{
    "disease_id": "DOID:14176", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:14176", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14176", 
            "name": "Immunoglobin G subclass deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14176", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14176", 
            "name": "Selective IgG Immunodeficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14176", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14176", 
            "name": "Selective Immunoglobulin G Subclass deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14176", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14176", 
            "name": "Selective deficiency of IgG"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14176", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14176", 
            "name": "Selective immunoglobulin G deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:14176", 
        "description": "A dysgammaglobulinemia that is characterized by isolated deficiency of an IgG subclass, normal total IgG levels, and subsequent increased susceptibility to recurrent infections, atopic disease, and autoimmune conditions.", 
        "resource": "Disease Ontology", 
        "id": "DOID:14176", 
        "name": "selective IgG deficiency disease"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/14176#disease-associations", 
            "id": "14176", 
            "database": "Alliance of Genome Resources"
        }
    ]
}