Human genes for Usher syndrome type 1C
Usher syndrome type 1C [DOID:0110830]
An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the USH1C gene on chromosome 11p15.
Synonyms: Usher syndrome type 1C, DOID:0110830, Usher syndrome type I Acadian variety, Usher syndrome type IC, Usher syndrome type I Acadian varieties ...