Term Name:	Usher syndrome type 2D
Synonyms:	USH2D, Usher syndrome type IID
Definition:	An Usher syndrome type 2 that has_material_basis_in by homozygous or compound heterozygous mutation in the WHRN gene on chromosome 9q32.
Ontology:	Human Disease [DOID:0110840]   ( DOID:0110840 )