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Disease Info Card
Abnormal Color Vision
Information about Abnormal Color Vision: 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 Abnormal Color Vision
Most recent studies have shown that Abnormal Color Vision shares some biological mechanisms with atrophy, blind-vision, cardiovascular-diseases, cataract, color-blindness, color-vision-defect, confusion, disorder-of-the-optic-nerve, dystrophy, erectile-dysfunction, flushing, headache, hemorrhage, night-blindness, retinal-degeneration, retinal-diseases, retinitis-pigmentosa, visual-impairment.
Among the many pathways, these few ones have gauged particular interests from scientists studying Abnormal Color Vision, and have been seen in publications frequently: Flight, Muscle Atrophy, Pathogenesis
Quite a number of genes have been found to play important roles in Abnormal Color Vision, such as ABCD1, ASCC2, CACNA1F, CS, ERG, FMOD, GOLGB1, KCNH2, MMEL1, NOL3, OSCAR, PDE5A, PLXNB1, PRPS1, RPE, SFSWAP, TNFSF14, TPX2. 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.
Pathways Related to Abnormal Color Vision
This information is being compiled and will come in a future update
| Flight | Muscle Atrophy | Pathogenesis |