{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013821", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013821", 
            "name": "intellectual disability, autosomal dominant 16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013821", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013821", 
            "name": "mental retardation, autosomal dominant 16; MRD16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013821", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013821", 
            "name": "mental retardation, autosomal dominant 16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013821", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013821", 
            "name": "MRD16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013821", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013821", 
            "name": "Coffin-Siris syndrome caused by mutation in SMARCA4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013821", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013821", 
            "name": "autosomal dominant mental retardation 16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013821", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013821", 
            "name": "mental retardation, autosomal dominant type 16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013821", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013821", 
            "name": "CSS4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013821", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013821", 
            "name": "COFFIN-SIRIS syndrome 4; CSS4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013821", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013821", 
            "name": "SMARCA4 Coffin-Siris syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070046", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070046", 
            "name": "CSS4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070046", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070046", 
            "name": "MRD16"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070046", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070046", 
            "name": "autosomal dominant mental retardation 16"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070046", 
        "description": "A Coffin-Siris syndrome that has_material_basis_in an autosomal dominant mutation of SMARCA4 on chromosome 19p13.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070046", 
        "name": "Coffin-Siris syndrome 4"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614609", 
            "id": "614609", 
            "database": "MIM"
        }
    ]
}