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Disease Info Card
Deafness Congenital
Information about Deafness Congenital: 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 Deafness Congenital
Most recent studies have shown that Deafness Congenital shares some biological mechanisms with blind-vision, cardiac-arrhythmia, complete-hearing-loss, congenital-abnormality, dog-diseases, dysplasia, goiter, hearing-problem, jervell-lange-nielsen-syndrome, long-qt-syndrome, meningitis, pendreds-syndrome, retinitis-pigmentosa, rubella, sensorineural-hearing-loss-(disorder), sudden-death, syncope, usher-syndrome, waardenburg-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Deafness Congenital, and have been seen in publications frequently: Aging, Cell Death, Cell Development, Cell Differentiation, Cell-cell Adhesion, Cellular Homeostasis, Ear Development, Endocytosis, Glycosylation, Hypersensitivity, Inner Ear Development, Localization, Mating, Ossification, Pathogenesis, Pigmentation, Reflex, Secretion, System Development, Transport
Quite a number of genes have been found to play important roles in Deafness Congenital, such as ABR, CAT, CDH23, CRAT, GJB2, GJB6, GLYAT, KCNE1, KCNQ1, MYO15A, MYO7A, PAX3, PCDH15, POU3F4, PTGDS, SLC26A4, TMPRSS3, USH1C. 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.