{
    "disease_id": "DOID:0061097",
    "recommended_name": {
        "id": "DOID:0061097",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061097",
        "name": "immunodeficiency 132B",
        "description": "A primary immunodeficiency disease that is characterized by recurrent upper and lower respiratory infections caused by various pathogens beginning in childhood, B-cell lymphoid hyperplasia, and dysregulation of T-cell subsets and function and that has_material_basis_in heterozygous loss-of-function mutation in the TRAF3 gene on chromosome 14q32."
    },
    "synonyms": [
        {
            "id": "MONDO:0976228",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0976228",
            "name": "immunodeficiency 132b",
            "description": ""
        },
        {
            "id": "MIM:621096",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/621096",
            "name": "Immunodeficiency 132B",
            "description": "Immunodeficiency 132B"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061097"
    ],
    "unlinked_id_list": []
}