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Disease Info Card
Limb Deformity
Information about Limb Deformity: 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 Limb Deformity
Most recent studies have shown that Limb Deformity shares some biological mechanisms with bone-diseases, bone-diseases-developmental, congenital-abnormality, deformity-of-lower-limb, degenerative-polyarthritis, dwarfism, dysplasia, familial-hypophosphatemia, foot-deformities, fracture, horse-diseases, leg-length-inequality, limb-deformities-congenital, muscle-contracture, muscle-spasticity, osteomyelitis, pain, rickets, scoliosis-unspecified, syndactyly.
Among the many pathways, these few ones have gauged particular interests from scientists studying Limb Deformity, and have been seen in publications frequently: Aging, Brain Development, Cardiac Conduction, Cell Death, Cell Proliferation, Chondrocyte Proliferation, Cytokinesis, Fertilization, Kidney Morphogenesis, Limb Development, Limb Morphogenesis, Localization, Mating, Ossification, Pathogenesis, Phagocytosis, Programmed Cell Death, Tooth Eruption, Translation, Transport
Quite a number of genes have been found to play important roles in Limb Deformity, such as FGF23, FGF4, FGF8, FMN1, FOXC2, GLI3, GPSM2, GREM1, HOXD13, IKBKG, PHEX, PRPF40A, SF1, SHH, WBP4. 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.