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Disease Info Card
Eye Diseases, Hereditary
Information about Eye Diseases, Hereditary: 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 Eye Diseases, Hereditary
Most recent studies have shown that Eye Diseases, Hereditary shares some biological mechanisms with age-related-macular-degeneration, atrophy, blind-vision, cataract, disorder-of-eye, dystrophy, eye-abnormalities, genetic-diseases-x-linked, glaucoma, myopia, night-blindness, retinal-degeneration, retinal-detachment, retinal-diseases, retinitis-pigmentosa, retinoschisis, stickler-syndrome-(disorder), visual-impairment.
Among the many pathways, these few ones have gauged particular interests from scientists studying Eye Diseases, Hereditary, and have been seen in publications frequently: Aging, Angiogenesis, Cell Death, Cell Differentiation, Dna Repair, Enucleation, Gene Silencing, Innervation, Localization, Mating, Muscle Cell Differentiation, Pathogenesis, Phototransduction, Pigmentation, Prenylation, Reflex, Regeneration, Striated Muscle Cell Differentiation, Translation, Transport
Quite a number of genes have been found to play important roles in Eye Diseases, Hereditary, such as ABCA4, BEST1, CACNA1F, CHM, COL11A1, COL18A1, COL2A1, ERG, FZD4, KCNH2, KIF21A, NDP, RDH5, RHO, RPE, RPE65, RS1, RSC1A1. 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.