igm deficiency Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormally decreased level of immunoglobulin IgM in blood. (Human Phenotype Ontology, HP_0002850)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002850
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10 genes associated with the igm deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BLM Bloom syndrome, RecQ helicase-like
CARD11 caspase recruitment domain family, member 11
CNBP CCHC-type zinc finger, nucleic acid binding protein
ICOS inducible T-cell co-stimulator
LAMTOR2 late endosomal/lysosomal adaptor, MAPK and MTOR activator 2
LRBA LPS-responsive vesicle trafficking, beach and anchor containing
PLCG2 phospholipase C, gamma 2 (phosphatidylinositol-specific)
TCN2 transcobalamin II
TNFRSF13B tumor necrosis factor receptor superfamily, member 13B
WAS Wiskott-Aldrich syndrome