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Disease Info Card
Mevalonic Aciduria
Information about Mevalonic Aciduria: 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 Mevalonic Aciduria
Most recent studies have shown that Mevalonic Aciduria shares some biological mechanisms with anemia, arthralgia, ataxia, cerebellar-ataxia, deficiency-of-mevalonate-kinase, exanthema, failure-to-thrive, familial-mediterranean-fever, hyper-igd-syndrome, hypergammaglobulinemia, inborn-errors-of-metabolism, inflammation, liver-diseases, metabolic-diseases, smith-lemli-opitz-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Mevalonic Aciduria, and have been seen in publications frequently: Cytokine Production, Excretion, Glycolysis, Inflammatory Response, Light Absorption, Localization, Pathogenesis, Protein Folding, Secretion
Quite a number of genes have been found to play important roles in Mevalonic Aciduria, such as ATP7A, CRP, ECHDC1, GALK1, GGT2, HMGCR, IL1B, MDK, MVK, RHOA, SEC23B, TYMP. 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 Mevalonic Aciduria
This information is being compiled and will come in a future update
| Cytokine Production | Excretion | Glycolysis |
| Inflammatory Response | Light Absorption | Localization |
| Pathogenesis | Protein Folding | Secretion |