5.3.1.8	6-phosphofructokinase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=139680&form=6&db=m	[Exercise-induced muscular weakness, myalgia and contractures. I. A clinical review]	causal interaction,unassigned	3,0	
5.3.1.8	6-phosphofructokinase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=847445&form=6&db=m	[Exercise-induced muscular weakness, myalgia and contractures. II. Casuistic contribution]	causal interaction,unassigned	4,0	
5.3.1.8	Adenocarcinoma	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=34511962&form=6&db=m	Phosphomannose Isomerase High Expression Associated with Better Prognosis in Pancreatic Ductal Adenocarcinoma.	causal interaction,diagnostic usage,unassigned	4,4,0	
5.3.1.8	Alcohol Withdrawal Delirium	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=5573906&form=6&db=m	Activity of aldolase, aminotransferases, phosphohexoisomerase and ceruloplasmin in the course of delirium tremens.	unassigned	-	
5.3.1.8	Alcohol Withdrawal Delirium	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=5805104&form=6&db=m	[Activity of aldolase, aminotransferases, phosphohexoisomerase and ceruloplasmin in the course of delirium tremens]	unassigned	-	
5.3.1.8	Anemia	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=13605990&form=6&db=m	[Erythrocyte enzymes; activity of glycolytic enzymes of erythrocytes in anemia: phosphoglucomutase, phosphohexoisomerase, diphosphofructaldolase, lactic acid dehydrogenase.]	ongoing research,unassigned	1,0	
5.3.1.8	Biliary Tract Diseases	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=5941685&form=6&db=m	[Serum iron and copper levels and serum activity of phosphohexoisomerase and glutamic-pyruvic transaminase in patients with liver and biliary tract disease]	diagnostic usage,ongoing research,unassigned	4,3,0	
5.3.1.8	Blindness	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24421398&form=6&db=m	Mannose supplements induce embryonic lethality and blindness in phosphomannose isomerase hypomorphic mice.	causal interaction,ongoing research,unassigned	3,1,0	
5.3.1.8	Congenital Disorders of Glycosylation	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9525984&form=6&db=m	Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy.	causal interaction,therapeutic application,unassigned	4,1,0	
5.3.1.8	Congenital Disorders of Glycosylation	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9585601&form=6&db=m	Phosphomannose isomerase deficiency: a carbohydrate-deficient glycoprotein syndrome with hepatic-intestinal presentation.	causal interaction,unassigned	3,0