{
    "disease_id": "DOID:0111863", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010511", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010511", 
            "name": "vas deferens, congenital bilateral aplasia of, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010511", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010511", 
            "name": "CBAVDX"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010511", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010511", 
            "name": "vas deferens, congenital bilateral aplasia of, X-linked; CBAVDX"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111863", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111863", 
            "name": "CBAVDX"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111863", 
        "description": "A congenital bilateral absence of vas deferens that has_material_basis_in mutation in ADGRG2 on chromosome Xp22.13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111863", 
        "name": "X-linked congenital bilateral absence of vas deferens"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111863#disease-associations", 
            "id": "0111863", 
            "database": "Alliance of Genome Resources"
        }
    ]
}