UMLS:C0848332 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0848332 (Spots)
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Human Gene/Protein
beige-like protein	16.1
SNC73	14.5
N-acetylneuraminic acid phosphate synthase	14.1
SFRS4	13.8
tyrosinase related protein-2	13.5
histone H2A.1	13.5
Phosphomonoesterase	12.4
neurobeachin	12.2
eIF-2 gamma	12.0
ribosomal protein L17	11.9
UFC1	11.7
LOK	11.7
Cenexin	11.6
phosphotyrosyl phosphatase activator	11.2
ATP6V1A	11.1
ERp46	11.1
OBFC1	11.1
PDIA6	11.0
GNB1	11.0
14-3-3 epsilon	11.0

Disease
AIN III	12.8
Calcifying aponeurotic fibroma	11.0
rash	10.5
Fibrous dysplasia of bone	10.5
Microaneurysms	10.1
ASAP	9.9
ARTS	9.8
Blight	9.7
Fusarium infection	8.9
Fibrous dysplasia	8.6
Sutton	8.5
Recklinghausen	8.4
Netherton syndrome	8.2
PARK7	8.1
precocious puberty	8.0
GALT	7.7
leukoderma	7.7
freckles	7.7
cerebral thrombosis	7.5
multinodular goiter	7.5

Enzyme
tetrahydroxynaphthalene reductase	12.9
N5,N10-methenyltetrahydromethanopterin cyclohydrolase	12.4
formylmethanofuran dehydrogenase	11.0
beta-glycerophosphatase	10.3
FTR	10.3
phosphoenolpyruvate synthase	10.1
aspartylglucosaminidase	9.3
nicotinamide mononucleotide adenylyltransferase	9.1
PWD	9.1
exopolyphosphatase	8.7
arginine deiminase	8.7
phosphomannomutase	8.2
clostripain	8.1
bile salt hydrolase	8.1
xylitol dehydrogenase	8.0
granule-bound starch synthase	7.8
glycerol kinase	7.6
succinyl-CoA synthetase	7.4
arginine kinase	7.3
acetate kinase	7.2