{
    "disease_id": "DOID:1928", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008678", 
            "name": "Williams syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008678", 
            "name": "deletion 7q11.23"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008678", 
            "name": "chromosome 7Q11.23 deletion syndrome, 1.5- to 1.8-Mb"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008678", 
            "name": "Williams-Beuren syndrome (WBS)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008678", 
            "name": "WBS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008678", 
            "name": "Fanconi Schlesinger syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008678", 
            "name": "monosomy 7q11.23"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008678", 
            "name": "WMS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008678", 
            "name": "Williams-Beuren syndrome; WBS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1928", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1928", 
            "name": "Fanconi Schlesinger syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:1928", 
        "description": "A syndrome that is characterized by mild to moderate intellectual disability, a broad forehead, a short nose with a broad tip, full cheeks, and a wide mouth with full lips and difficulty with visual-spatial tasks and has_material_basis_in hemizygous deletion of 1.5 to 1.8 Mb on chromosome 7q11.23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:1928", 
        "name": "Williams-Beuren syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/1928#disease-associations", 
            "id": "1928", 
            "database": "Alliance of Genome Resources"
        }
    ]
}