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Disease Info Card
Blindness Congenital
Information about Blindness Congenital: 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 Blindness Congenital
Most recent studies have shown that Blindness Congenital shares some biological mechanisms with amaurosis, atrophy, autistic-disorder, blind-vision, complete-hearing-loss, congenital-abnormality, dysplasia, dystrophy, leber-congenital-amaurosis, microphthalmos, norrie-disease, optic-atrophies-hereditary, retinal-degeneration, retinal-detachment, retinal-diseases, retinal-dysplasia, retinal-dystrophies, retinitis-pigmentosa, visual-impairment.
Among the many pathways, these few ones have gauged particular interests from scientists studying Blindness Congenital, and have been seen in publications frequently: Angiogenesis, Cell Adhesion, Cell Cycle, Cell Differentiation, Cell Proliferation, Cognition, Echolocation, Embryonic Organ Development, Excretion, Eye Development, G1 Phase, Immune Response, Localization, Neurogenesis, Pathogenesis, Phototransduction, Reflex, Regeneration, Sensory Processing, Visual Perception
Quite a number of genes have been found to play important roles in Blindness Congenital, such as AIPL1, CEP290, CLTA, CRB1, CRX, FAM49B, GUCA1A, GUCY2D, LRP5, MAOA, MAOB, NDP, PTPRC, RHO, RPE65, RPGR, RPGRIP1, VSX2. 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.