Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0027066 (
myoclonus
)
4,275
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
epsilon-sarcoglycan
0.009
SGCE
0.008
DYT11
0.006
EPM1
0.002
jerky
0.001
MERRF
0.001
EPM2A
0.001
Nova-1
0.001
Epsilon-sarcoglycan
0.001
malin
0.001
PME
0.001
laforin
0.001
DYT1
0.000
14-3-3 protein
0.000
stiff person syndrome
0.000
NEU1
0.000
dentatorubral-pallidoluysian atrophy
0.000
GOSR2
0.000
prion protein
0.000
KCTD17
0.000
DYT3
0.000
NGK2
0.000
Golgi SNAP
0.000
Na+,K+ ATPase
0.000
ANO3
0.000
KCTD7
0.000
Prion protein
0.000
CACNA1B
0.000
MRI
0.000
PR domain containing 8
0.000
GCH1
0.000
Contactin-associated protein 2
0.000
PRKRA
0.000
prion
0.000
dopa-responsive dystonia
0.000
PRNP
0.000
Cystatin B
0.000
CLN6
0.000
TUBB4
0.000
N33
0.000
THAP1
0.000
ATLD
0.000
HEPACAM2
0.000
MM1
0.000
Kv3.3
0.000
CIZ1
0.000
SAMD12
0.000
PrP
0.000
TBC1D24
0.000
PFKL
0.000
CSF
0.000
lysosomal sialidase
0.000
MT-TK
0.000
EBN1
0.000
PPEF1
0.000
PWI
0.000
ATP1A3
0.000
glutamic acid decarboxylase
0.000
CLN8
0.000
She
0.000
Kv8.1
0.000
PRDM8
0.000
SMEI
0.000
Bos1
0.000
LDE
0.000
SEP
0.000
GNAL
0.000
putative protein tyrosine phosphatase
0.000
atrophin 1
0.000
NANH
0.000
CLN7
0.000
PIGL
0.000
FAD1
0.000
TAF1
0.000
POLG protein
0.000
GCH
0.000
SCN1A
0.000
REM
0.000
amphiphysin
0.000
LIMP-2
0.000
RAPGEF2
0.000
SPG10
0.000
MM2
0.000
MTND4
0.000
PKC-gamma
0.000
MARCH6
0.000
ALG11
0.000
DPPX
0.000
JME
0.000
KCND3
0.000
MELAS
0.000
STX6
0.000
inhibitory glycine receptor
0.000
P25
0.000
EJM1
0.000
aminomethyltransferase
0.000
GYS1
0.000
LGI1
0.000
RARS2
0.000
ubiquitin-protein ligase E3A
0.000
GTT1
0.000
CACNB4
0.000
FARS2
0.000
GPR37L1
0.000
atrophin-1
0.000
GABA
0.000
14-3-3
0.000
DRPLA
0.000
mRNA decapping enzyme
0.000
presenilin 1
0.000
MT-ND6
0.000
NADH-coenzyme Q reductase
0.000
MNGIE
0.000
CAPN5
0.000
ADSL
0.000
CRMP5
0.000
tau protein
0.000
POLG
0.000
PSEN1
0.000
SCA8
0.000
SCA2
0.000
ZBTB38
0.000
CLN5
0.000
ADCK3
0.000
GAD
0.000
sialidase
0.000
SCARB2
0.000
SCA17
0.000
PCA1
0.000
PKAN
0.000
putative E3 ubiquitin ligase
0.000
CV2
0.000
neuraminidase
0.000
ALG6
0.000
SACS
0.000
PSD
0.000
KH1
0.000
Caspr2
0.000
GLRA1
0.000
Neuroserpin
0.000
SPTAN1
0.000
cathepsin A
0.000
NARP
0.000
PRICKLE1
0.000
Cyclin-dependent kinase inhibitor 3
0.000
c-Jun N-terminal kinase 2
0.000
chromosome 21
0.000
SCA1
0.000
CHMP2B
0.000
GIGYF2
0.000
EIF4G1
0.000
Synphilin-1
0.000
SHFM1
0.000
D2 dopamine receptor
0.000
5-HT receptor
0.000
CerS1
0.000
Glutamic acid decarboxylase
0.000
HuB
0.000
EFHC1
0.000
CST6
0.000
human leucocyte antigen D
0.000
S31
0.000
NMYC
0.000
voltage-gated potassium channel
0.000
Kv4
0.000
MOBP
0.000
GSD
0.000
puratrophin-1
0.000
SCA10
0.000
serotonin receptor
0.000
PRRT2
0.000
DQ2
0.000
MR-1
0.000
neuroserpin
0.000
NOVA
0.000
cathepsin Z
0.000
KCNC3
0.000
PIMT
0.000
SCN8A
0.000
Rett syndrome
0.000
GAD65
0.000
DDT
0.000
CLN1
0.000
KH2
0.000
B37
0.000
glucocerebrosidase
0.000
PME-1
0.000
voltage gated potassium channel
0.000
PSEN2
0.000
AFG3L2
0.000
EMP1
0.000
GLYT2
0.000
Hallervorden-Spatz syndrome
0.000
THPO
0.000
L2HGDH
0.000
Sialidase
0.000
ganglioside sialidase
0.000
5-HT1A
0.000
Aristaless-related homeobox
0.000
Ubiquitin C-terminal hydrolase
0.000
SLC1A2
0.000
HPCA
0.000
GRN
0.000
GPR37
0.000
KRIT1
0.000
GABRB3
0.000
SLC20A2
0.000
ATA
0.000
SCA6
0.000
PTG
0.000
adenylosuccinate lyase
0.000
ASAH1
0.000
5-hydroxytryptamine
0.000
TARDBP
0.000
thyroid peroxidase
0.000
TMEM106B
0.000
