{
    "disease_id": "DOID:0081140",
    "recommended_name": {
        "id": "DOID:0081140",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081140",
        "name": "agammaglobulinemia 8A",
        "description": "An agammaglobulinemia that has_material_basis_in heterozygous dominant-negative mutation in the TCF3 gene on chromosome 19p13."
    },
    "synonyms": [
        {
            "id": "MONDO:0014840",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014840",
            "name": "agammaglobulinemia 8, autosomal dominant",
            "description": "Any autosomal agammaglobulinemia in which the cause of the disease is a mutation in the TCF3 gene."
        },
        {
            "id": "MONDO:0014840",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014840",
            "name": "AGM8",
            "description": ""
        },
        {
            "id": "MONDO:0014840",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014840",
            "name": "TCF3 autosomal agammaglobulinemia",
            "description": ""
        },
        {
            "id": "MONDO:0014840",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014840",
            "name": "agammaglobulinemia 8, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0014840",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014840",
            "name": "agammaglobulinemia 8, autosomal dominant; AGM8",
            "description": ""
        },
        {
            "id": "MONDO:0014840",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014840",
            "name": "autosomal agammaglobulinemia caused by mutation in TCF3",
            "description": ""
        },
        {
            "id": "MIM:616941",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616941",
            "name": "Agammaglobulinemia 8A, autosomal dominant",
            "description": "Agammaglobulinemia 8A, autosomal dominant"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081140"
    ],
    "unlinked_id_list": []
}