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:C0700208 (
scoliosis
)
8,574
document(s) hit in 31,850,051 MEDLINE articles (0.01 seconds)
.
Concepts found in the documents ranked by [
Frequency
|
Pointwise Mutual Information
|
Symmetric Conditional Probability
] .
Human Gene/Protein
G protein-coupled receptor 126
0.001
AIS
0.001
SH3TC2
0.001
CMT4C
0.001
SRS
0.000
T12
0.000
LBX1
0.000
ladybird homeobox 1
0.000
Ras and Rab interactor 2
0.000
ROBO3
0.000
TBX6
0.000
SEPN1
0.000
RIN2
0.000
neurofibromatosis
0.000
Rett syndrome
0.000
Galactose-3-O-sulfotransferase 4
0.000
MYH7 protein
0.000
Hypothetical short protein
0.000
TMEM184C
0.000
26S protease regulatory subunit 8
0.000
GPR126
0.000
CLCF1
0.000
T10
0.000
T11
0.000
fibrillin 15
0.000
golgin, RAB6-interacting
0.000
olfactomedin-like 1
0.000
p59 subunit
0.000
SH3TC2 protein
0.000
ZNF541
0.000
MESP2
0.000
fibrillin-2
0.000
asymmetrical
0.000
COL27A1
0.000
EOS
0.000
horizontal gaze palsy with progressive scoliosis
0.000
TMEM51
0.000
PIGK
0.000
AHNAK nucleoprotein
0.000
FGD4
0.000
cage
0.000
KLHL7
0.000
PPP1R9B
0.000
LFNG
0.000
chromodomain helicase DNA binding protein 2
0.000
GZF1
0.000
frataxin
0.000
DSTYK
0.000
Golgi UDP-GlcNAc transporter
0.000
kyphoscoliosis peptidase
0.000
BNC2
0.000
FBN1
0.000
She
0.000
regulating synaptic membrane exocytosis 2
0.000
Golgi SNAP
0.000
potassium inwardly-rectifying channel
0.000
MEIS3
0.000
EXOC6B
0.000
GOSR2
0.000
CISS
0.000
MRI
0.000
Sotos syndrome
0.000
Chondroadherin
0.000
SNRPB
0.000
ECEL1
0.000
TUBGCP4
0.000
RIPPLY2
0.000
fused
0.000
Rod
0.000
Delta3
0.000
filamin B
0.000
IRX4
0.000
fibrillin
0.000
MECP2
0.000
strabismus
0.000
STAC3
0.000
FKBP10
0.000
PIGU
0.000
NXF5
0.000
SEDC
0.000
SLC8A2
0.000
LL)
0.000
MSTO1
0.000
TMBIM4
0.000
HYDIN2
0.000
myosin light chain, phosphorylatable, fast skeletal muscle
0.000
DA2B
0.000
NSD1
0.000
PLOD2
0.000
PHOSPHO1
0.000
IRX2
0.000
KIAA1217
0.000
SEDT
0.000
COL23A1
0.000
FLNB
0.000
MHC class 1 antigen
0.000
DHX34
0.000
G protein-regulated inducer of neurite outgrowth 1
0.000
MATN1
0.000
Spinocerebellar ataxia 7
0.000
Hes7
0.000
PTDSS1
0.000
TELO2
0.000
calmodulin-binding transcription activator 1
0.000
GNB4
0.000
EDS VI
0.000
CHRNG
0.000
melatonin receptor 1B
0.000
BRWD3
0.000
IER3IP1
0.000
RIMS2
0.000
ZC4H2
0.000
NFIX
0.000
cardiotrophin-like cytokine
0.000
neurofibromatosis type 1
0.000
CFTD
0.000
Homeobox protein
0.000
FSS
0.000
transforming growth factor beta receptor II
0.000
COL1A2
0.000
IRX1
0.000
PIGS
0.000
AICARFT
0.000
SH3PXD2B
0.000
B3GAT3
0.000
SOC3
0.000
MAGEL2
0.000
MEOX1
0.000
KIF22
0.000
TNNT3
0.000
exostosin
0.000
PMP22
0.000
AKAP220
0.000
NPAS1
0.000
GRIN2C
0.000
lysyl hydroxylase 1
0.000
POLE2
0.000
COL1A1
0.000
SLC35A3
0.000
neuronal growth regulator 1
0.000
COG7
0.000
ADAMTS-2
0.000
GPAA1
0.000
phosphatidylinositol-binding clathrin assembly protein
0.000
FRDA
0.000
IFITM5
0.000
LLGL1
0.000
CHRNA
0.000
B3GALT6
0.000
TMCO1
0.000
CHAD
0.000
X-linked recessive
0.000
NXF2
0.000
ubiquitin-protein ligase E3A
0.000
PIGT
0.000
TAL-H
0.000
ARHGAP10
0.000
Ymer
0.000
Filamin B
0.000
gigaxonin
0.000
bromodomain containing 4
0.000
PAX1
0.000
X-linked
0.000
RGMA
0.000
B4GALT7
0.000
ZFYVE26
0.000
KIF6
0.000
COG6
0.000
DTDST
0.000
lysyl hydroxylase
0.000
GAA
0.000
glucose-6-phosphate 1-dehydrogenase
0.000
CAMK2B
0.000
DMRT2
0.000
GORAB
0.000
FBLN1
0.000
SEC24D
0.000
CMT4A
0.000
RYR1
0.000
ZIC4
0.000
AAC1
0.000
MIM
0.000
