Usher Syndrome Type I

About the Disease
Usher Syndrome, Type I, also known as usher syndrome type 1, is related to usher syndrome, type ic and usher syndrome, type ij, and has symptoms including unspecified visual loss An important gene associated with Usher Syndrome, Type I is MYO7A (Myosin VIIA), and among its related pathways/superpathways are Olfactory Signaling Pathway and Sensory processing of sound. Affiliated tissues include eye, retina and cerebellum, and related phenotypes are intellectual disability and ataxia

Common Targets
MYO7A | FAM161A | PCDH15 | ESPN | USH2A | CIB2 | CLRN1 | USH1G | USH1C | CDH23

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