Disease Info Card

Occipital Encephalocele

Information about Occipital Encephalocele: 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 Occipital Encephalocele

Most recent studies have shown that Occipital Encephalocele shares some biological mechanisms with cleft-palate, congenital-abnormality, congenital-absence, congenital-cerebral-hernia, congenital-neurologic-anomalies, cystic-kidney-diseases, dandy-walker-syndrome, dysplasia, fetal-diseases, fibrosis, hernia, hydrocephalus, hypoplasia, meckel-gruber-syndrome, meningeal-disorder, meningocele, microcephaly, nervousness, polycystic-kidney-diseases, polydactyly.

Among the many pathways, these few ones have gauged particular interests from scientists studying Occipital Encephalocele, and have been seen in publications frequently: Angiogenesis, Bone Maturation, Cell Proliferation, Eye Development, Fertilization, Localization, Mesoderm Formation, Metaphase, Neural Tube Closure, Neural Tube Formation, Ossification, Paraxial Mesoderm Formation, Parturition, Pathogenesis, Transposition, Tube Closure, Tube Formation

Quite a number of genes have been found to play important roles in Occipital Encephalocele, such as AFP, B9D1, CC2D2A, CEP290, COL18A1, CSF2, FUZ, GFAP, INS, LAMC2, MKKS, MKS1, NPHP1, OXSM, RPGRIP1L, SHH, TIMM8A, 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.