{
    "disease_id": "DOID:0111677", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009235", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009235", 
            "name": "familial benign flecked retina"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009235", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009235", 
            "name": "FLECK retina, familial benign"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009235", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009235", 
            "name": "FRFB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009235", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009235", 
            "name": "FLECK retina, familial benign; FRFB"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111677", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111677", 
            "name": "FRFB"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111677", 
        "description": "A retinal disease characterized by a striking pattern of diffuse, yellow-white, fleck-like lesions extending to the far periphery of the retina but with no apparent visual or electrophysiologic deficits that has_material_basis_in homozygous or compound heterozygous mutation in PLA2G5 on chromosome 1p36.13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111677", 
        "name": "familial benign fleck retina"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111677#disease-associations", 
            "id": "0111677", 
            "database": "Alliance of Genome Resources"
        }
    ]
}