{
    "disease_id": "DOID:0081150",
    "recommended_name": {
        "id": "DOID:0081150",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0081150",
        "name": "common variable immunodeficiency 7",
        "description": "A common variable immunodeficiency that has_material_basis_in compound heterozygous mutation in the CD21 gene (CR2) on chromosome 1q32."
    },
    "synonyms": [
        {
            "id": "MONDO:0013862",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013862",
            "name": "immunodeficiency, common variable, 7",
            "description": ""
        },
        {
            "id": "MONDO:0013862",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013862",
            "name": "immunodeficiency, common variable, 7",
            "description": ""
        },
        {
            "id": "MONDO:0013862",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013862",
            "name": "immunodeficiency, common variable, type 7",
            "description": ""
        },
        {
            "id": "MONDO:0013862",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013862",
            "name": "CVID7",
            "description": ""
        },
        {
            "id": "MIM:614699",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614699",
            "name": "Immunodeficiency, common variable, 7",
            "description": "Immunodeficiency, common variable, 7"
        }
    ]
}