1.1.1.47	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	
1.1.1.47	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	
1.1.1.47	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	
1.1.1.47	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	
1.1.1.47	3alpha(or 20beta)-hydroxysteroid dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=15956339&form=6&db=m	Hexose-6-phosphate dehydrogenase confers oxo-reductase activity upon 11 beta-hydroxysteroid dehydrogenase type 1.	causal interaction,unassigned	4,0	
1.1.1.47	3alpha(or 20beta)-hydroxysteroid dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16091483&form=6&db=m	Genotypes at 11beta-hydroxysteroid dehydrogenase type 11B1 and hexose-6-phosphate dehydrogenase loci are not risk factors for apparent cortisone reductase deficiency in a large population-based sample.	causal interaction,unassigned	3,0	
1.1.1.47	3alpha(or 20beta)-hydroxysteroid dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17062770&form=6&db=m	Lack of Association of the 11beta-hydroxysteroid dehydrogenase type 1 gene 83,557insA and hexose-6-phosphate dehydrogenase gene R453Q polymorphisms with body composition, adrenal androgen production, blood pressure, glucose metabolism, and dementia.	causal interaction,ongoing research,therapeutic application,unassigned	3,2,1,0	
1.1.1.47	3alpha(or 20beta)-hydroxysteroid dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=18628520&form=6&db=m	Steroid biomarkers and genetic studies reveal inactivating mutations in hexose-6-phosphate dehydrogenase in patients with cortisone reductase deficiency.	causal interaction,unassigned	4,0	
1.1.1.47	3alpha(or 20beta)-hydroxysteroid dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19935835&form=6&db=m	Hexose-6-phosphate dehydrogenase: a new risk gene for multiple sclerosis.	causal interaction,therapeutic application,unassigned	3,4,0	
1.1.1.47	3alpha(or 20beta)-hydroxysteroid dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21050867&form=6&db=m	Mutations of the hexose-6-phosphate dehydrogenase gene rarely cause hyperandrogenemic polycystic ovary syndrome.	causal interaction,unassigned	3,0