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Disease Info Card
Mucopolysaccharidosis Type Iiic
Information about Mucopolysaccharidosis Type Iiic: 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 Mucopolysaccharidosis Type Iiic
Most recent studies have shown that Mucopolysaccharidosis Type Iiic shares some biological mechanisms with dementia, joint-stiffness, lysosomal-storage-diseases, mps-iii-a, mucolipidosis-type-iv, mucopolysaccharidoses, mucopolysaccharidosis-i, mucopolysaccharidosis-iii, mucopolysaccharidosis-mps-iv-a, mucopolysaccharidosis-type-iiib, mucopolysaccharidosis-type-iiid, mutation-out-of-frame, nerve-degeneration, nervousness, neurodegenerative-disorders, pfaundler-hurler-syndrome, regurgitation.
Among the many pathways, these few ones have gauged particular interests from scientists studying Mucopolysaccharidosis Type Iiic, and have been seen in publications frequently: Autophagy, Excretion, Glycosylation, Lipid Storage, Localization, Pathogenesis, Transport
Quite a number of genes have been found to play important roles in Mucopolysaccharidosis Type Iiic, such as GNS, GUSB, HGSNAT, LAMP2, MBL2, MBP, MCOLN1, MTSS1, NAGLU, PRG2, PSMD4, QPCT, SGSH. 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 Mucopolysaccharidosis Type Iiic
This information is being compiled and will come in a future update
| Autophagy | Excretion | Glycosylation |
| Lipid Storage | Localization | Pathogenesis |
| Transport |