{
    "disease_id": "DOID:0111569", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008662", 
            "name": "vitreoretinochoroidopathy, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008662", 
            "name": "vitreoretinochoroidopathy, autosomal dominant, with nanophthalmos"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008662", 
            "name": "microcornea, Rod-cone dystrophy, cataract, and posterior staphyloma"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008662", 
            "name": "VRCP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008662", 
            "name": "vitreoretinochoroidopathy dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008662", 
            "name": "vitreoretinochoroidopathy; VRCP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008662", 
            "name": "vitreoretinochoroidopathy with microcornea, glaucoma, and cataract"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008662", 
            "name": "VRCP autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008662", 
            "name": "vitreoretinochoroidopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008662", 
            "name": "ADVIRC"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111569", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111569", 
            "name": "ADVIRC"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111569", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111569", 
            "name": "VRCP autosomal dominant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111569", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111569", 
            "name": "vitreoretinochoroidopathy dominant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111569", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111569", 
            "name": "vitreoretinochoroidopathy, autosomal dominant, with nanophthalmos"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111569", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111569", 
            "name": "vitreoretinochoroidopathy with microcornea, glaucoma, and cataract"
        }, 
        {
            "url": "https://www.omim.org/entry/193220", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:193220", 
            "name": "Vitreoretinochoroidopathy, autosomal dominant"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111569", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111569", 
        "name": "autosomal dominant vitreoretinochoroidopathy"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/193220", 
            "id": "193220", 
            "database": "MIM"
        }
    ]
}