SLC2A1
0.000
Sep
0.000
GLYT1
0.000
DLX6
0.000
PTE
0.000
HSP10
0.000
Presenilin 1
0.000
Kufor-Rakeb syndrome
0.000
asymmetrical
0.000
hippocalcin
0.000
IGE
0.000
NADH-ubiquinone reductase
0.000
neuron-specific enolase
0.000
succinic semialdehyde dehydrogenase
0.000
NifU
0.000
UBE3A
0.000
SYNE1
0.000
NKX2.1
0.000
KCNJ10
0.000
CACNA1A
0.000
5-HT1D
0.000
NMD
0.000
PANK2
0.000
CXCL13
0.000
GTP cyclohydrolase I
0.000
FMR1 protein
0.000
dual-specificity phosphatase
0.000
dual specificity phosphatase
0.000
CBD
0.000
ARX
0.000
P33
0.000
PPT1
0.000
SPG7
0.000
SPG11
0.000
EIF2AK3
0.000
STXBP1
0.000
KCNQ3
0.000
CLN3
0.000
rasGAP
0.000
cysteine string protein
0.000
SCN1B
0.000
amyloid precursor protein
0.000
spinocerebellar ataxia type 2
0.000
DRD2
0.000
FUS
0.000
MM46
0.000
5-HT1B
0.000
EAAT4
0.000
alpha-synuclein
0.000
KH-type splicing regulatory protein
0.000
MECP2
0.000
POG
0.000
ACTH
0.000
SV2A
0.000
SEF
0.000
H-protein
0.000
SOX6
0.000
CLN
0.000
auxilin
0.000
PE1
0.000
tRNA
0.000
MIM
0.000
neuronatin
0.000
HTR2C
0.000
LBD
0.000
ATXN2
0.000
AED
0.000
HEXA
0.000
A4 protein
0.000
Wilson disease
0.000
adrenocorticotropic hormone
0.000
APRIL
0.000
COL6A3
0.000
FDG
0.000
ATXN3
0.000
cytochrome c oxidase
0.000
MEP
0.000
NK-2
0.000
C9orf72
0.000
PSN
0.000
LHON
0.000
P36
0.000
RELN
0.000
ceruloplasmin
0.000
GlyT2
0.000
dystrophin-associated glycoprotein
0.000
NSA
0.000
COL6A1
0.000
PLA2G6
0.000
P37
0.000
HTR1A
0.000
DLX5
0.000
WFS1
0.000
CLCN1
0.000
XDP
0.000
DNA polymerase gamma
0.000
biotinidase
0.000
5HT1A
0.000
5-HT2 receptor
0.000
potassium ion channel
0.000
spermine synthase
0.000
cysteine protease
0.000
sepiapterin reductase
0.000
BGM
0.000
VPS35
0.000
P22
0.000
NCL
0.000
Dopamine transporter
0.000
ATP13A2
0.000
Hexosaminidase
0.000
MAOB
0.000
P15
0.000
TDP-43
0.000
N14
0.000
COL1A2
0.000
IP10
0.000
galactocerebrosidase
0.000
thyroperoxidase
0.000
glycine decarboxylase
0.000
SCN4A
0.000
progranulin
0.000
neogenin
0.000
neurotransmitter receptor
0.000
LAS
0.000
calpain 3
0.000
cysteine proteinase inhibitor
0.000
PSP
0.000
DBS
0.000
carboxyl methyltransferase
0.000
enolase
0.000
EMP
0.000
GLUT-1
0.000
methyl CpG binding protein 2
0.000
sodium channel
0.000
CIT
0.000
beta-endorphin
0.000
BAFF
0.000
X-linked
0.000
CELF
0.000
GW182
0.000
GSS
0.000
SLS
0.000
HuC
0.000
axonal
0.000
chronic renal failure
0.000
B12
0.000
AC5
0.000
pallid
0.000
PEG10
0.000
ILS
0.000
GBP
0.000
DBA
0.000
pantothenate kinase
0.000
dominant)
0.000
CDKL5
0.000
glutaryl-CoA dehydrogenase
0.000
GCG
0.000
with Parkinsonism
0.000
HDS
0.000
hexosaminidase A
0.000
orphan G protein-coupled receptor
0.000
gephyrin
0.000
arylsulfatase A
0.000
LAMP2
0.000
cytochrome P450 1A2
0.000
A-T
0.000
GAT1
0.000
CADASIL
0.000
PSM
0.000
MX1
0.000
ECD
0.000
Neuraminidase
0.000
Cathepsin B
0.000
voltage-gated sodium channel
0.000
P14
0.000
p190
0.000
prosaposin
0.000
propionyl-CoA carboxylase
0.000
aldolase C
0.000
acid ceramidase
0.000
SNCA
0.000
dihydropteridine reductase
0.000
hnRNP K
0.000
ICAM-3
0.000
PDGFB
0.000
presenilin 2
0.000
CSF1R
0.000
matrix metalloproteinase 1
0.000
TREM2
0.000
chitotriosidase
0.000
parkin
0.000
PARKIN
0.000
HIP
0.000
IMP
0.000
X-receptor
0.000
HtrA2
0.000
PSG
0.000
P100
0.000
synuclein
0.000
P23
0.000
ALC
0.000
GABA transaminase
0.000
NONO
0.000
Met
0.000
ATM protein
0.000
PARK7
0.000
proline rich
0.000
CHAC
0.000
neuronal protein
0.000
AC1
0.000
DAT
0.000
RS1
0.000
thyroid transcription factor 1
0.000
extracellular superoxide dismutase
