{
    "disease_id": "DOID:0111960",
    "recommended_name": {
        "id": "DOID:0111960",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111960",
        "name": "immunodeficiency 15A",
        "description": "A combined T cell and B cell immunodeficiency characterized by immune dysregulation, combined T and B cell deficiency, inflammation, and epithelial defects that has_material_basis_in heterozygous missense mutation in the IKBKB gene on chromosome 8p11.21."
    },
    "synonyms": [
        {
            "id": "DOID:0111960",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111960",
            "name": "IMD15A",
            "description": ""
        },
        {
            "id": "MONDO:0032599",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032599",
            "name": "immunodeficiency 15a",
            "description": ""
        },
        {
            "id": "MONDO:0032599",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032599",
            "name": "IMD15A",
            "description": ""
        },
        {
            "id": "MIM:618204",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618204",
            "name": "Immunodeficiency 15A",
            "description": "Immunodeficiency 15A"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111960"
    ],
    "unlinked_id_list": []
}