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Disease Info Card
Talipes Cavus
Information about Talipes Cavus: 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 Talipes Cavus
Most recent studies have shown that Talipes Cavus shares some biological mechanisms with ataxia, atrophy, charcot-marie-tooth-disease, congenital-abnormality, congenital-clubfoot, congenital-flat-foot, congenital-foot-deformity, deformity-cavus, foot-deformities, foot-deformities-acquired, hereditary-motor-and-sensory-neuropathies, muscle-weakness, muscular-atrophy, pain, peripheral-neuropathy, scoliosis-unspecified, sensory-neuropathy, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Talipes Cavus, and have been seen in publications frequently: Cardiac Conduction, Cell Differentiation, Central Nervous System Development, Hypersensitivity, Innervation, Lipid Storage, Localization, Menopause, Muscle Atrophy, Muscle Hypertrophy, Nervous System Development, Pathogenesis, Pigmentation, Proprioception, Reflex, Regeneration, Schwann Cell Differentiation, Social Behavior, System Development, Transport
Quite a number of genes have been found to play important roles in Talipes Cavus, such as DNM2, EGR2, ELL, ENDOU, EXOSC6, FXN, GAA, GALC, GDI1, GJB1, KIF1B, MPZ, PES1, PMP22, PXMP2, RPLP0, S100A10, SPAST. 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.