{
    "disease_id": "DOID:0081153",
    "recommended_name": {
        "id": "DOID:0081153",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081153",
        "name": "common variable immunodeficiency 11",
        "description": "A common variable immunodeficiency that has_material_basis_in homozygous mutation in the IL21 gene on chromosome 4q27."
    },
    "synonyms": [
        {
            "id": "MONDO:0014338",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014338",
            "name": "IL21-related infantile inflammatory bowel disease",
            "description": ""
        },
        {
            "id": "MONDO:0014338",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014338",
            "name": "IL21-related infantile IBD",
            "description": ""
        },
        {
            "id": "MONDO:0014338",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014338",
            "name": "immunodeficiency, common variable, type 11",
            "description": ""
        },
        {
            "id": "MONDO:0014338",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014338",
            "name": "CVID11",
            "description": ""
        },
        {
            "id": "MONDO:0014338",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014338",
            "name": "immunodeficiency, common variable, 11",
            "description": ""
        },
        {
            "id": "MIM:615767",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615767",
            "name": "Immunodeficiency, common variable, 11",
            "description": "Immunodeficiency, common variable, 11"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081153"
    ],
    "unlinked_id_list": []
}