UMLS:C0029713 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0029713 (immaturity)
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Human Gene/Protein
SERPINE2 protein	11.8
TSEN34	10.8
KLEIP	10.8
HCDI	10.8
Hermansky-Pudlak syndrome type 1	10.5
SEN34	10.3
KPTN	10.3
pregnancy specific beta-1-glycoprotein	10.0
Dihydropyridine receptor	9.8
SLC38A5	9.4
Monad	9.4
edg-2	9.4
GPR146	9.4
TSEN2	9.4
collagenous Alzheimer amyloid plaque component	9.3
Neurogenin 1	9.1
SCTR	9.0
FATZ	9.0
Maltase-glucoamylase	9.0
pregnancy-specific beta-1 glycoprotein	9.0
concentrative nucleoside transporter 1	8.9
PARP-14	8.8
Acyloxyacyl hydrolase	8.8
Junctin	8.8
neuropeptide S receptor 1	8.6
NKG2B	8.6
RARS2	8.5
PIN1 protein	8.5
pp52	8.3
BAVM	8.3
peptide transporter 2	8.3
SREB2	8.2
TSEN54	8.1
ALTE	8.1
Cysteine-rich protein	8.0
HLA-2	8.0
2E4	8.0
paired box transcription factor	7.9
ARHGDIB	7.8
ANG2	7.7

Disease
Central nervous system vascular disorders	12.8
immaturity	12.8
Anoxic-ischemic encephalopathy	11.8
Sexual immaturity	11.8
personality problem	11.5
Pulmonary immaturity	11.3
Recurrent bronchitis	10.8
Ohdo blepharophimosis syndrome	10.5
Axenfeld's syndrome	10.3
Transient hypothyroxinemia	10.3
Generalized osteopenia	10.3
Neonatal hyperglycaemia	10.3
PCH5	10.0
Genitourinary infection	10.0
Benign Familial Neonatal Convulsions	9.8
Gallbladder sludge	9.7
PCH4	9.7
Penile Cancer	9.7
Neonatal respiratory distress syndrome	9.4
Transient tachypnea of newborn	9.3
Wilson-Mikity syndrome	9.2
Erythema toxicum neonatorum	9.1
Kohler's disease	9.0
Neonatal hypocalcemia	9.0
Funisitis	9.0
Acute basophilic leukemia	9.0
sideroblastosis	8.9
Sinding-Larsen-Johansson disease	8.8
Thyroid hyperplasia	8.8
PCH1	8.7
panmyelosis	8.6
Recurrent respiratory tract infections	8.5
infectious encephalomyelitis	8.5
hyaline membrane disease	8.5
Neonatal hyperbilirubinemia	8.5
Toriello-Carey syndrome	8.5
IgG1 deficiency	8.5
Solitary plasmacytoma of bone	8.3
Clonic seizures	8.3
Congenital myotonic dystrophy	8.3

Symptom
Nasal regurgitation	10.5
Dysdiadochokinesis	10.5
Procedural pain	9.8
change in skin color	9.1
Intermenstrual bleeding	7.8
Infantile colic	7.0
Q angle	6.8
Motor dysfunction	6.5
Periodic breathing	6.4
gumma	6.3
bedwetting	6.2
enuresis	6.0
Macula	6.0
Crushing	5.9
respiratory distress	5.8
Severe pain	5.5
breath holding	5.3
impaired motor coordination	5.3
irregular bleeding	5.3
tonic seizure	5.1
inanition	5.0
tachypnea	5.0
clumsiness	4.7
hyperoxia	4.6
thirsty	4.5
hypercapnia	4.3
Involuntary Movement	4.2
tonic-clonic seizure	4.1
Halo	4.0
sneezing	3.9
hypotonia	3.9
abdominal cramps	3.8
urinary frequency	3.7
night sweats	3.6
chronic constipation	3.5
Sedation	3.5
partial seizure	3.4
CSR	3.4
Neuropathic pain	3.4
hypothermia	3.3

Enzyme
splicing endonuclease	6.5
phosphoserine phosphatase	5.8
proline oxidase	5.8
arginyl-tRNA synthetase	5.7
lactase-phlorizin hydrolase	5.5
lactase-phlorizin hydrolase	5.1
TdT	5.1
PRT	5.0
lactase	4.8
CD13	4.7
CDH	4.7
PNL	4.4
chymase	4.0
sucrase	3.9
nucleotidase	3.8
cystathionine gamma-lyase	3.8
arginase	3.8
CNPase	3.8
ADPase	3.7
cytochrome P-450scc	3.7
1-hydroxylase	3.7
CD10	3.7
alpha-glucosidase	3.6
p-nitrophenylphosphatase	3.6
factor C	3.5
BMT	3.5
adenine phosphoribosyltransferase	3.4
GCA	3.4
fatty acid desaturase	3.4
phenylalanine hydroxylase	3.4
6-phosphogluconate dehydrogenase	3.3
ornithine aminotransferase	3.3
6-phosphogluconate dehydrogenase	3.3
insulin-degrading enzyme	3.3
caspase-2	3.3
caspase-2	3.2
dipeptidyl peptidase IV	3.1
succinic dehydrogenase	3.1
sucrase-isomaltase	3.1
prolyl hydroxylase	3.0