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Disease Info Card
Congenital Webbing
Information about Congenital Webbing: 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 Webbing
Most recent studies have shown that Congenital Webbing shares some biological mechanisms with cicatrix, cleft-palate, congenital-abnormality, congenital-hand-deformities, dwarfism, dysplasia, edema, flexed-fetal-attitude, hypoplasia, limb-deformities-congenital, multiple-pterygium-syndrome, muscle-contracture, orbital-separation-excessive, pterygium, pterygium-colli, stenosis, syndactyly, tissue-adhesions, turner-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Webbing, and have been seen in publications frequently: Cell Adhesion, Cell Death, Cell Proliferation, Chromosome Segregation, Development Of Secondary Sexual Characteristics, Excretion, Innervation, Limb Development, Limb Morphogenesis, Localization, Locomotion, Oviposition, Pathogenesis, Pigmentation, Programmed Cell Death, Swimming, Tissue Development, Transport, Transposition, Wound Healing
Quite a number of genes have been found to play important roles in Congenital Webbing, such as AFP, ALB, ASRGL1, BMP2, BMP4, DNAH5, DNAI1, FERMT1, FGF8, FMN1, FOXC2, GREM1, HOXD13, INS, KCNT1, PCBD1, RARB, SHH, TRIM26. 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.