Term Name:	Usher syndrome type 1D
Synonyms:	USH1D, Usher syndrome type ID
Definition:	An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the CDH23 gene on chromosome 10q22.
Ontology:	Human Disease [DOID:0110831]   ( DOID:0110831 )