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Disease Info Card
Meningocele
Information about Meningocele: 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 Meningocele
Most recent studies have shown that Meningocele shares some biological mechanisms with cerebrospinal-fluid-rhinorrhea, congenital-abnormality, congenital-cerebral-hernia, congenital-failure-of-fusion, congenital-sacral-meningocele, hernia, hydrocephalus, lipoma, meningeal-disorder, meningitis, meningoencephalocele, meningomyelocele, neoplasms, neurofibromatoses, neurofibromatosis-1, pain, pathologic-fistula, pseudomeningocele, spina-bifida, spina-bifida-occulta.
Among the many pathways, these few ones have gauged particular interests from scientists studying Meningocele, and have been seen in publications frequently: Bone Development, Brain Development, Cell Proliferation, Coagulation, Defecation, Dehiscence, Fertilization, Gastrulation, Localization, Locomotion, Metaphase, Muscle Atrophy, Neural Tube Closure, Ossification, Pathogenesis, Reflex, Segmentation, Spinal Cord Development, Transposition, Tube Closure
Quite a number of genes have been found to play important roles in Meningocele, such as ACHE, AFP, C2, CERS2, CRLF1, CSF2, HNRNPC, LAMC2, MNX1, NLRP5, PPFIBP1, RPL3, RPL5, SLC25A5, VIM, ZACN. 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.