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Disease Info Card
Hyperpipecolatemia
Information about Hyperpipecolatemia: 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 Hyperpipecolatemia
Most recent studies have shown that Hyperpipecolatemia shares some biological mechanisms with acatalasia, acidemia, adrenoleukodystrophy, adrenoleukodystrophy-neonatal, brain-diseases, chondrodysplasia-punctata, chondrodysplasia-punctata-rhizomelic, diffuse-cerebral-sclerosis-of-schilder, hepatomegaly, hyperoxaluria, inborn-errors-of-metabolism, infantile-refsum-disease-(disorder), liver-cirrhosis, liver-diseases, peroxisomal-disorders, peroxisomal-thiolase-deficiency, refsum-disease, zellweger-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hyperpipecolatemia, and have been seen in publications frequently: Cell Proliferation, Fatty Acid Beta-oxidation, Localization, Pathogenesis, Transport
Quite a number of genes have been found to play important roles in Hyperpipecolatemia, such as ABCD1, AMY2A, BLOC1S6, CAT, CSF2, DAO, DCXR, EPB42, ERG, FGD1, GNPAT, HPSE, KCNH2, PEX10, PEX13, PIPOX, PRH1, XPR1. 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 Hyperpipecolatemia
This information is being compiled and will come in a future update
| Cell Proliferation | Fatty Acid Beta oxidation | Localization |
| Pathogenesis | Transport |