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Disease Info Card
Cornelia De Lange Syndrome
Information about Cornelia De Lange 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 Cornelia De Lange Syndrome
Most recent studies have shown that Cornelia De Lange Syndrome shares some biological mechanisms with autistic-disorder, cleft-palate, congenital-abnormality, congenital-heart-defects, cytogenetic-abnormality, developmental-delay-(disorder), developmental-disabilities, dwarfism, fetal-growth-retardation, gastroesophageal-reflux-disease, growth-disorders, growth-retardation, hernia, hypertrichosis, limb-deformities-congenital, microcephaly, micrognathism, trisomy.
Among the many pathways, these few ones have gauged particular interests from scientists studying Cornelia De Lange Syndrome, and have been seen in publications frequently: Aging, Cell Cycle, Cell Division, Chromosome Condensation, Chromosome Segregation, Dna Repair, Dna Replication, Interphase, Localization, Meiosis, Metaphase, Mitosis, Pathogenesis, Reflex, Regulation Of Gene Expression, S Phase, Sister Chromatid Cohesion, Translation, Transport
Quite a number of genes have been found to play important roles in Cornelia De Lange Syndrome, such as CHAT, CTCF, ERMAP, ESCO2, IGF2, MAU2, MYC, NIPBL, PAPPA, PDS5A, PDS5B, RAD21, SH2D3C, SMC1A, SMC3, STAG1, STAG2. 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.