Genetic deficiency of g6pd. Medical search. Frequent questions

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Anatomy19

Cells, Cultured Fibroblasts Kidney Liver Macrophages Cell Line Erythrocytes Brain Mitochondria Skin T-Lymphocytes Spleen Bone and Bones Neurons B-Lymphocytes Lymphocytes Lung Muscle, Skeletal Neutrophils

Organisms8

Mice, Knockout Mice, Inbred C57BL Mice, Mutant Strains Mice, Transgenic Rats, Sprague-Dawley Animals, Newborn Mice, 129 Strain Rats, Inbred Strains

Diseases94

Leukodystrophy, Globoid Cell Disease Models, Animal Vitamin A Deficiency Deficiency Diseases alpha 1-Antitrypsin Deficiency Vitamin B 12 Deficiency Glucosephosphate Dehydrogenase Deficiency Vitamin D Deficiency Folic Acid Deficiency IgA Deficiency Thiamine Deficiency Magnesium Deficiency Anemia, Iron-Deficiency Vitamin E Deficiency Ascorbic Acid Deficiency Immunologic Deficiency Syndromes Protein C Deficiency IgG Deficiency Vitamin B 6 Deficiency Factor V Deficiency Riboflavin Deficiency Antithrombin III Deficiency Metabolism, Inborn Errors Vitamin K Deficiency Parkinson Disease 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 Yin Deficiency Lipid Metabolism, Inborn Errors Hypopituitarism Carbohydrate Metabolism, Inborn Errors Anemia, Hemolytic Purine-Pyrimidine Metabolism, Inborn Errors Dwarfism, Pituitary Body Weight Potassium Deficiency Platelet Storage Pool Deficiency Growth Disorders Dihydropyrimidine Dehydrogenase Deficiency Brain Diseases, Metabolic, Inborn Pyruvate Dehydrogenase Complex Deficiency Disease Mitochondrial Diseases Anemia Anemia, Hemolytic, Congenital Nonspherocytic Vitamin K Deficiency Bleeding Syndrome Scurvy Severe Combined Immunodeficiency Anemia, Macrocytic Homocystinuria Brain Diseases, Metabolic Xerophthalmia Rickets Agammaglobulinemia Glycogen Storage Disease Anemia, Megaloblastic Hyperlipoproteinemia Type I Yang Deficiency Multiple Carboxylase Deficiency Malabsorption Syndromes Mevalonate Kinase Deficiency Inflammation Multiple Acyl Coenzyme A Dehydrogenase Deficiency Goiter Hypogonadism Leigh Disease Adrenal Insufficiency Disease Susceptibility Hyperammonemia Pregnancy Complications Pregnancy Complications, Hematologic Anemia, Pernicious Muscular Diseases Lesch-Nyhan Syndrome Kidney Failure, Chronic Common Variable Immunodeficiency Genetic Predisposition to Disease Favism Anemia, Hemolytic, Congenital Peritonitis Congenital Hypothyroidism

Chemicals and Drugs68

Galactosylceramidase RNA, Messenger Iron Glucosephosphate Dehydrogenase Zinc Iodine Vitamin B 12 Ferritins Vitamin D alpha 1-Antitrypsin Fatty Acids, Essential Hemoglobins Steroid 21-Hydroxylase Human Growth Hormone Vitamin A Copper Iron, Dietary Palladium Folic Acid Selenium Methylmalonic Acid Carnitine Acyl-CoA Dehydrogenases Thiamine Membrane Proteins Acyl-CoA Dehydrogenase Carrier Proteins Homocysteine Complement C6 Biological Markers DNA DNA Primers Biotinidase alpha-Synuclein Growth Hormone Complement C2 Flavonoids Transcobalamins Adenosine Deaminase Transferrin DNA-Binding Proteins Sulfatases Transcription Factors Antiparkinson Agents Receptors, Transferrin Mannose-Binding Lectin Enzyme Inhibitors Pyridoxine Codon, Nonsense Hydroxocobalamin Trace Elements Pyrithiamine Complement C7 Protoporphyrins Phosphorus Methionine Cholesterol Complement C4 Glucose Transketolase Glutathione Peroxidase Ceruloplasmin Acyl-CoA Dehydrogenase, Long-Chain Biotin Lipids Cerebroside-Sulfatase Apolipoproteins E Fatty Acids

