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Disease Info Card
Digeorge Syndrome
Information about Digeorge 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 Digeorge Syndrome
Most recent studies have shown that Digeorge Syndrome shares some biological mechanisms with 22q11-deletion-syndrome, cleft-palate, congenital-abnormality, congenital-heart-defects, congenital-heart-disease, craniofacial-abnormalities, crest-syndrome, cytogenetic-abnormality, heart-diseases, hypocalcemia, hypoparathyroidism, hypoplasia, immunologic-deficiency-syndromes, mental-disorders, psychotic-disorders, schizophrenia, tetralogy-of-fallot, velopharyngeal-insufficiency, ventricular-septal-defects.
Among the many pathways, these few ones have gauged particular interests from scientists studying Digeorge Syndrome, and have been seen in publications frequently: Aging, Brain Development, Cell Development, Cell Differentiation, Cell Migration, Cell Proliferation, Cognition, Fertilization, Gastrulation, Heart Development, Interphase, Localization, Meiosis, Metaphase, Neural Crest Cell Migration, Pathogenesis, Prepulse Inhibition, Translation, Transport, Transposition
Quite a number of genes have been found to play important roles in Digeorge Syndrome, such as ADA, CD4, CD8A, CDC45, COMT, DGCR2, DGCR8, FGF8, GATA3, HIRA, PRODH, PTH, SS18L1, TBX1. 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.