{
    "disease_id": "DOID:0050660", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007412", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007412", 
            "name": "BSTVS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007412", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007412", 
            "name": "Beare Stevenson syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007412", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007412", 
            "name": "cutis gyrata syndrome of Beare and Stevenson"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007412", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007412", 
            "name": "Beare-Stevenson syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007412", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007412", 
            "name": "cutis gyrata - acanthosis nigricans - craniosynostosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007412", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007412", 
            "name": "Beare-Stevenson cutis gyrata syndrome; BSTVS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007412", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007412", 
            "name": "cutis gyrata-acanthosis nigricans-craniosynostosis syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050660", 
        "description": "A syndrome that is characterized by cutis gyrata, acanthosis nigricans and craniosynostosis, has_material_basis_in heterozygous mutation in the FGFR2 gene on chromosome 10q26.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050660", 
        "name": "Beare-Stevenson cutis gyrata syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050660#disease-associations", 
            "id": "0050660", 
            "database": "Alliance of Genome Resources"
        }
    ]
}