0.000
HTR2A
0.000
SLI
0.000
TL1A
0.000
ATX
0.000
MAOA
0.000
Beckwith-Wiedemann syndrome
0.000
neuronal nicotinic acetylcholine receptor
0.000
gamma2
0.000
phosphoglycerate dehydrogenase
0.000
PDGFRB
0.000
HT3
0.000
peptidylglycine alpha-amidating monooxygenase
0.000
VCP
0.000
MYCN
0.000
Aspartate aminotransferase
0.000
Kir4.1
0.000
CAE
0.000
tryptophan hydroxylase
0.000
CA1
0.000
bcl-x
0.000
parvalbumin
0.000
SCA3
0.000
glutamate receptor subunit
0.000
UCHL1
0.000
CLN2
0.000
GLD
0.000
asparagine synthetase
0.000
NMA
0.000
AP-3
0.000
glial fibrillary acidic protein
0.000
FTD
0.000
I-1
0.000
hnRNP
0.000
G-CSF receptor
0.000
recoverin
0.000
imiglucerase
0.000
dopamine transporter
0.000
argininosuccinate synthetase
0.000
aldolase A
0.000
alpha-enolase
0.000
N-acetylaspartate
0.000
PARK2
0.000
TPO
0.000
X-linked recessive
0.000
KCNQ2
0.000
APP
0.000
pseudoxanthoma elasticum
0.000
PHP
0.000
LEP
0.000
GBS
0.000
NMDA receptor
0.000
ALS
0.000
Tic
0.000
vesicular GABA transporter
0.000
pS2
0.000
TAU
0.000
lysosomal protein
0.000
MDS
0.000
thyroid transcription factor-1
0.000
pseudocholinesterase
0.000
protein phosphatase
0.000
Thyrotropin-releasing hormone
0.000
RAD50
0.000
TMS
0.000
P27
0.000
Proteinase
0.000
PINK1
0.000
ATP synthase
0.000
tyrosine protein kinase
0.000
PLP
0.000
SLC6A4
0.000
Trio
0.000
Kv4.3
0.000
creatine kinase
0.000
HTT
0.000
CAST
0.000
dach
0.000
dystrophin
0.000
AEP
0.000
T12
0.000
HGC
0.000
PON
0.000
HLA-DQB1
0.000
ARG
0.000
ataxin-3
0.000
Erb
0.000
GABA(A) receptor
0.000
prohibitin
0.000
SMS
0.000
apolipoprotein E
0.000
MCD
0.000
T10
0.000
GNAS
0.000
N-myc
0.000
MT-1
0.000
EC1
0.000
strabismus
0.000
CPR
0.000
MRE11
0.000
Choline acetyltransferase
0.000
NSE
0.000
EAAC1
0.000
urocortin
0.000
NPC1
0.000
Li-Fraumeni syndrome
0.000
ATRX
0.000
ubiquitin
0.000
MAR
0.000
STOP
0.000
integral membrane protein
0.000
AP4
0.000
heterogeneous nuclear ribonucleoprotein
0.000
calbindin
0.000
CCL22
0.000
PPT
0.000
ASA
0.000
ChAT
0.000
transcobalamin II
0.000
SPR
0.000
MCL
0.000
NSD
0.000
ALD
0.000
unknown function
0.000
TTF-1
0.000
voltage-dependent anion channel
0.000
5-HT4
0.000
NBS1
0.000
CSP
0.000
brain-derived
0.000
NF-L
0.000
DSP
0.000
P40
0.000
APH
0.000
RNA binding protein
0.000
SS-A
0.000
PTS
0.000
MAG
0.000
calretinin
0.000
huntingtin
0.000
P11
0.000
TCS
0.000
ND4
0.000
DOM
0.000
Parkin
0.000
AQP4
0.000
chloride channel
0.000
CCL19
0.000
MSA
0.000
ornithine aminotransferase
0.000
GABA transporter
0.000
ubiquitin ligase
0.000
cystatin C
0.000
5-HT2A
0.000
MSD
0.000
T11
0.000
thyrotropin-releasing hormone
0.000
CCP
0.000
AAG
0.000
SNARE
0.000
CXCR5
0.000
trkB
0.000
FANCD2
0.000
CGA
0.000
hereditary hemochromatosis
0.000
NADH dehydrogenase
0.000
acetylcholine receptor
0.000
dopa decarboxylase
0.000
AChR
0.000
HBA
0.000
CA2
0.000
PDS
0.000
M-protein
0.000
NPY
0.000
CD20
0.000
TMP
0.000
LRRK2
0.000
transmembrane glycoprotein
0.000
tyrosine hydroxylase
0.000
FM1
0.000
agrin
0.000
lipoamide dehydrogenase
0.000
IPS
0.000
vesicular monoamine transporter 2
0.000
SP2
0.000
CYP2D6
0.000
endoplasmic reticulum
0.000
ATC
0.000
CD55
0.000
homeobox gene
0.000
MCT
0.000
OTC
0.000
p15
0.000
metabotropic glutamate receptor
0.000
C protein
0.000
LAMP-1
0.000
dopamine D2 receptor
0.000
RDX
0.000
CA4
0.000
glycogen synthase
0.000
intrinsic factor
0.000
tap
0.000
DAG
0.000
glutamate transporter
0.000
G6PD
0.000
5-HT2C
0.000
EMD
0.000
SDH
0.000
autoantigen
0.000
GAD67
0.000
RNA-binding protein
0.000
more...
