|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
2 genes/proteins associated with the disease IgA Deficiency from the curated CTD Gene-Disease Associations dataset.