COH1
0.000
CANT1
0.000
CELSR3
0.000
DNA helicase B
0.000
CHST14
0.000
TPM2
0.000
DOK7
0.000
GNPTAB
0.000
type X collagen
0.000
CHM1
0.000
COL2A1
0.000
lysyl hydroxylase 2
0.000
XYLT2
0.000
FBLN5
0.000
choline kinase beta
0.000
F8C
0.000
TGFBR2
0.000
GEFH1
0.000
NEO1
0.000
SZP
0.000
LTBP3
0.000
SERPINH1
0.000
FHL1
0.000
NKAP
0.000
nuclear factor I/X
0.000
NXF
0.000
STRP
0.000
basonuclin
0.000
ST3GAL5
0.000
cartilage-associated protein
0.000
Fibronectin 1
0.000
USP9X
0.000
MED13L
0.000
NGLY1
0.000
syntaxin-binding protein 1
0.000
ROBO
0.000
Sep
0.000
GNB1
0.000
Ficolin-3
0.000
AJAP1
0.000
GMPPB
0.000
Cystatin B
0.000
ADAMTS-13
0.000
NALCN
0.000
GBS
0.000
TNNI2
0.000
HOXD8
0.000
LTBP4
0.000
MYH7
0.000
P4HB
0.000
WNT1
0.000
AGRN
0.000
PUF60
0.000
XT-I
0.000
collagen
0.000
P3H1
0.000
NF1
0.000
MACS
0.000
NGFI-C
0.000
Lysyl hydroxylase
0.000
IQSEC2
0.000
growth hormone
0.000
LAMA2
0.000
Hip
0.000
COL6A1
0.000
MAGI1
0.000
Nebulin
0.000
homeobox A9
0.000
SCRIB
0.000
TNIK
0.000
CHRNE
0.000
TGFB2
0.000
neurofibromin
0.000
MEGF10
0.000
FK506-binding protein 38
0.000
TN-C
0.000
ARCH
0.000
tropomyosin 3
0.000
supervillin
0.000
MUSK
0.000
CELSR1
0.000
VPS13B
0.000
SCO-spondin
0.000
ASH1L
0.000
GPI transamidase
0.000
Silver syndrome
0.000
TLH
0.000
FKBP22
0.000
Mot
0.000
FKBP65
0.000
DUET
0.000
TPM3
0.000
DLG4
0.000
COL6A2
0.000
ciliary neurotrophic factor receptor
0.000
MYH2
0.000
PSSA
0.000
CRTAP
0.000
ITGB5
0.000
GDF6
0.000
sit
0.000
ADO
0.000
merosin
0.000
MAPK7
0.000
TBC1D24
0.000
GLB1
0.000
Frataxin
0.000
Growth hormone
0.000
TGFB3
0.000
MT2
0.000
CELSR2
0.000
nesprin-2
0.000
SMARCE1
0.000
galactose-1-phosphate uridyl transferase
0.000
CMT2
0.000
serine/threonine kinase 11
0.000
HADHA
0.000
COLQ
0.000
MT4-MMP
0.000
alsin
0.000
deleted in colorectal carcinoma
0.000
MMACHC
0.000
cystathionine-beta-synthase
0.000
RPS6KA3
0.000
P5C
0.000
EPHA4
0.000
WISP3
0.000
Spot14
0.000
Rubinstein-Taybi syndrome
0.000
SMC1A
0.000
MASA
0.000
CMT1
0.000
PMCA4b
0.000
p11
0.000
DSR
0.000
lunatic fringe
0.000
FKBP38
0.000
GDF3
0.000
WDR45
0.000
EDF
0.000
ZIC3
0.000
RBM10
0.000
PQBP1
0.000
NDUFV1
0.000
pycnodysostosis
0.000
AO2
0.000
ZIP8
0.000
SGCA
0.000
Fibroblast growth factor receptor 3
0.000
CALM1
0.000
COL6A3
0.000
ACTA1
0.000
GAP protein
0.000
Aristaless-related homeobox
0.000
FLNA
0.000
Glypican-5
0.000
DNM2
0.000
TIS)
0.000
DUSP22
0.000
PTRF
0.000
FAT4
0.000
ESR2
0.000
Emery-Dreifuss muscular dystrophy
0.000
CHL1
0.000
CAMTA1
0.000
RAI1
0.000
PORCN
0.000
SHOC2
0.000
large aggregating proteoglycan
0.000
FOP
0.000
nesprin-1
0.000
OPLL
0.000
EDNRA
0.000
BMD
0.000
TBL1XR1
0.000
CHD2
0.000
TFAP2B
0.000
KIAA1549
0.000
senataxin
0.000
PIK3CA
0.000
FHL-1
0.000
myelo
0.000
MTM1
0.000
methyl-CpG binding protein 2
0.000
dopa-responsive dystonia
0.000
early growth response 2
0.000
kelch-like
0.000
IRAK3
0.000
9p22
0.000
ATIC
0.000
MTNR1A
0.000
DSCAM
0.000
SPAST
0.000
proteolipid protein 1
0.000
SCO1
0.000
proline hydroxylase
0.000
tyrosine kinase 2
0.000
ninein
0.000
EFEMP1
0.000
Spp1
0.000
TRPV4
0.000
GTB
0.000
EMX2
0.000
PTK7
0.000
EXT2
0.000
TUBB
0.000
periaxin
0.000
NCOR1
0.000
Pericentrin
0.000
site-1 protease
0.000
TARP
0.000
PWS
0.000
FLIR
0.000
myoadenylate deaminase
0.000
NAPA
0.000
RyR1
0.000
SCN4A
0.000
ALMS1
0.000
ABCC9
0.000
CMT1A
0.000
chondrocyte-derived
0.000
TGFBR1
0.000
SYNE1
0.000
CAMA
0.000
LBR
0.000
CREBBP
0.000
ACVR1
0.000
GCH
0.000
PDGFRB
0.000
SIN3A
0.000
ankylosing spondylitis
