agammaglobulinemia Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A B cell deficiency that is caused by a reduction in all types of gamma globulins. (Human Disease Ontology, DOID_2583)
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Genes

2 genes associated with the disease agammaglobulinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
BTK Bruton agammaglobulinemia tyrosine kinase
TNFRSF13B tumor necrosis factor receptor superfamily, member 13B