{
    "disease_id": "DOID:0081145",
    "recommended_name": {
        "id": "DOID:0081145",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081145",
        "name": "common variable immunodeficiency 2",
        "description": "A common variable immunodeficiency that has_material_basis_in heterozygous, homozygous, or compound heterozygous mutation in the TNFRSF13B gene, which encodes the transmembrane activator and CAML interactor (TACI), on chromosome 17p11.2."
    },
    "synonyms": [
        {
            "id": "MONDO:0009413",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009413",
            "name": "immunodeficiency, common variable, 2",
            "description": ""
        },
        {
            "id": "MONDO:0009413",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009413",
            "name": "immunodeficiency, common variable, 2",
            "description": ""
        },
        {
            "id": "MONDO:0009413",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009413",
            "name": "immunodeficiency, common variable, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0009413",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009413",
            "name": "CVID2",
            "description": ""
        },
        {
            "id": "MIM:240500",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/240500",
            "name": "Immunodeficiency, common variable, 2",
            "description": "Immunodeficiency, common variable, 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081145"
    ],
    "unlinked_id_list": []
}