1.1.1.53 11beta-hydroxysteroid dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12649576&form=6&db=m 11beta-hydroxysteroid dehydrogenase type 1 deficiency ('apparent cortisone reductase deficiency') in a 6-year-old boy. causal interaction,ongoing research,unassigned 3,1,0 1.1.1.53 3alpha(or 20beta)-hydroxysteroid dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8370690&form=6&db=m Defects in the HSD11 gene encoding 11 beta-hydroxysteroid dehydrogenase are not found in patients with apparent mineralocorticoid excess or 11-oxoreductase deficiency. causal interaction,unassigned 4,0 1.1.1.53 3alpha(or 20beta)-hydroxysteroid dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8923828&form=6&db=m Apparent cortisone reductase deficiency: a unique form of hypercortisolism. causal interaction,unassigned 4,0 1.1.1.53 3alpha(or 20beta)-hydroxysteroid dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10522997&form=6&db=m Apparent cortisone reductase deficiency: a functional defect in 11beta-hydroxysteroid dehydrogenase type 1. causal interaction,unassigned 4,0 1.1.1.53 3alpha(or 20beta)-hydroxysteroid dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11150889&form=6&db=m Apparent cortisone reductase deficiency: a rare cause of hyperandrogenemia and hypercortisolism. causal interaction,therapeutic application,unassigned 4,1,0 1.1.1.53 3alpha(or 20beta)-hydroxysteroid dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11469811&form=6&db=m Cortisol metabolism and the role of 11beta-hydroxysteroid dehydrogenase. causal interaction,unassigned 4,0 1.1.1.53 3alpha(or 20beta)-hydroxysteroid dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12858176&form=6&db=m Mutations in the genes encoding 11beta-hydroxysteroid dehydrogenase type 1 and hexose-6-phosphate dehydrogenase interact to cause cortisone reductase deficiency. causal interaction,unassigned 2,0 1.1.1.53 3alpha(or 20beta)-hydroxysteroid dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=15315958&form=6&db=m 11{beta}-Hydroxysteroid Dehydrogenase Type 1: A Tissue-Specific Regulator of Glucocorticoid Response. causal interaction,therapeutic application,unassigned 3,2,0 1.1.1.53 3alpha(or 20beta)-hydroxysteroid dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=15466942&form=6&db=m 11beta-hydroxysteroid dehydrogenase type 1: a tissue-specific regulator of glucocorticoid response. causal interaction,therapeutic application,unassigned 3,2,0 1.1.1.53 3alpha(or 20beta)-hydroxysteroid dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=15827106&form=6&db=m A study of the hexose-6-phosphate dehydrogenase gene R453Q and 11beta-hydroxysteroid dehydrogenase type 1 gene 83557insA polymorphisms in the polycystic ovary syndrome. ongoing research,unassigned 2,0