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Disease Info Card
Deficiency Of 3-hydroxyacyl-coa Dehydrogenase
Information about Deficiency Of 3-hydroxyacyl-coa Dehydrogenase: 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 Deficiency Of 3-hydroxyacyl-coa Dehydrogenase
Most recent studies have shown that Deficiency Of 3-hydroxyacyl-coa Dehydrogenase shares some biological mechanisms with acidosis, cardiomyopathies, fatty-liver, hellp-syndrome, hypoglycemia, inborn-errors-of-metabolism, liver-diseases, medium-chain-acyl-coenzyme-a-dehydrogenase-deficiency, metabolic-diseases, mitochondrial-trifunctional-protein-deficiency, muscle-hypotonia, pregnancy-complications, protein-deficiency, retinal-diseases, retinitis-pigmentosa, sudden-infant-death-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Deficiency Of 3-hydroxyacyl-coa Dehydrogenase, and have been seen in publications frequently: Central Nervous System Myelination, Dna Amplification, Excretion, Fatty Acid Beta-oxidation, Fatty Acid Oxidation, Fertilization, Hypersensitivity, Insulin Secretion, Localization, Myelination, Pathogenesis, Secretion
Quite a number of genes have been found to play important roles in Deficiency Of 3-hydroxyacyl-coa Dehydrogenase, such as ACADM, ACADVL, CDH15, ERG, GLUD1, HADH, HADHA, HSD17B10, INS, KCNH2, MCAT, MCPH1, MT1B, MTTP, QPCT, RPE, SLC16A1, TRIM39, VIM. 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.