This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
, No Gclids
Disease Info Card
Primary Hyperoxaluria Type 2
Information about Primary Hyperoxaluria Type 2: 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 Primary Hyperoxaluria Type 2
Most recent studies have shown that Primary Hyperoxaluria Type 2 shares some biological mechanisms with acidosis, acute-kidney-injury, cat-diseases, hereditary-diseases, hyperoxaluria, hyperoxaluria-primary, inborn-errors-of-metabolism, kidney-calculi, kidney-diseases, kidney-failure, kidney-failure-chronic, metabolic-diseases, nephrocalcinosis, nephrolithiasis, primary-hyperoxaluria-type-i, urolithiasis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Primary Hyperoxaluria Type 2, and have been seen in publications frequently: Excretion, Fatty Acid Oxidation, Glomerular Filtration, Glyoxylate Cycle, Light Absorption, Muscle Atrophy
Quite a number of genes have been found to play important roles in Primary Hyperoxaluria Type 2, such as AGT, AGXT, CAT, CRAT, DAO, DLC1, G6PC, GGT1, GLYAT, GPI, GRHPR, GSR, HAO2, NR3C1, PAH, PHC1, PHC2, PPARA, QPCT. 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.
Pathways Related to Primary Hyperoxaluria Type 2
This information is being compiled and will come in a future update
| Excretion | Fatty Acid Oxidation | Glomerular Filtration |
| Glyoxylate Cycle | Light Absorption | Muscle Atrophy |