Symptoms of 3 beta hydroxysteroid dehydrogenase deficiency. Medical search. Frequent questions

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Anatomy3

Liver Erythrocytes Cells, Cultured

Diseases22

Glucosephosphate Dehydrogenase Deficiency Multiple Acyl Coenzyme A Dehydrogenase Deficiency Dihydropyrimidine Dehydrogenase Deficiency Lipid Metabolism, Inborn Errors Brain Diseases, Metabolic, Inborn Favism Pyruvate Dehydrogenase Complex Deficiency Disease Amino Acid Metabolism, Inborn Errors Metabolism, Inborn Errors Anemia, Hemolytic Purine-Pyrimidine Metabolism, Inborn Errors Kernicterus Brain Diseases, Metabolic Reye Syndrome Jaundice, Neonatal Gilbert Disease Glycogen Storage Disease Type I Hemolysis Hirsutism Hyperbilirubinemia, Neonatal Hyperbilirubinemia Mitochondrial Diseases

Chemicals and Drugs62

Hydroxysteroid Dehydrogenases 11-beta-Hydroxysteroid Dehydrogenase Type 2 3-Hydroxysteroid Dehydrogenases 11-beta-Hydroxysteroid Dehydrogenase Type 1 17-Hydroxysteroid Dehydrogenases 11-beta-Hydroxysteroid Dehydrogenases 20-Hydroxysteroid Dehydrogenases Steroid 17-alpha-Hydroxylase 3-alpha-Hydroxysteroid Dehydrogenase (B-Specific)Hydrocortisone Estradiol Dehydrogenases Acyl-CoA Dehydrogenase Acyl-CoA Dehydrogenases Sulfotransferases Glucosephosphate Dehydrogenase Acyl-CoA Dehydrogenase, Long-Chain Cortisone Alcohol Oxidoreductases Steroids NAD Succinate-Semialdehyde Dehydrogenase Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase 3-Hydroxyacyl CoA Dehydrogenases Carnitine Glutaryl-CoA Dehydrogenase Butyryl-CoA Dehydrogenase Testosterone Dihydrouracil Dehydrogenase (NADP)L-Lactate Dehydrogenase Androsterone Alcohol Dehydrogenase Electron-Transferring Flavoproteins Pyruvate Dehydrogenase (Lipoamide)Glyceraldehyde-3-Phosphate Dehydrogenases Phosphoglycerate Dehydrogenase 20-alpha-Hydroxysteroid Dehydrogenase Primaquine Aldehyde Dehydrogenase Glutamate Dehydrogenase Dimethylglycine Dehydrogenase Malate Dehydrogenase Isocitrate Dehydrogenase Phosphoadenosine Phosphosulfate Arylsulfotransferase Methylphenazonium Methosulfate Ketosteroids Dihydrolipoamide Dehydrogenase NADP Succinate Dehydrogenase Carbohydrate Dehydrogenases L-Iditol 2-Dehydrogenase Oxidoreductases Dehydroepiandrosterone Mitochondrial Trifunctional Protein Oxidoreductases Acting on CH-CH Group Donors Glycerolphosphate Dehydrogenase 17-alpha-Hydroxypregnenolone Glucose 1-Dehydrogenase Ketoglutarate Dehydrogenase Complex Aldehyde Oxidoreductases Interleukin-1beta Isoenzymes

Analytical, Diagnostic and Therapeutic Techniques and Equipment2

Neonatal Screening Exchange Transfusion, Whole Blood

Phenomena and Processes7

Kinetics Base Sequence Mutation Hemolysis Substrate Specificity Oxidation-Reduction Amino Acid Sequence

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Named Groups1

Infant, Newborn

Health Care1

Neonatal Screening

Geographicals1

Mediterranean Islands

Anatomy Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes Information Science Named Groups Health Care Geographicals

Hydroxysteroid Dehydrogenases 11-beta-Hydroxysteroid Dehydrogenase Type 2 3-Hydroxysteroid Dehydrogenases 11-beta-Hydroxysteroid Dehydrogenase Type 1 17-Hydroxysteroid Dehydrogenases 11-beta-Hydroxysteroid Dehydrogenases Glucosephosphate Dehydrogenase Deficiency 20-Hydroxysteroid Dehydrogenases Steroid 17-alpha-Hydroxylase 3-alpha-Hydroxysteroid Dehydrogenase (B-Specific)Hydrocortisone Estradiol Dehydrogenases Multiple Acyl Coenzyme A Dehydrogenase Deficiency Dihydropyrimidine Dehydrogenase Deficiency Acyl-CoA Dehydrogenase Acyl-CoA Dehydrogenases Lipid Metabolism, Inborn Errors Sulfotransferases Glucosephosphate Dehydrogenase Acyl-CoA Dehydrogenase, Long-Chain Cortisone Brain Diseases, Metabolic, Inborn Alcohol Oxidoreductases Steroids Favism Pyruvate Dehydrogenase Complex Deficiency Disease NAD Succinate-Semialdehyde Dehydrogenase Neonatal Screening Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase 3-Hydroxyacyl CoA Dehydrogenases Carnitine Amino Acid Metabolism, Inborn Errors Metabolism, Inborn Errors Liver Glutaryl-CoA Dehydrogenase Kinetics Butyryl-CoA Dehydrogenase Testosterone Dihydrouracil Dehydrogenase (NADP)L-Lactate Dehydrogenase Mediterranean Islands Androsterone Anemia, Hemolytic Alcohol Dehydrogenase Electron-Transferring Flavoproteins Purine-Pyrimidine Metabolism, Inborn Errors Pyruvate Dehydrogenase (Lipoamide)Glyceraldehyde-3-Phosphate Dehydrogenases Kernicterus Phosphoglycerate Dehydrogenase 20-alpha-Hydroxysteroid Dehydrogenase Primaquine Aldehyde Dehydrogenase Glutamate Dehydrogenase Brain Diseases, Metabolic Dimethylglycine Dehydrogenase Malate Dehydrogenase Isocitrate Dehydrogenase Reye Syndrome Molecular Sequence Data Infant, Newborn Phosphoadenosine Phosphosulfate Arylsulfotransferase Methylphenazonium Methosulfate Jaundice, Neonatal Gilbert Disease Ketosteroids Base Sequence Mutation Dihydrolipoamide Dehydrogenase NADP Glycogen Storage Disease Type I Succinate Dehydrogenase Carbohydrate Dehydrogenases L-Iditol 2-Dehydrogenase Oxidoreductases Dehydroepiandrosterone Hemolysis Hirsutism Mitochondrial Trifunctional Protein Oxidoreductases Acting on CH-CH Group Donors Glycerolphosphate Dehydrogenase Hyperbilirubinemia, Neonatal Substrate Specificity Exchange Transfusion, Whole Blood Oxidation-Reduction 17-alpha-Hydroxypregnenolone Hyperbilirubinemia Amino Acid Sequence Glucose 1-Dehydrogenase Ketoglutarate Dehydrogenase Complex Aldehyde Oxidoreductases Mitochondrial Diseases Interleukin-1beta Isoenzymes Erythrocytes Cells, Cultured

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