UMLS:C0024523 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0024523 (malabsorption)
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Human Gene/Protein
microsomal triglyceride transfer protein large subunit	11.1
ADP-ribosylation factor-like 1	11.1
ADP-ribosylation factor related protein 1	10.5
MGA1	10.4
CUBN	9.5
sodium/bile acid cotransporter	9.5
ECRP	9.5
CEL protein	9.5
intrinsic factor-cobalamin receptor	9.5
SAR1B	9.2
NHLRC2	9.1
TREH	9.1
proton-coupled folate transporter	8.9
THSD1	8.9
intrinsic factor	8.9
Formiminotransferase-cyclodeaminase	8.8
EIF6	8.8
alpha heavy chain	8.7
lactase	8.6
pregastric lipase	8.6
cblD	8.4
HSD3B7	8.4
cubilin	8.4
HCP1	8.3
ARFRP1	8.3
organic solute transporter alpha	8.3
cblF	8.3
CD320	8.2
Cubilin	8.2
DNAJC21	8.2
thiamine transporter 1	8.2
dNT-2	8.1
PFIC	8.0
OSTbeta	8.0
seven in absentia homolog 1	7.9
ileal bile acid transporter	7.9
MYO5B	7.8
MTTP	7.8
FTCD	7.8
NOS1 protein	7.8

Disease
Dihydrofolate reductase deficiency	12.1
Drug-induced diabetes mellitus	12.1
Campylobacter gastritis	12.1
Colonic dysfunction	12.1
Juvenile dermatitis herpetiformis	12.1
Gastrointestinal inflammatory conditions	12.1
glucoglycinuria	12.1
malabsorption	12.1
malnutrition; mild	12.1
Hypogammaglobulinemic sprue	12.1
Osmotic diarrhea	11.6
Other obesity	11.5
Crohn's jejunitis	11.5
Brown bowel syndrome	11.4
Collagenous sprue	11.2
Imerslund	11.1
Diarrhea predominant irritable bowel syndrome	11.1
Diverticulosis of the jejunum	11.1
Late neonatal hypocalcemia	11.1
Intestinal ulceration	11.1
Mixed proteinuria	11.1
Bronchiectasis, recurrent	11.1
familial hypolipoproteinemia	11.1
tropical sprue	10.9
Enteric hyperoxaluria	10.6
R-binder deficiency	10.5
Childhood celiac disease	10.5
Diabetic diarrhea	10.5
hypercalcaemia due to parathyroid adenoma	10.5
hereditary neoplastic syndrome	10.5
Lymphosarcoma cell leukemia	10.5
Chronic peptic ulcer	10.5
Looser-Milkman	10.5
chylomicron retention disease	10.5
steatorrhea	10.3
Phrynoderma	10.3
Hepatic osteodystrophy	10.3
Secondary lactose intolerance	10.3
Gastrointestinal amyloidosis	10.3
Immunoproliferative small intestinal disease	10.2

Symptom
Neck discomfort	11.1
Gastrointestinal signs and symptoms	9.3
Gastrointestinal discomfort	8.5
Food intolerance	8.5
jaundice of the skin	8.1
Watery diarrhea	8.0
change in stool	7.8
bloating	7.6
ischuria	7.4
Lung hyperinflation	7.3
abnormal taste	7.2
Gastrointestinal symptoms	7.1
Wind	6.9
localized abdominal pain	6.9
diarrhea	6.9
hypoproteinemia	6.7
carpopedal spasm	6.6
koilonychia	6.4
belching	6.4
Beau's lines	6.4
infant diarrhea	6.3
decreased appetite	6.3
Severe diarrhea	6.3
clubbing	6.3
Chronic abdominal pain	6.3
hyperemesis	6.2
abdominal discomfort	6.0
abdominal cramps	6.0
Bitot's spots	6.0
intestinal angina	6.0
inanition	5.9
Neurologic symptoms	5.6
cachexia	5.5
intestinal bleeding	5.4
abdominal pain	5.4
autodigestion	5.4
emaciation	5.4
pedal edema	5.3
Joint hypermobility	5.1
anorexia	5.0

Enzyme
lactase	8.6
lactase-phlorizin hydrolase	7.1
ketohexokinase	7.0
triokinase	7.0
sucrase-isomaltase	6.8
lactase-phlorizin hydrolase	6.7
sucrase	6.6
conjugase	6.3
transglutaminase	6.2
trehalase	5.9
glyoxylate reductase	5.8
glyoxylate reductase	5.8
CYP8B1	5.6
alpha-glucosidase	5.5
3-oxoacid CoA-transferase	5.5
monoacylglycerol acyltransferase	5.4
methylenetetrahydrofolate dehydrogenase	5.3
DAP II	5.3
invertase	5.2
carnosinase	5.1
pantothenate kinase	5.1
enterokinase	5.0
formyltetrahydrofolate synthetase	4.9
methylenetetrahydrofolate dehydrogenase	4.9
lipase	4.8
hydroxypyruvate reductase	4.6
3alpha-hydroxysteroid dehydrogenase	4.6
hydroxypyruvate reductase	4.5
methionine synthase reductase	4.4
dihydropteridine reductase	4.4
methionine synthase	4.4
acetylesterase	4.4
cyclohydrolase	4.3
methionine synthase	4.3
PPH	4.2
CYP7A1	4.1
bile salt hydrolase	4.1
CPL	4.1
methylenetetrahydrofolate reductase	3.8
methylenetetrahydrofolate reductase	3.8