1.5.5.1	Acidosis	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8617498&form=6&db=m	Assignment of Etfdh, Etfb, and Etfa to chromosomes 3, 7, and 13: the mouse homologs of genes responsible for glutaric acidemia type II in human.	causal interaction,ongoing research,therapeutic application,unassigned	4,1,1,0	
1.5.5.1	Acidosis	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17912479&form=6&db=m	Cardiomyopathy in multiple Acyl-CoA dehydrogenase deficiency: a clinico-pathological correlation and review of literature.	causal interaction,therapeutic application,unassigned	2,1,0	
1.5.5.1	Acidosis	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17977044&form=6&db=m	Risk of sudden death and acute life-threatening events in patients with glutaric acidemia type II.	unassigned	-	
1.5.5.1	acyl-coa dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7360517&form=6&db=m	Multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II) with transient hypersarcosinemia and sarcosinuria; possible inherited deficiency of an electron transfer flavoprotein.	causal interaction,unassigned	3,0	
1.5.5.1	acyl-coa dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9889013&form=6&db=m	Isolated isobutyryl-CoA dehydrogenase deficiency: an unrecognized defect in human valine metabolism.	causal interaction,diagnostic usage,unassigned	1,3,0	
1.5.5.1	acyl-coa dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16165386&form=6&db=m	Identification of the human mitochondrial FAD transporter and its potential role in multiple acyl-CoA dehydrogenase deficiency.	causal interaction,ongoing research,unassigned	2,2,0	
1.5.5.1	acyl-coa dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16510302&form=6&db=m	Electron transfer flavoprotein deficiency: functional and molecular aspects.	causal interaction,diagnostic usage,therapeutic application,unassigned	4,2,1,0	
1.5.5.1	acyl-coa dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17050691&form=6&db=m	Structure of electron transfer flavoprotein-ubiquinone oxidoreductase and electron transfer to the mitochondrial ubiquinone pool.	causal interaction,ongoing research,unassigned	1,2,0	
1.5.5.1	acyl-coa dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17912479&form=6&db=m	Cardiomyopathy in multiple Acyl-CoA dehydrogenase deficiency: a clinico-pathological correlation and review of literature.	causal interaction,therapeutic application,unassigned	2,1,0	
1.5.5.1	acyl-coa dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19249206&form=6&db=m	ETFDH mutations, CoQ10 levels, and respiratory chain activities in patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.	causal interaction,diagnostic usage,unassigned	2,2,0