{
    "disease_id": "DOID:0111862",
    "recommended_name": {
        "id": "DOID:0111862",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111862",
        "name": "congenital bilateral absence of vas deferens",
        "description": "A male infertility that is characterized by bilateral absence of the vas deferens resulting in obstroctive azoospermia and male infertility."
    },
    "synonyms": [
        {
            "id": "DOID:0111862",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111862",
            "name": "CAVD",
            "description": ""
        },
        {
            "id": "DOID:0111862",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111862",
            "name": "CBAVD",
            "description": ""
        },
        {
            "id": "DOID:0111862",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111862",
            "name": "congenital bilateral agenesis of vas deferens",
            "description": ""
        },
        {
            "id": "DOID:0111862",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111862",
            "name": "congenital bilateral aplasia of vas deferens",
            "description": ""
        },
        {
            "id": "MONDO:0010178",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010178",
            "name": "congenital bilateral aplasia of vas deferens from CFTR mutation",
            "description": "An autosomal recessive disorder that is associated with mutation(s) in the CFTR gene, encoding cystic fibrosis transmembrane conductance regulator. Mutation(s) in the same gene are associated with cystic fibrosis."
        },
        {
            "id": "MONDO:0010178",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010178",
            "name": "congenital bilateral absence of vas deferens",
            "description": ""
        },
        {
            "id": "MONDO:0010178",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010178",
            "name": "congenital bilateral aplasia of the vas deferens",
            "description": ""
        },
        {
            "id": "MONDO:0010178",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010178",
            "name": "vas deferens, congenital bilateral aplasia of",
            "description": ""
        },
        {
            "id": "MONDO:0010178",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010178",
            "name": "CAVD",
            "description": ""
        },
        {
            "id": "MONDO:0010178",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010178",
            "name": "CBAVD",
            "description": ""
        },
        {
            "id": "MIM:277180",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/277180",
            "name": "Congenital bilateral absence of the vas deferens",
            "description": "Congenital bilateral absence of the vas deferens"
        }
    ],
    "children": [
        {
            "id": "DOID:0111863",
            "label": "X-linked congenital bilateral absence of vas deferens",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111864",
            "label": "autosomal recessive congenital bilateral absence of vas deferens",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0111863",
        "DOID:0111862",
        "DOID:0111864"
    ],
    "unlinked_id_list": []
}