Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4907
Gene Symbol: NT5E
NT5E
0.010 Biomarker disease BEFREE Sudden sensorineural hearing loss (SSNHL) is a common and alarming symptom that often prompts an urgent visit to an ENT specialist. 29396226 2018
Entrez Id: 3105
Gene Symbol: HLA-A
HLA-A
0.010 Biomarker disease BEFREE HLA-A and HLA-B typing using a standard microlymphocytotoxicity technique and HLA-DRB1 genotyping were performed in 35 patients with sudden sensorineural hearing loss and in 206 healthy controls. 11099146 2000
Entrez Id: 27306
Gene Symbol: HPGDS
HPGDS
0.010 GeneticVariation disease BEFREE Glutathione s-transferase gene polymorphisms in Italian patients with sudden sensorineural hearing loss. 16788422 2006
Entrez Id: 3383
Gene Symbol: ICAM1
ICAM1
0.020 AlteredExpression disease BEFREE Intercellular adhesion molecule 1 and VCAM-1 levels in sera of patients with SSHL were significantly higher than those of the matched control subjects (p < 0.001). 18401280 2008
Entrez Id: 2153
Gene Symbol: F5
F5
0.030 Biomarker disease BEFREE Factor V Leiden (FVL) is by far the most prevalent inherited thrombophilic abnormality in Western countries, and this genetic condition has been associated with sudden sensorineural hearing loss (SSHL). 24735015 2014
Entrez Id: 79977
Gene Symbol: GRHL2
GRHL2
0.010 GeneticVariation disease BEFREE GRHL2 genetic polymorphisms, rs611419 and rs10955255, have a protective role against SSHL and reduce the risk of SSHL. 26847018 2016
Entrez Id: 2878
Gene Symbol: GPX3
GPX3
0.010 Biomarker disease BEFREE GPX3 may be one of the aetiologies of sudden sensorineural hearing loss (SSNHL), which might be attributed to the genetic effect of GPX3 by influence reactive oxygen species (ROS). 28738977 2017
Entrez Id: 375611
Gene Symbol: SLC26A5
SLC26A5
0.010 Biomarker disease BEFREE Prestin autoantibodies screening in idiopathic sudden sensorineural hearing loss. 30606654 2019
Entrez Id: 4049
Gene Symbol: LTA
LTA
0.010 GeneticVariation disease BEFREE A significant increase was found for the TNF-beta allele 1 in SSNHL patients compared with the controls (chi( 2) = 7.251, P = .007, odds ratio [OR] = 1.534, confidence interval [CI] = 1.12-2.10). 19833626 2010
Entrez Id: 2147
Gene Symbol: F2
F2
0.040 GeneticVariation disease BEFREE According to our data, factor V G1691A, prothrombin G20210A, and MTHFR C677T variants should be not considered risk factors for SSNHL. 16572609 2006
Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
0.070 GeneticVariation disease BEFREE According to our data, factor V G1691A, prothrombin G20210A, and MTHFR C677T variants should be not considered risk factors for SSNHL. 16572609 2006
Entrez Id: 3569
Gene Symbol: IL6
IL6
0.030 AlteredExpression disease BEFREE Both the -174G/G polymorphism and elevated IL-6 levels in SSNHL patients could suggest that IL-6 plays a role in the inner ear involvement by atherosclerotic inflammatory events. 25345762 2015
Entrez Id: 9961
Gene Symbol: MVP
MVP
0.010 Biomarker disease BEFREE Chi-squared tests were used to compare differences in sociodemographic characteristics, while conditional logistic regression analyses were used to examine the association of SSNHL with previously diagnosed MVP. 30286192 2018
Entrez Id: 129831
Gene Symbol: RBM45
RBM45
0.020 GeneticVariation disease BEFREE Distribution of HLA-A, -B and -DRB1 alleles in patients with sudden sensorineural hearing loss. 11099146 2000
Entrez Id: 718
Gene Symbol: C3
C3
0.010 AlteredExpression disease BEFREE Fasting blood glucose levels, complement C3, C4, and fibrinogen may be closely related to childhood SSNHL. 30870353 2019
Entrez Id: 183
Gene Symbol: AGT
AGT
0.010 GeneticVariation disease BEFREE Furthermore, the AGT and GAC haplotypes were associated with a significantly higher prevalence of SSNHL than were the GAT, GGC and GGT haplotypes. 26051414 2015
Entrez Id: 2744
Gene Symbol: GLS
GLS
0.010 GeneticVariation disease BEFREE Furthermore, the AGT and GAC haplotypes were associated with a significantly higher prevalence of SSNHL than were the GAT, GGC and GGT haplotypes. 26051414 2015
Entrez Id: 2147
Gene Symbol: F2
F2
0.040 Biomarker disease BEFREE Hematologic investigation, including MTHFR, prothrombin, platelet, and V Leiden genotyping, may help to detect patients at potential risk of recurrent hearing loss and multiple microvascular diseases, and could be usefully performed in otherwise idiopathic sudden sensorineural hearing loss. 19374152 2009
Entrez Id: 3066
Gene Symbol: HDAC2
HDAC2
0.010 AlteredExpression disease BEFREE Here, we investigated the protective effects of aminophylline on HDAC2 expression and glucocorticoid sensitivity in lipopolysaccharide (LPS)-induced sudden sensorineural hearing loss in guinea pigs. 28578424 2017
Entrez Id: 3106
Gene Symbol: HLA-B
HLA-B
0.010 Biomarker disease BEFREE HLA-A and HLA-B typing using a standard microlymphocytotoxicity technique and HLA-DRB1 genotyping were performed in 35 patients with sudden sensorineural hearing loss and in 206 healthy controls. 11099146 2000
Entrez Id: 129831
Gene Symbol: RBM45
RBM45
0.020 Biomarker disease BEFREE Human leukocyte antigen-DQB1 and -DRB1 associations in patients with idiopathic sudden sensorineural hearing loss from a defined population of Northwest Spain. 16303674 2005
Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
0.020 Biomarker disease BEFREE Human leukocyte antigen-DQB1 and -DRB1 associations in patients with idiopathic sudden sensorineural hearing loss from a defined population of Northwest Spain. 16303674 2005
Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
0.070 GeneticVariation disease BEFREE Impact of methionine synthase gene and methylenetetrahydrofolate reductase gene polymorphisms on the risk of sudden sensorineural hearing loss. 16778415 2006
Entrez Id: 929
Gene Symbol: CD14
CD14
0.010 Biomarker disease BEFREE In addition, the percentage of CD14(+) monocytes expressing TLR2 in SNNHL patients was higher than in normal controls assessed by flow cytometry and significantly correlated with the hearing thresholds of the affected ear (P < 0.05). 25809471 2015
Entrez Id: 7097
Gene Symbol: TLR2
TLR2
0.010 AlteredExpression disease BEFREE In addition, the percentage of CD14(+) monocytes expressing TLR2 in SNNHL patients was higher than in normal controls assessed by flow cytometry and significantly correlated with the hearing thresholds of the affected ear (P < 0.05). 25809471 2015