Deficiency with secondary deficiency diseases. Medical search. Frequent questions

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Anatomy1

Organisms3

Mice, Knockout Mice, Inbred C57BL Mice, Mutant Strains

Diseases47

Mannosidase Deficiency Diseases Carbamoyl-Phosphate Synthase I Deficiency Disease Immunologic Deficiency Syndromes Multiple Sulfatase Deficiency Disease Pyruvate Carboxylase Deficiency Disease Deficiency Diseases Pyruvate Dehydrogenase Complex Deficiency Disease Ornithine Carbamoyltransferase Deficiency Disease Vitamin A Deficiency 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 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 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

Chemicals and Drugs7

Iron Iodine Zinc Vitamin B 12 Ferritins Vitamin D alpha 1-Antitrypsin

Analytical, Diagnostic and Therapeutic Techniques and Equipment2

Pedigree Disease Models, Animal

Phenomena and Processes6

Mutation Phenotype Homozygote Heterozygote Diet Base Sequence

Information Science2

Molecular Sequence Data Base Sequence

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

Mannosidase Deficiency Diseases Carbamoyl-Phosphate Synthase I Deficiency Disease Immunologic Deficiency Syndromes Multiple Sulfatase Deficiency Disease Pyruvate Carboxylase Deficiency Disease Deficiency Diseases Pyruvate Dehydrogenase Complex Deficiency Disease Ornithine Carbamoyltransferase Deficiency Disease Vitamin A Deficiency 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 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 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

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