Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: EC:1.3.99.3 (acyl-CoA dehydrogenase)
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Concepts found in the documents ranked by [ Frequency | Pointwise Mutual Information | Symmetric Conditional Probability ] .
Human Gene/Protein
acyl-CoA dehydrogenase 0.528
medium-chain acyl-CoA dehydrogenase 0.247
long-chain acyl-CoA dehydrogenase 0.134
short-chain acyl-CoA dehydrogenase 0.016
MCAD 0.010
very-long-chain acyl-CoA dehydrogenase 0.009
long chain acyl-CoA dehydrogenase 0.006
ETFDH 0.006
isovaleryl-CoA dehydrogenase 0.005
ACADM 0.004
VLCAD 0.004
3-hydroxyacyl-CoA dehydrogenase 0.004
LCAD 0.004
enoyl-CoA hydratase 0.004
flavoprotein 0.003
isobutyryl-CoA dehydrogenase 0.003
hSCAD 0.003
ETFB 0.003
electron transfer flavoprotein-ubiquinone oxidoreductase 0.003
acyl-CoA dehydrogenase 9 0.003
SCAD 0.003
acyl-CoA oxidase 0.002
Medium-chain acyl-CoA dehydrogenase 0.002
ACAD9 0.002
ETFA 0.002
ACADSB 0.002
ACAD9 protein 0.002
ETF 0.002
3-ketoacyl-CoA thiolase 0.002
ACAD11 0.002
carnitine palmitoyltransferase 0.002
ACADVL 0.001
FLAD1 0.001
FAD 0.001
SBCAD 0.001
Isovaleryl-CoA dehydrogenase 0.001
FAM78A protein 0.001
mitochondrial trans-2-enoyl-CoA reductase 0.001
glutaryl-CoA dehydrogenase 0.001
ETF-QO 0.001
CPT II 0.001
ACAD10 0.001
beta-ETF 0.001
citrate synthase 0.001
acyl-CoA synthetase 0.001
SACM1L 0.001
Rrh 0.001
NADH dehydrogenase flavoprotein 1 0.001
CDK5 regulatory subunit-associated protein 1 0.001
2,4-dienoyl-CoA reductase 0.001
M/SCHAD 0.001
acyl-CoA synthetase family member 2 0.001
ACSM4 0.001
ACAD8 0.000
ATP synthase gamma chain 0.000
electron transfer flavoprotein ubiquinone oxidoreductase 0.000
OXSM 0.000
carnitine palmitoyltransferase I 0.000
ubiquinol-cytochrome c reductase binding protein 0.000
dienoyl-CoA isomerase 0.000
DC12 0.000
mitochondrial 3-oxoacyl-CoA thiolase 0.000
estrogen-related receptor alpha 0.000
3-hydroxy-3-methylglutaryl-CoA lyase 0.000
L-3-hydroxyacyl-CoA dehydrogenase 0.000
GPR172B 0.000
MOGAT2 0.000
CABC1 0.000
NDUFB5 0.000
CPT2 0.000
crotonase 0.000
very long-chain acyl-CoA synthetase 0.000
COQ6 0.000
apolipoprotein A-I binding protein 0.000
acyl-CoA synthetase long-chain family member 3 0.000
Cytosolic malate dehydrogenase 0.000
long chain 0.000
carnitine palmitoyltransferase 1A 0.000
PDSS2 0.000
elongation of very long chain fatty acids protein 0.000
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Disease
MCAD deficiency 0.038
glutaric aciduria 0.002
Reye 0.001
Reye's syndrome 0.001
Fatty acid oxidation defects 0.001
Disorders of mitochondrial metabolism 0.000
hypoglycemia 0.000
propionic acidemia 0.000
glycinuria 0.000
methylmalonic acidemia 0.000
phenylketonuria 0.000
HMG-CoA lyase deficiency 0.000
Jordan's anomaly 0.000
Organic acidemias 0.000
riboflavin deficiency 0.000
maple syrup urine disease 0.000
Acute fatty liver 0.000
myopathy 0.000
MILS 0.000
homocystinuria 0.000
IVA 0.000
cardiomyopathy 0.000
Fazio-Londe 0.000
MCC deficiency 0.000
sudden infant death syndrome 0.000
Fasting hypoglycemia 0.000
metabolic disorder 0.000
pediatric disorder 0.000
tyrosinosis 0.000
Reactive hypoglycemia 0.000
CPS deficiency 0.000
lipidosis 0.000
ornithine transcarbamylase deficiency 0.000
fatty liver 0.000
