{
    "disease_id": "DOID:14179", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010421", 
            "name": "Bruton-type agammaglobulinemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010421", 
            "name": "Bruton's agammaglobulinaemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010421", 
            "name": "agammaglobulinemia, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010421", 
            "name": "agammaglobulinemia, BTK"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010421", 
            "name": "BTK deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010421", 
            "name": "Bruton agammaglobulinemia tyrosine kinase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010421", 
            "name": "hypogammaglobulinemia, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010421", 
            "name": "agammaglobulinemia, X-linked; XLA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010421", 
            "name": "Bruton's Sex-linked agammaglobulinemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010421", 
            "name": "agammaglobulinemia, Bruton tyrosine kinase"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010421", 
            "name": "Bruton's type agammaglobulinemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010421", 
            "name": "Bruton's agammaglobulinemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010421", 
            "name": "agammaglobulinemia, X-linked, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010421", 
            "name": "Bruton's X-linked agammaglobulinemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010421", 
            "name": "Bruton type agammaglobulinemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010421", 
            "name": "BTK-deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010421", 
            "name": "immunodeficiency 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010421", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010421", 
            "name": "XLA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14179", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14179", 
            "name": "BTK deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14179", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14179", 
            "name": "Bruton's Sex-Linked Agammaglobulinemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14179", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14179", 
            "name": "Bruton's agammaglobulinaemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14179", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14179", 
            "name": "Bruton's type agammaglobulinemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14179", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14179", 
            "name": "Bruton-type agammaglobulinemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14179", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14179", 
            "name": "Bruton agammaglobulinemia tyrosine kinase deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:14179", 
        "description": "An agammaglobulinemia that is that has_material_basis_in a mutation in the Bruton's tyrosine kinase (BTK) gene on the X chromosome resulting in X-linked agammaglobulinemia type 1, which is an immunodeficiency characterized by the failure to produce mature B lymphocytes, and associated with a failure of Ig heavy chain rearrangement.", 
        "resource": "Disease Ontology", 
        "id": "DOID:14179", 
        "name": "X-linked agammaglobulinemia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/14179#disease-associations", 
            "id": "14179", 
            "database": "Alliance of Genome Resources"
        }
    ]
}