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Disease Info Card
Hydrophthalmos
Information about Hydrophthalmos: 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 Hydrophthalmos
Most recent studies have shown that Hydrophthalmos shares some biological mechanisms with aqueous-humor-disorders, blind-vision, cataract, congenital-abnormality, corneal-diseases, disorder-of-eye, edema, eye-abnormalities, glaucoma, glaucoma-open-angle, intraocular-pressure-disorder, microphthalmos, myopia, neurofibromatoses, primary-congenital-glaucoma, primary-open-angle-glaucoma, retinal-detachment, scleral-diseases, secondary-glaucoma, visual-impairment.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hydrophthalmos, and have been seen in publications frequently: Cell Death, Cell Migration, Cell Proliferation, Coagulation, Dehiscence, Dna Repair, Enucleation, Excretion, Eye Development, Fertilization, Localization, Menarche, Neural Crest Cell Migration, Pathogenesis, Pigmentation, Reflex, Regeneration, Trabecular Meshwork Development, Translation, Transport
Quite a number of genes have been found to play important roles in Hydrophthalmos, such as BRCA1, CYP1B1, FOXC1, GLYAT, LTBP2, LTBP3, MYOC, PAX6, PITX2, RANGAP1, SLC17A5, SS18L1, TNFSF14, TYR. 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.