UMLS:C0020500 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0020500 (hyperoxaluria)
912 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

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

Human Gene/Protein
Sep	51
gut	37
lactate dehydrogenase	21
osteopontin	20
chronic renal failure	19
alkaline phosphatase	18
alanine-glyoxylate aminotransferase	18
PH1	17
proximal tubule	16
SLC26A6	16
Mol	15
catalase	14
parathyroid hormone	14
superoxide dismutase	13
AGXT	12
alanine:glyoxylate aminotransferase	10
hydroxypyruvate reductase	10
collagen	9
insulin	8
GSH	8

Disease
hyperoxaluria	912
urolithiasis	199
hypercalciuria	184
nephrolithiasis	144
primary hyperoxaluria	131
nephrocalcinosis	92
renal failure	84
renal disease	79
malabsorption	51
oxalosis	48
obesity	35
steatorrhea	33
cystinuria	33
chronic renal failure	30
renal tubular acidosis	27
urinary tract infection	25
Crohn's disease	22
primary hyperparathyroidism	19
proteinuria	18
acute renal failure	15

Enzyme
AGT	23
lactate dehydrogenase	22
catalase	18
alkaline phosphatase	18
superoxide dismutase	16
NADPH oxidase	10
NADPH oxidase	8
urease	7
glyoxylate reductase	7
glycolate oxidase	7
glyoxylate reductase	7
urease	7
hydroxypyruvate reductase	6
oxalate decarboxylase	6
hydroxypyruvate reductase	6
glutathione peroxidase	5
xanthine oxidase	5
oxalyl-CoA decarboxylase	4
peroxidase	4
gamma-glutamyl transpeptidase	4