UMLS:C0042875 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0042875 (vitamin E deficiency)
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Human Gene/Protein
ATLD	12.8
alpha-tocopherol transfer protein	12.7
IOSCA	12.1
ATTP	11.9
SANDO	11.8
POLG protein	11.5
Caytaxin	11.5
OSBP2	11.3
SACS	10.5
Type I iodothyronine deiodinase	10.3
SPTBN2	10.2
SRR	9.8
senataxin	9.8
TTP	9.8
DYT11	9.7
RRR	9.6
cellular retinaldehyde-binding protein	9.5
frataxin	9.5
DARS2	9.4
3-beta-hydroxysteroid dehydrogenase	9.2

Disease
vitamin E deficiency	15.1
Dietetic microangiopathy	15.1
Steatitis	14.1
Brown bowel syndrome	13.9
Nutritional muscular dystrophy	13.5
Exudative diathesis	13.5
Detergent sensitivity	13.1
ATLD	13.1
SCAE	13.1
Spastic ataxia	12.8
tocopherol deficiency	12.6
Early Onset Cerebellar Ataxia	12.5
DYT15	12.5
IOSCA	12.3
Pansteatitis	12.3
Pseudo-Bartter syndrome	12.3
VED	12.2
SANDO	11.8
Mitochondrial neurogastrointestinal encephalopathy	11.5
chylomicron retention disease	11.4

Enzyme
SRR	10.0
Delta6-desaturase	9.1
D-amino-acid oxidase	7.9
phospholipid hydroperoxide glutathione peroxidase	7.6
NAO	7.6
Lod	7.5
biotinidase	7.5
glutamic dehydrogenase	7.3
propionyl-CoA carboxylase	6.7
propionyl-CoA carboxylase	6.7
ficin	6.6
cathepsin H	6.6
beta-hydroxybutyrate dehydrogenase	6.5
methylmalonyl-CoA mutase	6.4
phospholipase A1	6.4
carnitine acetyltransferase	6.4
glutathione peroxidase	6.2
acyl-CoA oxidase	6.2
TGT	6.1
pyruvate kinase	6.1