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Disease Info Card
Dysautonomia
Information about Dysautonomia: 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 Dysautonomia
Most recent studies have shown that Dysautonomia shares some biological mechanisms with ataxia, atrophy, autonomic-nervous-system-disorders, diabetes-mellitus, dysautonomia-familial, guillain-barre-syndrome, hypertensive-disease, hypotension-adverse-event, multiple-system-atrophy, nervous-system-disorder, nervousness, pain, parkinson-disease, peripheral-neuropathy, pure-autonomic-failure, secondary-parkinson-disease, syncope.
Among the many pathways, these few ones have gauged particular interests from scientists studying Dysautonomia, and have been seen in publications frequently: Aging, Cell Cycle, Cell Migration, Cell Motility, Circadian Rhythm, Cognition, Excretion, Gastric Emptying, Glomerular Filtration, Histone Acetylation, Hypersensitivity, Innervation, Localization, Mrna Splicing, Pathogenesis, Reflex, Regeneration, Secretion, Synaptic Transmission, Vasoconstriction
Quite a number of genes have been found to play important roles in Dysautonomia, such as ABCB6, ACHE, C4BPA, CARD14, CFH, CSF2, DBH, GRIP1, GZMA, LAMC2, NGF, PRDX2, PRNP, REN, SNCA, SS18L1, TTR. 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.