EC:1.3.1.8 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:1.3.1.8 (acyl-CoA dehydrogenase)
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Human Gene/Protein
mitochondrial trans-2-enoyl-CoA reductase	15.3
acyl-CoA dehydrogenase	15.3
FAM78A protein	15.3
ACAD9 protein	14.9
acyl-CoA dehydrogenase 9	14.8
SBCAD	14.7
ACAD11	14.6
SACM1L	14.3
NADH dehydrogenase flavoprotein 1	14.3
Rrh	14.3
CDK5 regulatory subunit-associated protein 1	14.3
hSCAD	14.2
ETFDH	13.9
ETFB	13.9
ACADSB	13.9
acyl-CoA synthetase family member 2	13.7
isobutyryl-CoA dehydrogenase	13.7
ACSM4	13.7
long chain acyl-CoA dehydrogenase	13.7
FLAD1	13.6
Isovaleryl-CoA dehydrogenase	13.6
ETFA	13.5
ACAD9	13.4
very-long-chain acyl-CoA dehydrogenase	13.4
OXSM	13.3
electron transfer flavoprotein ubiquinone oxidoreductase	13.3
ACAD10	13.2
isovaleryl-CoA dehydrogenase	13.1
electron transfer flavoprotein-ubiquinone oxidoreductase	13.1
M/SCHAD	13.1
short-chain acyl-CoA dehydrogenase	13.1
ETF-QO	13.1
ubiquinol-cytochrome c reductase binding protein	13.0
DECR	12.8
ACAD8	12.8
GPR172B	12.5
SCAD	12.4
long-chain acyl-CoA dehydrogenase	12.4
MCAD	12.3
NDUFB5	12.3

Disease
Disorders of mitochondrial metabolism	13.3
MCAD deficiency	12.8
Jordan's anomaly	12.1
Fatty acid oxidation defects	12.0
glutaric aciduria	11.0
HMG-CoA lyase deficiency	11.0
Fazio-Londe	10.8
Reye	10.2
Conduction disorders	9.5
riboflavin deficiency	9.4
Complex I deficiency	9.4
pediatric disorder	9.1
Reye's syndrome	8.7
Acute fatty liver of pregnancy	8.7
lipidosis	8.6
GA I	8.3
hyperglycinemia	8.2
propionic acidemia	8.1
McArdle's disease	8.1
PKS	7.8
Forbes	7.8
LWS	7.7
paramyotonia	7.7
thalassemia minor	7.5
IVA	7.4
maple syrup urine disease	7.4
protein deficiency	7.3
hypoglycemic coma	7.2
enzyme deficiency	7.2
EMA	7.2
ornithine transcarbamylase deficiency	7.1
Canavan	7.1
homocystinuria	7.0
myopathy	6.9
metabolic disorder	6.8
LQT1	6.8
attention deficit disorder	6.6
RP11	6.6
AMD	6.5
ASAT	6.5

Symptom
Positive and Negative Symptoms	8.7
Spots	6.5
hypotonia	6.3
hepatomegaly	5.6
muscle cramps	5.5
hypertonia	5.0
myalgia	4.9
lethargy	4.8
weakness	4.7
stridor	4.1
starvation	4.0
vomiting	3.7
dysarthria	3.4
hyperoxia	3.0
exhaustion	2.6
seizures	2.5
ataxia	2.4
regurgitation	2.3
nausea and vomiting	2.1
sleepiness	1.7
fatigue	1.6
dyspnea	1.5
hypothermia	1.2
respiratory distress	1.0
angina	0.9
nausea	0.8
collapse	0.5
diarrhea	-0.5
pain	-2.7

Enzyme
acyl-CoA dehydrogenase	15.3
acyl-CoA dehydrogenase	14.4
EC 1.3.1.44	14.3
electron transfer flavoprotein dehydrogenase	13.6
branched-chain acyl-CoA dehydrogenase	13.2
isovaleryl-CoA dehydrogenase	13.1
anthranilate hydroxylase	13.0
anthranilate hydroxylase	13.0
melilotate hydroxylase	12.7
trans-2-enoyl-CoA reductase	12.7
butyryl-CoA dehydrogenase	12.5
anthranilate hydroxylase	12.2
4-N-trimethylaminobutyraldehyde dehydrogenase	12.1
2,4-dienoyl-CoA reductase	12.1
isobutyryl-CoA mutase	12.0
desulfinase	11.8
geranoyl-CoA carboxylase	11.7
glutaconyl-CoA decarboxylase	11.3
acyl-CoA elongase	11.2
glutaryl-CoA dehydrogenase	11.1
3-hydroxyacyl-CoA dehydrogenase	11.1
EC 3.1.2.14	11.1
EC 5.3.3.8	11.1
dimethylglycine dehydrogenase	11.0
3-hydroxyacyl-CoA dehydrogenase	10.9
long-chain acyl-coenzyme A dehydrogenase	10.9
acyl-CoA oxidase	10.8
ECH	10.7
3-hydroxybutyryl-CoA dehydrogenase	10.6
3-hydroxyacyl-CoA epimerase	10.5
NAO	10.4
glycine N-acyltransferase	10.3
3-hydroxy-3-methylglutaryl-CoA lyase	10.0
KAT	10.0
acyl-CoA synthetase	9.9
ornithine cyclodeaminase	9.9
ribulose 5-phosphate 3-epimerase	9.8
p-hydroxybenzoate hydroxylase	9.6
acyl-CoA synthetase	9.6
p-hydroxybenzoate hydroxylase	9.5