1.3.8.1	acetyl-coa c-acyltransferase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9848022&form=6&db=m	Clinical and biochemical features of fatty acid oxidation disorders.	causal interaction,unassigned	4,0	
1.3.8.1	acetyl-coa c-acyltransferase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10626578&form=6&db=m	Newborn screening with tandem mass spectrometry: 12 months' experience in NSW Australia.	causal interaction,unassigned	3,0	
1.3.8.1	acetyl-coa c-acyltransferase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16598811&form=6&db=m	Evaluation of electrospray-tandem mass spectrometry for the detection of phenylketonuria and other rare disorders.	causal interaction,diagnostic usage,unassigned	2,1,0	
1.3.8.1	Acidosis	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26045367&form=6&db=m	Reveal genes functionally associated with ACADS by a network study.	causal interaction,unassigned	1,0	
1.3.8.1	Acidosis, Lactic	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10626578&form=6&db=m	Newborn screening with tandem mass spectrometry: 12 months' experience in NSW Australia.	causal interaction,unassigned	3,0	
1.3.8.1	Acidosis, Lactic	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32143453&form=6&db=m	Inherited Metabolic Diseases and Cardiac Pathology in Adults: Diagnosis and Prevalence in a CardioMetabo Study.	causal interaction,diagnostic usage,unassigned	3,3,0	
1.3.8.1	acyl-coa dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2326316&form=6&db=m	Molecular cloning and nucleotide sequence of cDNAs encoding human short chain acyl-CoA dehydrogenase and study of the molecular basis of human short chain acyl-CoA dehydrogenase deficiency.	diagnostic usage,ongoing research,unassigned	3,2,0	
1.3.8.1	acyl-coa dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10490047&form=6&db=m	Mitochondrial fatty acid oxidation disorders and cyclic vomiting syndrome.	causal interaction,therapeutic application,unassigned	4,1,0	
1.3.8.1	acyl-coa dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12013984&form=6&db=m	[Short chain acyl-CoA dehydrogenase deficiency]	causal interaction,unassigned	4,0	
1.3.8.1	acyl-coa dehydrogenase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=14568186&form=6&db=m	A comparison of in vitro acylcarnitine profiling methods for the diagnosis of classical and variant short chain acyl-CoA dehydrogenase deficiency.	diagnostic usage,unassigned	2,0