{
    "disease_id": "DOID:0070044", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013819", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013819", 
            "name": "intellectual disability, autosomal dominant 14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013819", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013819", 
            "name": "CSS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013819", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013819", 
            "name": "ARID1A Coffin-Siris syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013819", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013819", 
            "name": "COFFIN-SIRIS syndrome 2; CSS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013819", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013819", 
            "name": "mental retardation, autosomal dominant 14; MRD14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013819", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013819", 
            "name": "MRD14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013819", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013819", 
            "name": "Coffin-Siris syndrome caused by mutation in ARID1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013819", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013819", 
            "name": "mental retardation, autosomal dominant 14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013819", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013819", 
            "name": "autosomal dominant mental retardation 14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013819", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013819", 
            "name": "mental retardation, autosomal dominant type 14"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070044", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070044", 
            "name": "CSS2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070044", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070044", 
            "name": "MRD14"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070044", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070044", 
            "name": "autosomal dominant mental retardation 14"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070044", 
        "description": "A Coffin-Siris syndrome that has_material_basis_in an autosomal dominant mutation of ARID1A on chromosome 1p36.11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070044", 
        "name": "Coffin-Siris syndrome 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070044#disease-associations", 
            "id": "0070044", 
            "database": "Alliance of Genome Resources"
        }
    ]
}