UMLS:C0024523 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts: Target Concepts:

Query: UMLS:C0024523 (malabsorption)
7,319 document(s) hit in 31,850,051 MEDLINE articles (0.01 seconds)

.

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

Human Gene/Protein
lactase	0.002
intrinsic factor	0.002
B12	0.002
proton-coupled folate transporter	0.001
tissue transglutaminase	0.000
MGA1	0.000
CUBN	0.000
gut	0.000
cubilin	0.000
microsomal triglyceride transfer protein large subunit	0.000
transcobalamin II	0.000
alpha heavy chain	0.000
brush border	0.000
SAR1B	0.000
B-12	0.000
ADP-ribosylation factor-like 1	0.000
DQ2	0.000
SGLT1	0.000
ADP-ribosylation factor related protein 1	0.000
reduced folate carrier	0.000
lipase	0.000
intrinsic factor-cobalamin receptor	0.000
pancreatic lipase	0.000
sucrase-isomaltase	0.000
IGS	0.000
IgA	0.000
CEL protein	0.000
sodium/bile acid cotransporter	0.000
ECRP	0.000
ASBT	0.000
Cubilin	0.000
TREH	0.000
NHLRC2	0.000
ileal bile acid transporter	0.000
cblF	0.000
THSD1	0.000
microsomal triglyceride transfer protein	0.000
cblD	0.000
EIF6	0.000
Formiminotransferase-cyclodeaminase	0.000

Disease
malabsorption	1.000
steatorrhea	0.014
celiac disease	0.008
lactose intolerance	0.005
pancreatic insufficiency	0.005
tropical sprue	0.004
short bowel syndrome	0.003
enteropathy	0.003
sprue	0.003
Imerslund	0.002
malnutrition	0.002
megaloblastic anemia	0.002
giardiasis	0.001
pernicious anemia	0.001
vitamin B12 deficiency	0.001
vitamin E deficiency	0.001
Whipple's disease	0.001
chylomicron retention disease	0.001
Collagenous sprue	0.001
osteomalacia	0.001
Immunoproliferative small intestinal disease	0.001
Brown bowel syndrome	0.001
folate deficiency	0.001
cystic fibrosis	0.001
protein-losing enteropathy	0.001
disaccharidase deficiency	0.001
Crohn's disease	0.001
hypovitaminosis	0.001
Osmotic diarrhea	0.001
acrodermatitis enteropathica	0.001
functional diarrhea	0.001
vitamin K deficiency	0.000
failure to thrive	0.000
vitamin D deficiency	0.000
chronic pancreatitis	0.000
hypobetalipoproteinemia	0.000
hyperoxaluria	0.000
irritable bowel syndrome	0.000
blind loop syndrome	0.000
Enteric hyperoxaluria	0.000

Symptom
diarrhea	0.006
bloating	0.000
abdominal pain	0.000
Wind	0.000
Neck discomfort	0.000
anorexia	0.000
vomiting	0.000
hypoproteinemia	0.000
Gastrointestinal symptoms	0.000
cachexia	0.000
Gastrointestinal signs and symptoms	0.000
constipation	0.000
abdominal discomfort	0.000
decreased appetite	0.000
Food intolerance	0.000
clubbing	0.000
nausea	0.000
Gastrointestinal discomfort	0.000
ataxia	0.000
Watery diarrhea	0.000
change in stool	0.000
jaundice of the skin	0.000
belching	0.000
weakness	0.000
abdominal cramps	0.000
ischuria	0.000
Lung hyperinflation	0.000
bone pain	0.000
lethargy	0.000
abnormal taste	0.000
hyperemesis	0.000
emaciation	0.000
hepatomegaly	0.000
localized abdominal pain	0.000
intestinal bleeding	0.000
carpopedal spasm	0.000
infant diarrhea	0.000
colic	0.000
pain	0.000
koilonychia	0.000

Enzyme
lactase	0.002
transglutaminase	0.000
sucrase	0.000
lipase	0.000
sucrase-isomaltase	0.000
alpha-glucosidase	0.000
invertase	0.000
lactase-phlorizin hydrolase	0.000
trehalase	0.000
lactase-phlorizin hydrolase	0.000
ketohexokinase	0.000
alkaline phosphatase	0.000
conjugase	0.000
triokinase	0.000
trypsin	0.000
ceruloplasmin	0.000
enterokinase	0.000
chymotrypsin	0.000
glyoxylate reductase	0.000
glyoxylate reductase	0.000
elastase	0.000
CYP8B1	0.000
3-oxoacid CoA-transferase	0.000
monoacylglycerol acyltransferase	0.000
methylenetetrahydrofolate dehydrogenase	0.000
pantothenate kinase	0.000
DAP II	0.000
diamine oxidase	0.000
carnosinase	0.000
methylenetetrahydrofolate reductase	0.000
methionine synthase	0.000
methylenetetrahydrofolate reductase	0.000
formyltetrahydrofolate synthetase	0.000
methionine synthase	0.000
methylenetetrahydrofolate dehydrogenase	0.000
CYP7A1	0.000
hydroxypyruvate reductase	0.000
beta-galactosidase	0.000
dihydropteridine reductase	0.000
3alpha-hydroxysteroid dehydrogenase	0.000