UMLS:C0728731 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0728731 (prematurity)
7,134 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
RDS	0.000
SAPL	0.000
SEN34	0.000
SLC27A4	0.000
erythropoietin	0.000
GSTT2B	0.000
FATP4	0.000
fatty acid transport protein	0.000
HLM-2	0.000
EEFSEC	0.000
SIDS	0.000
SP-A1	0.000
cysteine/histidine-rich 1	0.000
Erythropoietin	0.000
ABCA3 protein	0.000
SLC27A5	0.000
ALTE	0.000
histone family member	0.000
GATS	0.000
Ermin	0.000
VARS	0.000
strabismus	0.000
FREAC-1	0.000
RLF	0.000
TPSAB1	0.000
IVF	0.000
CPAP	0.000
neuropeptide S receptor 1	0.000
Siglec-14	0.000
MRX34	0.000
Thrombospondin-2	0.000
C16orf57	0.000
SLC12A1	0.000
very long-chain acyl-CoA synthetase	0.000
SP-A2	0.000
Leu-16	0.000
Fumarylacetoacetate hydrolase	0.000
Cad	0.000
PKK2	0.000
Pregnancy-specific beta 1-glycoprotein	0.000

Disease
prematurity	1.000
bronchopulmonary dysplasia	0.005
necrotizing enterocolitis	0.002
retinopathy of prematurity	0.001
premature rupture of membranes	0.001
chorioamnionitis	0.001
premature labor	0.001
hyaline membrane disease	0.001
preeclampsia	0.001
lung disease	0.001
cerebral palsy	0.001
immaturity	0.001
RDS	0.000
abortion	0.000
abruptio placentae	0.000
sepsis	0.000
sudden infant death syndrome	0.000
toxemia	0.000
Osteopenia of prematurity	0.000
sepsis	0.000
Chronic lung disease	0.000
fetal neoplasm	0.000
hyperbilirubinemia	0.000
eclampsia	0.000
postmaturity	0.000
anemia	0.000
Metabolic bone disease	0.000
Parotid abscess	0.000
Homozygous alpha thalassaemia	0.000
Haemophilus sepsis	0.000
Infantile hemiparesis	0.000
Neonatal nephrocalcinosis	0.000
gastroschisis	0.000
cervical incompetence	0.000
oligohydramnios	0.000
Transient hypothyroxinemia	0.000
neonatal jaundice	0.000
Delayed delivery	0.000
Periventricular leukomalacia	0.000
RSV infection	0.000

Symptom
respiratory distress	0.001
Pruritus of pregnancy	0.000
hyperoxia	0.000
wheezing	0.000
Poor weight gain	0.000
tachypnea	0.000
KIDNEY	0.000
Very Low Birth Weight	0.000
Bilious vomiting	0.000
Fetal tachycardia	0.000
false labor	0.000
cyanosis	0.000
Other pain	0.000
hypercapnia	0.000
seizures	0.000
abnormal taste	0.000
bigeminal	0.000
hypothermia	0.000
hyperemesis gravidarum	0.000
delayed language development	0.000
Periodic breathing	0.000
athetosis	0.000
stomach distension	0.000
Darier's sign	0.000
Reticulocytosis	0.000
hypotonia	0.000
diarrhea	0.000
Flare	0.000
anesthesia	0.000
cough	0.000
stridor	0.000
trigeminy	0.000
vomiting	0.000
torticollis	0.000
spasticity	0.000
monoplegia	0.000
nocturnal cough	0.000
microbial colonization	0.000
lethargy	0.000
Anoxia	0.000

Enzyme
PdxH	0.000
AOR	0.000
C5a peptidase	0.000
5-oxoprolinase	0.000
PRT	0.000
phosphatidylglycerophosphate synthase	0.000
sulfiredoxin	0.000
guanidinoacetate methyltransferase	0.000
glycine N-methyltransferase	0.000
glycine amidinotransferase	0.000
ScpA	0.000
adenylosuccinate lyase	0.000
valyl-tRNA synthetase	0.000
acyl-CoA synthetase	0.000
phosphocholine cytidylyltransferase	0.000
p100	0.000
PPH	0.000
alkaline phosphatase	0.000
lysophosphatidylcholine acyltransferase	0.000
fumarylacetoacetate hydrolase	0.000
EPT	0.000
3-hydroxyacyl-CoA dehydrogenase	0.000
3-hydroxyacyl-CoA dehydrogenase	0.000
methionine adenosyltransferase	0.000
renin	0.000
phospholipase A1	0.000
argininosuccinate lyase	0.000
ceruloplasmin	0.000
choline kinase	0.000
methylenetetrahydrofolate reductase	0.000
methylenetetrahydrofolate reductase	0.000
lecithin:cholesterol acyltransferase	0.000
meprin	0.000
acyl-CoA synthetase	0.000
CDH	0.000
gamma-glutamylcysteine synthetase	0.000
glutathione synthetase	0.000
monoacylglycerol lipase	0.000
argininosuccinate synthetase	0.000
type III procollagen	0.000