Term Name:	Usher syndrome type 3A
Synonyms:	USH3A, Usher syndrome type IIIA
Definition:	An Usher syndrome type 3 that has_material_basis_in homozygous or compound heterozygous mutation in the CLRN1 gene on chromosome 3q25.
Ontology:	Human Disease [DOID:0110841]   ( DOID:0110841 )