Term Name:	Usher syndrome type 1G
Synonyms:	USH1G, Usher syndrome type IG
Definition:	An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the USH1G gene on chromosome 17q25.
Ontology:	Human Disease [DOID:0110834]   ( DOID:0110834 )