Optic Atrophy, Autosomal Dominant

Overview of Optic Atrophy, Autosomal Dominant

Most recent studies have shown that Optic Atrophy, Autosomal Dominant shares some biological mechanisms with ataxia, atrophy, blind-vision, charcot-marie-tooth-disease, color-vision-defect, disorder-of-the-optic-nerve, glaucoma, glaucoma-open-angle, intraocular-pressure-disorder, low-tension-glaucoma, mitochondrial-diseases, nerve-degeneration, neurodegenerative-disorders, optic-atrophies-hereditary, optic-atrophy, optic-atrophy-hereditary-leber, pallor, sensorineural-hearing-loss-(disorder), visual-impairment.

Among the many pathways, these few ones have gauged particular interests from scientists studying Optic Atrophy, Autosomal Dominant, and have been seen in publications frequently: Aging, Autophagy, Cell Death, Electron Transport, Electron Transport Chain, Glycolysis, Localization, Membrane Fission, Membrane Fusion, Mitochondrial Fission, Mitochondrial Fusion, Mrna Splicing, Myelination, Oxidative Phosphorylation, Pathogenesis, Programmed Cell Death, Proteolysis, Reflex, Translation, Transport

Quite a number of genes have been found to play important roles in Optic Atrophy, Autosomal Dominant, such as BAX, COX5A, COX8A, CPOX, CRMP1, CYCS, DAPK2, DENR, DNM1L, ERG, KCNH2, MED12, MFN1, MFN2, OPA1, OPA3, PARL, SPG7, UTRN. 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.

Optic Atrophy, Autosomal Dominant Related Genes

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Pathways Related to Optic Atrophy, Autosomal Dominant

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

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