Gene: CDH23 ×
Source: INFERRED ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 64072
Gene Symbol: CDH23
CDH23 		0.100 CausalMutation disease CLINVAR Variable clinical features in patients with CDH23 mutations (USH1D-DFNB12). 15353998 2004
Entrez Id: 64072
Gene Symbol: CDH23
CDH23 		0.100 CausalMutation disease CLINVAR Mutations in the calcium-binding motifs of CDH23 and the 35delG mutation in GJB2 cause hearing loss in one family. 12522556 2003
Entrez Id: 64072
Gene Symbol: CDH23
CDH23 		0.100 CausalMutation disease CLINVAR CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness. 12075507 2002