UMLS:C0162316 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0162316 (iron deficiency anemia)
3,806 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
ankyrin repeat domain 37	12.4
TMPRSS6	11.7
transmembrane protease, serine 6	11.4
matriptase-2	11.3
hemochromatosis type 2	11.0
DCYTB	10.4
G1 to S phase transition 1	10.4
COPZ1	9.9
DDX42	9.9
NAP5	9.2
CACNA2D3	9.1
hemojuvelin	9.1
Hepcidin	8.9
ARHGEF3	8.8
TfR	8.7
AD 1	8.6
transferrin receptor 2	8.6
ferritin	8.5
IDA	8.4
hereditary hemochromatosis	8.2
ferroportin 1	8.1
Ferritin	8.1
GST-1	7.9
MSPL	7.9
FPN1	7.9
HFE2	7.8
DMT1	7.8
hephaestin	7.8
SLC39A14	7.7
divalent metal transporter 1	7.7
APR-1	7.6
SLC11A2	7.6
transferrin receptor	7.6
pyrimidine 5'-nucleotidase	7.6
SLC39A4	7.4
DCT1	7.4
BMP6	7.4
tissue factor pathway inhibitor-2	7.3
mitochondrial ferritin	7.3
HAMP	7.3

Disease
perverted appetite	13.0
vagabond's disease	13.0
iron deficiency anemia	13.0
Chronic iron deficiency anemia	13.0
Bantu siderosis	12.0
Angioectasia	12.0
Thrombosed haemorrhoids	12.0
Secondary autoimmune haemolytic anaemia	12.0
Iron deficiency without anemia	11.9
Plummer-Vinson syndrome	11.6
vitamin B12 deficiency anemia	11.2
folate deficiency anemia	11.1
Nutritional anemia	11.0
Alkaline reflux esophagitis	11.0
Gastrointestinal vascular malformations	11.0
Idiopathic pulmonary hemosiderosis	10.9
Hemorrhoidal bleeding	10.7
anemia of chronic disease	10.6
Gastric antral vascular ectasia	10.6
esophageal web	10.5
iron deficiency	10.3
anaemia in pregnancy	10.0
Microcytic hypochromic anemia	10.0
Secondary hemochromatosis	10.0
Adult celiac disease	10.0
disorders of iron metabolism	10.0
thalassemia trait	9.9
microcytic anemia	9.8
Secondary anemia	9.6
Uremic syndrome	9.6
Gastrointestinal angiodysplasia	9.6
Sports anemia	9.6
Red cell aplasia	9.6
hypochromic anemia	9.5
thalassemia minor	9.4
Anemia during pregnancy	9.3
nutritional disorder	9.2
Geophagia	9.1
Portal hypertensive gastropathy	9.1
duodenal polyp	9.0

Enzyme
EC 3.1.2.3	11.4
inulin fructotransferase	8.6
inulin fructotransferase	8.3
matriptase	6.8
matriptase	6.4
pyridoxal kinase	6.3
DMT	5.7
transglutaminase	5.2
3-mercaptopyruvate sulfurtransferase	5.1
iodothyronine 5'-deiodinase	4.9
ferrochelatase	4.8
acetoacetyl-CoA thiolase	4.7
inulinase	4.7
enterokinase	4.6
thyroid peroxidase	4.6
inulinase	4.6
guanylate kinase	4.5
ceruloplasmin	4.4
succinyl-CoA synthetase	4.3
SCP	4.2
HMG-CoA synthase	4.1
paraoxonase	3.9
AOR	3.8
phytase	3.7
phytase	3.7
3-hydroxyacyl-CoA dehydrogenase	3.6
paraoxonase	3.6
GAS	3.1
SCS	3.0
ALA synthase	3.0
heme oxygenase	3.0
3-hydroxy-3-methylglutaryl-CoA reductase	2.9
21-hydroxylase	2.8
glutathione peroxidase	2.8
alpha-ketoglutarate dehydrogenase	2.7
PGM	2.6
urease	2.5
glucocerebrosidase	2.5
3-hydroxy-3-methylglutaryl coenzyme A reductase	2.5
thromboplastin	2.5