Congenital Night Blindness

Overview of Congenital Night Blindness

Most recent studies have shown that Congenital Night Blindness shares some biological mechanisms with abnormal-degeneration, achromatopsia, age-related-macular-degeneration, atrophy, blind-vision, color-vision-defect, congenital-stationary-night-blindness, disorder-of-eye, dystrophy, eye-diseases-hereditary, genetic-diseases-x-linked, hemeralopia, myopia, night-blindness, pigmentary-retinal-dystrophy, retinal-degeneration, retinal-diseases, retinitis-pigmentosa.

Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Night Blindness, and have been seen in publications frequently: Aging, Cell Death, Endocytosis, Exocytosis, Light Absorption, Localization, Pathogenesis, Phototransduction, Pigmentation, Reflex, Regeneration, Sensitization, Synaptic Transmission, Translation

Quite a number of genes have been found to play important roles in Congenital Night Blindness, such as CACNA1F, DMBT1, ERG, GPR151, GRK1, GRM6, KCNH2, LGR6, MRGPRX1, NR2E3, NSF, OXER1, RDH5, RHO, RNF7, RPE, SAG, TNFSF14. 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.

Congenital Night Blindness Related Genes

click to see detail information for each gene

Pathways Related to Congenital Night Blindness

This information is being compiled and will come in a future update

Related Diseases