UMLS:C0026850 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts: Target Concepts:

Query: UMLS:C0026850 (muscular dystrophy)
5,870 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

.

Concepts found in the documents ranked by [ Frequency | Pointwise Mutual Information | Symmetric Conditional Probability ] .

Human Gene/Protein
dystrophin	0.034
merosin	0.023
Fukuyama-type congenital muscular dystrophy	0.011
DAG	0.011
fukutin-related protein	0.007
dysferlin	0.007
LAMA2	0.007
fukutin	0.006
dystrophin gene	0.005
POMT1	0.005
utrophin	0.005
Dystrophin	0.004
POMGnT1	0.004
LARGE	0.003
DMD	0.003
POMT2	0.003
Facioscapulohumeral muscular dystrophy	0.003
dystrophin-associated glycoprotein	0.003
delta-sarcoglycan	0.003
PLEC1	0.003
Emery-Dreifuss muscular dystrophy	0.002
plectin	0.002
gamma-sarcoglycan	0.002
sarcospan	0.002
DM1	0.002
calpain 3	0.001
choline kinase beta	0.001
creatine kinase	0.001
LMNA	0.001
LGMD2A	0.001
SGCA	0.001
Fukutin-related protein	0.001
DMPK	0.001
protein O-mannosyltransferase	0.001
Walker	0.001
DUX4	0.001
LGMD2B	0.001
DYSF	0.001
CCTG	0.001
lamin A/C	0.001

Disease
muscular dystrophy	1.000
Duchenne muscular dystrophy	0.025
limb-girdle muscular dystrophy	0.020
Fukuyama congenital muscular dystrophy	0.008
MDC1A	0.006
myopathy	0.005
DM1	0.004
BMD	0.003
Emery-Dreifuss muscular dystrophy	0.002
muscular atrophy	0.002
Congenital muscular dystrophy	0.002
CMD	0.002
CMD	0.002
MDC1C	0.002
FMD	0.001
Ullrich	0.001
LGMD2I	0.001
LGMD2A	0.001
lissencephaly	0.001
MD-EBS	0.001
LGMD2C	0.001
Type II lissencephaly	0.001
LGMD2B	0.001
cerebro-oculo-muscular syndrome	0.001
cardiomyopathy	0.001
Landouzy	0.001
LGMD1B	0.001
MDC1D	0.001
EDMD2	0.001
Myosclerosis	0.001
polymyositis	0.001
neuromuscular disorder	0.000
wasting	0.000
Severe childhood autosomal recessive muscular dystrophy	0.000
CMD1A	0.000
LGMD2H	0.000
epidermolysis bullosa	0.000
Kugelberg-Welander	0.000
Oculopharyngeal muscular dystrophy	0.000
dilated cardiomyopathy	0.000

Symptom
weakness	0.002
hypotonia	0.001
Flaccid dysarthria	0.000
impaired body balance	0.000
benign congenital hypotonia	0.000
Muscle fibrosis	0.000
Fatigability	0.000
cachexia	0.000
muscle stiffness	0.000
abiotrophy	0.000
growing pains	0.000
ophthalmoplegia	0.000
fatigue	0.000
myalgia	0.000
anesthesia	0.000
Hyperekplexia	0.000
abnormal gait	0.000
hypercapnia	0.000
respiratory problem	0.000
Exercise intolerance	0.000
Joint hypermobility	0.000
bigeminal	0.000
muscle cramps	0.000
ataxia	0.000
dystonia	0.000
cerebellar ataxia	0.000
torticollis	0.000
pachyonychia	0.000
seizures	0.000
giddiness	0.000
orthopnea	0.000
giddiness	0.000
asthenia	0.000
rundown	0.000
twitching	0.000
exhaustion	0.000
hypersomnia	0.000
muscle rigidity	0.000
body pain	0.000
paresis	0.000

Enzyme
calpain 3	0.002
calpain 3	0.002
creatine kinase	0.001
N-acetylglucosaminyltransferase	0.000
calpain 4	0.000
L-glycol dehydrogenase	0.000
phosphatidylinositol-3,4,5-trisphosphate 3-phosphatase	0.000
choline kinase	0.000
aldolase	0.000
glycerol kinase	0.000
galactosylhydroxylysyl glucosyltransferase	0.000
CMP-Neu5Ac hydroxylase	0.000
EC 2.4.1.11	0.000
acylglycerol kinase	0.000
serum carnosinase	0.000
phosphoinositide 5-phosphatase	0.000
guanidinoacetate methyltransferase	0.000
calpain 10	0.000
m-calpain	0.000
C1 esterase	0.000
glycine amidinotransferase	0.000
LIS	0.000
glutathione peroxidase	0.000
polypeptide N-acetylgalactosaminyltransferase	0.000
cancer procoagulant	0.000
nicotinamide N-methyltransferase	0.000
adenylate kinase	0.000
cathepsin C	0.000
proteasome	0.000
phosphatidylethanolamine N-methyltransferase	0.000
mu-calpain	0.000
acetylcholinesterase	0.000
cathepsin B	0.000
ATPase	0.000
iodothyronine 5'-deiodinase	0.000
protein kinase	0.000
N-acetylgalactosaminidase	0.000
hepsin	0.000
hepsin	0.000
aspartate aminotransferase	0.000