severe b lymphocytopenia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A severe form of B lymphocytopenia in which the count of B cells is very low or absent. (Human Phenotype Ontology, HP_0005365)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005365
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Genes

4 genes associated with the severe b lymphocytopenia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADA adenosine deaminase
DCLRE1C DNA cross-link repair 1C
RAG1 recombination activating gene 1
RAG2 recombination activating gene 2