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Rare Disease Database

2 Search Results for: USH3


NORD Rare Disease Database

Usher Syndrome

Summary Usher syndrome is a rare genetic disorder primarily characterized by deafness due to an impaired ability of the inner ear and auditory nerves to transmit...

Subdivisions: Usher syndrome type 1, Usher syndrome type 2, Usher syndrome type 3

NIH GARD Information

Usher syndrome type 3A

Usher syndrome is a genetic disorder characterized by sensorineural hearing loss or deafness and progressive vision loss due to retinitis pigmentosa....