Genetic diseases of steroid metabolism.

Medicine & Life Sciences

• Inborn Genetic Diseases 93%
• Steroids 75%
• Mineralocorticoids 72%
• Congenital Adrenal Hyperplasia 44%
• Short Chain Dehydrogenase-Reductases 36%
• Cholesterol Side-Chain Cleavage Enzyme 33%
• Enzymes 24%
• NADP 24%
• 17-Hydroxysteroid Dehydrogenase Deficiency 24%
• Cytochrome P-450 Enzyme System 21%
• Adrenal hyperplasia, congenital, type 5 21%
• Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency 20%
• Oxidoreductases 20%
• Androgens 20%
• 3b-Hydroxysteroid Dehydrogenase Deficiency 20%
• Glucocorticoids 20%
• Hydrocortisone 19%
• 17-Hydroxysteroid Dehydrogenases 19%
• 3-Hydroxysteroid Dehydrogenases 19%
• Cholestenone 5 alpha-Reductase 18%
• Molecular Weight 18%
• 3-Oxo-5-alpha-Steroid 4-Dehydrogenase 18%
• Estrogens 18%
• Physiological Sexual Dysfunctions 18%
• Electrons 17%
• Steroid 21-Hydroxylase 16%
• Steroid 17-alpha-Hydroxylase 16%
• Congenital adrenal hyperplasia due to 21 hydroxylase deficiency 15%
• Male Genitalia 14%
• Aromatase 13%
• Adrenal Cortex 13%
• Dihydrotestosterone 13%
• Steroid Receptors 13%
• Gonads 12%
• Heme 12%
• Progestins 12%
• NAD 11%
• Lysine 10%
• Tyrosine 10%
• Catalytic Domain 10%
• Testosterone 9%
• Membrane Proteins 9%
• Cholesterol 8%
• Oxygen 8%
• Hormones 7%
• Proteins 4%

Chemical Compounds

• Mineralocorticoid 100%
• Steroid 93%
• Pharmacological Metabolism 78%
• Gonadal Steroid Hormone 55%
• Cholesterol 33%
• Glucocorticoid 32%
• Cortisol 32%
• Androgen 31%
• Estrogen 27%
• Cytochrome P450 27%
• Disorder 21%
• Hydride 21%
• Biosynthesis 21%
• Progestin 19%
• Steroid Hormone 16%
• Bioconversion 15%
• Testosterone 14%
• Tyrosine Residue 14%
• Lysine Residue 14%
• Electron Particle 13%
• Weight 13%
• Protein 10%
• Dioxygen 6%
• Amount 5%