Deficiency of lysosomal enzyme. Medical search. Frequent questions

Home page Questions and answers Statistics Donations Contact

Anatomy25

Lysosomes Liver Fibroblasts Neutrophils Cells, Cultured Golgi Apparatus Macrophages Cell Line Subcellular Fractions Endosomes Organoids Vacuoles Kidney Cytoplasmic Granules Ascitic Fluid Brain Leukocytes Coated Pits, Cell-Membrane Skin Intracellular Membranes trans-Golgi Network Phagosomes Spleen Cell Membrane Endoplasmic Reticulum

Organisms10

Mice, Knockout Dictyostelium Mice, Inbred C57BL Mice, Mutant Strains Rats, Inbred Strains Rabbits Cricetinae Cattle Hepatitis Viruses Mice, Transgenic

Diseases63

Mucolipidoses Lysosomal Storage Diseases Vitamin A Deficiency Deficiency Diseases alpha 1-Antitrypsin Deficiency Gaucher Disease Vitamin B 12 Deficiency Mucopolysaccharidosis I Vitamin D Deficiency Glycogen Storage Disease Type II Fabry Disease Folic Acid Deficiency IgA Deficiency Thiamine Deficiency Gangliosidoses Mucopolysaccharidosis IV Mucopolysaccharidoses Glucosephosphate Dehydrogenase Deficiency Leukodystrophy, Globoid Cell Magnesium Deficiency Metabolism, Inborn Errors Leukodystrophy, Metachromatic Anemia, Iron-Deficiency Vitamin E Deficiency Ascorbic Acid Deficiency Mucopolysaccharidosis II Immunologic Deficiency Syndromes Protein C Deficiency IgG Deficiency Tay-Sachs Disease Protein Deficiency Chediak-Higashi Syndrome Vitamin B 6 Deficiency Mucopolysaccharidosis III Neuronal Ceroid-Lipofuscinoses Sandhoff Disease Disease Models, Animal Factor V Deficiency Mucopolysaccharidosis VII Riboflavin Deficiency Antithrombin III Deficiency Mucopolysaccharidosis VI Vitamin K Deficiency Aspartylglucosaminuria Factor VII Deficiency Lipidoses Factor XI Deficiency Fucosidosis Anemia, Hypochromic Vitamin B Deficiency Factor XIII Deficiency Sphingolipidoses Leukocyte-Adhesion Deficiency Syndrome Factor X Deficiency Ornithine Carbamoyltransferase Deficiency Disease Adrenal Hyperplasia, Congenital Choline Deficiency Tuberculosis, Cutaneous Cytochrome-c Oxidase Deficiency Amino Acid Metabolism, Inborn Errors Togaviridae Infections Lecithin Acyltransferase Deficiency Biotinidase Deficiency

Chemicals and Drugs113

Glucuronidase Mannosephosphates Acetylglucosaminidase Receptor, IGF Type 2 Cathepsin D Acid Phosphatase Hexosaminidases beta-N-Acetylhexosaminidases Cerebroside-Sulfatase alpha-Mannosidase Arylsulfatases Mannosidases Cathepsins Transferases (Other Substituted Phosphate Groups)alpha-L-Fucosidase Hydrolases Sulfatases beta-Glucosidase Hexosephosphates alpha-Galactosidase Galactosidases Glucosidases Zymosan Iduronidase Glucosylceramidase Cathepsin B Glycoside Hydrolases alpha-Glucosidases Ammonium Chloride Cathepsin L Cytochalasin B beta-Galactosidase Galactosylceramidase Oligosaccharides N-Acetylgalactosamine-4-Sulfatase Aspartylglucosylaminase Methylmannosides Mannosyl-Glycoprotein Endo-beta-N-Acetylglucosaminidase Cathepsin C Chondro-4-Sulfatase Mannose Dipeptidyl-Peptidases and Tripeptidyl-Peptidases Hexosaminidase A Iduronate Sulfatase Thiolester Hydrolases Enzyme Precursors Antipain alpha-N-Acetylgalactosaminidase Esterases L-Lactate Dehydrogenase Muramidase Colchicine N-Formylmethionine Iron Glucan 1,4-alpha-Glucosidase Saposins Glycoproteins Psychosine Receptors, Cell Surface Phosphotransferases Chloroquine Phosphoric Diester Hydrolases Chondroitinsulfatases Enzymes Leucyl Aminopeptidase Lipofuscin Sphingomyelin Phosphodiesterase Acetylglucosamine Cysteine Endopeptidases Proteins Endopeptidases Lysosome-Associated Membrane Glycoproteins Peptide Hydrolases Mannose-Binding Lectins G(M2) Ganglioside RNA, Messenger Glycosaminoglycans Taurodeoxycholic Acid Carrier Proteins Cations Serine Proteases Uridine Diphosphate N-Acetylglucosamine Metalloproteins Iodine Zinc Acridine Orange Antigen-Antibody Complex Lysosomal-Associated Membrane Protein 2 Bromhexine Sphingolipid Activator Proteins Hexosaminidase B Peroxidase Cathepsin H Monensin Ribonucleases Sulfuric Acids Alkaline Phosphatase Disaccharidases Membrane Proteins Peroxidases Pepstatins Recombinant Proteins Leupeptins Cathepsin A Lipase Carbohydrates Phospholipases A1 N-Formylmethionine Leucyl-Phenylalanine Adaptor Protein Complex 1 DNA Phospholipases Sucrose Polystyrenes

