{
    "disease_id": "DOID:0111959", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014267", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014267", 
            "name": "severe combined immunodeficiency due to IKK2 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014267", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014267", 
            "name": "IMD15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014267", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014267", 
            "name": "immunodeficiency type 15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014267", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014267", 
            "name": "immunodeficiency 15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014267", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014267", 
            "name": "SCID due to IKK2 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014267", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014267", 
            "name": "immunodeficiency 15; IMD15"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111959", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111959", 
            "name": "IMD15B"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111959", 
        "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 IKBKB on chromosome 8p11.21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111959", 
        "name": "immunodeficiency 15B"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111959#disease-associations", 
            "id": "0111959", 
            "database": "Alliance of Genome Resources"
        }
    ]
}