0.000
PEDF
0.000
NMD
0.000
KCC3
0.000
GRK1
0.000
Holt-Oram syndrome
0.000
forkhead/winged helix transcription factor
0.000
PANK2
0.000
MIS
0.000
GALNS
0.000
filamin C
0.000
ARX
0.000
HSPG2
0.000
UTE
0.000
SBDS
0.000
COMP
0.000
SH2B1
0.000
DTD
0.000
MEP
0.000
CHD8
0.000
SPG7
0.000
TMX
0.000
Creatine kinase
0.000
KID
0.000
HUWE1
0.000
COL11A2
0.000
FED
0.000
GDAP1
0.000
GAN
0.000
ITGB4
0.000
GREM1
0.000
MTNR1B
0.000
EIF2AK3
0.000
type I collagen
0.000
DMR
0.000
MAP3K7
0.000
DOCK8
0.000
MFT
0.000
bone)
0.000
ISS
0.000
BMP1
0.000
TGIF
0.000
OCRL1
0.000
DEGS1
0.000
EXT
0.000
AML3
0.000
ALS2
0.000
dystrophin
0.000
SMA
0.000
HOXA1
0.000
LMX1B
0.000
EPM1
0.000
Cx47
0.000
aldehyde dehydrogenase 1A1
0.000
LMNA
0.000
FEV
0.000
TPH1
0.000
stiff person syndrome
0.000
SPRY4
0.000
MID1
0.000
CLP36
0.000
SOX9
0.000
tenascin-X
0.000
E25
0.000
peripheral myelin protein 22
0.000
CCA
0.000
PSF
0.000
Kir2.1
0.000
PHF6
0.000
JAG1
0.000
SP7
0.000
FAN
0.000
TGR
0.000
ASB
0.000
PMM2
0.000
EDAR
0.000
SOX6
0.000
Trio
0.000
LH2
0.000
TRPS1
0.000
CAD
0.000
thyroid hormone responsive
0.000
NIN
0.000
FISH
0.000
creatine kinase
0.000
FGS
0.000
ROR2
0.000
GM3 synthase
0.000
DBL
0.000
ATXN2
0.000
MLT
0.000
PAX9
0.000
extracellular signal-regulated kinase 5
0.000
ASAP
0.000
axonemal dynein
0.000
NF90
0.000
IRK1
0.000
TDT
0.000
NOTCH2
0.000
RALDH2
0.000
fukutin
0.000
MYOD
0.000
SOX5
0.000
GRIN2A
0.000
CNTNAP2
0.000
NRXN1
0.000
EP300
0.000
ARID1B
0.000
Fibroblast growth factor receptor
0.000
NEB
0.000
LRP4
0.000
ELN
0.000
fibulin-1
0.000
CMM
0.000
contractile protein
0.000
P37
0.000
PLA2G6
0.000
kid
0.000
panhypopituitarism
0.000
UBE3A
0.000
LIMK
0.000
lysosomal alpha-mannosidase
0.000
Lamin A/C
0.000
LBP
0.000
SNRPN
0.000
AF10
0.000
NIPBL
0.000
PTPN11
0.000
Delta-like 1
0.000
neuronal apoptosis inhibitory protein
0.000
FGFR3
0.000
voltage-dependent anion channel 1
0.000
DMD
0.000
DUSP6
0.000
axonal
0.000
neuron-specific protein
0.000
reserved
0.000
myelin protein zero
0.000
SEP
0.000
TES
0.000
ACTN3
0.000
Pendrin
0.000
ALR
0.000
COL5A1
0.000
FLG
0.000
p36
0.000
GTX
0.000
kinesin-like protein
0.000
MEF
0.000
signal protein
0.000
PICALM
0.000
CPO
0.000
prune
0.000
NOTCH3
0.000
ATK
0.000
COL10A1
0.000
Alagille syndrome
0.000
lumican
0.000
Fukuyama-type congenital muscular dystrophy
0.000
BIN1
0.000
GRIP1
0.000
NPR-B
0.000
LH1
0.000
Polo-like kinase 4
0.000
ALDH1A3
0.000
type I procollagen
0.000
NADH-ubiquinone reductase
0.000
lamin A/C
0.000
PTCH
0.000
MMP-3
0.000
FN1
0.000
NADH diaphorase
0.000
SATB2
0.000
CDH13
0.000
RAD21
0.000
CYP2
0.000
A27
0.000
MAC
0.000
gamma-sarcoglycan
0.000
EGR2
0.000
proteoglycan core protein
0.000
HSS
0.000
PEF
0.000
ASK
0.000
myotubularin
0.000
ANOVA
0.000
CRHR1
0.000
MEIS1
0.000
TEF
0.000
FOXC1
0.000
GRIN2B
0.000
aggrecan
0.000
ALDH1A2
0.000
methyl CpG binding protein 2
0.000
CMAP
0.000
DPS
0.000
myosin
0.000
MRX
0.000
tissue-nonspecific alkaline phosphatase
0.000
leptin
0.000
ADAMTS-4
0.000
insulin-like growth factor 1 receptor
0.000
CAM
0.000
swan
0.000
osteogenic
0.000
Y14
0.000
matrix protein
0.000
signal transducer and activator of transcription 3
0.000
LIMK1
0.000
proteoglycan
0.000
pallid
0.000
CTM
0.000
SMARCB1
0.000
pseudocholinesterase
0.000
ESR1
0.000
rapsyn
0.000
necdin
0.000
RSK2
0.000
protein kinase C delta
0.000
pantothenate kinase
0.000
ABCC6
0.000
T13
0.000
FOXC2
0.000
Mol
0.000
CDKL5
0.000
KCNQ3
0.000
osteocalcin
0.000
NT3
0.000
more...
