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Disease Info Card
Congenital Nystagmus
Information about Congenital Nystagmus: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Congenital Nystagmus
Most recent studies have shown that Congenital Nystagmus shares some biological mechanisms with albinism, albinism-ocular, albinism-oculocutaneous, blind-vision, cataract, disorder-of-eye, esotropia, genetic-diseases-x-linked, horizontal-nystagmus, hypoplasia, myopia, nystagmus, ocular-motility-disorders, pendular-nystagmus, refractive-errors, retinal-diseases, strabismus, visual-impairment.
Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Nystagmus, and have been seen in publications frequently: Brain Development, Cell Differentiation, Cognition, Hormone Transport, Innervation, Localization, Myelination, Pathogenesis, Pigment Accumulation, Pigmentation, Proprioception, Reflex, Sex Determination, Swimming, Swimming Behavior, Translation, Transport, Transposition, Visual Behavior, Visual Perception
Quite a number of genes have been found to play important roles in Congenital Nystagmus, such as CACNA1A, COMP, COX5A, ERG, FRMD7, GPR143, INS, KCNH2, MAPT, MB, PAX6, PDXP, RPE65, TNFSF14, TYR, TYRP1. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.