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Disease Info Card
Congenital Cerebellar Hypoplasia
Information about Congenital Cerebellar Hypoplasia: 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 Cerebellar Hypoplasia
Most recent studies have shown that Congenital Cerebellar Hypoplasia shares some biological mechanisms with ataxia, atrophy, cerebellar-ataxia, cerebellar-diseases, congenital-abnormality, congenital-absence, congenital-disorders-of-glycosylation, developmental-delay-(disorder), dysplasia, dystrophy, epilepsy, fetal-diseases, hydrocephalus, hypoplasia, lissencephaly, microcephaly, muscle-hypotonia, nervousness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Cerebellar Hypoplasia, and have been seen in publications frequently: Brain Development, Cell Adhesion, Cell Death, Cell Migration, Cell Proliferation, Coagulation, Cognition, Glycosylation, Localization, Locomotion, Mating, Myelination, Neuroblast Migration, Neurogenesis, Pathogenesis, Pigmentation, Protein Glycosylation, Reflex, Startle Response, Transport
Quite a number of genes have been found to play important roles in Congenital Cerebellar Hypoplasia, such as AHI1, ARX, CASK, CSN3, DCX, FLNA, GFAP, GUK1, OPHN1, PAFAH1B1, PLA2G7, PMM2, RELN, TF, UBA2, VLDLR. 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.