Term Name:	Usher syndrome type 1F
Synonyms:	USH1F, Usher syndrome type IF
Definition:	An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the PCDH15 gene on chromosome 10q.
Ontology:	Human Disease [DOID:0110832]   ( DOID:0110832 )