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Disease Info Card
Optic Atrophies, Hereditary
Information about Optic Atrophies, 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 Optic Atrophies, Hereditary
Most recent studies have shown that Optic Atrophies, Hereditary shares some biological mechanisms with amaurosis, atrophy, blind-vision, disorder-of-the-optic-nerve, hereditary-motor-and-sensory-neuropathies, leber-congenital-amaurosis, melas-syndrome, mitochondrial-diseases, multiple-sclerosis, neuritis, optic-atrophy, optic-atrophy-autosomal-dominant, optic-atrophy-hereditary-leber, optic-neuritis, retinal-diseases, retinitis-pigmentosa, sclerosis, visual-impairment.
Among the many pathways, these few ones have gauged particular interests from scientists studying Optic Atrophies, Hereditary, and have been seen in publications frequently: Aging, Cardiac Conduction, Cell Death, Electron Transport, Electron Transport Chain, Excretion, Immune Response, Localization, Myelination, Nuclear Transport, Oogenesis, Ossification, Oxidative Phosphorylation, Pathogenesis, Phototransduction, Pigmentation, Programmed Cell Death, Reflex, Regeneration, Transport
Quite a number of genes have been found to play important roles in Optic Atrophies, Hereditary, such as AIPL1, CLTA, CRX, ERG, GUCY2D, IVNS1ABP, KCNH2, MED12, MFN2, NDP, OPA1, PTPRC, RHO, RPE65. 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.