Disease
myoclonus epilepsy
0.009
Opsoclonus
0.008
DYT11
0.007
PME
0.004
Creutzfeldt-Jakob disease
0.004
Opsoclonus-myoclonus syndrome
0.003
movement disorder
0.003
sialidosis
0.002
LBD
0.002
Opsoclonus myoclonus
0.002
epilepsy
0.002
Benign neonatal sleep myoclonus
0.001
mutism
0.001
MERRF
0.001
encephalopathy
0.001
Progressive myoclonic epilepsy
0.001
juvenile myoclonic epilepsy
0.001
Corticobasal degeneration
0.001
parkinsonism
0.001
choreoathetosis
0.001
dementia
0.001
EPM2B
0.001
apraxia
0.001
DYT10
0.001
Dystonia
0.001
DYT1
0.001
Reading epilepsy
0.000
CJD
0.000
status epilepticus
0.000
cerebellar syndrome
0.000
DYT4
0.000
subacute sclerosing panencephalitis
0.000
mitochondrial encephalomyopathy
0.000
Epilepsia partialis continua
0.000
paraneoplastic syndrome
0.000
pathological emotionality
0.000
Encephalopathies toxic and metabolic
0.000
Pure photosensitive epilepsy
0.000
Post-anoxic myoclonus
0.000
SHFM1D
0.000
Intermittent confusion
0.000
Other CNS disorders
0.000
Symptomatic myoclonus
0.000
Peripheral vestibular nystagmus
0.000
Panencephalitis
0.000
Dentatorubropallidoluysian atrophy
0.000
encephalitis
0.000
DYT15
0.000
torsion dystonia
0.000
DYT2
0.000
SPS
0.000
restless legs syndrome
0.000
Alcoholic pellagra
0.000
familial striatal degeneration
0.000
Familial essential myoclonus
0.000
Pallidoluysian atrophy
0.000
Focal clonic seizures
0.000
Myoclonic Encephalopathy
0.000
kuru
0.000
SCA14
0.000
neuronal ceroid lipofuscinosis
0.000
Ocular bobbing
0.000
Gerstmann
0.000
paramyoclonus multiplex
0.000
Dialysis dementia
0.000
Pseudodystonia
0.000
CRCL
0.000
Galactosialidosis
0.000
fits
0.000
petit mal
0.000
Kufs' disease
0.000
abnormal involuntary movements
0.000
hallucinations
0.000
Epileptic encephalopathy
0.000
CNS degenerative disease
0.000
Paraneoplastic encephalomyelitis
0.000
progressive supranuclear palsy
0.000
reflex epilepsy
0.000
CLN6
0.000
Kozhevnikov's epilepsy
0.000
ATLD
0.000
SCAE
0.000
DRD
0.000
olivopontocerebellar atrophy
0.000
DYT7
0.000
brain atrophy
0.000
Hashimoto's thyroiditis
0.000
Progressive rubella panencephalitis
0.000
Neurologic Diseases
0.000
Early onset cerebellar ataxia with retained tendon reflexes
0.000
Akinetic mutism
0.000
torsion spasm
0.000
Olivary hypertrophy
0.000
DYT13
0.000
coma
0.000
hereditary chorea
0.000
nystagmus
0.000
disorientation
0.000
dyskinesia
0.000
XDP
0.000
adult GM1 gangliosidosis
0.000
moria
0.000
SCA21
0.000
DYT14
0.000
confusion
0.000
Rasmussen encephalitis
0.000
CLN8
0.000
Lambert-Eaton myasthenic syndrome
0.000
Whipple's disease
0.000
Atypical benign partial epilepsy
0.000
Epilepsy with myoclonic absences
0.000
Alzheimer's disease with early onset
0.000
Benign myoclonic epilepsy in infancy
0.000
delirium
0.000
HPNS
0.000
generalized seizure
0.000
aphasia
0.000
Alexander disease
0.000
Transient amnesia
0.000
Cytochrome c oxidase deficiency
0.000
Cerebellar degeneration
0.000
neuroblastoma
0.000
encephalomyelitis
0.000
hypsarhythmia
0.000
Neuroleptic-induced tardive dyskinesia
0.000
Sylvian aqueduct syndrome
0.000
blepharoclonus
0.000
cancer associated retinopathy
0.000
mitochondrial myopathy
0.000
FFI
0.000
EME
0.000
tardive dyskinesia
0.000
neurological disease
0.000
photosensitivity
0.000
stereotypies
0.000
spongiform encephalopathy
0.000
sleep disorders
0.000
SCA19
0.000
Millard-Gubler syndrome
0.000
optic atrophy
0.000
Lennox-Gastaut syndrome
0.000
Striatonigral degeneration
0.000
Eating epilepsy
0.000
epileptic twilight state
0.000
Uremic syndrome
0.000
Juvenile Parkinsonism
0.000
Secondary parkinsonism
0.000
Leigh syndrome
0.000
Lennox-Gastaut syndrome
0.000
