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Disease Info Card
Agenesis Of Corpus Callosum
Information about Agenesis Of Corpus Callosum: 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 Agenesis Of Corpus Callosum
Most recent studies have shown that Agenesis Of Corpus Callosum shares some biological mechanisms with acrocallosal-syndrome, aicardis-syndrome, atrophy, brain-diseases, brain-neoplasms, congenital-abnormality, congenital-absence, congenital-neurologic-anomalies, developmental-delay-(disorder), developmental-disabilities, dysplasia, epilepsy, holoprosencephaly, hydrocephalus, hypoplasia, infantile-spasms, microcephaly, nervousness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Agenesis Of Corpus Callosum, and have been seen in publications frequently: Axon Guidance, Brain Development, Cell Adhesion, Cell Migration, Cell Proliferation, Central Nervous System Development, Cognition, Corpus Callosum Development, Localization, Myelination, Nervous System Development, Neural Tube Closure, Neurogenesis, Ossification, Pathogenesis, Pigmentation, Secretion, System Development, Transport, Tube Closure
Quite a number of genes have been found to play important roles in Agenesis Of Corpus Callosum, such as ACACA, AKT3, ARX, AVP, CSF2, DCC, DCX, FAM49B, L1CAM, LAMC2, MB, PAFAH1B1, POMC, SLC12A6, SPG11, UBA2, VCAM1, ZEB2. 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.