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Disease Info Card
Congenital Anomaly Of Brain
Information about Congenital Anomaly Of Brain: 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 Anomaly Of Brain
Most recent studies have shown that Congenital Anomaly Of Brain shares some biological mechanisms with agenesis-of-corpus-callosum, brain-diseases, congenital-abnormality, congenital-absence, congenital-muscular-dystrophy-(disorder), congenital-neurologic-anomalies, dysplasia, dystrophy, ectopic-tissue, epilepsy, holoprosencephaly, hydrocephalus, hypoplasia, lissencephaly, microcephaly, muscular-dystrophy, nervousness, polymicrogyria.
Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Anomaly Of Brain, and have been seen in publications frequently: Brain Development, Brain Morphogenesis, Cell Adhesion, Cell Cycle, Cell Death, Cell Division, Cell Migration, Cell Proliferation, Eye Development, Glycosylation, Localization, Myelination, Neural Tube Closure, Neurogenesis, Ossification, Pathogenesis, Protein Glycosylation, Segmentation, Transport, Tube Closure
Quite a number of genes have been found to play important roles in Congenital Anomaly Of Brain, such as ARX, DAG1, DCX, FKRP, FKTN, FLNA, GLUL, PAFAH1B1, PLA2G7, POMGNT1, POMT1, POMT2, RELN, SHH, SIX3, TGIF1, UBA2, ZIC2. 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.