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Disease Info Card
Sensory Neuropathy, Hereditary
Information about Sensory Neuropathy, Hereditary: 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 Sensory Neuropathy, Hereditary
Most recent studies have shown that Sensory Neuropathy, Hereditary shares some biological mechanisms with absence-of-sensation, anhidrosis, ataxia, charcot-marie-tooth-disease, congenital-pain-insensitivity, hereditary-motor-and-sensory-neuropathies, hereditary-sensory-and-autonomic-neuropathies, hereditary-sensory-autonomic-neuropathy-type-1, hsan-type-iv, hypohidrosis, nerve-degeneration, nervous-system-disorder, nervousness, pain, peripheral-neuropathy, sensory-neuropathy, ulcer, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Sensory Neuropathy, Hereditary, and have been seen in publications frequently: Cell Cycle Phase, Cell Death, Cell Proliferation, Cytoskeleton Organization, Dna Methylation, Gastric Emptying, Hypersensitivity, Innervation, Localization, Methylation, Mismatch Repair, Neural Tube Closure, Neurogenesis, Pathogenesis, Reflex, Regeneration, Response To Pain, Swimming, Transport, Tube Closure
Quite a number of genes have been found to play important roles in Sensory Neuropathy, Hereditary, such as AGXT, ATL1, BDNF, DNMT1, DST, KIF1B, NAA50, NGF, NGFR, NINJ1, NTRK1, NTRK2, RAB7A, RAB7B, SPTLC1, SPTLC2, 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.