EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
1.3.8.1 | acetyl-coa c-acyltransferase deficiency |
9848022 |
Clinical and biochemical features of fatty acid oxidation disorders. |
causal interaction unassigned |
4 0 |
1.3.8.1 | acetyl-coa c-acyltransferase deficiency |
10626578 |
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 |
16598811 |
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 |
26045367 |
Reveal genes functionally associated with ACADS by a network study. |
causal interaction unassigned |
1 0 |
1.3.8.1 | Acidosis, Lactic |
10626578 |
Newborn screening with tandem mass spectrometry: 12 months' experience in NSW Australia. |
causal interaction unassigned |
3 0 |
1.3.8.1 | Acidosis, Lactic |
32143453 |
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 |
2326316 |
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 |
10490047 |
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 |
12013984 |
[Short chain acyl-CoA dehydrogenase deficiency] |
causal interaction unassigned |
4 0 |
1.3.8.1 | acyl-coa dehydrogenase deficiency |
14568186 |
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 |