Multiple Sulfatase Deficiency Disease

Overview of Multiple Sulfatase Deficiency Disease

Most recent studies have shown that Multiple Sulfatase Deficiency Disease shares some biological mechanisms with deficiency-of-arylsulfatase, deficiency-of-sulfatase, gangliosidoses, gaucher-disease, hydrocephalus, ichthyoses, ichthyosis-x-linked, inborn-errors-of-metabolism, leukodystrophy, leukodystrophy-metachromatic, lysosomal-storage-diseases, mucolipidoses, mucopolysaccharidoses, mucopolysaccharidosis-iv, mucopolysaccharidosis-vi, nerve-degeneration, neurodegenerative-disorders, sphingolipidoses, storage-disease.

Among the many pathways, these few ones have gauged particular interests from scientists studying Multiple Sulfatase Deficiency Disease, and have been seen in publications frequently: Autophagy, Bone Development, Cell Death, Cell Development, Cellular Process, Endocytosis, Excretion, Exocytosis, Intracellular Transport, Lipid Storage, Localization, Lymphocyte Differentiation, Macroautophagy, Pathogenesis, Regeneration, Reverse Transcription, Secretion, Secretory Pathway, Translation, Transport

Quite a number of genes have been found to play important roles in Multiple Sulfatase Deficiency Disease, such as ABCB6, ARSA, ARSB, ARSH, BBS9, CTLA4, DEGS1, GALNS, HLA-DQA1, LMAN1, NOD2, SGSH, SLURP1, STS, SUMF1, SUMF2. 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.

Multiple Sulfatase Deficiency Disease Related Genes

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Pathways Related to Multiple Sulfatase Deficiency Disease

This information is being compiled and will come in a future update

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