Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4275242
Disease: Sudden sensorineural hearing loss
Sudden sensorineural hearing loss
0.020 GeneticVariation disease BEFREE This is the first approach to analyze gene polymorphism and efficacy of clinical treatment of patients with SSNHL, although the observations do not confirm the effect of the GSTM1/T1 and CYP1A1 genotypes as a risk factor for SSNHL. 21389901 2011
CUI: C4275242
Disease: Sudden sensorineural hearing loss
Sudden sensorineural hearing loss
0.020 GeneticVariation disease BEFREE We investigated 80 Italian patients with SSNHL for the frequency of GSTT1 and GSTM1 polymorphisms. 16788422 2006