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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...

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....