{
    "disease_id": "DOID:0060025", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012291", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012291", 
            "name": "immunoglobulin A deficiency 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012291", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012291", 
            "name": "TNFRSF13B selective IgA deficiency disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012291", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012291", 
            "name": "IMMUNOGLOBULIN A deficiency 2; IGAD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012291", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012291", 
            "name": "selective IgA deficiency disease caused by mutation in TNFRSF13B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012291", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012291", 
            "name": "Immunoglobulin a deficiency type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012291", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012291", 
            "name": "IGAD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012291", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012291", 
            "name": "Immunoglobulin A, selective deficiency of, TACI-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012291", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012291", 
            "name": "IgA, selective deficiency of, TACI-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012291", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012291", 
            "name": "Immunoglobulin A, selective deficiency of, TACI related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012291", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012291", 
            "name": "IgA, selective deficiency of, TACI related"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060025", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060025", 
            "name": "IgA deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060025", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060025", 
            "name": "gamma-A-globulin deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060025", 
        "description": "A B cell deficiency that is an autosomal recessive disorder that has_material_basis_in mutation in the IgA (CD79 alpha) antigen receptor.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060025", 
        "name": "immunoglobulin alpha deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060025#disease-associations", 
            "id": "0060025", 
            "database": "Alliance of Genome Resources"
        }
    ]
}