{
    "disease_id": "DOID:0111999", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010296", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010296", 
            "name": "AGMX2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010296", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010296", 
            "name": "agammaglobulinemia, X-linked, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010296", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010296", 
            "name": "agammaglobulinemia X-linked type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010296", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010296", 
            "name": "XLA2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010296", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010296", 
            "name": "agammaglobulinemia, X-linked, type 2; AGMX2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111999", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111999", 
            "name": "IMD61"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111999", 
        "description": "A B cell deficiency characterized by onset in early childhood of recurrent infections due to an intrinsic defect in the ability of B cells to produce antibodies that has_material_basis_in hemizygous mutation in SH3KBP1 on chromosome Xp22.12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111999", 
        "name": "immunodeficiency 61"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111999#disease-associations", 
            "id": "0111999", 
            "database": "Alliance of Genome Resources"
        }
    ]
}