Disease
scoliosis
1.000
spondylolisthesis
0.002
Horizontal gaze palsy
0.002
IS1
0.001
Scheuermann's disease
0.001
Neuromuscular scoliosis
0.001
arachnodactyly
0.001
diastematomyelia
0.001
syringomyelia
0.001
CMT4C
0.001
AIS
0.000
spinal stenosis
0.000
Infantile idiopathic scoliosis
0.000
SRS
0.000
Klippel
0.000
Marfan syndrome
0.000
arthrodesis
0.000
spondylolysis
0.000
cerebral palsy
0.000
osteogenesis imperfecta
0.000
Kyphosis and lordosis
0.000
Proteus syndrome
0.000
CISS1
0.000
Bruck syndrome
0.000
neurofibromatosis
0.000
CISS2
0.000
dysplasia
0.000
Rett syndrome
0.000
Duchenne muscular dystrophy
0.000
disc degeneration
0.000
Friedreich's ataxia
0.000
myopathy
0.000
MURCS ASSOCIATION
0.000
Postoperative pneumothorax
0.000
Drug-induced diabetes mellitus
0.000
Biconcave vertebrae
0.000
VACTERL ASSOCIATION
0.000
Scoliosis associated with other conditions
0.000
Resolving infantile idiopathic scoliosis
0.000
macrocephaly
0.000
Posterior
0.000
degenerative disc disease
0.000
developmental delay
0.000
neurofibromatosis type 1
0.000
muscular atrophy
0.000
Generalized osteopenia
0.000
Protrusio acetabuli
0.000
Neuropathic arthritis
0.000
Man-in-the-barrel syndrome
0.000
BRKS1
0.000
BRKS2
0.000
partial monosomy 2q
0.000
Iliac vein thrombosis
0.000
Thoracolumbar scoliosis
0.000
osteoma
0.000
Thoracic
0.000
funnel chest
0.000
SPONASTRIME
0.000
spondyloepiphyseal dysplasia
0.000
EOS
0.000
EOS
0.000
Charcot-Marie-Tooth disease
0.000
Distal arthrogryposis
0.000
mental retardation
0.000
mental retardation
0.000
Anterior
0.000
Amyloid neuropathy
0.000
Peripheral sensorimotor neuropathy
0.000
Progression of rheumatoid arthritis
0.000
Miles-Carpenter syndrome
0.000
camptocormia
0.000
Congenital fiber type disproportion
0.000
muscular dystrophy
0.000
paraplegia
0.000
Jarcho-Levin syndrome
0.000
spondylosis
0.000
Hydrosyringomyelia
0.000
Sponastrime dysplasia
0.000
CMT1E
0.000
Localized tetanus
0.000
osteoarthritis of the lumbar spine
0.000
Pisa syndrome
0.000
Marshall-Smith syndrome
0.000
Osteoblastoma
0.000
osteoporosis
0.000
Superior mesenteric artery syndrome
0.000
genetic disorder
0.000
dentinogenesis imperfecta
0.000
Esophageal atresia/tracheoesophageal fistula
0.000
Choanal stenosis
0.000
Multiple joint contractures
0.000
Progressive pulmonary hypertension
0.000
DA7
0.000
acrorenal syndrome
0.000
facet joint degeneration
0.000
radiculopathy
0.000
Hepatic osteodystrophy
0.000
Restrictive lung disease
0.000
Neuhauser syndrome
0.000
HIES
0.000
neuromuscular disorder
0.000
FSS
0.000
respiratory failure
0.000
Sotos syndrome
0.000
recombinant 8 syndrome
0.000
CMT2B1
0.000
Staphylococcus epidermidis meningitis
0.000
Scapuloperoneal spinal muscular atrophy
0.000
diploid/triploid mixoploidy
0.000
labile personality
0.000
severe mental retardation
0.000
polio
0.000
Linear and whorled nevoid hypermelanosis
0.000
ring chromosome 12
0.000
Wilms' tumor stage
0.000
XLAG
0.000
de Barsy syndrome
0.000
congenital dislocation of the hip
0.000
cleft palate
0.000
anal atresia
0.000
Vertebral column
0.000
Vertebral column
0.000
LQT7
0.000
spondyloperipheral dysplasia
0.000
Spinal instability
0.000
spondylopathy
0.000
Ehlers-Danlos syndrome
0.000
familial dysautonomia
0.000
uniparental disomy of chromosome 14
0.000
tetraplegia
0.000
Hajdu-Cheney syndrome
0.000
14q deletion syndrome
0.000
CMT2B2
0.000
tetrasomy 18p
0.000
protruded disk
0.000
brachycephaly
0.000
mitral valve prolapse
0.000
Wildervanck syndrome
0.000
heritable connective tissue disorder
0.000
CACP
0.000
trisomy 19q
0.000
Bronchial compression
0.000
tetrasomy 15q
0.000
Vertebral anomalies
0.000
Ullrich
0.000
malignant hyperthermia
0.000
flatback syndrome
0.000
SMA II
0.000
FRDA
0.000
trisomy 15q
0.000
epiphysis
0.000
CM1
0.000
Rebound hypertension
0.000
partial monosomy 6q
0.000
ter Haar syndrome
0.000
Brachyolmia
0.000
Blount
0.000
Leg length discrepancy
0.000
prolapse
0.000
Goldenhar syndrome
0.000
MPS IVB
0.000
hydrocephalus
0.000
Osteoid osteoma
0.000
lumbar spondylosis
0.000
EDS VI
0.000
Angelman syndrome
0.000
partial trisomy 6q
0.000
floppy baby syndrome
0.000
Jaffe-Campanacci syndrome
0.000
Atlantoaxial instability
0.000
Degenerative lumbar spinal stenosis
0.000
Central core disease
0.000
tracheomalacia
0.000
connective tissue disease
0.000
megalocornea
0.000
lipoma
0.000
Rud syndrome
0.000
Spondyloepiphyseal dysplasia tarda
0.000
Lumbar spinal stenosis
0.000
esophageal atresia
0.000
Martsolf syndrome
0.000
spinal degeneration
0.000
Roussy-Levy
0.000
CMT2K
0.000
Intervertebral disc calcification
0.000
Morquio
0.000
enchondromatosis
0.000
nerve root compression
0.000
strabismus
0.000
cutis laxa
0.000
achondroplasia
0.000
pseudocroup
0.000
Meningocele
0.000
Dysostosis
0.000
hypomelanosis of Ito
0.000
Kugelberg-Welander
0.000
ganglioneuroma
0.000
degenerative disease
0.000
DTD
0.000
decubitus
0.000
Mayer-Rokitansky-Kuster-Hauser syndrome
0.000
MWS
0.000
osteodysplastic primordial dwarfism
0.000
familial hypophosphatemia
0.000
OIC
0.000
Cardiorespiratory failure
0.000
sacralization
0.000
nystagmus
0.000
chondrodysplasia
0.000
Speckled lentiginous nevus
0.000
Cohen syndrome
0.000
gastroesophageal reflux disease
0.000
Andermann syndrome
0.000
Neuroaxonal dystrophy
0.000
craniosynostosis
0.000
herniated disc
0.000
MOPD II
0.000
Skeletal dysplasia
0.000
CMT4A
0.000
epidermal nevus syndrome
0.000
hypertrichosis
0.000
hernia
0.000
Giant axonal neuropathy
0.000
cardiomyopathy
0.000
trisomy 10q
0.000
cor pulmonale
0.000
sensory disturbance
0.000
trisomy 8q
0.000
myopia
0.000
VATER association
0.000
Klippel-Trenaunay syndrome
0.000
blepharophimosis
0.000
partial trisomy 2p
0.000
unable to remember
0.000
Amniotic band
0.000
cafe au lait spots
0.000
Mucolipidosis
0.000
Spinal muscular atrophy
0.000
foot drop
0.000
COL2A1
0.000
Coffin-Siris syndrome
0.000
SGS
0.000
Kniest dysplasia
0.000
hyperostosis
0.000
hemolymphangioma
0.000
Premature adrenarche
0.000
Brown-Sequard
0.000
back disorder
0.000
RSS
0.000
pulmonary insufficiency
0.000
claudication
0.000
LGMD2D
0.000
Hurler-Scheie syndrome
0.000
triplegia
0.000
hereditary motor and sensory neuropathy
0.000
spondylitis
0.000
Dandy-Walker malformation
0.000
epilepsy
0.000
MDC1A
0.000
Gastric dilatation
0.000
spinal cord compression
0.000
myelopathy
0.000
Costello syndrome
0.000
congenital disorder
0.000
osteoarthropathy
0.000
Tarlov cyst
0.000
Degenerative spondylolisthesis
0.000
nevoid basal cell carcinoma syndrome
