Term Name:	Usher syndrome type 1B
Synonyms:	USH1B, Usher syndrome type IB
Definition:	An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the MYO7A gene on chromosome 11q13.
Ontology:	Human Disease [DOID:0070655]   ( DOID:0070655 )