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MeSH keywords -> Related genes, diseases (OMIM)


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01 Spine [NCBI]

Gene


 Gene Link Information
Gain		 01
AIS [NCBI] 0.00952492
FOP [NCBI] 0.000479488
SPOAN [NCBI] 0.000331755
HFM [NCBI] 0.000269618
PAX1 [NCBI] 0.000150052
MS [NCBI] 0.000100317
DLL3 [NCBI] 8.20206e-05
VDR [NCBI] 7.06989e-05
PTH [NCBI] 6.23852e-05
BMP2 [NCBI] 3.1368e-05
ESR1 [NCBI] 2.51915e-05
FGFR3 [NCBI] 2.11024e-05
ACP5 [NCBI] 1.91899e-05
SEPN1 [NCBI] 1.69402e-05
FLNB [NCBI] 1.65478e-05
COL2A1 [NCBI] 1.58036e-05
HOXC8 [NCBI] 1.57934e-05
COL1A1 [NCBI] 1.55343e-05
LRP5 [NCBI] 1.47573e-05
CBX4 [NCBI] 1.35942e-05
TBX6 [NCBI] 1.3409e-05
GDF11 [NCBI] 1.10694e-05
HOXB8 [NCBI] 1.07254e-05
TGFB1 [NCBI] 1.00873e-05
TRAPPC2 [NCBI] 1.00226e-05
MGP [NCBI] 9.92792e-06
ROR2 [NCBI] 9.34002e-06
DLL1 [NCBI] 9.18836e-06
HIP1 [NCBI] 8.71432e-06
ALPL [NCBI] 8.67635e-06
FOXC2 [NCBI] 8.23937e-06
PDLIM7 [NCBI] 8.01169e-06
GDF5 [NCBI] 7.55747e-06
ZFP90 [NCBI] 7.22635e-06
TNFRSF1B [NCBI] 7.22436e-06
COL11A2 [NCBI] 7.15355e-06
NOG [NCBI] 7.08943e-06
ENPP1 [NCBI] 7.0685e-06
HOXA9 [NCBI] 7.01919e-06
GLI3 [NCBI] 6.84831e-06
HES7 [NCBI] 6.70259e-06
SLC35A3 [NCBI] 6.36252e-06
MESP2 [NCBI] 6.36252e-06
WDR8 [NCBI] 5.90826e-06
ESR2 [NCBI] 5.48447e-06
HOXC5 [NCBI] 5.4721e-06
NKX3-2 [NCBI] 5.4721e-06
CHST3 [NCBI] 5.3608e-06
LEP [NCBI] 5.21761e-06
CHST1 [NCBI] 5.16971e-06
ADCY10 [NCBI] 5.16971e-06
GDF6 [NCBI] 4.93803e-06
HOXD9 [NCBI] 4.93803e-06
MATN1 [NCBI] 4.89026e-06
TNFRSF19 [NCBI] 4.87141e-06
HNRNPR [NCBI] 4.87141e-06
MMP13 [NCBI] 4.82179e-06
HIP1R [NCBI] 4.80897e-06
FBN2 [NCBI] 4.75022e-06
COL10A1 [NCBI] 4.69474e-06
ZIC1 [NCBI] 4.69474e-06
JAG1 [NCBI] 4.6117e-06
IGF1 [NCBI] 4.57058e-06
SIM1 [NCBI] 4.49943e-06
COL9A3 [NCBI] 4.45607e-06
BMP7 [NCBI] 4.28256e-06
PCSK5 [NCBI] 4.19625e-06
COL6A1 [NCBI] 4.16412e-06
HOXD10 [NCBI] 4.13301e-06
BGLAP [NCBI] 4.13301e-06
GAS6 [NCBI] 4.13301e-06
LECT1 [NCBI] 4.10285e-06
