4.1.3.16	Hyperoxaluria, Primary	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20797690&form=6&db=m	Mutations in DHDPSL are responsible for primary hyperoxaluria type III.	causal interaction,unassigned	3,0	
4.1.3.16	Hyperoxaluria, Primary	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21896830&form=6&db=m	Primary hyperoxaluria type III gene HOGA1 (formerly DHDPSL) as a possible risk factor for idiopathic calcium oxalate urolithiasis.	diagnostic usage,unassigned	3,0	
4.1.3.16	Urolithiasis	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21896830&form=6&db=m	Primary hyperoxaluria type III gene HOGA1 (formerly DHDPSL) as a possible risk factor for idiopathic calcium oxalate urolithiasis.	diagnostic usage,unassigned	3,0	
4.1.3.16	Hyperoxaluria, Primary	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21998747&form=6&db=m	Structural and biochemical studies of human 4-hydroxy-2-oxoglutarate aldolase: implications for hydroxyproline metabolism in primary hyperoxaluria.	diagnostic usage,ongoing research,unassigned	3,2,0	
4.1.3.16	Hyperoxaluria, Primary	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22115483&form=6&db=m	Re: Mutations in DHDPSL are Responsible for Primary Hyperoxaluria Type III.	causal interaction,unassigned	4,0	
4.1.3.16	Hyperoxaluria, Primary	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22325509&form=6&db=m	Re: primary hyperoxaluria type III gene HOGA1 (formerly DHDPSL) as a possible risk factor for idiopathic calcium oxalate urolithiasis.	diagnostic usage,therapeutic application,unassigned	3,1,0	
4.1.3.16	Urolithiasis	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22325509&form=6&db=m	Re: primary hyperoxaluria type III gene HOGA1 (formerly DHDPSL) as a possible risk factor for idiopathic calcium oxalate urolithiasis.	diagnostic usage,therapeutic application,unassigned	3,1,0	
4.1.3.16	Hyperoxaluria, Primary	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22391140&form=6&db=m	The enzyme 4-hydroxy-2-oxoglutarate aldolase is deficient in primary hyperoxaluria type 3.	causal interaction,diagnostic usage,ongoing research,unassigned	4,3,2,0	
4.1.3.16	4-hydroxy-2-oxoglutarate aldolase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22729392&form=6&db=m	Primary hyperoxaluria type III-a model for studying perturbations in glyoxylate metabolism.	causal interaction,unassigned	4,0	
4.1.3.16	Hyperoxaluria, Primary	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22729392&form=6&db=m	Primary hyperoxaluria type III-a model for studying perturbations in glyoxylate metabolism.	causal interaction,unassigned	4,0