Analytical, Diagnostic and Therapeutic Techniques and Equipment25

Disease Models, Animal Immunohistochemistry Pedigree Peritoneal Dialysis Body Weight Erythrocyte Indices DNA Mutational Analysis Polymerase Chain Reaction Blotting, Western Prevalence Reference Values Reverse Transcriptase Polymerase Chain Reaction Organ Size Hematocrit Models, Biological Case-Control Studies Risk Factors Analysis of Variance Heterozygote Detection Crosses, Genetic Genetic Complementation Test Flow Cytometry Neonatal Screening Gene Targeting Severity of Illness Index

Phenomena and Processes41

Mutation Phenotype Gene Expression Regulation Signal Transduction Homozygote Heterozygote Base Sequence Diet Time Factors Body Weight Pregnancy Genotype Consanguinity Point Mutation Erythrocyte Indices Nutritional Status Mutation, Missense Alleles Gene Deletion Amino Acid Sequence Exons Apoptosis Homeostasis Oxidative Stress Organ Size Genes, Recessive Gene Expression Aging Hematocrit Cell Differentiation Cell Proliferation Dose-Response Relationship, Drug Lipid Metabolism Disease Susceptibility Nutritional Requirements Frameshift Mutation Codon, Nonsense Phosphorylation Genetic Predisposition to Disease Oxidation-Reduction Kinetics

Disciplines and Occupations1

Immunohistochemistry

Technology, Industry, Agriculture3

Dietary Supplements Food, Fortified Trace Elements

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Prevalence

Named Groups1

Infant, Newborn

Health Care8

Nutritional Status Prevalence Case-Control Studies Risk Factors Analysis of Variance Neonatal Screening Severity of Illness Index Age Factors

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

Galactosylceramidase Mice, Knockout Mice, Inbred C57BL Leukodystrophy, Globoid Cell Disease Models, Animal Mutation Mice, Mutant Strains Mice, Transgenic Cells, Cultured Phenotype Fibroblasts Kidney Gene Expression Regulation Immunohistochemistry Signal Transduction Liver Macrophages Cell Line RNA, Messenger Molecular Sequence Data Vitamin A Deficiency Deficiency Diseases alpha 1-Antitrypsin Deficiency Vitamin B 12 Deficiency Glucosephosphate Dehydrogenase Deficiency Vitamin D Deficiency Folic Acid Deficiency IgA Deficiency Thiamine Deficiency Magnesium Deficiency Anemia, Iron-Deficiency Vitamin E Deficiency Ascorbic Acid Deficiency Immunologic Deficiency Syndromes Protein C Deficiency IgG Deficiency Vitamin B 6 Deficiency Factor V Deficiency Iron Riboflavin Deficiency Antithrombin III Deficiency Metabolism, Inborn Errors Vitamin K Deficiency Parkinson Disease Factor VII Deficiency Glucosephosphate Dehydrogenase Factor XI Deficiency Protein Deficiency Anemia, Hypochromic Vitamin B Deficiency Factor XIII Deficiency Leukocyte-Adhesion Deficiency Syndrome Zinc Iodine Factor X Deficiency Ornithine Carbamoyltransferase Deficiency Disease Homozygote Adrenal Hyperplasia, Congenital Heterozygote Choline Deficiency Pedigree Cytochrome-c Oxidase Deficiency Amino Acid Metabolism, Inborn Errors Lecithin Acyltransferase Deficiency Biotinidase Deficiency Vitamin B 12 Ferritins Base Sequence Diet Peritoneal Dialysis Yin Deficiency Vitamin D Lipid Metabolism, Inborn Errors alpha 1-Antitrypsin Hypopituitarism Carbohydrate Metabolism, Inborn Errors Anemia, Hemolytic Fatty Acids, Essential Purine-Pyrimidine Metabolism, Inborn Errors Hemoglobins Steroid 21-Hydroxylase Erythrocytes Human Growth Hormone Vitamin A Copper Infant, Newborn Time Factors Iron, Dietary Dwarfism, Pituitary Body Weight Pregnancy Potassium Deficiency Platelet Storage Pool Deficiency Genotype Palladium Folic Acid Dietary Supplements Selenium Consanguinity Growth Disorders

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