Hereditary Fructose Intolerance Syndrome

Overview of Hereditary Fructose Intolerance Syndrome

Most recent studies have shown that Hereditary Fructose Intolerance Syndrome shares some biological mechanisms with abdominal-bloating, abdominal-pain, acidosis, dental-caries, diarrhea, fructose-16-diphosphatase-deficiency, galactosemias, glycogen-storage-disease, hepatolenticular-degeneration, hepatomegaly, hypoglycemia, inborn-errors-of-metabolism, irritable-bowel-syndrome, lactose-intolerance, liver-cirrhosis, liver-diseases, malabsorption-syndrome, metabolic-diseases, pain, vomiting.

Among the many pathways, these few ones have gauged particular interests from scientists studying Hereditary Fructose Intolerance Syndrome, and have been seen in publications frequently: Coagulation, Diuresis, Dna Amplification, Excretion, Fatty Acid Oxidation, Fermentation, Glomerular Filtration, Gluconeogenesis, Glycolysis, Glycosylation, Hypersensitivity, Immune Response, Intestinal Absorption, Localization, Ossification, Pathogenesis, Protein Glycosylation, Secretion, Transport, Urea Cycle

Quite a number of genes have been found to play important roles in Hereditary Fructose Intolerance Syndrome, such as AGA, ALDOB, CRP, G6PC, GCG, GLB1, GPI, GSTP1, INS, KHK, LCT, PAH, QPCT, SERPINA1, SLC16A1, SUOX, TALDO1, TBPL1, TF, TYRP1. 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.

Hereditary Fructose Intolerance Syndrome Related Genes

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Pathways Related to Hereditary Fructose Intolerance Syndrome

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

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