1.1.1.270	11beta-hydroxysteroid dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10915016&form=6&db=m	Epidemiologic study of adrenal gland disorders in Japan.	causal interaction,unassigned	3,0	
1.1.1.270	3(or 17)beta-hydroxysteroid dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=184011&form=6&db=m	Male pseudohermaphroditism consistent with 17,20-desmolase deficiency.	diagnostic usage,unassigned	1,0	
1.1.1.270	3(or 17)beta-hydroxysteroid dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10599696&form=6&db=m	New insight into the molecular basis of 3beta-hydroxysteroid dehydrogenase deficiency: identification of eight mutations in the HSD3B2 gene eleven patients from seven new families and comparison of the functional properties of twenty-five mutant enzymes.	causal interaction,ongoing research,unassigned	4,2,0	
1.1.1.270	3(or 17)beta-hydroxysteroid dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10770215&form=6&db=m	Characterization of two novel homozygous missense mutations involving codon 6 and 259 of type II 3beta-hydroxysteroid dehydrogenase (3betaHSD) gene causing, respectively, nonsalt-wasting and salt-wasting 3betaHSD deficiency disorder.	causal interaction,ongoing research,therapeutic application,unassigned	4,1,1,0	
1.1.1.270	3(or 17)beta-hydroxysteroid dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16148681&form=6&db=m	Masculinizing genitoplasty in intersex patients.	unassigned	-	
1.1.1.270	3-oxo-5alpha-steroid 4-dehydrogenase (acceptor) deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16148681&form=6&db=m	Masculinizing genitoplasty in intersex patients.	unassigned	-	
1.1.1.270	3beta-hydroxy-delta5-steroid dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12608938&form=6&db=m	Carriers for type II 3beta-hydroxysteroid dehydrogenase (HSD3B2) deficiency can only be identified by HSD3B2 genotype study and not by hormone test.	causal interaction,diagnostic usage,ongoing research,unassigned	3,1,2,0	
1.1.1.270	3beta-hydroxysteroid 3-dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=4835137&form=6&db=m	Testicular endocrine function in a pubertal boy with 3beta-hydroxysteroid dehydrogenase deficiency.	causal interaction,unassigned	4,0	
1.1.1.270	3beta-hydroxysteroid 3-dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9402240&form=6&db=m	Definitive diagnosis of enzymatic deficiencies of steroidogenesis in at-risk newborns and infants by urinary marker analysis using GC/MS-SIM.	causal interaction,diagnostic usage,unassigned	4,4,0	
1.1.1.270	3beta-hydroxysteroid 3-dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10208955&form=6&db=m	An inborn error of bile acid synthesis (3beta-hydroxy-delta5-C27-steroid dehydrogenase deficiency) presenting as malabsorption leading to rickets.	unassigned	-