Component deficiency. Medical search. Frequent questions

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Anatomy20

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

Organisms8

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

Diseases95

Vitamin A Deficiency Deficiency Diseases alpha 1-Antitrypsin Deficiency Vitamin B 12 Deficiency Vitamin D Deficiency Folic Acid Deficiency IgA Deficiency Thiamine Deficiency Glucosephosphate Dehydrogenase 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 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 Disease Models, Animal Lecithin Acyltransferase Deficiency Biotinidase Deficiency Yin Deficiency Lipid Metabolism, Inborn Errors Hypopituitarism Carbohydrate Metabolism, Inborn Errors Purine-Pyrimidine Metabolism, Inborn Errors Dwarfism, Pituitary Anemia, Hemolytic Potassium Deficiency Platelet Storage Pool Deficiency Body Weight Growth Disorders Dihydropyrimidine Dehydrogenase Deficiency Brain Diseases, Metabolic, Inborn Pyruvate Dehydrogenase Complex Deficiency Disease Mitochondrial Diseases Anemia, Hemolytic, Congenital Nonspherocytic Vitamin K Deficiency Bleeding Scurvy Severe Combined Immunodeficiency Anemia Syndrome 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 Multiple Acyl Coenzyme A Dehydrogenase Deficiency Goiter Hypogonadism Leigh Disease Adrenal Insufficiency Hyperammonemia Inflammation Pregnancy Complications Pregnancy Complications, Hematologic Anemia, Pernicious Muscular Diseases Disease Susceptibility Lesch-Nyhan Syndrome Common Variable Immunodeficiency Congenital Hypothyroidism Blood Coagulation Disorders Anemia, Hemolytic, Congenital Fructose-1,6-Diphosphatase Deficiency Acquired Immunodeficiency Syndrome Pyruvate Carboxylase Deficiency Disease Hemorrhagic Disorders Dwarfism Hypothyroidism

Chemicals and Drugs71

Iron Iodine Zinc Vitamin B 12 Ferritins Vitamin D alpha 1-Antitrypsin Fatty Acids, Essential Steroid 21-Hydroxylase Vitamin A Human Growth Hormone Hemoglobins Iron, Dietary RNA, Messenger Copper Folic Acid Selenium Methylmalonic Acid Carnitine Acyl-CoA Dehydrogenases Glucosephosphate Dehydrogenase Thiamine Acyl-CoA Dehydrogenase Membrane Proteins Complement C6 Homocysteine Carrier Proteins Biotinidase Growth Hormone Complement C2 Transcobalamins Adenosine Deaminase DNA Primers Transferrin DNA Biological Markers Sulfatases Receptors, Transferrin DNA-Binding Proteins Mannose-Binding Lectin Pyridoxine Codon, Nonsense Hydroxocobalamin Trace Elements Pyrithiamine Complement C7 Protoporphyrins Complement C4 Ceruloplasmin Methionine Acyl-CoA Dehydrogenase, Long-Chain Biotin Transcription Factors Cerebroside-Sulfatase Cholesterol Transketolase Phosphorus Fatty Acids Glutathione Peroxidase Apolipoproteins E Iron-Binding Proteins Ascorbic Acid Lipids Riboflavin 17-alpha-Hydroxyprogesterone Methylmalonyl-CoA Decarboxylase Cystathionine beta-Synthase Cation Transport Proteins Purine-Nucleoside Phosphorylase Vitamins Cytokines

Analytical, Diagnostic and Therapeutic Techniques and Equipment23

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

Phenomena and Processes38

Mutation Phenotype Homozygote Heterozygote Diet Base Sequence Body Weight Consanguinity Pregnancy Genotype Erythrocyte Indices Point Mutation Mutation, Missense Nutritional Status Alleles Gene Deletion Signal Transduction Time Factors Gene Expression Regulation Exons Amino Acid Sequence Homeostasis Organ Size Genes, Recessive Apoptosis Hematocrit Aging Gene Expression Oxidative Stress Nutritional Requirements Lipid Metabolism Disease Susceptibility Frameshift Mutation Cell Differentiation Codon, Nonsense Cell Proliferation Sunlight DNA Repair

Disciplines and Occupations1

Immunohistochemistry

Technology, Industry, Agriculture4

Dietary Supplements Food, Fortified Trace Elements Vitamins

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Prevalence

Named Groups1

Infant, Newborn

Health Care6

Nutritional Status Prevalence Neonatal Screening Sunlight Risk Factors Case-Control Studies

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

Vitamin A Deficiency Deficiency Diseases alpha 1-Antitrypsin Deficiency Vitamin B 12 Deficiency Vitamin D Deficiency Folic Acid Deficiency IgA Deficiency Thiamine Deficiency Glucosephosphate Dehydrogenase Deficiency Magnesium Deficiency Anemia, Iron-Deficiency Vitamin E Deficiency Ascorbic Acid Deficiency Mice, Knockout Immunologic Deficiency Syndromes Protein C Deficiency IgG Deficiency Vitamin B 6 Deficiency Factor V Deficiency Iron Riboflavin Deficiency Mutation Antithrombin III Deficiency Mice, Inbred C57BL Metabolism, Inborn Errors Vitamin K Deficiency Factor VII Deficiency Factor XI Deficiency Protein Deficiency Anemia, Hypochromic Vitamin B Deficiency Factor XIII Deficiency Leukocyte-Adhesion Deficiency Syndrome Iodine Zinc Phenotype Factor X Deficiency Ornithine Carbamoyltransferase Deficiency Disease Adrenal Hyperplasia, Congenital Homozygote Choline Deficiency Liver Cytochrome-c Oxidase Deficiency Amino Acid Metabolism, Inborn Errors Heterozygote Pedigree Disease Models, Animal Lecithin Acyltransferase Deficiency Biotinidase Deficiency Vitamin B 12 Ferritins Diet Yin Deficiency Molecular Sequence Data Base Sequence Lipid Metabolism, Inborn Errors Vitamin D alpha 1-Antitrypsin Mice, Mutant Strains Hypopituitarism Carbohydrate Metabolism, Inborn Errors Fatty Acids, Essential Purine-Pyrimidine Metabolism, Inborn Errors Steroid 21-Hydroxylase Cells, Cultured Vitamin A Human Growth Hormone Mice, Transgenic Fibroblasts Hemoglobins Iron, Dietary Dwarfism, Pituitary RNA, Messenger Copper Erythrocytes Infant, Newborn Anemia, Hemolytic Potassium Deficiency Platelet Storage Pool Deficiency Folic Acid Dietary Supplements Body Weight Selenium Consanguinity Pregnancy Growth Disorders Methylmalonic Acid Genotype Erythrocyte Indices Point Mutation Carnitine Dihydropyrimidine Dehydrogenase Deficiency Mutation, Missense Brain Diseases, Metabolic, Inborn Nutritional Status Acyl-CoA Dehydrogenases Pyruvate Dehydrogenase Complex Deficiency Disease Alleles Glucosephosphate Dehydrogenase Gene Deletion

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