Disease Info Card

Sensory Hearing Loss

Information about Sensory Hearing Loss: 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 Hearing Loss

Most recent studies have shown that Sensory Hearing Loss shares some biological mechanisms with acoustic-neuroma, cochlear-diseases, complete-hearing-loss, conductive-hearing-loss, deafness-sudden, ear-diseases, ear-inflammation, hearing-loss-bilateral, hearing-loss-high-frequency, hearing-problem, hyperacusis, labyrinthine-disorder, meniere-disease, neoplasms, neural-hearing-loss, noise-induced-hearing-loss, otitis-media, presbycusis, sensorineural-hearing-loss-(disorder), vertigo.

Among the many pathways, these few ones have gauged particular interests from scientists studying Sensory Hearing Loss, and have been seen in publications frequently: Aging, Cell Differentiation, Cell Division, Cell Proliferation, Cognition, Hyperphosphorylation, Hypersensitivity, Insulin Secretion, Keratinization, Lipid Storage, Localization, Ossification, Oxygen Transport, Pathogenesis, Platelet Aggregation, Reflex, Regeneration, Secretion, Swimming, Transport

Quite a number of genes have been found to play important roles in Sensory Hearing Loss, such as ABR, CPA1, DSP, FMOD, GJB2, HES1, HMGCL, INS, LAMC2, LIPC, MTFMT, MYO7A, NDUFB6, PTGDR, SGPL1, SLC17A5, TFF2. 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.