Human genes for Usher syndrome type 1F
Usher syndrome type 1F [DOID:0110832]
An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the PCDH15 gene on chromosome 10q.
Synonyms: Usher syndrome type 1F, DOID:0110832, USH1F, Usher syndrome type IF, Usher syndrome type IFs