NADH dehydrogenase | Lactate dehydrogenase | NADPH dehydrogenase | Malate dehydrogenase | Lactate dehydrogenase elevating virus | IMP dehydrogenase | Glucose-6-phosphate dehydrogenase deficiency | Succinate dehydrogenase complex subunit C | Pyruvate dehydrogenase | Phosphogluconate dehydrogenase | methylenetetrahydrofolate dehydrogenase (NADP+) | lactate dehydrogenase | Glucose-6-phosphate dehydrogenase | Corticosteroid 11-beta-dehydrogenase isozyme 2 | Aspartate-semialdehyde dehydrogenase | Aryl-alcohol dehydrogenase | Aldehyde dehydrogenase | Alcohol dehydrogenase | 3-hydroxybenzyl-alcohol dehydrogenase | 1,2-dihydroxy-6-methylcyclohexa-3,5-dienecarboxylate dehydrogenase |
3β-Hydroxysteroid dehydrogenase II deficient congenital adrenal hyperplasia (3β-HSD CAH) is an uncommon form of congenital adrenal hyperplasia (CAH) resulting from a mutation in the gene for one of the key enzymes in cortisol synthesis by the adrenal gland, 3β-hydroxysteroid dehydrogenase (3β-HSD) type II (HSD3B2).