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Disease Info Card
Polysyndactyly
Information about Polysyndactyly: 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 Polysyndactyly
Most recent studies have shown that Polysyndactyly shares some biological mechanisms with acrocallosal-syndrome, acrocephalosyndactylia, congenital-abnormality, congenital-absence, congenital-foot-deformity, congenital-hand-deformities, congenital-heart-defects, craniosynostosis, dysplasia, greig-cephalopolysyndactyly-syndrome, hamartoma, hypoplasia, hypothalamic-diseases, limb-deformities-congenital, orbital-separation-excessive, orofaciodigital-syndromes, polydactyly, radial-polydactyly, syndactyly.
Among the many pathways, these few ones have gauged particular interests from scientists studying Polysyndactyly, and have been seen in publications frequently: Cell Growth, Central Nervous System Myelination, Embryonic Morphogenesis, Eye Development, Gastrulation, Hair Follicle Development, Limb Development, Lung Morphogenesis, Lymphocyte Activation, Myelination, Ossification, Pathogenesis, Pigmentation, Protein Processing, Tooth Eruption, Translation, Transport, Transposition, Vesicle Transport
Quite a number of genes have been found to play important roles in Polysyndactyly, such as ATP6V0A1, BMP4, CORIN, EGFL7, FGF8, GLI3, IHH, LDLR, LMBR1, LRP4, LRP5, LRP6, PCBD1, RAB23, RFC1, RFC2, SHH, SMOC1. 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.