008662",
            "name": "vitreoretinochoroidopathy with microcornea, glaucoma, and cataract",
            "description": ""
        },
        {
            "id": "MONDO:0008662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008662",
            "name": "VRCP autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008662",
            "name": "vitreoretinochoroidopathy",
            "description": ""
        },
        {
            "id": "MONDO:0008662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008662",
            "name": "ADVIRC",
            "description": ""
        },
        {
            "id": "MIM:193220",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/193220",
            "name": "Vitreoretinochoroidopathy",
            "description": "Vitreoretinochoroidopathy"
        }
    ]
}