Genetics of congenital adrenal hyperplasia

Keyphrases

• Congenital Adrenal Hyperplasia 100%
• Electron Donor 50%
• Hydroxylase 50%
• Cytochrome P450 Reductase 50%
• CYP21A2 50%
• CYP17A1 50%
• Gene mutation 25%
• Clinical Phenotype 25%
• Hydroxysteroid Dehydrogenase 25%
• Cytochrome P450 (CYP450) 25%
• Autosomal Recessive 25%
• Steroidogenic Enzymes 25%
• Complex Phenotypes 25%
• Biochemical Phenotype 25%
• P450 Oxidoreductase Deficiency 25%
• Genital Ambiguity 25%
• CYP11B1 25%
• HSD3B2 25%
• Steroid 21-hydroxylase 25%
• Skeletal Malformations 25%
• Steroid Biosynthesis 25%
• Steroidogenic 25%
• Inherited Metabolic Diseases 25%
• Adrenal Steroidogenesis 25%
• Gonadal Steroids 25%
• Cortisol Biosynthesis 25%
• Specific Enzyme Activity 25%

Biochemistry, Genetics and Molecular Biology

• Genetics 100%
• Cytochrome P450 Reductase 100%
• Enzyme 66%
• Oxygenase 66%
• Steroid Biosynthesis 66%
• CYP17A1 66%
• Enzyme Activity 33%
• Gene Mutation 33%
• Cortisol 33%
• Hydroxysteroid Dehydrogenase 33%
• Anabolism 33%
• Cytochrome P450 33%
• Autosomal Recessive Disorder 33%
• 21-Hydroxylase 33%
• Steroidogenic Enzymes 33%
• HSD3B2 33%

Medicine and Dentistry

• Congenital Adrenal Hyperplasia 100%
• Cytochrome P450 Reductase 50%
• Steroidogenesis 50%
• CYP17A1 50%
• Gene Mutation 25%
• Hydrocortisone 25%
• Enzyme Activity 25%
• Cytochrome P450 25%
• Steroidogenic Enzymes 25%
• Autosomal Recessive Disorder 25%
• 21-Hydroxylase 25%
• P450 Oxidoreductase Deficiency 25%
• Steroid 17alpha Monooxygenase 25%
• Ambiguous Genitalia 25%
• Steroid 11beta Monooxygenase 25%
• 3(or 17)beta Hydroxysteroid Dehydrogenase 25%
• Skeleton Malformation 25%
• Enzyme Defect 25%
• Metabolic Disorder 25%