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Disease Info Card
Inborn Errors Of Metabolism
Information about Inborn Errors Of Metabolism: 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 Inborn Errors Of Metabolism
Most recent studies have shown that Inborn Errors Of Metabolism shares some biological mechanisms with acidemia, acidosis, anemia, congenital-abnormality, cytogenetic-abnormality, galactosemias, genetic-diseases-inborn, hereditary-diseases, homocystinuria, hyperammonemia, hypoglycemia, liver-diseases, metabolic-diseases, methylmalonic-acidemia, mucopolysaccharidoses, nervous-system-disorder, phenylketonurias.
Among the many pathways, these few ones have gauged particular interests from scientists studying Inborn Errors Of Metabolism, and have been seen in publications frequently: Coagulation, Conjugation, Electron Transport, Excretion, Fatty Acid Beta-oxidation, Fatty Acid Oxidation, Gluconeogenesis, Glycolysis, Glycosylation, Lipid Storage, Localization, Methylation, Myelination, Oxidative Phosphorylation, Pathogenesis, Regeneration, Secretion, Translation, Transport, Urea Cycle
Quite a number of genes have been found to play important roles in Inborn Errors Of Metabolism, such as ADA, BCHE, BTD, CAT, CSF2, DLD, G6PD, GCDH, GH1, GSR, GSS, IGF1, INS, LAMC2, OTC, PAH, POMC, SERPINA1. 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.