nocturnal leg cramps
0.000
cognitive impairment
0.000
Progressive dementia
0.000
MELAS
0.000
Cortical laminar necrosis
0.000
Jacksonian epilepsy
0.000
Ocular flutter
0.000
Recurrent depression
0.000
sleep epilepsy
0.000
Alpers
0.000
Paraneoplastic cerebellar degeneration
0.000
GM1 gangliosidosis
0.000
Pick's disease with Pick bodies
0.000
Focal motor seizures
0.000
Microdysgenesis
0.000
CAPOS
0.000
Parkinson's disease and parkinsonism
0.000
Jacksonian seizures
0.000
Gaucher disease
0.000
mental retardation
0.000
MELAS
0.000
Adenylosuccinate lyase deficiency
0.000
mental retardation
0.000
CLN7
0.000
Huntington's disease
0.000
dysautonomia
0.000
Multiple symmetrical lipomatosis
0.000
hemiparesis
0.000
familial disorder
0.000
eye movement disorder
0.000
gangliosidosis
0.000
bruxism
0.000
BFNC
0.000
Foville syndrome
0.000
Internuclear ophthalmoplegia
0.000
hemichorea
0.000
extrapyramidal disorder
0.000
Alzheimer's disease
0.000
Metabolic encephalopathy
0.000
3-Methylglutaconic aciduria
0.000
RDP
0.000
Parkinson's disease
0.000
Landau-Kleffner syndrome
0.000
neuromyotonia
0.000
vLINCL
0.000
mitochondrial disease
0.000
Tourette syndrome
0.000
Gaze-evoked nystagmus
0.000
Immune reconstitution syndrome
0.000
Photosensitive epilepsy
0.000
EPMR
0.000
SCA28
0.000
Sandifer syndrome
0.000
catatonic stupor
0.000
parasomnia
0.000
EJM1
0.000
Hypophagia
0.000
Balint's syndrome
0.000
slow virus infection
0.000
akinesia
0.000
ALS6
0.000
frontal lobe syndrome
0.000
Mild depression
0.000
cerebral ischemia/hypoxia
0.000
spinal cord neoplasm
0.000
brain anoxia
0.000
IGE
0.000
lactic acidosis
0.000
Morvan
0.000
Limbic encephalitis
0.000
hereditary ataxia
0.000
MNGIE
0.000
Generalized epilepsy
0.000
SCA8
0.000
Hallervorden-Spatz disease
0.000
sleep apnea
0.000
Staring
0.000
sleep disturbances
0.000
measles
0.000
REM sleep behavior disorder
0.000
A-V malformation
0.000
Ohtahara syndrome
0.000
Sydenham's chorea
0.000
Dementia with Lewy bodies
0.000
Angelman syndrome
0.000
CLN5
0.000
infectious encephalitis
0.000
Spinocerebellar ataxia
0.000
global aphasia
0.000
developmental delay
0.000
atonic seizure
0.000
Aspiration pneumonitis
0.000
Pick's disease
0.000
SCA2
0.000
pseudobulbar palsy
0.000
Pisa syndrome
0.000
adult HD
0.000
pellagra
0.000
astereognosis
0.000
Downbeat nystagmus
0.000
SCA17
0.000
Meige syndrome
0.000
psychosis
0.000
GM2 gangliosidosis
0.000
Soft palate
0.000
Biermer
0.000
progressive bulbar palsy
0.000
MGA3
0.000
GAD
0.000
Central pontine myelinolysis
0.000
hallucinosis
0.000
Withdrawal syndrome
0.000
ring chromosome 20
0.000
Infantile neuronal ceroid lipofuscinosis
0.000
Sepsis-associated encephalopathy
0.000
SCA1
0.000
Lennox syndrome
0.000
Autoimmune encephalitis
0.000
Progressive Aphasia
0.000
Primary insomnia
0.000
Nonconvulsive status epilepticus
0.000
Tic
0.000
encephalomyelopathy
0.000
Kluver-Bucy syndrome
0.000
gluten sensitivity
0.000
focal epilepsy
0.000
dysphagia
0.000
SACS
0.000
progressive chorea
0.000
INAD
0.000
narcolepsy
0.000
Multiple system atrophy
0.000
sleep terrors
0.000
delusions
0.000
angiokeratoma
0.000
Meige
0.000
Rosenthal
0.000
propionic acidemia
0.000
Convulsive status epilepticus
0.000
agnosia
0.000
tic
0.000
lysosomal storage disease
0.000
intellectual impairment
0.000
CLN1
0.000
Wilson's disease
0.000
Narcolepsy with cataplexy
0.000
Oppenheim
0.000
disinhibition
0.000
carcinoid syndrome
0.000
Rett syndrome
0.000
SCA6
0.000
disorders of carbohydrate metabolism
0.000
grand mal epilepsy
0.000
peripheral neuropathy
0.000
Altered mental status
0.000
Hypertrophic
0.000
myelinopathy
0.000
Pontocerebellar hypoplasia
0.000
