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Disease Info Card
Deficiency Of Sulfatase
Information about Deficiency Of Sulfatase: 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 Deficiency Of Sulfatase
Most recent studies have shown that Deficiency Of Sulfatase shares some biological mechanisms with chondrodysplasia-punctata, dwarfism, fetal-death, ichthyoses, ichthyosis-x-linked, inborn-errors-of-metabolism, leukodystrophy, leukodystrophy-metachromatic, lysosomal-storage-diseases, mucopolysaccharidoses, mucopolysaccharidosis-ii, mucopolysaccharidosis-iv, multiple-sulfatase-deficiency-disease, placenta-disorders, pregnancy-complications, sphingolipidoses, steroid-sulfatase-deficiency-disease.
Among the many pathways, these few ones have gauged particular interests from scientists studying Deficiency Of Sulfatase, and have been seen in publications frequently: Autophagy, Bone Development, Cell Death, Cell Maturation, Dosage Compensation, Endocytosis, Excretion, Keratinization, Lactation, Lipid Storage, Localization, Macroautophagy, Meiosis, Metaphase, Pathogenesis, Reverse Transcription, Secretion, Secretory Pathway, Translation, Transport
Quite a number of genes have been found to play important roles in Deficiency Of Sulfatase, such as AFP, ARSA, ARSB, ARSH, CYP19A1, DHDDS, DHPS, G6PD, GALNS, NOD2, OXSM, POMC, PRPH2, 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.