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
PP13439	11.5
OR2L8	11.5
3-hydroxymethyl-3-methylglutaryl-Coenzyme A lyase	11.5
Eukaryotic translation initiation factor 4A, isoform 2	11.5
CTNNBIP1 protein	11.5
ANKRD56	11.5
SET domain-containing protein 6	11.5
FLJ00279	11.5
carnosinase 1	10.9
MIOX protein	10.5
OR2AK2	10.5
LGP1	10.5
Engulfment and cell motility protein 1	10.5
SFRS15	10.5
bone morphogenic protein type II receptor	10.5
CNDP1	10.4
UbA52	10.2
ZNF236	10.2
FRMD3	10.1
engulfment and cell motility 1	10.0
TMEM212	9.9
Endosulfine alpha	9.9
C6orf167	9.9
IHG-1	9.9
hemicentin 1	9.9
ALDR1	9.9
TCEAL6	9.9
MFAP3	9.9
forkhead box O4	9.7
GPR149	9.5
TGFR-3	9.5
Homeodomain interacting protein kinase 2	9.5
PLEKHH2	9.5
collagen, type IV, alpha 1	9.2
MAPK organizer 1	9.2
myosin, heavy chain 9, non-muscle	9.2
FAM101A	9.2
TTC39C	9.2
APOL3	9.2
Small ubiquitin-like modifier 4	9.2

Disease
Chronic proliferative glomerulonephritis	11.5
nephropathy; hereditary	11.5
Hypercholesterolemia aggravated	11.5
diabetic nephropathy	11.5
Nodular diabetic glomerulosclerosis	11.5
Adult Fanconi syndrome	11.5
Renal failure and impairment	11.5
Incipient diabetic nephropathy	10.9
Clinical diabetic nephropathy	10.9
Nodular glomerulosclerosis	10.4
Acute on chronic renal failure	9.9
Residual proteinuria	9.9
GFND	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
hypertensive nephropathy	8.8
Immune complex glomerulonephritis	8.6
nephrosclerosis	8.6
IDDM6	8.5
Diabetic cystopathy	8.5
Lipoatrophic diabetes	8.5
Armanni-Ebstein lesion	8.5
Penile necrosis	8.4
Nephroangiosclerosis	8.4
chronic glomerulonephritis	8.3
glomerulosclerosis	8.3
Diabetic complications	8.2
Mesangioproliferative glomerulonephritis	8.2
IDDM10	8.1
Proliferative retinopathy	8.0
Diabetic microangiopathy	8.0
Uremic pericarditis	7.9
congenital hyperbilirubinemia	7.8
renal disease	7.8
Henoch-Schoenlein nephritis	7.7

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
NADPH oxidase	5.1
AMP-activated kinase	5.0
NADPH oxidase	5.0
neurolysin	5.0
prolyl-tRNA synthetase	4.8
angiotensin-converting enzyme 2	4.8
ketohexokinase	4.8
alanine aminopeptidase	4.8
meprin	4.7
proteinase-3	4.7
eEF2 kinase	4.6
chymase	4.6
nucleotide pyrophosphatase	4.6
AGT	4.5
GTP cyclohydrolase I	4.5
GLO	4.4
tissue kallikrein	4.4
aminopeptidase A	4.4
hepsin	4.3
hepsin	4.3