{
    "disease_id": "DOID:0061088",
    "recommended_name": {
        "id": "DOID:0061088",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061088",
        "name": "immunodeficiency 122",
        "description": "A T cell, B cell, and NK cell deficiency that is characterized by early-infantile onset of recurrent viral and bacterial infections of the respiratory tract and skin and that has_material_basis_in homozygous mutation in the POLD3 gene on chromosome 11q13."
    },
    "synonyms": [
        {
            "id": "MONDO:0971151",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0971151",
            "name": "immunodeficiency 122",
            "description": ""
        },
        {
            "id": "MIM:620869",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620869",
            "name": "Immunodeficiency 122",
            "description": "Immunodeficiency 122"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061088"
    ],
    "unlinked_id_list": []
}