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Disease Info Card
Hereditary Sensory And Autonomic Neuropathies
Information about Hereditary Sensory And Autonomic Neuropathies: 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 Hereditary Sensory And Autonomic Neuropathies
Most recent studies have shown that Hereditary Sensory And Autonomic Neuropathies shares some biological mechanisms with anhidrosis, atrophy, charcot-marie-tooth-disease, congenital-pain-insensitivity, hereditary-motor-and-sensory-neuropathies, hsan-type-iv, hypohidrosis, inherited-neuropathy, muscular-atrophy, nervousness, pain, peripheral-neuropathy, polyneuropathy, sensory-neuropathy, sensory-neuropathy-hereditary, ulcer.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hereditary Sensory And Autonomic Neuropathies, and have been seen in publications frequently: Cardiac Conduction, Cell Death, Cell Proliferation, Excretion, Hypersensitivity, Innervation, Localization, Meiosis, Mrna Splicing, Muscle Atrophy, Myelination, Neurogenesis, Pathogenesis, Proprioception, Reflex, Regeneration, Response To Pain, Sensory Perception, Transport, Wound Healing
Quite a number of genes have been found to play important roles in Hereditary Sensory And Autonomic Neuropathies, such as AGXT, BDNF, CEL, FAP, KIF1B, MAD2L1BP, MPZ, NAA50, NGF, NGFR, NTRK1, PMP22, PXMP2, SPTLC1, SPTLC2, TTR, WNK1. 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.