{{Rsnum
|rsid=111033270
|Chromosome=10
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CDH23
|position=71779316
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CDH23
}}{{omim
|id=605516
|rsnum=111033270
|variant=0002
}}{{ClinVar
|rsid=111033270
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=73539073
|CHROM=10
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050068000000000002110100
|GENEINFO=CDH23:64072
|GENE_NAME=CDH23
|GENE_ID=64072
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.73539073G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605516.0002
|CLNSIG=5
|CLNCUI=C1832845
|CLNDBN=Usher syndrome, type 1D; Hereditary hearing loss and deafness; Retinitis pigmentosa-deafness syndrome
|Disease=Usher syndrome; Hereditary hearing loss and deafness; Retinitis pigmentosa-deafness syndrome
|CLNACC=RCV000005198.1; RCV000039205.1
|Tags=PM;PMC;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet; GeneReviews:MedGen:SNOMED_CT; MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1265:C1832845:601067:231169:886; NBK1434:C0236038:95827002; C0271097:500004:231183:886:57838006
}}{{PMID|11138009}} Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.

{{PMID|12075507|OA=1
}} CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness.

{{PMID|18273900}} Usher syndrome type 1 due to missense mutations on both CDH23 alleles: investigation of mRNA splicing.