Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2936664
Disease: Acquired Hypogammaglobulinemia
Acquired Hypogammaglobulinemia
0.370 AlteredExpression disease BEFREE In contrast, circulating follicular helper T-cell frequency and expression of inducible T-cell co-stimulator and chemokine receptors were only significantly altered in patients with common variable immunodeficiency. 27634199 2017
CUI: C2936664
Disease: Acquired Hypogammaglobulinemia
Acquired Hypogammaglobulinemia
0.370 GeneticVariation disease BEFREE Three different classifications, B lymphocyte subpopulations, TNFRSF13B (TACI), TNFRSF13C (BAFF-R), TNFSF13 (APRIL) gene mutations, CTLA-4 and ICOS gene polymorphisms in Turkish patients with common variable immunodeficiency. 22699762 2012
CUI: C2936664
Disease: Acquired Hypogammaglobulinemia
Acquired Hypogammaglobulinemia
0.370 Biomarker disease BEFREE The role of costimulation in antibody deficiencies: ICOS and common variable immunodeficiency. 19426217 2009
CUI: C2936664
Disease: Acquired Hypogammaglobulinemia
Acquired Hypogammaglobulinemia
0.370 Biomarker disease BEFREE Human ICOS deficiency abrogates the germinal center reaction and provides a monogenic model for common variable immunodeficiency. 16384931 2006
CUI: C2936664
Disease: Acquired Hypogammaglobulinemia
Acquired Hypogammaglobulinemia
0.370 Biomarker disease BEFREE ICOS deficiency in patients with common variable immunodeficiency. 15507387 2004
CUI: C2936664
Disease: Acquired Hypogammaglobulinemia
Acquired Hypogammaglobulinemia
0.370 GeneticVariation disease BEFREE Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency. 12577056 2003
CUI: C2936664
Disease: Acquired Hypogammaglobulinemia
Acquired Hypogammaglobulinemia
0.370 GeneticVariation disease BEFREE Recently, the authors discovered that the homozygous loss of the ICOS in humans presents as common variable immunodeficiency, the most prevalent treated primary immunodeficiency in man. 14612664 2003
CUI: C2936664
Disease: Acquired Hypogammaglobulinemia
Acquired Hypogammaglobulinemia
0.370 Biomarker disease CTD_human