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Disease Info Card
Pure Autonomic Failure
Information about Pure Autonomic Failure: 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 Pure Autonomic Failure
Most recent studies have shown that Pure Autonomic Failure shares some biological mechanisms with ataxia, atrophy, autonomic-nervous-system-disorders, diabetes-mellitus, diabetes-mellitus-insulin-dependent, dysautonomia, hypertensive-disease, hypoglycemia, hypotension-adverse-event, multiple-system-atrophy, nervous-system-disorder, nervousness, neurodegenerative-disorders, parkinson-disease, secondary-parkinson-disease, shy-drager-syndrome, syncope.
Among the many pathways, these few ones have gauged particular interests from scientists studying Pure Autonomic Failure, and have been seen in publications frequently: Aging, Cognition, Diuresis, Excretion, Flight, Gastric Emptying, Hypersensitivity, Innervation, Micturition, Natriuresis, Pathogenesis, Pressure Natriuresis, Reflex, Regulation Of Blood Pressure, Response To Food, Secretion, Synaptic Transmission, Transport, Vasoconstriction, Vasodilation
Quite a number of genes have been found to play important roles in Pure Autonomic Failure, such as AVP, DBH, ELANE, EPO, GCG, GGH, GH1, INS, POMC, PPY, REN, SNCA, SST, TH, TPO, 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.