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Disease Info Card
Congenital Hand Deformities
Information about Congenital Hand Deformities: 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 Congenital Hand Deformities
Most recent studies have shown that Congenital Hand Deformities shares some biological mechanisms with aplasia-nos, brachydactyly, cleft-lip, cleft-palate, congenital-abnormality, congenital-foot-deformity, congenital-heart-defects, craniofacial-abnormalities, cytogenetic-abnormality, dwarfism, dysplasia, ectodermal-dysplasia, ectrodactyly, growth-disorders, holt-oram-syndrome, hypoplasia, limb-deformities-congenital, polydactyly, syndactyly.
Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Hand Deformities, and have been seen in publications frequently: Bone Development, Bone Maturation, Bone Resorption, Endochondral Ossification, Excretion, Innervation, Limb Development, Limb Morphogenesis, Localization, Menarche, Muscle Atrophy, Ossification, Pathogenesis, Pigmentation, Regeneration, Secretion, Segmentation, Translation, Transposition, Wound Healing
Quite a number of genes have been found to play important roles in Congenital Hand Deformities, such as ATP6V0A1, CKAP4, FBXW4, FGFR2, GDF5, GRIP1, HOXA13, HOXD13, IHH, LIMS1, RFC1, RFC2, RFC4, 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.