UMLS:C0270736 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0270736 (Essential tremor)
404 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
KV9.2	16.3
brain link protein-2	15.3
LINGO4	15.3
ETM2	14.7
Kv9.2	14.3
HAPLN4	14.3
LINGO2	13.8
STK32B	13.7
Teneurin-4	12.5
potassium channel 1	12.4
D3nf	11.7
SLC1A2	11.7
USP46	11.6
FTM	11.1
KARS	11.0
SCA12	10.9
SCN11A	10.8
mitochondrial serine protease	10.6
SCA5	10.5
CTNNA3	10.4
SLIT3	10.3
CACNA1G	9.8
KIF5A	9.7
axon guidance molecule	9.2
Cav3.1	8.9
CALM	8.9
HtrA2	8.9
FUS	8.9
SCN4A	8.5
SCA3	8.5
NGR	8.4
TUB	8.4
fus	8.3
SCA6	8.3
dopamine D3 receptor	8.3
aspartoacylase	8.3
SCA2	8.1
PPARGC1A	8.1
DBS	8.1
NPL	7.8
DRD3	7.8
NTRK1	7.8
SCA1	7.8
NOS3	7.7
IIS	7.6
HCN1	7.4
CIT	7.4
TBS	7.4
DYT1	7.3
VIM	7.3
TLS	7.2
gamma-amino butyric acid	7.1
sortilin	7.1
EAT	7.0
DMN	6.9
STN	6.8
asp	6.7
interacting protein	6.6
SERT	6.6
MSA	6.6
mover	6.5
functional)	6.5
version 1	6.4
CA IX	6.3
CRS	6.3
BK channel	6.1
glutamate transporter	6.0
neurofilament protein	5.9
TOR	5.9
DAT	5.7
dopamine transporter	5.7
BID	5.6
adenosine A1 receptor	5.6
RNA binding protein	5.5
catechol-O-methyltransferase	5.5
p75	5.5
MIM	5.5
methylenetetrahydrofolate reductase	5.3
GBS	5.2
STS	5.1

Disease
Essential tremor	16.3
Isolated head tremor	15.7
FET1	14.3
Vascular parkinsonism	12.3
ETM	11.4
SCA5	11.1
extrapyramidal disorder	11.1
SCA12	10.9
movement disorder	10.6
organic psychosis	9.4
Cerebellum	8.9
FUS	8.9
SCA6	8.6
Multiple system atrophy	8.6
REM sleep behavior disorder	8.4
torsion dystonia	8.4
SCA2	8.1
pseudobulbar palsy	8.1
Dystonia	7.8
TRS	7.8
Bielschowsky	7.7
SCA1	7.7
parkinsonism	7.6
DYT1	7.5
Machado-Joseph disease	7.5
TBS	7.2
pyomyositis	7.1
disabling disease	7.1
thyroid disorder	7.0
Parkinson's disease	7.0
neurological disease	6.9
spondylosis	6.9
Tic	6.8
akinesia	6.7
MSA	6.5
brain disorder	6.5
Tongue	6.4
dysphonia	6.2
Tourette syndrome	6.2
progressive supranuclear palsy	6.1
Wilson's disease	6.0
Klinefelter's syndrome	6.0
Charcot-Marie-Tooth disease	5.7
Dementia with Lewy bodies	5.6
peripheral neuropathy	5.5
restless legs syndrome	5.4
ichthyosis	5.4
Friedreich's ataxia	5.2
premature aging	5.2
ichthyosis	5.2
social phobia	5.1
Disorder	5.0
STS	5.0
complex partial seizures	4.9
dyskinesia	4.9
degenerative disease	4.8
tetraplegia	4.8
tic	4.6
hypogonadotropic hypogonadism	4.6
cognitive impairment	4.6
craniosynostosis	4.5
memory impairment	4.4
migraine	4.2
dementia	4.1
PCA	4.1
MRS	4.1
mania	4.0
herpes zoster	4.0
retinitis pigmentosa	3.9
Posterior	3.9
sleep disturbances	3.8
muscular dystrophy	3.7
psychological stress	3.7
neuroticism	3.6
polio	3.5
dysphagia	3.3
polyneuropathy	3.3
wasting	3.3
genetic disorder	3.1
cerebral palsy	3.1

Enzyme
Lod	9.7
aspartoacylase	8.7
Omi/HtrA2	7.8
NPL	7.4
TRS	7.2
DAT	5.7
TOR	5.7
methylenetetrahydrofolate reductase	5.2
methylenetetrahydrofolate reductase	5.2
carbonic anhydrase	4.4
creatine kinase	2.1
caspase-3	1.1
ERK	-0.3