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Disease Info Card
Limb Deformities, Congenital
Information about Limb Deformities, 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 Limb Deformities, Congenital
Most recent studies have shown that Limb Deformities, Congenital shares some biological mechanisms with atresia, brachydactyly, cleft-lip, cleft-palate, congenital-abnormality, congenital-foot-deformity, congenital-hand-deformities, congenital-heart-defects, craniofacial-abnormalities, cytogenetic-abnormality, dwarfism, dysplasia, eye-abnormalities, hypoplasia, limb-defect, microcephaly, polydactyly, syndactyly, teratogenic-effect.
Among the many pathways, these few ones have gauged particular interests from scientists studying Limb Deformities, Congenital, and have been seen in publications frequently: Bone Development, Cell Death, Cell Division, Cell Proliferation, Endochondral Ossification, Fertilization, Gastrulation, Innervation, Limb Development, Limb Morphogenesis, Localization, Mating, Metaphase, Ossification, Pathogenesis, Programmed Cell Death, Regeneration, Segmentation, Translation, Transport
Quite a number of genes have been found to play important roles in Limb Deformities, Congenital, such as BMP2, BMP4, CKAP4, FBXW4, FGF4, FGF8, GDF5, GJA1, GLI3, HOXA13, HOXD13, IHH, ROR2, RPE65, SHH, TBX5, TP63, UVRAG. 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.