Caused by a deficiency of arylsulfatase. Medical search. Frequent questions

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Anatomy12

Lysosomes Fibroblasts Liver Cells, Cultured Cell Line Skin Leukocytes Eosinophils Placenta Spermatozoa Kidney Hybrid Cells

Organisms15

Klebsiella Mycobacterium scrofulaceum Citrobacter Mice, Knockout Chlorophyta Mycobacterium Klebsiella pneumoniae Mice, Inbred C57BL Chlamydomonas reinhardtii Enterobacter Sea Urchins Cricetinae Cats Rhodococcus Rats, Inbred Strains

Diseases45

Leukodystrophy, Metachromatic Mucopolysaccharidosis VI Mucopolysaccharidoses Mucopolysaccharidosis IV Vitamin A Deficiency Deficiency Diseases alpha 1-Antitrypsin Deficiency Vitamin B 12 Deficiency Vitamin D Deficiency Folic Acid Deficiency IgA Deficiency Thiamine Deficiency Chondrodysplasia Punctata Glucosephosphate Dehydrogenase Deficiency Magnesium Deficiency Anemia, Iron-Deficiency Vitamin E Deficiency Ascorbic Acid Deficiency Lysosomal Storage Diseases Immunologic Deficiency Syndromes Protein C Deficiency IgG Deficiency Vitamin B 6 Deficiency Factor V Deficiency Riboflavin Deficiency Antithrombin III Deficiency Disease Models, Animal Metabolism, Inborn Errors Vitamin K Deficiency Cat Diseases Factor VII Deficiency Factor XI Deficiency Protein Deficiency Anemia, Hypochromic Vitamin B Deficiency Factor XIII Deficiency Leukocyte-Adhesion Deficiency Syndrome Factor X Deficiency Ornithine Carbamoyltransferase Deficiency Disease Adrenal Hyperplasia, Congenital Choline Deficiency Cytochrome-c Oxidase Deficiency Amino Acid Metabolism, Inborn Errors Lecithin Acyltransferase Deficiency Biotinidase Deficiency

Chemicals and Drugs56

Arylsulfatases Cerebroside-Sulfatase Sulfatases Chondro-4-Sulfatase N-Acetylgalactosamine-4-Sulfatase Steryl-Sulfatase Tyramine Sulfoglycosphingolipids Sulfates Saposins Sphingolipid Activator Proteins Diazomethane Galactolipids Monoamine Oxidase Sulfur Autacoids Transferases (Other Substituted Phosphate Groups)Acid Phosphatase Cathepsin D Ammonium Chloride Nitrosoguanidines Methionine Mannosyl-Glycoprotein Endo-beta-N-Acetylglucosaminidase Iron Oligosaccharides SRS-A Tryptamines Glucuronidase Hydrolases Mycolic Acids RNA, Messenger Thiosulfates DNA Cathepsins Isoenzymes Uridine Diphosphate N-Acetylglucosamine Glycosaminoglycans Cysteine Neuraminidase Iodine Zinc Carbohydrates DNA Probes Oxidoreductases Acting on CH-NH Group Donors Mannose DNA Primers Fucose Arabinose Oligonucleotide Probes DNA, Complementary Glycine Glycoside Hydrolases Amino Acid Oxidoreductases Recombinant Proteins Vitamin B 12 Ferritins

Analytical, Diagnostic and Therapeutic Techniques and Equipment20

Photofluorography Enzyme Replacement Therapy Cloning, Molecular Pedigree Isoelectric Focusing Restriction Mapping Immunodiffusion Immunoelectrophoresis, Two-Dimensional Electrophoresis, Polyacrylamide Gel Chromatography, Ion Exchange Disease Models, Animal Chromatography Genetic Complementation Test Polymerase Chain Reaction Chemical Precipitation Histocytochemistry Electrophoresis Enzyme Stability Transfection Blotting, Western

Phenomena and Processes29

Enzyme Repression Mutation Base Sequence Amino Acid Sequence Genes Homozygote Phenotype Alleles Hydrogen-Ion Concentration Glycosylation Chemical Phenomena Kinetics Genes, Regulator Sperm-Ovum Interactions Exons Chemical Precipitation Molecular Weight Pregnancy Heterozygote Species Specificity Enzyme Stability Gene Expression Regulation Transfection Genetic Linkage Sequence Homology Substrate Specificity Genetic Vectors Sequence Homology, Amino Acid Diet

Disciplines and Occupations3

Immunochemistry Chemistry Histocytochemistry

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes Disciplines and Occupations Information Science

Arylsulfatases Cerebroside-Sulfatase Sulfatases Chondro-4-Sulfatase Leukodystrophy, Metachromatic N-Acetylgalactosamine-4-Sulfatase Mucopolysaccharidosis VI Steryl-Sulfatase Tyramine Sulfoglycosphingolipids Sulfates Mucopolysaccharidoses Mucopolysaccharidosis IV Lysosomes Vitamin A Deficiency Saposins Deficiency Diseases Klebsiella Sphingolipid Activator Proteins alpha 1-Antitrypsin Deficiency Photofluorography Diazomethane Enzyme Repression Vitamin B 12 Deficiency Molecular Sequence Data Galactolipids Monoamine Oxidase Vitamin D Deficiency Mutation Folic Acid Deficiency IgA Deficiency Thiamine Deficiency Chondrodysplasia Punctata Sulfur Autacoids Base Sequence Mycobacterium scrofulaceum Glucosephosphate Dehydrogenase Deficiency Citrobacter Fibroblasts Magnesium Deficiency Anemia, Iron-Deficiency Vitamin E Deficiency Immunochemistry Amino Acid Sequence Liver Ascorbic Acid Deficiency Mice, Knockout Lysosomal Storage Diseases Immunologic Deficiency Syndromes Enzyme Replacement Therapy Transferases (Other Substituted Phosphate Groups)Acid Phosphatase Cathepsin D Protein C Deficiency Genes Ammonium Chloride IgG Deficiency Homozygote Phenotype Cloning, Molecular Nitrosoguanidines Vitamin B 6 Deficiency Methionine Alleles Mannosyl-Glycoprotein Endo-beta-N-Acetylglucosaminidase Pedigree Hydrogen-Ion Concentration Isoelectric Focusing Restriction Mapping Factor V Deficiency Immunodiffusion Cells, Cultured Iron Oligosaccharides SRS-A Riboflavin Deficiency Immunoelectrophoresis, Two-Dimensional Glycosylation Chlorophyta Tryptamines Mycobacterium Electrophoresis, Polyacrylamide Gel Antithrombin III Deficiency Chromatography, Ion Exchange Chemistry Glucuronidase Klebsiella pneumoniae Disease Models, Animal Chemical Phenomena Mice, Inbred C57BL Cell Line Kinetics Metabolism, Inborn Errors Chlamydomonas reinhardtii Hydrolases Mycolic Acids Genes, Regulator Enterobacter RNA, Messenger

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