IgA Deficiency Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A B cell deficiency that is an autosomal recessive disorder caused by mutation in the IgA (CD79 alpha) antigen receptor. (Human Disease Ontology, DOID_0060025)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D017098
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2 genes/proteins associated with the disease IgA Deficiency from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
IFIH1 interferon induced with helicase C domain 1 2.88009
CLEC16A C-type lectin domain family 16, member A 2.88009