{
    "disease_id": "DOID:0111863",
    "recommended_name": {
        "id": "DOID:0111863",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111863",
        "name": "X-linked congenital bilateral absence of vas deferens",
        "description": "A congenital bilateral absence of vas deferens that has_material_basis_in mutation in ADGRG2 on chromosome Xp22.13."
    },
    "synonyms": [
        {
            "id": "DOID:0111863",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111863",
            "name": "CBAVDX",
            "description": ""
        },
        {
            "id": "MONDO:0010511",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010511",
            "name": "vas deferens, congenital bilateral aplasia of, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010511",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010511",
            "name": "CBAVDX",
            "description": ""
        },
        {
            "id": "MONDO:0010511",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010511",
            "name": "vas deferens, congenital bilateral aplasia of, X-linked; CBAVDX",
            "description": ""
        },
        {
            "id": "MONDO:0010511",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010511",
            "name": "vas deferens, congenital bilateral aplasia of, X-linked",
            "description": ""
        },
        {
            "id": "MIM:300985",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300985",
            "name": "Congenital bilateral aplasia of the vas deferens, X-linked",
            "description": "Congenital bilateral aplasia of the vas deferens, X-linked"
        }
    ]
}