Human genes for Usher syndrome type 1G
Usher syndrome type 1G [DOID:0110834]
An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the USH1G gene on chromosome 17q25.
Synonyms: Usher syndrome type 1G, DOID:0110834, Usher syndrome type IG, Usher syndrome type IGs