congenital hypogammaglobulinemia Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
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Genes

10 genes co-occuring with the disease congenital hypogammaglobulinemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
IGHG2 immunoglobulin heavy constant gamma 2 (G2m marker) 1.53216
IGHG1 immunoglobulin heavy constant gamma 1 (G1m marker) 1.44957
IGLL1 immunoglobulin lambda-like polypeptide 1 1.4184
BLNK B-cell linker 1.20396
BTK Bruton agammaglobulinemia tyrosine kinase 1.01047
CD19 CD19 molecule 0.604591
CD79A CD79a molecule, immunoglobulin-associated alpha 0.481325
IL1A interleukin 1, alpha 0.313915
IL4 interleukin 4 0.306672
TNF tumor necrosis factor 0.167682