0.000
Askin tumor
0.000
Baastrup
0.000
Nevus comedonicus
0.000
lung disease
0.000
HMSN II
0.000
multicore
0.000
cardiofaciocutaneous syndrome
0.000
metastatic Wilms' tumor
0.000
Metallosis
0.000
lipomatosis
0.000
hematomyelia
0.000
tetrasomy 9p
0.000
stereotypies
0.000
neurobehavioral problems
0.000
osteochondrosis
0.000
49,XXXXY syndrome
0.000
Lumbar disc herniation
0.000
HCG
0.000
moderate mental retardation
0.000
primary amenorrhea
0.000
Cerebro-costo-mandibular syndrome
0.000
3p- syndrome
0.000
atrial septal defect
0.000
syringobulbia
0.000
mild mental retardation
0.000
hereditary ataxia
0.000
Congenital anomalies
0.000
Pycnodysostosis
0.000
velocardiofacial syndrome
0.000
AIC
0.000
trisomy
0.000
external genitalia
0.000
mole
0.000
trisomy 14
0.000
Hopkins syndrome
0.000
Taybi
0.000
Piriformis syndrome
0.000
Lowe
0.000
hypogonadism
0.000
chronic urinary tract infection
0.000
neuropathy
0.000
Floating-Harbor syndrome
0.000
INAD
0.000
SWS
0.000
BMD
0.000
osteoarthritis
0.000
Dubowitz
0.000
Osteopathia striata with cranial sclerosis
0.000
multiple nevi
0.000
dup(3q) syndrome
0.000
discitis
0.000
osteochondrodysplasia
0.000
musculoskeletal disease
0.000
Turner syndrome
0.000
Neonatal encephalopathy
0.000
Larsen
0.000
Body image disturbance
0.000
heart disease
0.000
Syndrome
0.000
conotruncal anomaly face syndrome
0.000
congenital cardiovascular anomaly
0.000
incomplete paraplegia
0.000
hereditary sensory neuropathy
0.000
Kaposiform hemangioendothelioma
0.000
Brown-Sequard syndrome
0.000
LCP
0.000
Carpenter syndrome
0.000
neurofibroma
0.000
hematometra
0.000
pneumothorax
0.000
Epidermal nevus syndrome
0.000
Metabolic bone disease
0.000
goniodysgenesis
0.000
osteochondritis
0.000
ventricular septal defect
0.000
ganglioneuromatosis
0.000
Pyle
0.000
osteomyelitis
0.000
arthropathy
0.000
Postural orthostatic tachycardia syndrome
0.000
Wolcott-Rallison syndrome
0.000
monosomy 9p
0.000
mucopolysaccharidosis
0.000
profound mental retardation
0.000
Pseudoachondroplasia
0.000
pelvic instability
0.000
FGS
0.000
psychological disturbance
0.000
Tapia
0.000
Southeast Asian ovalocytosis
0.000
Parathyroid adenoma
0.000
mixed deafness
0.000
Postoperative infection
0.000
Amniotic band syndrome
0.000
Fukuyama congenital muscular dystrophy
0.000
hereditary neuropathy
0.000
Unicameral bone cyst
0.000
LGMD2C
0.000
Spondyloarthritis
0.000
plexiform neurofibroma
0.000
chylothorax
0.000
arachnoiditis
0.000
Recklinghausen
0.000
CMT1A
0.000
thoracic outlet syndrome
0.000
ML III
0.000
rickets
0.000
oligohydramnios
0.000
progressive muscular atrophy
0.000
spondyloarthropathy
0.000
Juvenile hyaline fibromatosis
0.000
Kenny-Caffey syndrome
0.000
Conradi
0.000
obesity
0.000
Escherichia coli meningitis
0.000
bronchomalacia
0.000
osteosclerosis
0.000
Emery-Dreifuss muscular dystrophy
0.000
Mesenchymal hamartoma
0.000
Allan-Herndon-Dudley syndrome
0.000
WT1
0.000
AN2
0.000
Oropharyngeal dysphagia
0.000
radioulnar synostosis
0.000
Robin
0.000
OPLL
0.000
homocystinuria
0.000
quadriparesis
0.000
Fibrodysplasia ossificans progressiva
0.000
sclera
0.000
Myofascial pain syndrome
0.000
osteochondroma
0.000
Pulmonary actinomycosis
0.000
hemangioma
0.000
Brachydactyly
0.000
chondrolysis
0.000
SMS
0.000
trisomy 8
0.000
Congenital muscular dystrophy
0.000
Becker's nevus
0.000
periostitis
0.000
failure to thrive
0.000
CCV
0.000
Pelizaeus-Merzbacher
0.000
delayed puberty
0.000
Mongolian spots
0.000
phosphaturic mesenchymal tumor
0.000
SPG7
0.000
neurofibrosarcoma
0.000
Perthes disease
0.000
trisomy 9
0.000
elective mutism
0.000
generalized lipodystrophy
0.000
coxarthrosis
0.000
Cornelia de Lange syndrome
0.000
Robinow syndrome
0.000
deafness
0.000
Central retinal artery occlusion
0.000
periostosis
0.000
chromosome disorder
0.000
TRPS1
0.000
immaturity
0.000
Maffucci's syndrome
0.000
Growth failure
0.000
Alexander disease
0.000
precocious puberty
0.000
EXT2
0.000
Pilocytic astrocytoma
0.000
mitochondrial myopathy
0.000
optic atrophy
0.000
MBS
0.000
trismus
0.000
Fibrous dysplasia
0.000
disabling disease
0.000
gum disease
0.000
Seckel syndrome
0.000
TAR syndrome
0.000
tumor
0.000
18q- syndrome
0.000
polyneuropathy
0.000
hypophosphatasia
0.000
conductive hearing loss
0.000
Ruvalcaba syndrome
0.000
Morquio A syndrome
0.000
apophysitis
0.000
Poland
0.000
sleep apnea
0.000
Dental disease
0.000
Portopulmonary hypertension
0.000
delayed speech
0.000
ankylosing spondylitis
0.000
delayed language
0.000
FED
0.000
Aneurysmal bone cyst
0.000
CLS
0.000
periodic paralysis
0.000
ileus
0.000
6th nerve palsy
0.000
FDH
0.000
sirenomelia
0.000
poliosis
0.000
Abdominal compartment syndrome
0.000
sphingolipidosis
0.000
Bornholm
0.000
Cranial nerves
0.000
Cranial nerves
0.000
Axenfeld-Rieger syndrome
0.000
emotional upset
0.000
trisomy 1q
0.000
chondroblastic osteosarcoma
0.000
ganglioglioma
0.000
eye movement disorder
0.000
Ossifying fibroma
0.000
gangliosidosis
0.000
Bone sarcomas
0.000
apraxia
0.000
myelodysplastic syndrome
0.000
aspiration pneumonia
0.000
ICC
0.000
hydronephrosis
0.000
fibrothorax
0.000
gastroschisis
0.000
postpolio syndrome
0.000
ICC
0.000
sensorineural hearing loss
0.000
dysphagia
0.000
Werdnig-Hoffmann disease
0.000
spastic paraplegia
0.000
learning disability
0.000
Freiberg
0.000
radiculitis
0.000
acroosteolysis
0.000
dental abscess
0.000
TTP
0.000
DRD
0.000
Osteoradionecrosis
0.000
LMS
0.000
LMS
0.000
Cornelia de Lange
0.000
hemangiomatosis
0.000
conduction aphasia
0.000
natal teeth
0.000
growth hormone deficiency
0.000
ALS2
0.000
anhidrosis
0.000
osteopetrosis
0.000
optic nerve glioma
0.000
LDS
0.000
melanosis coli
0.000
Pineal
0.000
hypotrichosis
0.000
bone disease
0.000
Caffey's disease
0.000
eczema
0.000
Oculopharyngeal muscular dystrophy
0.000
encephalopathy
0.000
Vascular lesions
0.000
orphan disease
0.000
pulmonary hypertension
0.000
Trachea
0.000
Trachea
0.000
wasting
0.000
Morel
0.000
Trachea
0.000
anarthria
0.000
DiGeorge syndrome
0.000
Mandible
0.000
chronic pain
0.000
leukodystrophy
0.000
ASAP
0.000
spastic diplegia
0.000
Steinbrocker
0.000
Weber syndrome
0.000
secondary amenorrhea
0.000
Upper airway obstruction
0.000
acanthosis nigricans
0.000
polyneuritis
0.000
pachygyria
0.000
osteodystrophy
0.000
recurrent cystitis
0.000
cleft lip/palate
0.000
Ewing's sarcoma
0.000
Lowe syndrome
0.000
familial hemophagocytic lymphohistiocytosis
0.000
myelomalacia
0.000
biventricular failure
0.000
LGS
0.000
SHS
0.000
