Usher syndrome type 1C

A form of Usher syndrome type I that is caused by homozygous or compound heterozygous mutation in the gene encoding harmonin on chromosome 11p15. It is inherited in an autosomal recessive manner.

Also known as: USH1C, Usher syndrome type 1C, USHER syndrome, type IC, Usher syndrome, Acadian variety, Usher syndrome, type 1C, Usher syndrome, type I, Acadian variety

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