UMLS:C0154251 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts: Target Concepts:

Query: UMLS:C0154251 (lipid disorder)
795 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

.

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

Human Gene/Protein
Cytochrome b5 reductase 3	15.3
Mitochondrial trans-2-enoyl-CoA reductase	14.3
copine 6	13.7
hydroxysteroid (17-beta) dehydrogenase 4	13.3
ATP binding cassette transporter 1	12.4
Acyl-CoA synthetase 4	12.3
SPACA3	12.1
BTNL3	11.8
PAHX	11.8
HSD3B7	11.6
mitochondrial 3-oxoacyl-CoA thiolase	11.4
MECR	11.4
LIM domain containing 2	11.4
SLC35C1	11.1
ACAA2	11.1
ATP-binding cassette transporter-1	11.0
HVCN1	11.0
ACAA1	11.0
CD69 molecule	10.8
BSP1	10.8

Disease
lipid disorder	15.3
Peripheral and visceral atherosclerosis	15.3
Disorders of mitochondrial metabolism	13.3
Tendon xanthoma	13.0
Familial combined hyperlipidemia	12.9
FHBL2	12.5
Jordan's anomaly	12.1
Combined hyperlipidemia	11.5
Hyperapobetalipoproteinemia	11.0
hypolipoproteinemia	11.0
arcus senilis	10.8
Type V hyperlipoproteinemia	10.6
Hepatobiliary disease	10.6
familial hypertriglyceridemia	10.4
Homozygous familial hypercholesterolemia	10.2
Familial defective apolipoprotein B-100	10.2
Heterozygous familial hypercholesterolemia	9.8
Familial hypercholesterolemia	9.8
anthracosilicosis	9.7
lipoprotein disorder	9.6

Enzyme
phosphoethanolamine N-methyltransferase	10.0
KAR	8.9
gluconate dehydrogenase	8.8
phospholipid methyltransferase	8.7
sterol carrier protein	8.4
glycogenin	8.1
fatty-acid synthase	8.0
proprotein convertase	8.0
CYP7A1	7.9
acrosin	7.9
fatty acid elongase	7.3
lipoprotein lipase	7.3
LPL	7.2
iodothyronine 5'-deiodinase	7.2
phospholipid hydroperoxide glutathione peroxidase	6.8
ACAT	6.8
PMT	6.6
lecithin:cholesterol acyltransferase	6.6
acetyl-CoA carboxylase	6.6
CPT	6.6