DISEASES

Disease-gene associations mined from literature

Human genes for Usher syndrome type 2D

Usher syndrome type 2D [DOID:0110840]

An Usher syndrome type 2 that has_material_basis_in by homozygous or compound heterozygous mutation in the WHRN gene on chromosome 9q32.

Synonyms:  Usher syndrome type 2D,  DOID:0110840,  USH2D,  Usher syndrome type IID,  Usher syndrome type IIDs