{
    "disease_id": "DOID:0061054",
    "recommended_name": {
        "id": "DOID:0061054",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061054",
        "name": "immunodeficiency 84",
        "description": "A primary immunodeficiency disease that is characterized by recurrent sinopulmonary infections from childhood associated with low levels of B cells and impaired early B-cell development and that has_material_basis_in heterozygous mutation in the IKZF3 gene on chromosome 17q12-q21."
    },
    "synonyms": [
        {
            "id": "MONDO:0030333",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030333",
            "name": "immunodeficiency 84",
            "description": ""
        },
        {
            "id": "MONDO:0030333",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030333",
            "name": "IMD84",
            "description": ""
        },
        {
            "id": "MONDO:0030333",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030333",
            "name": "immunodeficiency 84",
            "description": ""
        },
        {
            "id": "MONDO:0030333",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030333",
            "name": "immunodeficiency due to IKZF3 deficiency",
            "description": ""
        },
        {
            "id": "MIM:619437",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619437",
            "name": "Immunodeficiency 84",
            "description": "Immunodeficiency 84"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061054"
    ],
    "unlinked_id_list": []
}