1.1.1.36	acetoacetyl-coa reductase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10497229&form=6&db=m	Yeast peroxisomal multifunctional enzyme: (3R)-hydroxyacyl-CoA dehydrogenase domains A and B are required for optimal growth on oleic acid.	unassigned	-	
1.1.1.36	acetoacetyl-coa reductase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11964182&form=6&db=m	The role of alpha-methylacyl-CoA racemase in bile acid synthesis.	causal interaction,unassigned	1,0	
1.1.1.36	Adrenoleukodystrophy	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11356171&form=6&db=m	Clinical consequences of defects in peroxisomal beta-oxidation.	causal interaction,unassigned	3,0	
1.1.1.36	alpha-methylacyl-coa racemase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11356171&form=6&db=m	Clinical consequences of defects in peroxisomal beta-oxidation.	causal interaction,unassigned	3,0	
1.1.1.36	Neoplasms	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26222439&form=6&db=m	Substrate Specificity, Inhibitor Selectivity and Structure-Function Relationships of Aldo-Keto Reductase 1B15: A Novel Human Retinaldehyde Reductase.	causal interaction,unassigned	3,0	
1.1.1.36	Neoplasms	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31028727&form=6&db=m	Engineering aldo-keto reductase 1B10 to mimic the distinct 1B15 topology and specificity towards inhibitors and substrates, including retinoids and steroids.	therapeutic application,unassigned	1,0	
1.1.1.36	Tuberculosis	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=14766307&form=6&db=m	Selection of an Escherichia coli host that expresses mutant forms of Mycobacterium tuberculosis 2-trans enoyl-ACP(CoA) reductase and 3-ketoacyl-ACP(CoA) reductase enzymes.	ongoing research,therapeutic application,unassigned	2,3,0