Acyl-coa Dehydrogenase, Very Long-chain Deficiency

Overview of Acyl-coa Dehydrogenase, Very Long-chain Deficiency

Most recent studies have shown that Acyl-coa Dehydrogenase, Very Long-chain Deficiency shares some biological mechanisms with cardiomyopathies, hepatomegaly, hypertrophic-cardiomyopathy, hypertrophy, hypoglycemia, inborn-errors-of-metabolism, long-chain-acyl-coa-dehydrogenase-deficiency, medium-chain-acyl-coenzyme-a-dehydrogenase-deficiency, metabolic-diseases, mitochondrial-diseases, muscle-hypotonia, myalgia, myopathy, pain, rhabdomyolysis, sudden-death, sudden-infant-death-syndrome, weakness.

Among the many pathways, these few ones have gauged particular interests from scientists studying Acyl-coa Dehydrogenase, Very Long-chain Deficiency, and have been seen in publications frequently: Aging, Carnitine Shuttle, Fatty Acid Beta-oxidation, Fatty Acid Oxidation, Gluconeogenesis, Glycolysis, Lipid Storage, Localization, Menopause, Oxidative Phosphorylation, Pathogenesis

Quite a number of genes have been found to play important roles in Acyl-coa Dehydrogenase, Very Long-chain Deficiency, such as ACADL, ACADM, ACADS, ACADVL, BRCA2, CALD1, CDH15, CHKA, CHKB, CPT2, FANCD2, MCAT, MCPH1, NBN, PPARG, SLC16A1. 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.

Acyl-coa Dehydrogenase, Very Long-chain Deficiency Related Genes

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Pathways Related to Acyl-coa Dehydrogenase, Very Long-chain Deficiency

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

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