Inborn errors of cholesterol biosynthesis

Medicine & Life Sciences

• Cholesterol 100%
• Lathosterolosis 41%
• Simvastatin 34%
• Mevalonate Kinase Deficiency 32%
• 7,8-didehydrocimigenol 31%
• Desmosterolosis 29%
• Sterols 28%
• HEM dysplasia 20%
• Cytochrome P-450 Enzyme System 18%
• Congenital Ichthyosiform Erythroderma 17%
• Desmosterol 16%
• Smith-Lemli-Opitz Syndrome 15%
• Lanosterol 15%
• Extremities 14%
• Mutation 13%
• Disorders of Sex Development 12%
• Lovastatin 12%
• coenzyme Q10 12%
• Bile Acids and Salts 10%
• cholesta-5,8-dien-3 beta-ol 9%
• Blood-Brain Barrier 9%
• Weights and Measures 9%
• Antley-Bixler Syndrome Phenotype 8%
• Oxidoreductases 8%
• lamin B receptor 8%
• 7-dehydrocholesterol reductase 8%
• mevalonate kinase 8%
• Leukotriene Receptors 8%
• Chondrodysplasia Punctata 8%
• Hemizygote 8%
• zafirlukast 8%
• lathosterol 7%
• Fever 7%
• Therapeutics 7%
• Dietary Cholesterol 6%
• Serum 6%
• Hydrops Fetalis 6%
• Cholesterol Esters 5%
• Genes 5%
• Gastrostomy 5%
• Cholestasis 5%
• Enteral Nutrition 5%
• Heterozygote 5%
• Vitamin E 5%
• Missense Mutation 5%
• Dietary Supplements 4%
• Growth 4%
• Energy Intake 4%
• Granulocytes 4%
• Ascorbic Acid 4%
• Life Expectancy 4%
• Hydroxymethylglutaryl-CoA Reductase Inhibitors 4%
• Skin Diseases 4%
• Intellectual Disability 4%
• Siblings 4%
• Epilepsy 4%
• Adipose Tissue 4%
• Adrenal Cortex Hormones 3%
• Reactive Oxygen Species 3%
• Electrons 3%
• Accidental Falls 3%
• Tissue Donors 3%
• Steroids 3%
• Head 3%
• Aptitude 3%
• Lipids 3%
• Pathology 3%
• Phenotype 2%
• Skin 2%
• Enzymes 2%
• Child 2%