{
    "disease_id": "DOID:0050662", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012733", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012733", 
            "name": "autosomal recessive bestrophinopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012733", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012733", 
            "name": "bestrophinopathy, autosomal recessive; ARB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012733", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012733", 
            "name": "bestrophinopathy, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012733", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012733", 
            "name": "retinopathy, Burgess-Black type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012733", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012733", 
            "name": "ARB"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050662", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050662", 
            "name": "autosomal recessive bestrophinopathy"
        }, 
        {
            "url": "https://www.omim.org/entry/611809", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:611809", 
            "name": "Bestrophinopathy, autosomal recessive"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050662", 
        "description": "A macular degeneration that is characterized by central vision loss, an absent electrooculogram light rise and a reduced electroretinogram, has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the BEST1 gene on chromosome 11q12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050662", 
        "name": "bestrophinopathy"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/611809", 
            "id": "611809", 
            "database": "MIM"
        }
    ]
}