Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 64072
Gene Symbol: CDH23
CDH23
0.320 GeneticVariation disease BEFREE The aim of the present study was to elucidate the role of the non‑syndromic autosomal recessive deafness 12 allelic variant of cadherin 23 (CDH23) in Chinese patients with non‑syndromic hearing loss. 31322239 2019
Entrez Id: 64072
Gene Symbol: CDH23
CDH23
0.320 GeneticVariation disease BEFREE Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23. 11090341 2001
Entrez Id: 64072
Gene Symbol: CDH23
CDH23
0.320 Biomarker disease GENOMICS_ENGLAND