Zellweger syndrome 0.000
enzyme deficiency 0.000
GA I 0.000
Conduction disorders 0.000
Complex I deficiency 0.000
protein deficiency 0.000
galactosemia 0.000
congenital hypothyroidism 0.000
Neonatal diabetes mellitus 0.000
Carnitine deficiency 0.000
citrullinemia 0.000
EMA 0.000
glycogen storage disease 0.000
Inborn errors of metabolism 0.000
Forbes 0.000
encephalopathy 0.000
McArdle's disease 0.000
hyperphenylalaninemia 0.000
Acute fatty liver of pregnancy 0.000
GSD I 0.000
hypoglycemic coma 0.000
orotic aciduria 0.000
congenital adrenal hyperplasia 0.000
hyperglycinemia 0.000
tyrosinemia 0.000
Central diabetes insipidus 0.000
SHS 0.000
SHS 0.000
hyperargininemia 0.000
coma 0.000
developmental delay 0.000
LWS 0.000
paramyotonia 0.000
mitochondrial disease 0.000
thalassemia minor 0.000
ketosis 0.000
AMD 0.000
Barth syndrome 0.000
lactic acidosis 0.000
MCD 0.000
PRS 0.000
alcoholic fatty liver 0.000
Canavan 0.000
Copper deficiency 0.000
cystic fibrosis 0.000
lipid disorder 0.000
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Symptom
hypotonia 0.000
hepatomegaly 0.000
weakness 0.000
Positive and Negative Symptoms 0.000
lethargy 0.000
inanition 0.000
ketonuria 0.000
myalgia 0.000
vomiting 0.000
starvation 0.000
Spots 0.000
seizures 0.000
muscle cramps 0.000
hypertonia 0.000
sleepiness 0.000
stridor 0.000
fatigue 0.000
hypothermia 0.000
exhaustion 0.000
cyanosis 0.000
dysarthria 0.000
hyperoxia 0.000
nausea 0.000
dyspnea 0.000
ataxia 0.000
regurgitation 0.000
nausea and vomiting 0.000
Ill 0.000
collapse 0.000
erythema 0.000
functional recovery 0.000
diarrhea 0.000
respiratory distress 0.000
angina 0.000
cough 0.000
overweight 0.000
pain 0.000
anesthesia 0.000
Drug
FAD 0.001
Riboflavin 0.000
Rifater 0.000
Rifater 0.000
Sodium phenylbutyrate 0.000
Coconut oil 0.000
Flavin 0.000
NADH 0.000
Lipidex 0.000
Liraglutide 0.000
Tween 60 0.000
Bezafibrate 0.000
Palmitoyl 0.000
EDR 0.000
Rosiglitazone 0.000
SMP 0.000
lysine 0.000
Bosentan 0.000
Bosentan 0.000
Glutamic acid 0.000
Dihydro 0.000
Clofibrate 0.000
citric acid 0.000
Gel 0.000
PFA 0.000
AraC 0.000
Doxycycline 0.000
RFP 0.000
Serum albumin 0.000
ALA 0.000
IL-1ra 0.000
Vitamin K 0.000
Glycyrrhiza 0.000
Tacrolimus 0.000
Fructose 0.000
ROS 0.000
ACT 0.000
Estrogens 0.000
Glutathione 0.000
pyridoxal phosphate 0.000
Retinoic acid 0.000
Kenyan 0.000
Glucagon 0.000
ABC 0.000
Ethanol 0.000
Asn 0.000
CAM 0.000
MAP 0.000
THF 0.000
DNase I 0.000
CTX 0.000
Leaf 0.000
CSF 0.000
Enzyme
acyl-CoA dehydrogenase 0.999
acyl-CoA dehydrogenase 0.508
isovaleryl-CoA dehydrogenase 0.005
electron transfer flavoprotein dehydrogenase 0.005
3-hydroxyacyl-CoA dehydrogenase 0.004
3-hydroxyacyl-CoA dehydrogenase 0.003
acyl-CoA oxidase 0.003
butyryl-CoA dehydrogenase 0.003
ECH 0.002
long-chain acyl-coenzyme A dehydrogenase 0.001
KAT 0.001
CPT 0.001
acyl-CoA synthetase 0.001
branched-chain acyl-CoA dehydrogenase 0.001
citrate synthase 0.001
acyl-CoA synthetase 0.001
anthranilate hydroxylase 0.001
anthranilate hydroxylase 0.001
2,4-dienoyl-CoA reductase 0.001
glutaryl-CoA dehydrogenase 0.001
holocarboxylase-synthetase 0.001
anthranilate hydroxylase 0.000
desulfinase 0.000
melilotate hydroxylase 0.000
EC 5.3.3.8 0.000
4-N-trimethylaminobutyraldehyde dehydrogenase 0.000
3-hydroxy-3-methylglutaryl-CoA lyase 0.000
