Term Name:	Usher syndrome type 1C
Synonyms:	USH1C, Usher syndrome type I Acadian variety, Usher syndrome type IC
Definition:	An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the USH1C gene on chromosome 11p15.
Ontology:	Human Disease [DOID:0110830]   ( DOID:0110830 )