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Disease Info Card
Complete Trisomy 18 Syndrome
Information about Complete Trisomy 18 Syndrome: 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 Complete Trisomy 18 Syndrome
Most recent studies have shown that Complete Trisomy 18 Syndrome shares some biological mechanisms with aneuploidy, atresia, brain-diseases, congenital-abnormality, congenital-heart-defects, cytogenetic-abnormality, down-syndrome, edema, embryonic-mosaic, fetal-death, fetal-diseases, fetal-growth-retardation, growth-retardation, high-risk-pregnancy, monosomy, patau-syndrome, triploidy, trisomy, turner-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Complete Trisomy 18 Syndrome, and have been seen in publications frequently: Cell Division, Cell Proliferation, Centromere Separation, Dna Methylation, Fertilization, Interphase, Meiosis, Meiosis I, Meiosis Ii, Metaphase, Methylation, Mitosis, Oncogenesis, Oogenesis, Ossification, Pachytene, Pathogenesis, Pigmentation, Transport, Transposition
Quite a number of genes have been found to play important roles in Complete Trisomy 18 Syndrome, such as AFP, BCL2, CGA, DAND5, GGT1, IL31RA, MALT1, MEFV, NT5E, NTM, NTS, PAPPA, PGF, PSG1, SLPI, SP1, 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.