Disease Info Card

Meningoencephalocele

Information about Meningoencephalocele: 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 Meningoencephalocele

Most recent studies have shown that Meningoencephalocele shares some biological mechanisms with cerebrospinal-fluid-leak, cerebrospinal-fluid-otorrhea, cerebrospinal-fluid-rhinorrhea, cleft-lip, cleft-palate, congenital-abnormality, congenital-absence, congenital-cerebral-hernia, dysplasia, hernia, hydrocephalus, meningeal-disorder, meningitis, meningocele, meningomyelocele, neoplasms, nervousness, orbital-separation-excessive, pathologic-fistula, rhinorrhea.

Among the many pathways, these few ones have gauged particular interests from scientists studying Meningoencephalocele, and have been seen in publications frequently: Bone Development, Cell Killing, Cell Proliferation, Chondrocyte Proliferation, Coagulation, Dehiscence, Enucleation, Fertilization, Fibrinolysis, Insemination, Localization, Metaphase, Pathogenesis, Wound Healing

Quite a number of genes have been found to play important roles in Meningoencephalocele, such as CRAT, CSF2, ENO2, FMN1, FOXC2, FUT3, GLYAT, HNRNPC, HPS4, LAMC2, MKS1, NLRP5, RANGAP1, SLC17A5, SS18L1, TF, TMEM67. 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.