UMLS:C0011881 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0011881 (diabetic nephropathy)
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Human Gene/Protein
3-hydroxymethyl-3-methylglutaryl-Coenzyme A lyase	11.5
OR2L8	11.5
PP13439	11.5
FLJ00279	11.5
ANKRD56	11.5
SET domain-containing protein 6	11.5
CTNNBIP1 protein	11.5
Eukaryotic translation initiation factor 4A, isoform 2	11.5
carnosinase 1	10.9
bone morphogenic protein type II receptor	10.5
LGP1	10.5
OR2AK2	10.5
MIOX protein	10.5
SFRS15	10.5
Engulfment and cell motility protein 1	10.5
CNDP1	10.4
ZNF236	10.2
UbA52	10.2
FRMD3	10.1
engulfment and cell motility 1	10.0

Disease
Adult Fanconi syndrome	11.5
Chronic proliferative glomerulonephritis	11.5
nephropathy; hereditary	11.5
Hypercholesterolemia aggravated	11.5
Nodular diabetic glomerulosclerosis	11.5
diabetic nephropathy	11.5
Renal failure and impairment	11.5
Clinical diabetic nephropathy	10.9
Incipient diabetic nephropathy	10.9
Nodular glomerulosclerosis	10.4
GFND	9.9
Acute on chronic renal failure	9.9
Residual proteinuria	9.9
microalbuminuria	9.6
Microproteinuria	9.5
kidney hypertrophy	9.4
Segmental glomerulosclerosis	9.2
Hepatic calcification	9.2
von Willebrand disease type 2A	8.9
von Willebrand disease type 2A	8.9

Enzyme
serum carnosinase	9.1
carnosinase	8.7
meprin B	7.6
HK2	7.4
myo-inositol oxygenase	7.2
EC 2.4.2.26	7.1
5,10-methenyltetrahydrofolate synthetase	7.0
NSY	6.7
calpain 10	6.5
aldose reductase	6.4
carnosine synthetase	6.3
pantetheinase	6.3
ACE	6.3
aspartyl aminopeptidase	6.2
renin	6.0
dimethylarginine dimethylaminohydrolase	5.8
beta-D-fucosidase	5.5
FPS	5.4
3-hydroxy-3-methylglutaryl-CoA lyase	5.2
thrombin-activatable fibrinolysis inhibitor	5.1