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Disease Info Card
Mucopolysaccharidosis Vii
Information about Mucopolysaccharidosis Vii: 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 Vii
Most recent studies have shown that Mucopolysaccharidosis Vii shares some biological mechanisms with congenital-abnormality, corneal-diseases, dog-diseases, dysplasia, edema, fetal-diseases, gaucher-disease, hydrops-fetalis, lysosomal-storage-diseases, metabolic-diseases, mucopolysaccharidoses, mucopolysaccharidosis-i, mucopolysaccharidosis-ii, nervousness, pathological-dilatation, pfaundler-hurler-syndrome, storage-disease.
Among the many pathways, these few ones have gauged particular interests from scientists studying Mucopolysaccharidosis Vii, and have been seen in publications frequently: Acute Inflammatory Response, Bone Maturation, Bone Resorption, Brain Development, Complement Activation, Endocytosis, Excretion, Glycosylation, Immune Response, Localization, Mating, Ossification, Pathogenesis, Regeneration, Secretion, Transcytosis, Translation, Transport, Transposition, Viral Replication
Quite a number of genes have been found to play important roles in Mucopolysaccharidosis Vii, such as CAT, CD34, CRAT, ELF3, FCGRT, GLB1, GLYAT, GUSB, HGF, HNRNPC, IGF2, MPO, ORC3, RPE, SPNS1, TLR4. 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.