Disease: hearing impairment ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.330 Biomarker phenotype BEFREE Here we examined the ethnic differences, allele and genotype frequencies of the NAT2, GRM7, and GRHL2 genes pooled samples of healthy Hungarian and healthy and hearing impaired Roma people. 29455378 2019
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.330 Biomarker phenotype GENOMICS_ENGLAND Mutations in GRHL2 result in an autosomal-recessive ectodermal Dysplasia syndrome. 25152456 2014
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.330 GeneticVariation phenotype BEFREE The grainyhead-like 2 gene (GRHL2) single nucleotide polymorphism is not associated with age-related hearing impairment in Han Chinese. 21557239 2011
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.330 GeneticVariation phenotype BEFREE The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment. 17921507 2008