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Disease Info Card
Fabry Disease
Information about Fabry Disease: 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 Fabry Disease
Most recent studies have shown that Fabry Disease shares some biological mechanisms with angiokeratoma, cardiomyopathies, cerebrovascular-accident, corneal-diseases, gaucher-disease, heart-diseases, hypertrophic-cardiomyopathy, hypertrophy, kidney-diseases, kidney-failure, kidney-failure-chronic, left-ventricular-hypertrophy, lysosomal-storage-diseases, metabolic-diseases, nervousness, pain, proteinuria-of-undiagnosed-cause, storage-disease.
Among the many pathways, these few ones have gauged particular interests from scientists studying Fabry Disease, and have been seen in publications frequently: Cardiac Conduction, Cell Adhesion, Endocytosis, Excretion, Glomerular Filtration, Glycosylation, Immune Response, Innervation, Lipid Storage, Localization, Methylation, Pathogenesis, Platelet Activation, Receptor-mediated Endocytosis, Reflex, Secretion, Translation, Transport, Urea Cycle, Vasodilation
Quite a number of genes have been found to play important roles in Fabry Disease, such as ARSA, CTH, ELF3, FOS, GALC, GBA, GLA, GLB1, NAGA, NAT8, PGR, QPCT, RAPGEF5, SMPD1, TMEM37, VSIG2. 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.