Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
0.800 Biomarker disease MGD
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
0.800 GermlineCausalMutation disease ORPHANET Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome. 17676033 2007
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
0.800 GermlineCausalMutation disease ORPHANET STAT3 mutations in the hyper-IgE syndrome. 17881745 2007
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
0.800 GeneticVariation disease BEFREE In 2007, mutations in signal transducer and activator of transcription 3 (STAT3) were determined to be the cause of autosomal-dominant HIES. 18978467 2008
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
0.800 Biomarker disease BEFREE Since STAT-3 plays a role in B cell development and differentiation, we analyzed memory B cells in 20 patients with HIES, 17 of which had STAT-3 mutations. 18835223 2008
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
0.800 GeneticVariation disease BEFREE Recently it was shown that heterozygous signal transducer and activator of transcription 3 (STAT3) mutations cause autosomal-dominant HIES. 18602572 2008
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
0.800 Biomarker disease BEFREE Conversely, IEC-specific Stat3 deficiency enhances susceptibility to chemically induced epithelial damage and subsequent mucosal inflammation, while excessive Stat3 activation confers resistance to colitis. 19185844 2009
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
0.800 Biomarker disease BEFREE In this article, we will review how the study of STAT3 deficiency in humans and mice has highlighted nonredundant roles of STAT3, and of specific cytokines, in diverse cellular processes such as antimicrobial immunity and protection at epithelial barriers, the generation of functional humoral immune responses, bone formation, and keratinocyte biology. 19109129 2009
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
0.800 Biomarker disease BEFREE In addition, we discuss animal models of STAT3 deficiency that provide insight into the pathogenesis of HIES. 19190525 2009
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
0.800 GeneticVariation disease BEFREE Mutations in STAT3 cause autosomal dominant HIES (Job's syndrome), which is unique in its diversity of connective tissue, skeletal, and vascular abnormalities. 21178271 2010
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
0.800 GeneticVariation disease BEFREE By contrast, CMC is one of the few key infections in patients with autosomal dominant hyper IgE syndrome (mutations in STAT3), and in rare patients with autosomal recessive predisposition to mucocutaneous and invasive fungal infections (mutation in CARD9). 20674321 2010
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
0.800 GeneticVariation disease BEFREE Rapid molecular analysis of the STAT3 gene in Job syndrome of hyper-IgE and recurrent infectious diseases. 20093388 2010
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
0.800 GeneticVariation disease BEFREE Recently, it was shown that heterozygous mutations in signal transducer and activator of transcription 3 (STAT3), can cause autosomal-dominant HIES. 20149460 2010
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
0.800 GeneticVariation disease BEFREE Mutations in STAT3 are associated with AD-HIES, whereas mutations in DOCK8, or rarely TYK2, are associated with AR-HIES. 21970826 2011
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
0.800 GeneticVariation disease BEFREE Patients with autosomal-dominant hyper-IgE syndrome (AD-HIES) carry dominant-negative STAT3 mutations and are susceptible to a variety of bacterial and fungal infections. 22118528 2011
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
0.800 GeneticVariation disease BEFREE Autosomal dominant HIES (AD-HIES) is a primary immunodeficiency caused by dominant negative mutations in STAT3 clustered in the DNA binding and SH2 domains. 21288777 2011
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
0.800 AlteredExpression disease BEFREE STAT3 activation also induced expression of receptor activator of nuclear factor kappa B ligand (RANKL), a cytokine essential for osteoclastogenesis, and STAT3 deficiency or pharmacological inhibition promoted significant reduction in expression of both IL-6 family cytokines and RANKL in vitro. 21937456 2011
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
0.800 GeneticVariation disease BEFREE Autosomal-dominant hyper-IgE syndrome (AD-HIES) is a primary immunodeficiency caused by STAT3 mutations. 21792878 2011
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
0.800 GeneticVariation disease BEFREE Autosomal dominant HIES has been shown to be mainly due to STAT3 mutations and additionally results in connective tissue, skeletal, vascular and dental abnormalities. 23210525 2012
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
0.800 GeneticVariation disease BEFREE Autosomal dominant hyper-IgE syndrome (AD-HIES) or Job's syndrome is a primary immunodeficiency with a wide array of clinical features caused by dominant negative mutations in STAT3. 22268731 2012
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
0.800 Biomarker disease BEFREE STAT3 mosaicism accounts for a milder phenotype and allows for further investigation into the pathogenesis of AD-HIES. 23623265 2013
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
0.800 GeneticVariation disease BEFREE Signal transducer and activator of transcription 3 (STAT3) mutations underlying autosomal dominant hyper-IgE syndrome impair human CD8(+) T-cell memory formation and function. 23830147 2013
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
0.800 GeneticVariation disease BEFREE Autosomal dominant hyper-IgE syndrome (AD-HIES) due to heterozygous STAT3 mutation is a primary immunodeficiency characterized by eczema, elevated serum IgE, recurrent infections, and connective tissue and skeletal findings. 23584561 2013
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
0.800 Biomarker disease BEFREE This in vitro phenotype was reproduced in mice infused with STAT3 inhibitors and mice with platelet-specific STAT3 deficiency. 23266857 2013
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
0.800 GeneticVariation disease BEFREE Nearly every patient with autosomal-dominant hyper-IgE syndrome (AD-HIES) due to signal transducer and activator of transcription 3 (STAT3) mutations has a history of eczematous dermatitis and elevated IgE; however, clinical atopy has never been systematically studied. 24184145 2013