{
    "disease_id": "DOID:0060758", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011528", 
            "name": "hyper-IgM syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011528", 
            "name": "HIGM2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011528", 
            "name": "immunodeficiency with hyper IgM type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011528", 
            "name": "immunodeficiency with hyper-IgM, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011528", 
            "name": "hyper-IgM syndrome caused by mutation in AICDA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011528", 
            "name": "immunodeficiency with hyper-IgM, type 2; HIGM2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011528", 
            "name": "aid deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011528", 
            "name": "hyper-IgM syndrome 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011528", 
            "name": "activation-induced cytidine deaminase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011528", 
            "name": "hyper IgM syndrome 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011528", 
            "name": "AICDA hyper-IgM syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060758", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060758", 
            "name": "AID deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060758", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060758", 
            "name": "HIGM2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060758", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060758", 
            "name": "activation-induced cytidine deaminase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060758", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060758", 
            "name": "hyper-IgM syndrome type 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060758", 
        "description": "A hyper IgM syndrome that is characterized by normal or elevated serum IgM levels with absence of IgG, IgA, and IgE, resulting in a profound susceptibility to bacterial infections that has_material_basis_in homozygous or compound heterozygous mutation in the AICDA gene on chromosome 12p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060758", 
        "name": "immunodeficiency with hyper-IgM type 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060758#disease-associations", 
            "id": "0060758", 
            "database": "Alliance of Genome Resources"
        }
    ]
}