Usher Syndrome, Type Ij (USH1J)

Usher Syndrome, Type Ij, also known as usher syndrome type 1j, is related to rare genetic deafness and sensorineural hearing loss. An important gene associated with Usher Syndrome, Type Ij is CIB2 (Calcium And Integrin Binding Family Member 2), and among its related pathways/superpathways are Olfactory Signaling Pathway and Sensory processing of sound. Affiliated tissues include retina and eye, and related phenotypes are motor delay and rod-cone dystrophy