1.14.14.19	17alpha-hydroxyprogesterone deacetylase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9177409&form=6&db=m	A 5'-splice site mutation in the cytochrome P450 steroid 17alpha-hydroxylase gene in 17alpha-hydroxylase deficiency.	causal interaction,unassigned	4,0	
1.14.14.19	17alpha-hydroxyprogesterone deacetylase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11549876&form=6&db=m	New compound heterozygous mutation in the CYP17 gene in a 46,XY girl with 17 alpha-hydroxylase/17,20-lyase deficiency.	causal interaction,diagnostic usage,ongoing research,unassigned	4,4,3,0	
1.14.14.19	17alpha-hydroxyprogesterone deacetylase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12466376&form=6&db=m	Differential inhibition of 17alpha-hydroxylase and 17,20-lyase activities by three novel missense CYP17 mutations identified in patients with P450c17 deficiency.	causal interaction,diagnostic usage,therapeutic application,unassigned	4,2,1,0	
1.14.14.19	17alpha-hydroxyprogesterone deacetylase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12706306&form=6&db=m	A complex heterozygous mutation of His373Leu and Asp487-Ser488-Phe489 deletion in human cytochrome P450c17 causes 17alpha-hydroxylase/17,20-lyase deficiency in three Chinese sisters.	causal interaction,ongoing research,unassigned	4,1,0	
1.14.14.19	17alpha-hydroxyprogesterone deacetylase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=14504283&form=6&db=m	CYP17 mutation E305G causes isolated 17,20-lyase deficiency by selectively altering substrate binding.	causal interaction,unassigned	3,0	
1.14.14.19	17alpha-hydroxyprogesterone deacetylase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19793597&form=6&db=m	Novel CYP17A1 mutation in a Japanese patient with combined 17alpha-hydroxylase/17,20-lyase deficiency.	causal interaction,diagnostic usage,ongoing research,unassigned	4,4,3,0	
1.14.14.19	17alpha-hydroxyprogesterone deacetylase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21340176&form=6&db=m	Distinctive profile of the 17-hydroxylase and 17,20-lyase activities revealed by urinary steroid metabolomes of patients with CYP17 deficiency.	causal interaction,diagnostic usage,unassigned	3,1,0	
1.14.14.19	Addison Disease	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29982238&form=6&db=m	Three new Brazilian cases of 17?-hydroxylase deficiency: clinical, molecular, hormonal, and treatment features.	causal interaction,diagnostic usage,therapeutic application,unassigned	3,2,1,0	
1.14.14.19	Adenoma	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8137519&form=6&db=m	In-vitro evidence for the regulation of 17,20-lyase activity by cytochrome b5 in adrenocortical adenomas from patients with Cushing's syndrome.	causal interaction,diagnostic usage,ongoing research,therapeutic application	4,1,3,1	
1.14.14.19	Adenoma	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8288710&form=6&db=m	Mechanism of abnormal production of adrenal androgens in patients with adrenocortical adenomas and carcinomas.	causal interaction,diagnostic usage,ongoing research,therapeutic application	4,4,2,1