DISEASES

Disease-gene associations mined from literature

Human genes for Usher syndrome type 2

Usher syndrome type 2 [DOID:0110827]

An Usher syndrome characterized by mild to severe congenital hearing impairment, normal vestibular function and later development of retinitis pigmentosa.

Synonyms:  Usher syndrome type 2,  DOID:0110827,  USH2