{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013288", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013288", 
            "name": "agammaglobulinemia 3, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013288", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013288", 
            "name": "agammaglobulinemia 3, autosomal recessive; AGM3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013288", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013288", 
            "name": "autosomal agammaglobulinemia caused by mutation in CD79A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013288", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013288", 
            "name": "AGM3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013288", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013288", 
            "name": "agammaglobulinemia, autosomal recessive, due to Cd79A defect"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013288", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013288", 
            "name": "CD79A autosomal agammaglobulinemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2583", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2583", 
            "name": "IGHM"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2583", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2583", 
            "name": "hypogammaglobulinemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2583", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2583", 
            "name": "mu heavy chain deficiency"
        }, 
        {
            "url": "https://www.omim.org/entry/613501", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:613501", 
            "name": "Agammaglobulinemia 3, autosomal recessive"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2583", 
        "description": "A B cell deficiency that is caused by a reduction in all types of gamma globulins.", 
        "resource": "Disease Ontology", 
        "id": "DOID:2583", 
        "name": "agammaglobulinemia"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613501", 
            "id": "613501", 
            "database": "MIM"
        }
    ]
}