Papillomatosis
0.000
sCJD
0.000
myelitis
0.000
Parinaud's syndrome
0.000
dysphonia
0.000
Cerebellum
0.000
monosomy 9p
0.000
sensory disturbance
0.000
dysphasia
0.000
myopathy
0.000
complex partial seizures
0.000
neuropathy
0.000
psycho-organic syndrome
0.000
stroke
0.000
leukoencephalitis
0.000
FAME
0.000
depression
0.000
FAME
0.000
acalculia
0.000
psychomotor epilepsy
0.000
Hypoxic-ischemic brain injury
0.000
SME
0.000
PDC
0.000
speech disorder
0.000
lymphocytic thymoma
0.000
radiculitis
0.000
audiogenic epilepsy
0.000
early onset schizophrenia
0.000
Systemic inflammatory response syndrome (SIRS)
0.000
Economo
0.000
polyneuropathy
0.000
Kearns-Sayre syndrome
0.000
myelomalacia
0.000
small cell lung cancer
0.000
viral CNS infection
0.000
neuronitis
0.000
Neuroblastoma
0.000
Neuroblastoma
0.000
aseptic meningitis
0.000
febrile convulsions
0.000
neurological infection
0.000
unknown primary cancer
0.000
dyscalculia
0.000
emotional stress
0.000
anteroseptal myocardial infarction
0.000
obsessive-compulsive disorder
0.000
cerebral degeneration
0.000
flutter
0.000
Cortical dysplasia
0.000
autoimmune thyroiditis
0.000
Brain stem
0.000
SPG7
0.000
presenile dementia
0.000
lipidosis
0.000
Acute encephalopathy
0.000
mild mental retardation
0.000
vCJD
0.000
CNS diseases
0.000
cataplexy
0.000
hypomania
0.000
glutaric aciduria
0.000
SUDEP
0.000
solvent abuse
0.000
pachygyria
0.000
autonomic disorder
0.000
sleepwalking
0.000
Inborn errors of metabolism
0.000
aspiration pneumonia
0.000
Bielschowsky
0.000
deafness
0.000
psychogenic disorders
0.000
meningoencephalomyelitis
0.000
motor aphasia
0.000
psychomotor impairment
0.000
SIADH
0.000
Transverse myelitis
0.000
fugue
0.000
tetraplegia
0.000
Wolfram syndrome
0.000
renal failure
0.000
Machado-Joseph disease
0.000
Tay-Sachs disease
0.000
alcoholic neuropathy
0.000
leukodystrophy
0.000
pseudopseudohypoparathyroidism
0.000
scrapie
0.000
sphingolipidosis
0.000
Migraine with aura
0.000
Cranial nerves
0.000
Cranial nerves
0.000
behavior disorder
0.000
nervous system infection
0.000
multiple sclerosis
0.000
vestibular nystagmus
0.000
Hurler
0.000
Oral ulcers
0.000
SPG11
0.000
FANCD1
0.000
herpangina
0.000
respiratory failure
0.000
KRS
0.000
pinealoma
0.000
Complex regional pain syndrome
0.000
Pulmonary infiltrates
0.000
CSE
0.000
pinealoma
0.000
ganglioneuroma
0.000
GCE
0.000
spastic paraplegia
0.000
breast cancer stage
0.000
organic psychosis
0.000
diplopia
0.000
Frontotemporal dementia
0.000
incontinence
0.000
blindness
0.000
perseveration
0.000
conduction aphasia
0.000
Duodenum
0.000
Duodenum
0.000
Wernicke's encephalopathy
0.000
Immune reconstitution inflammatory syndrome
0.000
memory impairment
0.000
schizencephaly
0.000
CLN3
0.000
FUS
0.000
Syndrome
0.000
Friedreich's ataxia
0.000
memory disorder
0.000
Demented
0.000
Lyme carditis
0.000
Canavan
0.000
metabolic disorder
0.000
throat infection
0.000
laryngospasm
0.000
Neurodegenerative Disorders
0.000
streptococcal infection
0.000
audiogenic seizure
0.000
alpha thalassemia
0.000
anarthria
0.000
hyperglycinemia
0.000
leukoencephalopathy
0.000
Canine distemper
0.000
Papilledema
0.000
Nystagmus
0.000
hypohidrosis
0.000
Leber's hereditary optic neuropathy
0.000
Lymphocytic infiltration
0.000
Neonatal seizures
0.000
hyperornithinemia
0.000
organic impotence
0.000
amnesia
0.000
thymoma
0.000
Central diabetes insipidus
0.000
Down syndrome
0.000
severe mental retardation
0.000
PSN
0.000
muscular atrophy
0.000
idiopathic disorder
0.000
Pneumocystis jiroveci pneumonia
0.000
cervical spondylosis
0.000
herpes zoster
0.000
Capgras syndrome
0.000
psychogenic impotence
