Severe deficiencies. Medical search. Frequent questions

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Anatomy13

X Chromosome Cells, Cultured Mitochondria Fibroblasts Liver Brain Pituitary Gland Chromosomes Cell Line B-Lymphocytes T-Lymphocytes Sex Chromosomes Erythrocytes

Organisms6

Mice, Knockout Mice, Inbred C57BL Drosophila melanogaster Mice, Mutant Strains Mice, Transgenic Caenorhabditis

Diseases84

Avitaminosis Deficiency Diseases Immunologic Deficiency Syndromes IgG Deficiency Vitamin A Deficiency Folic Acid Deficiency Vitamin E Deficiency Vitamin B Deficiency Hypopituitarism Anemia, Iron-Deficiency Mitochondrial Diseases Malnutrition Protein S Deficiency Antithrombin III Deficiency Nutrition Disorders Ascorbic Acid Deficiency Vitamin B 12 Deficiency Magnesium Deficiency Protein C Deficiency Dysgammaglobulinemia Metabolism, Inborn Errors Mitochondrial Myopathies Mitochondrial Encephalomyopathies Agammaglobulinemia Thrombophilia Lower Extremity Deformities, Congenital Malabsorption Syndromes Coagulation Protein Disorders Child Nutrition Disorders IgA Deficiency Protein-Energy Malnutrition Limb Deformities, Congenital Vitamin B 6 Deficiency Color Vision Defects Blood Coagulation Disorders, Inherited Blood Coagulation Disorders Growth Disorders Anemia Spherocytosis, Hereditary Common Variable Immunodeficiency Factor XII Deficiency Thiamine Deficiency Dwarfism, Pituitary Parasitic Diseases Disease Models, Animal Scurvy Pregnancy Complications Obesity, Morbid Purine-Pyrimidine Metabolism, Inborn Errors Lysosomal Storage Diseases White Muscle Disease Pituitary Diseases Infant Nutrition Disorders Lipid Metabolism, Inborn Errors Severe Combined Immunodeficiency Blood Platelet Disorders Hemorrhagic Disorders Carbohydrate Metabolism, Inborn Errors Afibrinogenemia Activated Protein C Resistance Hyperargininemia Congenital Disorders of Glycosylation Argininosuccinic Aciduria Hyper-IgM Immunodeficiency Syndrome, Type 1 Glucosephosphate Dehydrogenase Deficiency Hyperhomocysteinemia Disease Susceptibility Stomatitis, Aphthous Factor V Deficiency Anemia, Megaloblastic Potassium Deficiency Body Weight Peroxisomal Disorders Mucopolysaccharidoses Albinism Vitamin D Deficiency Chromosome Deletion Platelet Storage Pool Deficiency Multiple Sulfatase Deficiency Disease Infection Hyper-IgM Immunodeficiency Syndrome Neoplasms Craniopharyngioma Hypoprothrombinemias

Chemicals and Drugs62

Micronutrients Zinc Vitamins Trace Elements Iron Selenium Vitamin A Folic Acid Vitamin B 12 Iodine Complement C4a Complement C6 Minerals Copper Pituitary Hormones Cathepsin Z Iron, Dietary Complement C7 Hemoglobins Protein S Interleukin-12 Receptor beta 1 Subunit Riboflavin Complement C2 Elements Vitamin B Complex Human Growth Hormone Homocysteine Acyl-CoA Dehydrogenase, Long-Chain Ubiquinone Ferritins Complement C4 Pituitary Hormones, Anterior Prothrombin Thymus Hormones DNA-Binding Proteins Factor V Protein C Fatty Acids, Essential Vitamin B 6 DNA, Mitochondrial Membrane Proteins Complement System Proteins Blood Coagulation Factor Inhibitors RNA, Messenger Guanidinoacetate N-Methyltransferase beta Carotene Nuclear Proteins Cerebroside-Sulfatase Antithrombins Amidinotransferases Thiamine Transcription Factors Ethyl Methanesulfonate Drosophila Proteins Carrier Proteins Electron Transport Complex I Adenylosuccinate Lyase UTP-Hexose-1-Phosphate Uridylyltransferase Pyridoxine Mannose-6-Phosphate Isomerase Immunoglobulin G Complement C4b

Analytical, Diagnostic and Therapeutic Techniques and Equipment29

Crosses, Genetic Genetic Complementation Test Color Perception Tests Chromosome Mapping Nursing Records Complement Hemolytic Activity Assay Disease Models, Animal Obesity, Morbid Models, Biological Nutritional Support Prevalence Pituitary Function Tests Zygote Intrafallopian Transfer Risk Factors Bariatric Surgery Anthropometry FIGLU Test Case-Control Studies Cross-Sectional Studies Pedigree Body Weight Gastric Bypass Enzyme Assays Questionnaires Blood Coagulation Tests Nutrition Assessment Ilizarov Technique Partial Thromboplastin Time Retrospective Studies