CMTX
0.000
intellectual impairment
0.000
GAN
0.000
teratoma
0.000
CCD
0.000
cervical spondylosis
0.000
ectodermal dysplasia
0.000
hearing disability
0.000
astrocytoma
0.000
developmental disabilities
0.000
Hurler
0.000
protein deficiency
0.000
postphlebitic syndrome
0.000
dyschondroplasia
0.000
Roth
0.000
DMC
0.000
SPG4
0.000
Spinal cord ischemia
0.000
empyema
0.000
mitral regurgitation
0.000
Angle Class II
0.000
Opitz
0.000
cauda equina syndrome
0.000
Behavioral problems
0.000
hypertrophic cardiomyopathy
0.000
trisomy 22
0.000
hemiparkinsonism
0.000
Kartagener's syndrome
0.000
enchondroma
0.000
Menetrier's disease
0.000
reactive airway disease
0.000
movement disorder
0.000
Meigs' syndrome
0.000
Cavernous hemangioma
0.000
neurodermatitis
0.000
external ear
0.000
incontinence
0.000
malnutrition
0.000
pathological fracture
0.000
Ogilvie's syndrome
0.000
neurological disease
0.000
fibromyalgia
0.000
fibromatosis
0.000
pneumonia
0.000
megacolon
0.000
gingivostomatitis
0.000
DSS
0.000
skin ulcers
0.000
arthritis of the knee
0.000
ARF
0.000
Best
0.000
chylopericardium
0.000
neurogenic bladder
0.000
septal defect
0.000
paramyotonia
0.000
FMD
0.000
idiopathic cardiomyopathy
0.000
diffuse sclerosis
0.000
Esophageal perforation
0.000
Spontaneous pneumothorax
0.000
EVA
0.000
Pfeiffer syndrome
0.000
leptomeningitis
0.000
kidney hypertrophy
0.000
retrograde menstruation
0.000
Lequesne
0.000
autism
0.000
taurodontism
0.000
MAC
0.000
ischemic optic neuropathy
0.000
onychodystrophy
0.000
Vidal
0.000
dyskinesia
0.000
panhypopituitarism
0.000
CHARGE syndrome
0.000
torsion dystonia
0.000
ichthyosis
0.000
benign tumor
0.000
angioid streaks
0.000
cri-du-chat syndrome
0.000
psychological impairment
0.000
bronchiectasis
0.000
Deafness
0.000
Quervain
0.000
more...
Symptom
back pain
0.001
hypotonia
0.000
weakness
0.000
torticollis
0.000
distraction
0.000
pain
0.000
low back pain
0.000
spasticity
0.000
leg pain
0.000
prominent nose
0.000
Halo
0.000
anesthesia
0.000
paraparesis
0.000
Generalized fatigue
0.000
musculoskeletal back pain
0.000
poor balance and coordination
0.000
Antecollis
0.000
Tandem gait
0.000
chest restriction
0.000
ataxia
0.000
Easy bruising
0.000
hypertrophic breast
0.000
Night pain
0.000
lumbar instability
0.000
Persistent vomiting
0.000
Lasegue's sign
0.000
Neurogenic pain
0.000
Sensory ataxia
0.000
Ankle stiffness
0.000
Quadriceps weakness
0.000
abnormal gait
0.000
rib pain
0.000
thoracic back pain
0.000
iridodonesis
0.000
Pyramidal signs
0.000
Poor weight gain
0.000
dystonia
0.000
ophthalmoplegia
0.000
seizures
0.000
hypertonia
0.000
analgesia
0.000
Q angle
0.000
neck pain
0.000
delayed language development
0.000
finger pain
0.000
lumbar back pain
0.000
dysarthria
0.000
physical appearance
0.000
ataxic gait
0.000
Radicular pain
0.000
chronic back pain
0.000
coccygodynia
0.000
monoplegia
0.000
loss of balance
0.000
Plantar flexion
0.000
sciatica
0.000
Central pain
0.000
abnormal breathing
0.000
Referred pain
0.000
Joint hypermobility
0.000
abnormal reflex
0.000
paresis
0.000
Organ failure
0.000
nerve root irritation
0.000
Spontaneous nystagmus
0.000
athetosis
0.000
constipation
0.000
discomfort
0.000
numbness
0.000
discomfort
0.000
cerebellar ataxia
0.000
drooling
0.000
thigh pain
0.000
Spastic
0.000
abiotrophy
0.000
Lhermitte's sign
0.000
asthenia
0.000
Postoperative pain
0.000
dyspnea
0.000
hypercapnia
0.000
sighing
0.000
growing pains
0.000
Buckling
0.000
cyanosis
0.000
cardiovascular impairment
0.000
Platypnea
0.000
clonus
0.000
myoclonus
0.000
female puberty
0.000
fatigue
0.000
arthralgia
0.000
Catch
0.000
hyperesthesia
0.000
collapse
0.000
thinning
0.000
hip pain
0.000
Physical findings
0.000
Severe pain
0.000
cough
0.000
exertional dyspnea
0.000
leg edema
0.000
scaly skin
0.000
hypalgesia
0.000
respiratory distress
0.000
enuresis
0.000
pachyonychia
0.000
Regurgitation
0.000
arm weakness
0.000
vomiting
0.000
groin pain
0.000
bone pain
0.000
Spots
0.000
inanition
0.000
disturbed balance
0.000
headache
0.000
ACHE
0.000
clumsiness
0.000
paresthesia
0.000
spasm
0.000
blepharospasm
0.000
shortness of breath
0.000
joint stiffness
0.000
hypothermia
0.000
neck stiffness
0.000
cachexia
0.000
abdominal pain
0.000
incoordination
0.000
rales
0.000
limb pain
0.000
elbow pain
0.000
chronic constipation
0.000
myalgia
0.000
Psychiatric symptoms
0.000
metatarsalgia
0.000
prostration
0.000
stridor
0.000
tremor
0.000
clubbing
0.000
bloating
0.000
dysesthesia
0.000
neuralgia
0.000
hemiplegia
0.000
vertigo
0.000
Respiratory symptoms
0.000
hepatomegaly
0.000
nausea and vomiting
0.000
muscle rigidity
0.000
hemoptysis
0.000
regurgitation
0.000
skin irritation
0.000
overweight
0.000
muscle stiffness
0.000
adenitis
0.000
Gastrointestinal symptoms
0.000
atypical chest pain
0.000
nausea
0.000
anorexia
0.000
shoulder pain
0.000
photophobia
0.000
livedo
0.000
epigastric pain
0.000
lethargy
0.000
flank pain
0.000
acute pain
0.000
Stiffness
0.000
pelvic pain
0.000
dry skin
0.000
bradykinesia
0.000
hot flashes
0.000
chest pain
0.000
hepatosplenomegaly
0.000
pallor
0.000
nasal congestion
0.000
knee pain
0.000
tingling
0.000
fasciculation
0.000
syncope
0.000
splenomegaly
0.000
menopausal symptoms
0.000
hypocapnia
0.000
oliguria
0.000
twitching
0.000
tense
0.000
exhaustion
0.000
rhinorrhea
0.000
hopelessness
0.000
tachypnea
0.000
Wind
0.000
sore throat
0.000
snoring
0.000
hoarseness
0.000
polyuria
0.000
acute abdomen
0.000
sleepiness
0.000
apathy
0.000
chills
0.000
dizziness
0.000
insomnia
0.000
wheezing
0.000
ENT
0.000
hunger
0.000
stigma
0.000
functional recovery
0.000
flushing
0.000
diarrhea
0.000
Ill
0.000
agitation
0.000
erythema
0.000
starvation
0.000
Drug
Deflazacort
0.000
Arfonad
0.000
Growth hormone
0.000
Growth hormone
0.000
Somatropin
0.000
Arfonad
0.000
CXM
0.000
Sulla
0.000
Posture
0.000
Triptorelin
0.000
TMX
0.000
Metrizamide
0.000
Cobalamin
0.000
Aprotinin
0.000
Frontal
0.000
Conray
0.000
Thiopentone
0.000
Monit
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Bayer
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vitamin E
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lysyl hydroxylase
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galactosyltransferase I
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coagulation factor VIIa
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hatching enzyme
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CAD
