{
    "disease_id": "DOID:0060535", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013252", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013252", 
            "name": "WABS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013252", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013252", 
            "name": "WARSAW breakage syndrome; WABS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060535", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060535", 
            "name": "WABS"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060535", 
        "description": "A syndrome mainly characterized by severe congenital microcephaly, growth restriction, and sensorineural hearing loss due to cochlear hypoplasia and that has_material_basis_in homozygous or compound heterozygous mutation in the DDX11 gene on chromosome 12p11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060535", 
        "name": "Warsaw breakage syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060535#disease-associations", 
            "id": "0060535", 
            "database": "Alliance of Genome Resources"
        }
    ]
}