Psychiatry and Psychology2

Dissent and Disputes Child, Gifted

Phenomena and Processes41

Mutation Nutritional Status Genes, Lethal Phenotype Pregnancy Nutritional Physiological Phenomena Heterozygote Homozygote Genes, Recessive Diet DNA Repair Base Sequence Nutritional Requirements X Chromosome Growth Time Factors Alleles Obesity, Morbid Signal Transduction Aging Amino Acid Sequence Gene Deletion Recombination, Genetic Genotype Mutagenesis Gene Expression Regulation, Developmental Disease Susceptibility Consanguinity Genes, Insect Chromosomes Sex Chromosomes Body Weight DNA Damage Tooth Calcification Maternal Nutritional Physiological Phenomena Cell Differentiation Chromosome Deletion Haploinsufficiency Point Mutation Complement Activation Partial Thromboplastin Time

Disciplines and Occupations1

Radiation Genetics

Anthropology, Education, Sociology and Social Phenomena2

Nutrition Policy Developing Countries

Technology, Industry, Agriculture6

Micronutrients Vitamins Trace Elements Dietary Supplements Food, Fortified Flour

Information Science6

Molecular Sequence Data Nursing Records Base Sequence Amino Acid Sequence Prevalence Questionnaires

Named Groups3

Infant, Newborn Nursing Staff Child, Gifted

Health Care22

Nutritional Status Health Facilities, Proprietary Nursing Records Nursing Homes Nursing Staff Quality of Health Care Nutrition Policy Radiation Genetics Medical Audit Prevalence Risk Factors Anthropometry Case-Control Studies Cross-Sectional Studies Questionnaires Age Factors Water Pollution Nutrition Assessment Rural Population Swimming Pools Guidelines as Topic Retrospective Studies

Geographicals7

Bhutan Nepal United States Oman Indonesia Mexico Mongolia

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Anthropology, Education, Sociology and Social Phenomena Technology, Industry, Agriculture Information Science Named Groups Health Care Geographicals

Avitaminosis Micronutrients Deficiency Diseases Immunologic Deficiency Syndromes IgG Deficiency Vitamin A Deficiency Mutation Zinc Folic Acid Deficiency Vitamin E Deficiency Nutritional Status Genes, Lethal Vitamin B Deficiency Vitamins Hypopituitarism Trace Elements Iron Anemia, Iron-Deficiency Mitochondrial Diseases Phenotype Malnutrition Protein S Deficiency Antithrombin III Deficiency Nutrition Disorders Ascorbic Acid Deficiency Vitamin B 12 Deficiency Magnesium Deficiency Mice, Knockout Protein C Deficiency Selenium Dysgammaglobulinemia Metabolism, Inborn Errors Vitamin A Dietary Supplements Mitochondrial Myopathies Mitochondrial Encephalomyopathies Mice, Inbred C57BL Agammaglobulinemia Drosophila melanogaster Pregnancy Nutritional Physiological Phenomena Food, Fortified Folic Acid Vitamin B 12 Crosses, Genetic Thrombophilia Lower Extremity Deformities, Congenital Malabsorption Syndromes Coagulation Protein Disorders Child Nutrition Disorders IgA Deficiency Protein-Energy Malnutrition Mice, Mutant Strains Genetic Complementation Test Iodine Color Perception Tests Heterozygote Limb Deformities, Congenital Vitamin B 6 Deficiency Chromosome Mapping Color Vision Defects Blood Coagulation Disorders, Inherited Complement C4a Infant, Newborn Blood Coagulation Disorders Homozygote Growth Disorders Complement C6 Minerals Anemia Spherocytosis, Hereditary Molecular Sequence Data Common Variable Immunodeficiency Factor XII Deficiency Health Facilities, Proprietary Genes, Recessive Copper Pituitary Hormones Nursing Records Diet Cathepsin Z Bhutan Nursing Homes DNA Repair Base Sequence Iron, Dietary Nursing Staff Nepal Thiamine Deficiency Complement C7 Nutritional Requirements Dwarfism, Pituitary Hemoglobins Protein S Quality of Health Care Complement Hemolytic Activity Assay Dissent and Disputes Parasitic Diseases Disease Models, Animal Interleukin-12 Receptor beta 1 Subunit

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