UMLS:C0026827 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0026827 (hypotonia)
5,860 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
PREPL	0.002
MTM1	0.002
merosin	0.001
Prolyl endopeptidase-like	0.001
NALCN	0.001
X-linked	0.001
AHDC1	0.001
C2orf34	0.001
UNC80	0.001
PIGN	0.001
RASGEF1B	0.001
MAGEL2	0.001
strabismus	0.001
FAM36A	0.001
ACTA1	0.000
MECP2	0.000
SHANK3	0.000
PIGT	0.000
AHI1	0.000
PIGK	0.000
myotubularin	0.000
OCRL	0.000
MED13L	0.000
FBXL4	0.000
purine-rich element binding protein A	0.000
solute carrier family 25, member 12	0.000
CDKL5	0.000
SUCLA2	0.000
MIM	0.000
LAMA2	0.000
Succinic semialdehyde dehydrogenase	0.000
AP4B1	0.000
CDG Ia	0.000
ASXL3	0.000
SLC3A1	0.000
SNRPN	0.000
EHMT1	0.000
HIBCH	0.000
SLC16A2	0.000
RAI1	0.000

Disease
developmental delay	0.027
Joubert syndrome	0.004
failure to thrive	0.004
mental retardation	0.004
macrocephaly	0.004
mental retardation	0.003
myopathy	0.002
Cohen syndrome	0.002
severe mental retardation	0.001
Congenital muscular dystrophy	0.001
Leigh syndrome	0.001
Nemaline myopathy	0.001
FGS	0.001
delayed speech	0.001
encephalopathy	0.001
centronuclear myopathy	0.001
Zellweger syndrome	0.001
hypogonadism	0.001
congenital muscle disorder	0.001
Fumarase deficiency	0.001
Adenylosuccinate lyase deficiency	0.001
hyperglycinemia	0.001
Allan-Herndon-Dudley syndrome	0.001
optic atrophy	0.001
Toriello-Carey syndrome	0.001
Lowe syndrome	0.001
uniparental disomy of chromosome 14	0.001
lactic acidosis	0.001
Congenital myotonic dystrophy	0.001
muscular dystrophy	0.001
Neuhauser syndrome	0.000
EDS VI	0.000
SMAX2	0.000
brachycephaly	0.000
epilepsy	0.000
floppy baby syndrome	0.000
Congenital fiber type disproportion	0.000
moderate mental retardation	0.000
FGS2	0.000
MDC1A	0.000

Symptom
hypotonia	1.000
seizures	0.002
ataxia	0.002
weakness	0.002
hypertonia	0.001
benign congenital hypotonia	0.001
spasticity	0.001
lethargy	0.001
dystonia	0.000
athetosis	0.000
Abnormal muscle tone	0.000
Tongue fasciculations	0.000
hepatomegaly	0.000
dysarthria	0.000
cerebellar ataxia	0.000
clumsiness	0.000
chorea	0.000
Hyperirritability	0.000
respiratory distress	0.000
abnormal breathing	0.000
abnormal head movement	0.000
ophthalmoplegia	0.000
hepatosplenomegaly	0.000
Dysdiadochokinesis	0.000
constipation	0.000
cyanosis	0.000
vomiting	0.000
drooling	0.000
ataxic gait	0.000
Respiratory abnormalities	0.000
intention tremor	0.000
tremor	0.000
incoordination	0.000
sleepiness	0.000
myoclonus	0.000
Intermittent fever	0.000
staggering gait	0.000
Hypersomnolence	0.000
Sensory ataxia	0.000
tachypnea	0.000

Enzyme
biotinidase	0.000
aspartoacylase	0.000
phosphatidylinositol N-acetylglucosaminyltransferase	0.000
glutaryl-CoA dehydrogenase	0.000
phosphomannomutase	0.000
lysyl hydroxylase	0.000
complex I	0.000
ribonuclease alpha	0.000
dihydroxyacetone phosphate acyltransferase	0.000
cytochrome oxidase	0.000
methylglutaconyl coenzyme A hydratase	0.000
3-hydroxyisobutyryl-CoA hydrolase	0.000
creatine kinase	0.000
adenylosuccinate lyase	0.000
pyruvate dehydrogenase	0.000
3-hydroxy-3-methylglutaryl-CoA lyase	0.000
pterin-4alpha-carbinolamine dehydratase	0.000
galactosyltransferase II	0.000
mannosyl-oligosaccharide glucosidase	0.000
acyl-CoA dehydrogenase	0.000
spermine synthase	0.000
succinic semialdehyde dehydrogenase	0.000
methylcrotonyl-CoA carboxylase	0.000
branching enzyme	0.000
branched-chain acyl-CoA dehydrogenase	0.000
sepiapterin reductase	0.000
guanidinoacetate methyltransferase	0.000
EC 2.4.99.4	0.000
acyl-CoA dehydrogenase	0.000
glycine decarboxylase	0.000
electron transfer flavoprotein dehydrogenase	0.000
methylmalonyl-CoA mutase	0.000
alkylglycerol monooxygenase	0.000
PRPP synthetase	0.000
propionyl-CoA carboxylase	0.000
AIR synthetase	0.000
glycerate kinase	0.000
2-oxoglutarate decarboxylase	0.000
deoxyguanosine kinase	0.000
propionyl-CoA carboxylase	0.000