{
    "disease_id": "DOID:0061125",
    "recommended_name": {
        "id": "DOID:0061125",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061125",
        "name": "immunodeficiency 131",
        "description": "A primary immunodeficiency disease that is characterized by low IgM, IgG, and IgA serum levels, low plasma cell counts, abnormal T-cell subsets, and early graying of hair that has_material_basis_in heterozygous or homozygous mutation in the IRF4 gene on chromosome 6p25."
    },
    "synonyms": [
        {
            "id": "MONDO:0976229",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0976229",
            "name": "immunodeficiency 131",
            "description": ""
        },
        {
            "id": "MIM:621097",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/621097",
            "name": "Immunodeficiency 131",
            "description": "Immunodeficiency 131"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061125"
    ],
    "unlinked_id_list": []
}