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Disease Info Card
Congenital Omphalocele
Information about Congenital Omphalocele: 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 Omphalocele
Most recent studies have shown that Congenital Omphalocele shares some biological mechanisms with anencephaly, anus-imperforate, atresia, beckwith-wiedemann-syndrome, bladder-exstrophy, congenital-abnormality, congenital-exomphalos, congenital-heart-defects, cytogenetic-abnormality, diaphragmatic-hernia, down-syndrome, fetal-death, fetal-diseases, gastroschisis, hernia, hypoplasia, spina-bifida, trisomy, ventral-hernia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Omphalocele, and have been seen in publications frequently: Cell Adhesion, Cell Death, Cell Migration, Cell Proliferation, Coagulation, Dehiscence, Fertilization, Localization, Neural Tube Closure, Ossification, Parturition, Pathogenesis, Reverse Transcription, Segmentation, Somite Development, Somitogenesis, Transport, Transposition, Tube Closure, Wound Healing
Quite a number of genes have been found to play important roles in Congenital Omphalocele, such as ACHE, AFP, ALPI, ASAH1, CDKN1C, CTLA4, FLNA, FREM1, HLA-DQA1, IGF2, INS, MTHFR, NME1, NOD2, SHH, SLC17A5, TCN2, 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.