Disease: Immunoglobulin A deficiency (disorder) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0162538
Disease: Immunoglobulin A deficiency (disorder)
Immunoglobulin A deficiency (disorder) 		0.070 GeneticVariation disease BEFREE Therefore, our work seems to discard a role of TNFRSF13B mutations in IgAD, concordantly with the most recent published studies. 19392801 2009
CUI: C0162538
Disease: Immunoglobulin A deficiency (disorder)
Immunoglobulin A deficiency (disorder) 		0.070 GeneticVariation disease BEFREE Mutations in TACI were also found in relatives of patients with CVID who suffered from IgA deficiency (IgAD) as well as in a patient with isolated IgAD. 17917015 2007
CUI: C0162538
Disease: Immunoglobulin A deficiency (disorder)
Immunoglobulin A deficiency (disorder) 		0.070 GeneticVariation disease LHGDN Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency. 17392797 2007
CUI: C0162538
Disease: Immunoglobulin A deficiency (disorder)
Immunoglobulin A deficiency (disorder) 		0.070 GeneticVariation disease LHGDN Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency. 17392798 2007
CUI: C0162538
Disease: Immunoglobulin A deficiency (disorder)
Immunoglobulin A deficiency (disorder) 		0.070 GeneticVariation disease BEFREE Recently, patients with CVID and IGAD have been found to have mutations of the gene TNFRSF13B encoding the TACI (transmembrane activator and calcium-modulator and cyclophilin-ligand interactor), a member of the tumor necrosis factor-receptor superfamily. 16899196 2006
CUI: C0162538
Disease: Immunoglobulin A deficiency (disorder)
Immunoglobulin A deficiency (disorder) 		0.070 AlteredExpression disease BEFREE Common variable immunodeficiency, CVID, is a primary antibody deficiency characterized by decreased levels of serum immunoglobulin G (IgG), decreased IgA and/or IgM and recurrent infections. 15963052 2005
CUI: C0162538
Disease: Immunoglobulin A deficiency (disorder)
Immunoglobulin A deficiency (disorder) 		0.070 GeneticVariation disease LHGDN These results suggest that TACI mutations can result in CVID and IgAD. 16007086 2005
CUI: C0162538
Disease: Immunoglobulin A deficiency (disorder)
Immunoglobulin A deficiency (disorder) 		0.070 GeneticVariation disease BEFREE These results suggest that TACI mutations can result in CVID and IgAD. 16007086 2005