Usher syndrome type 1D

A form of Usher syndrome type I that is caused by homozygous or compound heterozygous mutation in the gene encoding cadherin-23 (CDH23) on chromosome 10q22. It is inherited in an autosomal recessive manner.

Also known as: USH1D, Usher syndrome, type 1D/F digenic, USHER syndrome, type ID, Ush1D/F, Cdh23/Pcdh15, digenic, Usher syndrome, type 1D, Usher syndrome, type Id/F, Cdh23/Pcdh15, digenic

1 clinical trial for this condition and its sub-types.