Disease Info Card

Intraocular Pressure Disorder

Information about Intraocular Pressure Disorder: 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 Intraocular Pressure Disorder

Most recent studies have shown that Intraocular Pressure Disorder shares some biological mechanisms with angle-closure-glaucoma, aqueous-humor-disorders, blind-vision, bulla, cataract, corneal-diseases, disorder-of-eye, disorder-of-the-optic-nerve, edema, glaucoma, glaucoma-open-angle, hemorrhage, hypertensive-disease, ocular-hypertension, ocular-hypotension, primary-open-angle-glaucoma, retinal-detachment, retinal-diseases, scleral-diseases.

Among the many pathways, these few ones have gauged particular interests from scientists studying Intraocular Pressure Disorder, and have been seen in publications frequently: Aging, Blood Circulation, Cell Death, Circadian Rhythm, Coagulation, Dehiscence, Enucleation, Inflammatory Response, Innervation, Localization, Neuroprotection, Pathogenesis, Pigmentation, Reflex, Regeneration, Secretion, Transport, Vasoconstriction, Vasodilation, Wound Healing

Quite a number of genes have been found to play important roles in Intraocular Pressure Disorder, such as BRCA1, CAT, CRAT, DCT, EDN1, ERG, F2, FUT2, GLYAT, KCNH2, MYOC, PLXNA2, RANGAP1, SLC17A5, SQLE, TNFSF14, VEGFA. 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.

Intraocular Pressure Disorder Related Genes

click to see detail information for each gene

BRCA1 CAT CRAT
DCT EDN1 ERG
F2 FUT2 GLYAT
KCNH2 MYOC PLXNA2
RANGAP1 SLC17A5 SQLE
TNFSF14 VEGFA