Disease Info Card

Intracranial Hypotension

Information about Intracranial Hypotension: 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 Intracranial Hypotension

Most recent studies have shown that Intracranial Hypotension shares some biological mechanisms with cerebrospinal-fluid-leak, headache, hematoma, hematoma-subdural, hematoma-subdural-chronic, hemorrhage, hernia, hydrocephalus, hypertensive-disease, hypotension-adverse-event, intracranial-hypertension, meningeal-disorder, nausea, orthostatic-headache, pain, spontaneous-intracranial-hypotension, subarachnoid-hemorrhage, subdural-effusion, thrombosis, vomiting.

Among the many pathways, these few ones have gauged particular interests from scientists studying Intracranial Hypotension, and have been seen in publications frequently: Aging, Blood Coagulation, Cell Death, Coagulation, Cognition, Developmental Process, Diuresis, Estrus, Excretion, Fibroblast Migration, Hemostasis, Inflammatory Response, Leukocyte Activation, Localization, Pathogenesis, Reflex, Swimming, Transport, Vasoconstriction, Wound Healing

Quite a number of genes have been found to play important roles in Intracranial Hypotension, such as ARHGAP4, C2, CSF2, DMBT1, EBP, GLB1, HNRNPC, HSF4, LAMC2, NLRP5, PFDN4, RNF7, SAG, SDHB, SDS, SDSL, SH3D19, SLC25A5, SLC26A5. 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.