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CAD
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creatine kinase
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phosphatidylinositol-4,5-bisphosphate 3-kinase
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pantothenate kinase
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proline oxidase
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alkaline phosphatase
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nucleotide pyrophosphatase
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rhodopsin kinase
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methylmalonyl-CoA mutase
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chymopapain
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nucleotidase
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myosin ATPase
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lysyl oxidase
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endothelin-converting enzyme
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DAT
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ubiquitin-protein ligase
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cathepsin K
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methionine synthase
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methionine synthase
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acyl-CoA dehydrogenase
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thromboplastin
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triphosphatase
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apyrase
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sialyltransferase
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mitogen-activated protein kinase
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succinic dehydrogenase
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glycerol-3-phosphate dehydrogenase
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acetylcholinesterase
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glycerol-3-phosphate dehydrogenase
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prolyl hydroxylase
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citrate synthase
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cholinesterase
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succinate dehydrogenase
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methylenetetrahydrofolate reductase
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methylenetetrahydrofolate reductase
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pepsin
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focal adhesion kinase
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phosphoglycerate kinase
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matrix metalloproteinase 9
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phosphorylase
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lipase
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carboxylesterase
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isocitrate dehydrogenase
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luciferase
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furin
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proteasome
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isocitrate dehydrogenase
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beta-galactosidase
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thrombin
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cytochrome oxidase
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renin
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phosphoinositide 3-kinase
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catalase
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ribonuclease
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ribonuclease
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lactate dehydrogenase
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caspase-9
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beta-glucuronidase
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glucose-6-phosphate dehydrogenase
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collagenase
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guanylate cyclase
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complex I
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gamma-glutamyl transpeptidase
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elastase
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alcohol dehydrogenase
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aspartate aminotransferase
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phosphatidylinositol 3-kinase
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protein kinase
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phospholipase A2
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neuraminidase
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superoxide dismutase
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caspase-3
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phosphodiesterase
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glutathione S-transferase
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alanine aminotransferase
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reverse transcriptase
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protein kinase C
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MB 1
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titanium
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Dec
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Trimethaphan
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dihydrosphingosine-1-phosphate
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2-hydroxy-3-methoxybenzaldehyde
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AICA-riboside
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SD 25
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keratan sulfate
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calcium
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TIF
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vitamin D
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ASK