geranoyl-CoA carboxylase 0.000
NAO 0.000
biotinidase 0.000
glutaconyl-CoA decarboxylase 0.000
FAD pyrophosphatase 0.000
dimethylglycine dehydrogenase 0.000
acyl-CoA elongase 0.000
EC 3.1.2.14 0.000
isobutyryl-CoA mutase 0.000
dephospho-CoA kinase 0.000
malonyl-CoA decarboxylase 0.000
3-hydroxybutyryl-CoA dehydrogenase 0.000
p-hydroxybenzoate hydroxylase 0.000
sarcosine dehydrogenase 0.000
acetyl-CoA carboxylase 0.000
trans-2-enoyl-CoA reductase 0.000
p-hydroxybenzoate hydroxylase 0.000
3-hydroxyacyl-CoA epimerase 0.000
rubredoxin reductase 0.000
glycine N-acyltransferase 0.000
acetoacetyl-CoA thiolase 0.000
acetylornithine aminotransferase 0.000
SsuE 0.000
CPT 0.000
ornithine cyclodeaminase 0.000
ribulose 5-phosphate 3-epimerase 0.000
CPT 0.000
pyruvate dehydrogenase 0.000
pyruvate dehydrogenase 0.000
pyruvate dehydrogenase 0.000
HMG-CoA synthase 0.000
hexokinase 0.000
complex I 0.000
carnitine acetyltransferase 0.000
LipB 0.000
malate synthase 0.000
phosphofructokinase 0.000
aromatic amino acid aminotransferase 0.000
lipoprotein lipase 0.000
heterodisulfide reductase 0.000
diacylglycerol acyltransferase 0.000
methylmalonyl-CoA mutase 0.000
succinate dehydrogenase 0.000
pantothenate kinase 0.000
acetyl-CoA synthetase 0.000
AlkA 0.000
glucose-6-phosphate dehydrogenase 0.000
pyruvate carboxylase 0.000
ATP synthase 0.000
membrane-bound hydrogenase 0.000
creatine kinase 0.000
riboflavin kinase 0.000
phosphoserine phosphatase 0.000
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Compound
octanoyl-CoA 0.019
CoA 0.006
butyryl-CoA 0.003
dec-4-enoic acid 0.002
FAD 0.001
palmitoyl-CoA 0.001
alpha-Methylbutyryl CoA 0.001
2-methylmalonamide 0.001
4-cis-Decenoyl-CoA 0.001
Crotonyl-CoA 0.001
3-methylcrotonyl-CoA 0.001
Octanoylcarnitine 0.001
undecylbenzene 0.000
acetoacetyl-CoA 0.000
L-carnitine 0.000
glutaryl-CoA 0.000
Ethylmalonic acid 0.000
C11H13NO3 0.000
Decanoyl-CoA 0.000
Lauroyl-CoA 0.000
Hypoglycin A 0.000
Carnitine 0.000
3-hydroxybutyryl-CoA 0.000
3-Hydroxyglutaric acid 0.000
MEZ 0.000
2-octynoic acid 0.000
Riboflavin 0.000
Acyl-CoA 0.000
tetradecanedioic acid 0.000
Palmitoyl-L-carnitine 0.000
5-hydroxyhexanoic acid 0.000
4-methylhexanoic acid 0.000
acetyl-CoA 0.000
K486 0.000
FMN 0.000
10-hydroxydecanoic acid 0.000
propionyl-coenzyme A 0.000
10-hydroxydecanoic acid 0.000
3-hydroxypropionyl-CoA 0.000
decanoic acid 0.000
2-methyl-2-butenoic acid 0.000
decanoic acid 0.000
3-hydroxyoctanoic acid 0.000
octanoic acid 0.000
Biguanide 0.000
Oleoyl-CoA 0.000
alpha-hydroxyisovaleric acid 0.000
octanoic acid 0.000
octanoic acid 0.000
octanoic acid 0.000
octanoic acid 0.000
4-pentenoic acid 0.000
dodecanedioic acid 0.000
CPT 0.000
1,2,4-butanetriol 0.000
Normetanephrine 0.000
CPT 0.000
hexanedioic acid 0.000
palmitic acid 0.000
ubiquinone 0.000
Hydroxyphenylacetate 0.000
3-buten-2-one 0.000
hexanedioic acid 0.000
3-buten-2-one 0.000
4-heptanone 0.000
glucose 0.000
Benazepril 0.000
palmitic acid 0.000
6-APA 0.000
docosanoic acid 0.000
3-heptanone 0.000
9,12-octadecadienoic acid 0.000
3-heptanone 0.000
2-ethylhexanoic acid 0.000
2-ethylhexanoic acid 0.000
MAD 0.000
malonyl-CoA 0.000
2-ethylhexanoic acid 0.000
HCI 0.000
myristic acid 0.000
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