0.000
Congenital central hypoventilation syndrome
0.000
temporal lobe epilepsy
0.000
myelopathy
0.000
ganglioglioma
0.000
brain dysfunction
0.000
regional pain syndrome
0.000
Behavioral problems
0.000
rare disease
0.000
stuttering
0.000
Aspartylglucosaminuria
0.000
hyperventilation syndrome
0.000
Essential tremor
0.000
trismus
0.000
echolalia
0.000
Middle ear
0.000
vascular disease
0.000
CAPA
0.000
vitamin B12 deficiency
0.000
Fahr's disease
0.000
cerebral palsy
0.000
mania
0.000
TRPS1
0.000
gastrointestinal dysfunction
0.000
cognitive deficit
0.000
Marchiafava-Bignami disease
0.000
Giant
0.000
Krabbe disease
0.000
pachymeningitis
0.000
Facial palsy
0.000
encephalomalacia
0.000
learning disorder
0.000
Norrie disease
0.000
incontinence
0.000
leptomeningitis
0.000
prolapse
0.000
psychotic depression
0.000
meningitis
0.000
tumor
0.000
hypertensive encephalopathy
0.000
onychodystrophy
0.000
Fibrodysplasia ossificans progressiva
0.000
lung carcinoma
0.000
fucosidosis
0.000
PSP
0.000
Niemann-Pick
0.000
agraphia
0.000
NMS
0.000
alcoholism
0.000
SLS
0.000
arteriovenous malformation
0.000
cognitive disorder
0.000
retinopathy
0.000
degenerative disease
0.000
celiac disease
0.000
migraine
0.000
anomia
0.000
uremia
0.000
quadriparesis
0.000
Acute disseminated encephalomyelitis
0.000
scoliosis
0.000
SLS
0.000
chorioretinitis
0.000
Miller Fisher syndrome
0.000
self-injurious behavior
0.000
West
0.000
epidermal nevus syndrome
0.000
autoimmune thyroid disease
0.000
CAA
0.000
arachnodactyly
0.000
CAE
0.000
hepatic coma
0.000
autoimmune disease
0.000
color blindness
0.000
iatrogenic disease
0.000
myasthenia gravis
0.000
HIV encephalopathy
0.000
genetic disorder
0.000
familial Alzheimer disease
0.000
hemiplegic migraine
0.000
bronchopneumonia
0.000
gynecologic cancer
0.000
Degos
0.000
drug withdrawal
0.000
CAE
0.000
diffuse goiter
0.000
Hand, foot, and mouth disease
0.000
Menkes
0.000
ATM
0.000
panic attacks
0.000
dysgraphia
0.000
PARK7
0.000
paralytic ileus
0.000
conversion reaction
0.000
hepatic encephalopathy
0.000
refractory cancer
0.000
metabolic alkalosis
0.000
CADASIL
0.000
Subclinical hypothyroidism
0.000
teratoma
0.000
metastatic neuroblastoma
0.000
osteodystrophy
0.000
scrub typhus
0.000
DBA
0.000
brain edema
0.000
middle ear
0.000
cancer
0.000
Relapsing polychondritis
0.000
neurogenic bladder
0.000
sensory neuropathy
0.000
moderate mental retardation
0.000
CMD
0.000
bilateral cataracts
0.000
CMD
0.000
impotence
0.000
DNT
0.000
Lipoma
0.000
AIDS dementia complex
0.000
chronic renal failure
0.000
citrullinemia
0.000
Stuttering
0.000
sinus tachycardia
0.000
exotropia
0.000
Horner syndrome
0.000
hypermagnesemia
0.000
wasting
0.000
retinitis pigmentosa
0.000
metachromatic leukodystrophy
0.000
motor neuron disease
0.000
common migraine
0.000
ACTH deficiency
0.000
ERS
0.000
CAA
0.000
invasive thymoma
0.000
glycogen storage disease
0.000
amnesic syndrome
0.000
rash
0.000
generalized lipodystrophy
0.000
brachial plexopathy
0.000
enzyme deficiency
0.000
plaque
0.000
glossitis
0.000
Sleep disturbance
0.000
cerebral artery aneurysm
0.000
tuberculous pleurisy
0.000
DWI
0.000
vasculitis
0.000
DES
0.000
hypertension
0.000
retrograde amnesia
0.000
MBS
0.000
CLN2
0.000
lipoma
0.000
myxedema
0.000
EBM
0.000
amaurosis
0.000
pneumonia
0.000
postherpetic neuralgia
0.000
amyotrophic lateral sclerosis
0.000
mannosidosis
0.000
thyroid storm
0.000
brain disorder
0.000
hydrocephalus
0.000
senile dementia
0.000
paraplegia
0.000
agammaglobulinemia
0.000
Binswanger
0.000
sideroblastic anemia
0.000
FTLD
0.000
hypersexuality
0.000
autonomic neuropathy
0.000
more...
