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Disease Info Card
Somatosensory Disorders
Information about Somatosensory Disorders: 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 Somatosensory Disorders
Most recent studies have shown that Somatosensory Disorders shares some biological mechanisms with absence-of-sensation, anxiety-disorders, cerebrovascular-accident, cranial-nerve-injuries, depressive-disorder, diabetes-mellitus, gait-disorders-neurologic, hyperalgesia, impairment-(finding), malnutrition, nerve-damage, nervousness, neuralgia, numbness, pain, paresis, paresthesia, peripheral-neuropathy, trigeminal-nerve-injuries.
Among the many pathways, these few ones have gauged particular interests from scientists studying Somatosensory Disorders, and have been seen in publications frequently: Aging, Brain Development, Cognition, Dehiscence, Hypersensitivity, Innervation, Localization, Locomotion, Mastication, Muscle Contraction, Ossification, Pathogenesis, Proprioception, Reflex, Regeneration, Sensitization, Sensory Perception, Sensory Processing, Translation, Transposition
Quite a number of genes have been found to play important roles in Somatosensory Disorders, such as ACLY, AURKA, C3, CARD16, DHDDS, FUT3, GRIP1, HPS4, MMEL1, PLXNB1, PMEL, PPP5C, PPT1, SCN10A, SI, SLC17A5, TAC1, 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.