{
    "disease_id": "DOID:0081143",
    "recommended_name": {
        "id": "DOID:0081143",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081143",
        "name": "agammaglobulinemia 8B",
        "description": "An agammaglobulinemia that is characterized by onset of recurrent infections in early childhood and that has_material_basis_in homozygous loss-of-function mutation in the TCF3 gene on chromosome 19p13."
    },
    "synonyms": [
        {
            "id": "MONDO:0859234",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0859234",
            "name": "agammaglobulinemia 8b, autosomal recessive",
            "description": ""
        },
        {
            "id": "MIM:619824",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619824",
            "name": "Agammaglobulinemia 8B, autosomal recessive",
            "description": "Agammaglobulinemia 8B, autosomal recessive"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081143"
    ],
    "unlinked_id_list": []
}