Mucopolysaccharidosis Type Ivb

Overview of Mucopolysaccharidosis Type Ivb

Most recent studies have shown that Mucopolysaccharidosis Type Ivb shares some biological mechanisms with beta-galactosidase-deficiency, dwarfism, dysostoses, dysplasia, galactosialidosis, gangliosidoses, gangliosidosis-generalized-gm1-type-1-(disorder), gangliosidosis-gm1, inborn-errors-of-metabolism, lactose-intolerance, lysosomal-storage-diseases, metabolic-bone-disorder, mucopolysaccharidoses, mucopolysaccharidosis-i, mucopolysaccharidosis-iv, mucopolysaccharidosis-mps-iv-a, mucopolysaccharidosis-type-iiib, nervousness, neurodegenerative-disorders, pfaundler-hurler-syndrome.

Among the many pathways, these few ones have gauged particular interests from scientists studying Mucopolysaccharidosis Type Ivb, and have been seen in publications frequently: Bone Resorption, Endocytosis, Excretion, Intracellular Transport, Lipid Storage, Localization, Pathogenesis, Protein Transport, Translation, Transport

Quite a number of genes have been found to play important roles in Mucopolysaccharidosis Type Ivb, such as ARSB, ARSH, CHRM1, CTSA, EGFL7, ELN, GALNS, GLA, GLB1, GUSB, IK, ITGA2B, ITGB3, MTCH1, MTSS1, NEU1, SH3D19, SP1, ST8SIA4, ZFYVE9. 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.

Mucopolysaccharidosis Type Ivb Related Genes

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Pathways Related to Mucopolysaccharidosis Type Ivb

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

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