UMLS:C0242706 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0242706 (hyperoxia)
5,219 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
CO2	0.000
ATA	0.000
antioxidant enzyme	0.000
MFN1 protein	0.000
superoxide dismutase	0.000
glutathione peroxidase	0.000
surfactant protein C	0.000
catalase	0.000
MnSOD	0.000
NARFL	0.000
extracellular superoxide dismutase	0.000
P14	0.000
P12	0.000
PIGF protein	0.000
manganese superoxide dismutase	0.000
SP-C	0.000
transmembrane protein 100	0.000
heme oxygenase-1	0.000
SP-B	0.000
Mol	0.000
p17	0.000
thioredoxin-like 6	0.000
rod-derived cone viability factor	0.000
parathyroid hormone-related protein receptor	0.000
GPNMB protein	0.000
EC-SOD	0.000
vascular endothelial growth factor	0.000
Novel transcript	0.000
SFTA2	0.000
PASKIN	0.000
Angiogenic factor with G patch and FHA domains 1	0.000
glutathione reductase	0.000
Retinol dehydrogenase 13	0.000
GSH	0.000
LW-1	0.000
SOD3	0.000
Extracellular superoxide dismutase	0.000
importin 8	0.000
RAB24	0.000
histone family member	0.000

Disease
bronchopulmonary dysplasia	0.009
Oxygen toxicity	0.003
retinopathy of prematurity	0.001
Carotid body	0.000
Carotid body	0.000
Carotid body	0.000
pulmonary edema	0.000
lung disease	0.000
retinopathy	0.000
Compensated respiratory acidosis	0.000
embryo hypoxia	0.000
Gas bubble disease	0.000
pulmonary hypertension	0.000
Diffuse alveolar damage	0.000
prematurity	0.000
respiratory acidosis	0.000
persistent pulmonary hypertension of the newborn	0.000
Vascular degeneration	0.000
ischemia	0.000
adult respiratory distress syndrome	0.000
respiratory failure	0.000
GSH	0.000
Platelet sequestration	0.000
Woakes' syndrome	0.000
alkalosis	0.000
pulmonary fibrosis	0.000
Retinol deficiency	0.000
pulmonary insufficiency	0.000
Secondary pulmonary hypertension	0.000
vitamin E deficiency	0.000
ventricular hypertrophy	0.000
hyaline membrane disease	0.000
Central retinal artery occlusion	0.000
Posterior vitreous detachment	0.000
Extremely low birth weight	0.000
metabolic alkalosis	0.000
carboxyhemoglobinemia	0.000
Congenital central hypoventilation syndrome	0.000
stroke	0.000
AD4	0.000

Symptom
hyperoxia	1.000
hypercapnia	0.003
hypocapnia	0.001
respiratory distress	0.000
bradypnea	0.000
Periodic breathing	0.000
anesthesia	0.000
impaired motor coordination	0.000
hypothermia	0.000
Anoxia	0.000
Gasping	0.000
breath holding	0.000
exhaustion	0.000
sighing	0.000
Positive and Negative Symptoms	0.000
cyanosis	0.000
cardiovascular impairment	0.000
tachypnea	0.000
seizures	0.000
fatigue	0.000
labored breathing	0.000
CSR	0.000
Excitability	0.000
starvation	0.000
thinning	0.000
dyspnea	0.000
wheezing	0.000
excessive sweating	0.000
presyncope	0.000
cough	0.000
acute stress	0.000
functional recovery	0.000
hypersomnia	0.000
microbial colonization	0.000
analgesia	0.000
collapse	0.000
exertional dyspnea	0.000
incoordination	0.000
discomfort	0.000
agitation	0.000

Enzyme
superoxide dismutase	0.000
glutathione peroxidase	0.000
catalase	0.000
strombine dehydrogenase	0.000
glutathione reductase	0.000
glucose-6-phosphate dehydrogenase	0.000
NADH kinase	0.000
sulfiredoxin	0.000
indole 2,3-dioxygenase	0.000
heme oxygenase	0.000
aconitase	0.000
lactate dehydrogenase	0.000
aryl sulfotransferase IV	0.000
caspase-3	0.000
carnosine synthetase	0.000
NO synthase	0.000
NADPH oxidase	0.000
xanthine oxidase	0.000
NADPH oxidase	0.000
thioredoxin reductase	0.000
NQO1	0.000
15-hydroxyprostaglandin dehydrogenase	0.000
PGE2 isomerase	0.000
complex I	0.000
TdT	0.000
mitogen-activated protein kinase	0.000
biliverdin reductase	0.000
10-formyltetrahydrofolate dehydrogenase	0.000
elastase	0.000
ubiquinol-cytochrome c oxidoreductase	0.000
xanthine dehydrogenase	0.000
cytochrome oxidase	0.000
peroxidase	0.000
peroxiredoxin	0.000
gamma-glutamylcysteine synthetase	0.000
prolyl hydroxylase	0.000
NOS	0.000
succinate dehydrogenase	0.000
dynamin GTPase	0.000
methionine sulfoxide reductase	0.000