{
    "disease_id": "DOID:0111959",
    "recommended_name": {
        "id": "DOID:0111959",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111959",
        "name": "immunodeficiency 15B",
        "description": "A severe combined immunodeficiency characterized by onset in infancy of life-threatening bacterial, fungal, and viral infections, failure to thrive, impaired differentiation and activation of immune cells, and hypo- or agammaglobulinemia but relatively normal B and T cell numbers that has_material_basis_in homozygous or compound heterozygous mutation in the IKBKB gene on chromosome 8p11.21."
    },
    "synonyms": [
        {
            "id": "DOID:0111959",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111959",
            "name": "IMD15B",
            "description": ""
        },
        {
            "id": "MONDO:0014267",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014267",
            "name": "severe combined immunodeficiency due to IKK2 deficiency",
            "description": "Severe combined immunodeficiency due to IKK2 deficiency is a rare, genetic form of primary immunodeficiency characterized by life-threatening bacterial, fungal and viral infections with the onset in infancy, and failure to thrive. Typically, hypogammaglobulinemia or agammaglobulinemia and normal levels of T and B cells are present."
        },
        {
            "id": "MONDO:0014267",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014267",
            "name": "SCID due to IKK2 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0014267",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014267",
            "name": "immunodeficiency 15B",
            "description": ""
        },
        {
            "id": "MONDO:0014267",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014267",
            "name": "immunodeficiency type 15",
            "description": ""
        },
        {
            "id": "MONDO:0014267",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014267",
            "name": "IMD15",
            "description": ""
        },
        {
            "id": "MONDO:0014267",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014267",
            "name": "immunodeficiency 15",
            "description": ""
        },
        {
            "id": "MIM:615592",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615592",
            "name": "Immunodeficiency 15B",
            "description": "Immunodeficiency 15B"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111959"
    ],
    "unlinked_id_list": []
}