UNIPROT:P02794 - FACTA Search

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

Query: UNIPROT:P02794 (ferritin)
17,525 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
ferritin	1.000
Ferritin	0.064
transferrin	0.026
transferrin receptor	0.011
ferroxidase	0.008
hemochromatosis	0.005
HFE	0.004
hemoglobin	0.004
Hepcidin	0.002
ferritin heavy chain	0.002
TfR	0.002
IRP1	0.002
hereditary hemochromatosis	0.002
IRP2	0.002
mitochondrial ferritin	0.002
erythropoietin	0.002
ferritin light chain	0.002
Transferrin	0.001
ferroportin 1	0.001
C-reactive protein	0.001
ferritin repressor protein	0.001
divalent metal transporter 1	0.001
iron regulatory protein 1	0.001
IRE	0.001
ceruloplasmin	0.001
nuclear receptor coactivator 4	0.001
Hemochromatosis	0.001
transferrin receptor 2	0.001
IRP	0.001
DMT1	0.001
SLC40A1	0.000
ferritin L-chain	0.000
FTH	0.000
FTH1	0.000
aconitase	0.000
FTL	0.000
ferroportin1	0.000
B12	0.000
hemojuvelin	0.000
ferritin light polypeptide	0.000

Disease
iron deficiency	0.029
iron overload	0.026
iron deficiency anemia	0.009
hemochromatosis	0.008
anemia	0.005
hereditary hemochromatosis	0.003
thalassemia	0.003
thalassemia major	0.002
anemia of chronic disease	0.002
hemophagocytic lymphohistiocytosis	0.001
siderosis	0.001
Still's disease	0.001
microcytic anemia	0.001
hemosiderosis	0.001
Adult-onset Still's disease	0.001
DMT1	0.000
disorders of iron metabolism	0.000
beta thalassemia	0.000
Macrophage activation syndrome	0.000
anaemia in pregnancy	0.000
hypochromic anemia	0.000
restless legs syndrome	0.000
Iron deficiency without anemia	0.000
Hepatic siderosis	0.000
HFE4	0.000
sideroblastic anemia	0.000
thalassemia trait	0.000
sickle cell disease	0.000
pancytopenia	0.000
HFE2	0.000
Hepatic hemosiderosis	0.000
Secondary hemosiderosis	0.000
myelodysplastic syndrome	0.000
folate deficiency	0.000
Cardiac siderosis	0.000
hemoglobinopathies	0.000
rash	0.000
porphyria cutanea tarda	0.000
cirrhosis	0.000
Autoimmune leukopenia	0.000

Symptom
hepatosplenomegaly	0.000
splenomegaly	0.000
arthralgia	0.000
fever of unknown origin	0.000
sore throat	0.000
hepatomegaly	0.000
Gastrointestinal distress	0.000
Paroxysmal hypertension	0.000
fatigue	0.000
starvation	0.000
toe pain	0.000
overweight	0.000
unable to sleep	0.000
Poor weight gain	0.000
Bitot's spots	0.000
nausea	0.000
pallor	0.000
myalgia	0.000
Postural tremor	0.000
male puberty	0.000
abdominal pain	0.000
cardiovascular impairment	0.000
respiratory distress	0.000
diarrhea	0.000
Reticulocytosis	0.000
pedal edema	0.000
hypoproteinemia	0.000
Flu-like symptoms	0.000
exhaustion	0.000
Gasping	0.000
cerebellar ataxia	0.000
generalized rash	0.000
brittle nails	0.000
Grimace	0.000
menometrorrhagia	0.000
dyspnea	0.000
night sweats	0.000
weakness	0.000
impaired motor coordination	0.000
bone pain	0.000

Enzyme
ceruloplasmin	0.003
aconitase	0.000
heme oxygenase	0.000
peroxidase	0.000
alanine aminotransferase	0.000
lactate dehydrogenase	0.000
aspartate aminotransferase	0.000
ALA synthase	0.000
superoxide dismutase	0.000
catalase	0.000
IDS3	0.000
neuraminidase	0.000
trimetaphosphatase	0.000
nicotianamine synthase	0.000
gamma-glutamyl transpeptidase	0.000
proprotein convertase 7	0.000
alkaline phosphatase	0.000
ribonucleotide reductase	0.000
ribonucleotide reductase	0.000
glutathione peroxidase	0.000
acid phosphatase	0.000
AST	0.000
ferrochelatase	0.000
biliverdin reductase	0.000
lysozyme	0.000
uroporphyrinogen decarboxylase	0.000
arginine kinase	0.000
xanthine oxidase	0.000
DMT	0.000
lactic acid dehydrogenase	0.000
enolase	0.000
CEAS	0.000
lactic acid dehydrogenase	0.000
chondroitinase	0.000
glutathione reductase	0.000
chondroitinase	0.000
heparinase	0.000
hyaluronidase	0.000
trypsin	0.000
lactic acid dehydrogenase	0.000