{
    "disease_id": "DOID:0070045", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013820", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013820", 
            "name": "intellectual disability, autosomal dominant 15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013820", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013820", 
            "name": "mental retardation, autosomal dominant 15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013820", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013820", 
            "name": "MRD15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013820", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013820", 
            "name": "SMARCB1 Coffin-Siris syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013820", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013820", 
            "name": "autosomal dominant mental retardation 15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013820", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013820", 
            "name": "mental retardation, autosomal dominant type 15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013820", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013820", 
            "name": "Coffin-Siris syndrome caused by mutation in SMARCB1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013820", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013820", 
            "name": "CSS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013820", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013820", 
            "name": "COFFIN-SIRIS syndrome 3; CSS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013820", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013820", 
            "name": "mental retardation, autosomal dominant 15; MRD15"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070045", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070045", 
            "name": "CSS3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070045", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070045", 
            "name": "MRD15"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070045", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070045", 
            "name": "autosomal dominant mental retardation 15"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070045", 
        "description": "A Coffin-Siris syndrome that has_material_basis_in an autosomal dominant mutation of SMARCB1 on chromosome 22q11.23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070045", 
        "name": "Coffin-Siris syndrome 3"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614608", 
            "id": "614608", 
            "database": "MIM"
        }
    ]
}