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Botulinum toxin type A
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oxygen
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hexuronic acid
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hexuronic acid
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hexuronic acid
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hexuronic acid
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DLT
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TGT
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6-12
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PID
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barium
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SET
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Toluidine blue
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Isoform
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Deoxyribonucleic acid
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ASA
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pentosidine
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homocysteine
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piperidine
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piperidine
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betaine
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phosphate
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zinc
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selenium
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water
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retinoic acid
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sulfate
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TCP
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TCP
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TCP
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TCP
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boric acid
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hyaluronic acid
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PPi
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CAT
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25-dihydroxycholecalciferol
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valine
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creatinine
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coenzyme Q10
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leucine
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isoxazole
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copper
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nicotinamide
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iron
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phosphorus
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cobalt
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aluminum
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glucose
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silver
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cadmium
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serine
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nicotinic acid
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retinol
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aflatoxin B1
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galactose
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phosphocreatine
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proline
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hydroxylamine
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strontium
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manganese
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hydroxylamine
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aspartic acid
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FK506
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hexose
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hexose
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cAMP
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bromide
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gamma-aminobutyric acid
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fluorine
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nickel
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alcohol dehydrogenase
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tryptophan
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tryptophan
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hexose
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TCA
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tryptophan
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isopropanol
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nitrogen
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isoleucine
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phosphoric acid
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tryptophan
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isoleucine
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aldosterone
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threonine
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salicylic acid
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sodium chloride
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formaldehyde
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silicon
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formaldehyde
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pyrimidine
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hydrogen
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phenol
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acetate
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noradrenaline
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acetic acid
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nitric oxide
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iodine
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nitrate
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methionine
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methanol
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BMC
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