Symptom
myoclonus
1.000
dystonia
0.008
ataxia
0.005
Palatal myoclonus
0.004
tremor
0.003
chorea
0.003
cerebellar ataxia
0.003
seizures
0.003
asterixis
0.002
Action myoclonus
0.002
Negative myoclonus
0.001
Objective tinnitus
0.001
athetosis
0.001
tonic-clonic seizure
0.000
clonus
0.000
dysarthria
0.000
Segmental Myoclonus
0.000
Vesical tenesmus
0.000
Hyperekplexia
0.000
intention tremor
0.000
ataxic gait
0.000
Marked rigidity
0.000
startle reaction
0.000
bradykinesia
0.000
clumsiness
0.000
spasticity
0.000
Involuntary Movement
0.000
insomnia
0.000
twitching
0.000
heaviness of the head
0.000
tonic seizure
0.000
Rest tremor
0.000
Diffuse pain
0.000
Persistent insomnia
0.000
ophthalmoplegia
0.000
tinnitus
0.000
muscle rigidity
0.000
Tandem gait
0.000
Jitteriness
0.000
agitation
0.000
abnormal gait
0.000
muscle stiffness
0.000
sleepiness
0.000
Acute dystonia
0.000
Extrapyramidal symptoms
0.000
consciousness disturbance
0.000
hypertonia
0.000
hypotonia
0.000
Mental status changes
0.000
Hemiballism
0.000
weakness
0.000
spasm
0.000
dyslalia
0.000
abnormal reflex
0.000
Drop attacks
0.000
paraparesis
0.000
Other pain
0.000
torticollis
0.000
neurological pain
0.000
Subjective tinnitus
0.000
blepharospasm
0.000
Abdominal tenderness
0.000
cancer pain
0.000
forgetfulness
0.000
partial seizure
0.000
hyperesthesia
0.000
Cervical dystonia
0.000
dizziness
0.000
memory loss
0.000
paresis
0.000
headache
0.000
catatonia
0.000
astasia
0.000
anesthesia
0.000
vertigo
0.000
Spasmodic dysphonia
0.000
pain
0.000
personality change
0.000
Pulsatile tinnitus
0.000
nausea
0.000
hepatosplenomegaly
0.000
incoordination
0.000
hemiplegia
0.000
Ataxic
0.000
visual hallucination
0.000
muscle cramps
0.000
Kayser-Fleischer ring
0.000
lethargy
0.000
Excitability
0.000
Psychiatric symptoms
0.000
pallor
0.000
hypersomnia
0.000
Parkinsonian tremor
0.000
vomiting
0.000
Crawling
0.000
sighing
0.000
Visual symptoms
0.000
motor symptom
0.000
nausea and vomiting
0.000
facial droop
0.000
photopsia
0.000
apathy
0.000
retching
0.000
leg cramps
0.000
meningism
0.000
tachypnea
0.000
paresthesia
0.000
blurred vision
0.000
hypalgesia
0.000
arm weakness
0.000
giddiness
0.000
giddiness
0.000
Opposition
0.000
diarrhea
0.000
hypothermia
0.000
neurological disability
0.000
Decreased activity
0.000
aphonia
0.000
breath holding
0.000
excessive sweating
0.000
stridor
0.000
auditory hallucination
0.000
emaciation
0.000
eds
0.000
Postoperative nausea and vomiting
0.000
body pain
0.000
constipation
0.000
drooling
0.000
fatigue
0.000
snoring
0.000
fasciculation
0.000
Physical findings
0.000
hyperacusis
0.000
Poor sleep
0.000
anorexia
0.000
dyspnea
0.000
enuresis
0.000
dysesthesia
0.000
blackout
0.000
tenesmus
0.000
analgesia
0.000
syncopal episodes
0.000
ketonuria
0.000
numbness
0.000
syncope
0.000
Sedation
0.000
neck stiffness
0.000
limb pain
0.000
anosmia
0.000
CSR
0.000
Ill
0.000
neuralgia
0.000
bone pain
0.000
respiratory distress
0.000
polydipsia
0.000
chills
0.000
urinary frequency
0.000
nasal congestion
0.000
decreased appetite
0.000
asthenia
0.000
tingling
0.000
hepatomegaly
0.000
cough
0.000
physical appearance
0.000
photophobia
0.000
myalgia
0.000
cyanosis
0.000
acute pain
0.000
oliguria
0.000
sneezing
0.000
acute abdominal pain
0.000
skin irritation
0.000
collapse
0.000
distraction
0.000
low back pain
0.000
sore throat
0.000
flushing
0.000
polyuria
0.000
regurgitation
0.000
neck pain
0.000
chest pain
0.000
splenomegaly
0.000
wheezing
0.000
abdominal pain
0.000
thinning
0.000
shortness of breath
0.000
back pain
0.000
functional recovery
0.000
discomfort
0.000
arthralgia
0.000
hypercapnia
0.000
discomfort
0.000
overweight
0.000
erythema
0.000
stigma
0.000
exhaustion
0.000
angina
0.000
Drug
Piracetam
0.000
Sodium valproate
0.000
IHMS
0.000
CSF
0.000
Abecarnil
0.000
Paxil
0.000
Cogentin
0.000
Cogentin
0.000
Paxil
0.000
Paxil
0.000
Hypnomidate
0.000
Xyrem
0.000
Metoclopramide hydrochloride
0.000
Exelon
0.000
Exelon
0.000
Progabide
0.000
Isoprinosine
0.000
Innovar
0.000
Stiripentol
0.000
Cordarone
0.000
Primperan
0.000
Zoloft
0.000
Pregabalin
0.000
Gabapentin
0.000
Cordarone
0.000
Naftidrofuryl
0.000
Buscopan
0.000
Propofol
0.000
DHT
0.000
DHT
0.000
Valproic Acid
0.000
Zonisamide
0.000
Botox
0.000
Anafranil
0.000
Gallamine
0.000
Prozac
0.000
Lisuride
0.000
HPMPC
0.000
GVG
0.000
Conray
0.000
Camphor
0.000
Camphor
0.000
Sinemet
0.000
DBS
0.000
Rituximab
0.000
Sinemet
0.000
Ranolazine
0.000
Ranolazine
0.000
Metrizamide
0.000
Zmax
0.000
Triazolam
0.000
Pilocarpine
0.000
Fentanyl
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SQ 10643
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