Analytical, Diagnostic and Therapeutic Techniques and Equipment14

Microscopy, Electron Enzyme Replacement Therapy Cell Fractionation Histocytochemistry Disease Models, Animal Neonatal Screening Centrifugation, Isopycnic Centrifugation, Density Gradient Blood Specimen Collection Pedigree Clinical Enzyme Tests Electrophoresis, Polyacrylamide Gel DNA Mutational Analysis Models, Biological

Phenomena and Processes24

Endocytosis Pinocytosis Phagocytosis Mutation Cell Compartmentation Kinetics Biological Transport Hydrogen-Ion Concentration Time Factors Phenotype Protein Processing, Post-Translational Amino Acid Sequence Base Sequence Glycosylation Phosphorylation Exocytosis Homozygote Tissue Distribution Molecular Weight Autophagy Heterozygote Chemotaxis, Leukocyte Pregnancy Protein Transport

Disciplines and Occupations2

Histocytochemistry Cell Biology

Technology, Industry, Agriculture1

Information Science3

Molecular Sequence Data Amino Acid Sequence Base Sequence

Named Groups1

Infant, Newborn

Health Care1

Neonatal Screening

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

Lysosomes Glucuronidase Mannosephosphates Acetylglucosaminidase Receptor, IGF Type 2 Cathepsin D Acid Phosphatase Hexosaminidases Mucolipidoses beta-N-Acetylhexosaminidases Cerebroside-Sulfatase alpha-Mannosidase Arylsulfatases Mannosidases Cathepsins Transferases (Other Substituted Phosphate Groups)Lysosomal Storage Diseases alpha-L-Fucosidase Hydrolases Sulfatases beta-Glucosidase Hexosephosphates alpha-Galactosidase Galactosidases Vitamin A Deficiency Deficiency Diseases Glucosidases Zymosan Iduronidase Glucosylceramidase Cathepsin B alpha 1-Antitrypsin Deficiency Gaucher Disease Vitamin B 12 Deficiency Glycoside Hydrolases alpha-Glucosidases Ammonium Chloride Mucopolysaccharidosis I Liver Fibroblasts Cathepsin L Vitamin D Deficiency Glycogen Storage Disease Type II Endocytosis Fabry Disease Folic Acid Deficiency Pinocytosis Cytochalasin B beta-Galactosidase IgA Deficiency Thiamine Deficiency Galactosylceramidase Oligosaccharides Gangliosidoses N-Acetylgalactosamine-4-Sulfatase Mice, Knockout Aspartylglucosylaminase Methylmannosides Mannosyl-Glycoprotein Endo-beta-N-Acetylglucosaminidase Neutrophils Phagocytosis Cathepsin C Mucopolysaccharidosis IV Cells, Cultured Chondro-4-Sulfatase Microscopy, Electron Golgi Apparatus Mutation Dictyostelium Mucopolysaccharidoses Glucosephosphate Dehydrogenase Deficiency Macrophages Leukodystrophy, Globoid Cell Enzyme Replacement Therapy Mannose Magnesium Deficiency Metabolism, Inborn Errors Leukodystrophy, Metachromatic Cell Compartmentation Anemia, Iron-Deficiency Vitamin E Deficiency Dipeptidyl-Peptidases and Tripeptidyl-Peptidases Cell Fractionation Ascorbic Acid Deficiency Mice, Inbred C57BL Mucopolysaccharidosis II Kinetics Hexosaminidase A Iduronate Sulfatase Thiolester Hydrolases Cell Line Molecular Sequence Data Immunologic Deficiency Syndromes Histocytochemistry Protein C Deficiency Enzyme Precursors IgG Deficiency Tay-Sachs Disease Biological Transport Hydrogen-Ion Concentration

No FAQ available that match "deficiency of lysosomal enzyme"