{
    "disease_id": "DOID:0070042", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007617", 
            "name": "CSS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007617", 
            "name": "fifth digit syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007617", 
            "name": "COFFIN-SIRIS syndrome 1; CSS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007617", 
            "name": "COFFIN-SIRIS syndrome; CSS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007617", 
            "name": "COFFIN-SIRIS syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070042", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070042", 
            "name": "CSS1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070042", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070042", 
            "name": "MRD12"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070042", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070042", 
            "name": "autosomal dominant mental retardation 12"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070042", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070042", 
            "name": "fifth digit syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070042", 
        "description": "A Coffin-Siris syndrome that has_material_basis_in an autosomal dominant mutation of ARID1B on chromosome 6q25.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070042", 
        "name": "Coffin-Siris syndrome 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070042#disease-associations", 
            "id": "0070042", 
            "database": "Alliance of Genome Resources"
        }
    ]
}