UMLS:C0029713 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0029713 (immaturity)
4,335 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
SERPINE2 protein	0.000
KLEIP	0.000
HCDI	0.000
TSEN34	0.000
Hermansky-Pudlak syndrome type 1	0.000
RDS	0.000
SEN34	0.000
KPTN	0.000
pregnancy specific beta-1-glycoprotein	0.000
Dihydropyridine receptor	0.000
Monad	0.000
SLC38A5	0.000
TSEN2	0.000
edg-2	0.000
GPR146	0.000
collagenous Alzheimer amyloid plaque component	0.000
Neurogenin 1	0.000
pregnancy-specific beta-1 glycoprotein	0.000
Maltase-glucoamylase	0.000
FATZ	0.000
SCTR	0.000
concentrative nucleoside transporter 1	0.000
Acyloxyacyl hydrolase	0.000
PARP-14	0.000
Junctin	0.000
neuropeptide S receptor 1	0.000
NKG2B	0.000
CD7	0.000
SP-B	0.000
RARS2	0.000
PIN1 protein	0.000
pp52	0.000
BAVM	0.000
peptide transporter 2	0.000
SREB2	0.000
TSEN54	0.000
ALTE	0.000
CD33	0.000
Cysteine-rich protein	0.000
2E4	0.000

Disease
immaturity	1.000
prematurity	0.001
hyaline membrane disease	0.001
Central nervous system vascular disorders	0.000
necrotizing enterocolitis	0.000
personality problem	0.000
RDS	0.000
Anoxic-ischemic encephalopathy	0.000
Sexual immaturity	0.000
bronchopulmonary dysplasia	0.000
Pulmonary immaturity	0.000
Recurrent bronchitis	0.000
Transient hypothyroxinemia	0.000
Ohdo blepharophimosis syndrome	0.000
retinopathy of prematurity	0.000
Neonatal hyperglycaemia	0.000
Axenfeld's syndrome	0.000
Generalized osteopenia	0.000
Neonatal respiratory distress syndrome	0.000
PCH5	0.000
Genitourinary infection	0.000
Benign Familial Neonatal Convulsions	0.000
Wilson-Mikity syndrome	0.000
Penile Cancer	0.000
PCH4	0.000
Gallbladder sludge	0.000
sudden infant death syndrome	0.000
Transient tachypnea of newborn	0.000
Erythema toxicum neonatorum	0.000
Kohler's disease	0.000
Neonatal hypocalcemia	0.000
Acute basophilic leukemia	0.000
Funisitis	0.000
sideroblastosis	0.000
panmyelosis	0.000
Sinding-Larsen-Johansson disease	0.000
Thyroid hyperplasia	0.000
Neonatal hyperbilirubinemia	0.000
PCH1	0.000
Recurrent respiratory tract infections	0.000

Symptom
respiratory distress	0.000
Procedural pain	0.000
Dysdiadochokinesis	0.000
Nasal regurgitation	0.000
change in skin color	0.000
enuresis	0.000
Intermenstrual bleeding	0.000
Infantile colic	0.000
hyperoxia	0.000
hypercapnia	0.000
Q angle	0.000
tachypnea	0.000
bedwetting	0.000
Motor dysfunction	0.000
Periodic breathing	0.000
gumma	0.000
hypothermia	0.000
seizures	0.000
Macula	0.000
Crushing	0.000
hypotonia	0.000
breath holding	0.000
Severe pain	0.000
irregular bleeding	0.000
impaired motor coordination	0.000
tonic seizure	0.000
inanition	0.000
clumsiness	0.000
weakness	0.000
sneezing	0.000
anesthesia	0.000
thirsty	0.000
tonic-clonic seizure	0.000
regurgitation	0.000
Involuntary Movement	0.000
pain	0.000
exhaustion	0.000
Halo	0.000
diarrhea	0.000
vomiting	0.000

Enzyme
CD13	0.000
TdT	0.000
splicing endonuclease	0.000
lactase	0.000
CD10	0.000
proline oxidase	0.000
phosphoserine phosphatase	0.000
arginyl-tRNA synthetase	0.000
lactase-phlorizin hydrolase	0.000
peroxidase	0.000
lactase-phlorizin hydrolase	0.000
PRT	0.000
arginase	0.000
CDH	0.000
alpha-glucosidase	0.000
sucrase	0.000
chymase	0.000
PNL	0.000
acid phosphatase	0.000
alkaline phosphatase	0.000
BMT	0.000
nucleotidase	0.000
cystathionine gamma-lyase	0.000
CNPase	0.000
ADPase	0.000
cytochrome P-450scc	0.000
adenosine deaminase	0.000
1-hydroxylase	0.000
adenosine deaminase	0.000
glutathione peroxidase	0.000
phenylalanine hydroxylase	0.000
p-nitrophenylphosphatase	0.000
factor C	0.000
6-phosphogluconate dehydrogenase	0.000
6-phosphogluconate dehydrogenase	0.000
diaphorase	0.000
adenine phosphoribosyltransferase	0.000
GCA	0.000
fatty acid desaturase	0.000
ornithine aminotransferase	0.000