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Disease Info Card
Benign Paroxysmal Positional Vertigo
Information about Benign Paroxysmal Positional Vertigo: 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 Benign Paroxysmal Positional Vertigo
Most recent studies have shown that Benign Paroxysmal Positional Vertigo shares some biological mechanisms with anxiety-disorders, craniocerebral-trauma, dizziness, ear-diseases, labyrinthine-disorder, labyrinthitis, lithiasis, meniere-disease, migraine-disorders, neuritis, nystagmus, positional-nystagmus, sensorineural-hearing-loss-(disorder), vertigo, vertigo-positional, vestibular-diseases, vestibular-neuronitis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Benign Paroxysmal Positional Vertigo, and have been seen in publications frequently: Aging, Cardiac Conduction, Cell Adhesion, Dehiscence, Flight, Habituation, Localization, Locomotion, Menopause, Otolith Formation, Pathogenesis, Proprioception, Reflex, Regeneration, Response To Gravity, Senescence, Swimming, Translation, Transport, Water Homeostasis
Quite a number of genes have been found to play important roles in Benign Paroxysmal Positional Vertigo, such as ABR, ACTA1, ASAH1, AURKA, CACNA1A, CP, CRP, CSRP1, MPZ, MSX2, NDUFB6, PTGDR, PYCARD, RUNX2, SCG2, SIGLEC1, STS. 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.