UMLS:C0020473 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0020473 (hyperlipidemia)
15,891 document(s) hit in 31,850,051 MEDLINE articles (0.01 seconds)

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Concepts found in the documents ranked by [ Frequency | Pointwise Mutual Information | Symmetric Conditional Probability ] .

Human Gene/Protein
HDL	0.004
lipoprotein lipase	0.002
insulin	0.002
apolipoprotein B	0.001
LDL receptor	0.001
HMG-CoA reductase	0.001
apolipoprotein	0.001
hepatic lipase	0.001
apoE	0.001
Lp(a)	0.000
apoB-100	0.000
apolipoprotein E	0.000
HDL2	0.000
peroxisome proliferator-activated receptor	0.000
CYP7A1	0.000
proprotein convertase subtilisin/kexin type 9	0.000
cholesteryl ester transfer protein	0.000
low-density lipoprotein receptor	0.000
adiponectin	0.000
SREBP-1c	0.000
LDLR	0.000
SREBP-2	0.000
leptin	0.000
microsomal triglyceride transfer protein	0.000
fatty acid synthase	0.000
reductase	0.000
LPL	0.000
HLP	0.000
A-I	0.000
Upstream transcription factor 1	0.000
PPAR	0.000
low density lipoprotein receptor	0.000
peroxisome proliferator-activated receptor alpha	0.000
C-reactive protein	0.000
FLJ20584	0.000
ATP synthase mitochondrial F1 complex assembly factor 1	0.000
acetyl-Coenzyme A acetyltransferase 2	0.000
LSR protein	0.000
A-II	0.000
calcineurin inhibitor	0.000

Disease
hyperlipidemia	1.000
hypertension	0.007
hypercholesterolemia	0.006
atherosclerosis	0.005
diabetes	0.005
obesity	0.004
hyperglycemia	0.003
dyslipidemia	0.002
cardiovascular disease	0.002
metabolic syndrome	0.002
Familial combined hyperlipidemia	0.002
coronary heart disease	0.002
hyperlipoproteinemia	0.001
fatty liver	0.001
coronary artery disease	0.001
type 2 diabetes	0.001
familial hypertriglyceridemia	0.001
hyperinsulinemia	0.001
glucose intolerance	0.001
nephrotic syndrome	0.001
lipid disorder	0.001
Combined hyperlipidemia	0.001
xanthoma	0.001
familial hyperlipidemia	0.001
lipodystrophy	0.001
hyperuricemia	0.001
proteinuria	0.000
renal disease	0.000
Type III hyperlipoproteinemia	0.000
Secondary hyperlipidemia	0.000
arteriosclerosis	0.000
myocardial infarction	0.000
hyperchylomicronemia	0.000
Lipemia retinalis	0.000
Zieve's syndrome	0.000
Nonalcoholic fatty liver	0.000
vascular disease	0.000
xanthomatosis	0.000
atherosclerotic cardiovascular disease	0.000
stroke	0.000

Symptom
overweight	0.000
angina	0.000
hepatomegaly	0.000
hypoproteinemia	0.000
Homan's sign	0.000
cardiovascular disability	0.000
chest pain	0.000
Cushingoid	0.000
hepatosplenomegaly	0.000
jaundice of the skin	0.000
Cushingoid	0.000
abdominal pain	0.000
chyluria	0.000
Upper abdominal pain	0.000
ketonuria	0.000
unable to sleep	0.000
myalgia	0.000
weakness	0.000
constipation	0.000
Sudden deafness	0.000
fatigue	0.000
exertional chest pain	0.000
vertigo	0.000
musculoskeletal impairment	0.000
pain	0.000
headache	0.000
polyuria	0.000
Acute chest pain	0.000
Amaurosis fugax	0.000
polydipsia	0.000
vomiting	0.000
nausea	0.000
diarrhea	0.000
facial droop	0.000
flushing	0.000
dysarthria	0.000
cachexia	0.000
emaciation	0.000
intestinal angina	0.000
corpulence	0.000

Enzyme
lipoprotein lipase	0.002
CYP7A1	0.000
3-hydroxy-3-methylglutaryl coenzyme A reductase	0.000
lipase	0.000
cholesterol acyltransferase	0.000
alanine aminotransferase	0.000
LPL	0.000
AMP-activated protein kinase	0.000
aspartate aminotransferase	0.000
acetyl-CoA carboxylase	0.000
superoxide dismutase	0.000
3-hydroxy-3-methylglutaryl-CoA reductase	0.000
lecithin:cholesterol acyltransferase	0.000
glucose-6-phosphatase	0.000
AST	0.000
AMPK	0.000
proprotein convertase	0.000
ACE	0.000
creatine kinase	0.000
AMPK	0.000
glutathione peroxidase	0.000
ACAT	0.000
calcineurin	0.000
hormone-sensitive lipase	0.000
catalase	0.000
carnitine O-octanoyltransferase	0.000
acyl-CoA oxidase	0.000
CPT	0.000
CYP27A1	0.000
citryl-CoA lyase	0.000
diacylglycerol acyltransferase	0.000
renin	0.000
tissue plasminogen activator	0.000
CAD	0.000
CAD	0.000
paraoxonase	0.000
CAD	0.000
cholesterol esterase	0.000
gamma-glutamyl transpeptidase	0.000
creatinine iminohydrolase	0.000