{
    "disease_id": "DOID:0111864", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010178", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010178", 
            "name": "congenital bilateral aplasia of vas deferens from CFTR mutation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010178", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010178", 
            "name": "vas deferens, congenital bilateral aplasia of; CBAVD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010178", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010178", 
            "name": "congenital bilateral aplasia of the vas deferens"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010178", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010178", 
            "name": "CAVD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010178", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010178", 
            "name": "CBAVD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010178", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010178", 
            "name": "vas deferens, congenital bilateral aplasia of"
        }, 
        {
            "url": "https://www.omim.org/entry/277180", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:277180", 
            "name": "Congenital bilateral absence of the vas deferens"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111864", 
        "description": "A congenital bilateral absence of vas deferens that has_material_basis_in homozygous or compound heterozygous mutation in CFTR on chromosome 7q31.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111864", 
        "name": "autosomal recessive congenital bilateral absence of vas deferens"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/277180", 
            "id": "277180", 
            "database": "MIM"
        }
    ]
}