Nystagmus 3, Congenital, Autosomal Dominant (NYS3)

Nystagmus 3, Congenital, Autosomal Dominant, also known as congenital nystagmus 3, is related to neuropathy, hereditary sensory, type id and nystagmus 6, congenital, x-linked. An important gene associated with Nystagmus 3, Congenital, Autosomal Dominant is NYS3 (Nystagmus 3, Congenital Autosomal Dominant), and among its related pathways/superpathways is GPR143 in melanocytes and retinal pigment epithelium cells. Affiliated tissues include eye and brain, and related phenotypes are visual impairment and horizontal jerk nystagmus