GALNS [NCBI] 4.10285e-06
BMP4 [NCBI] 4.04736e-06
MLLT3 [NCBI] 4.01751e-06
PAX9 [NCBI] 4.01751e-06
WNT3A [NCBI] 3.99063e-06
CLEC3B [NCBI] 3.93896e-06
HSPB8 [NCBI] 3.86621e-06
TGFBR1 [NCBI] 3.84538e-06
ACP1 [NCBI] 3.8431e-06
CALCR [NCBI] 3.82053e-06
HOXB7 [NCBI] 3.79846e-06
SLC26A2 [NCBI] 3.77687e-06
GC [NCBI] 3.75575e-06
ALOX12 [NCBI] 3.75575e-06
PAPPA [NCBI] 3.71481e-06
ATF1 [NCBI] 3.58365e-06
TAC1 [NCBI] 3.56627e-06
TNFRSF11B [NCBI] 3.52717e-06
TLX1 [NCBI] 3.48369e-06
ALOX15 [NCBI] 3.48369e-06
NR6A1 [NCBI] 3.4223e-06
TNFRSF11A [NCBI] 3.41449e-06
EWSR1 [NCBI] 3.40754e-06
TYRO3 [NCBI] 3.32337e-06
GAA [NCBI] 3.25839e-06
PTH1R [NCBI] 3.19747e-06
EDA [NCBI] 3.18574e-06
FBN1 [NCBI] 3.18574e-06
TNFSF11 [NCBI] 3.17991e-06
GRID2 [NCBI] 3.12909e-06
NCOA3 [NCBI] 3.09662e-06
DCN [NCBI] 3.06522e-06
LGALS3 [NCBI] 3.04483e-06
NF1 [NCBI] 3.03479e-06
F5 [NCBI] 2.97669e-06
DYSF [NCBI] 2.87849e-06
LEPR [NCBI] 2.84513e-06
ETS2 [NCBI] 2.72948e-06
BMI1 [NCBI] 2.67996e-06
ERF [NCBI] 2.67996e-06
CHI3L1 [NCBI] 2.67309e-06
MMP3 [NCBI] 2.60065e-06
MYOG [NCBI] 2.59433e-06
CASR [NCBI] 2.55728e-06
F2 [NCBI] 2.54525e-06
CDX2 [NCBI] 2.53337e-06
WNT4 [NCBI] 2.52748e-06
MTHFR [NCBI] 2.51004e-06
BAG1 [NCBI] 2.51004e-06
SPP1 [NCBI] 2.5043e-06
FGFR2 [NCBI] 2.47057e-06
FGF23 [NCBI] 2.46506e-06
CNTN2 [NCBI] 2.45415e-06
IGFBP3 [NCBI] 2.38111e-06
ISL1 [NCBI] 2.33223e-06
PAX3 [NCBI] 2.29949e-06
GHR [NCBI] 2.28128e-06
RUNX2 [NCBI] 2.26343e-06
LMNA [NCBI] 2.19529e-06
CAT [NCBI] 2.02116e-06
T [NCBI] 2.01018e-06
NTN1 [NCBI] 1.90598e-06
ALB [NCBI] 1.903e-06
PMP22 [NCBI] 1.79942e-06
FGF2 [NCBI] 1.76828e-06
MARCKS [NCBI] 1.58116e-06
RELN [NCBI] 1.50669e-06
HGF [NCBI] 1.49395e-06
COMT [NCBI] 1.44182e-06
MLL [NCBI] 1.39796e-06
XRCC5 [NCBI] 1.36577e-06
MOG [NCBI] 1.21664e-06
PTHLH [NCBI] 1.16005e-06
TNF [NCBI] 1.06081e-06
CTGF [NCBI] 1.03947e-06
AHR [NCBI] 1.01518e-06
PAX6 [NCBI] 1.00726e-06
ACHE [NCBI] 8.95505e-07
TJP1 [NCBI] 8.92285e-07
SOD1 [NCBI] 8.75007e-07
AFP [NCBI] 6.20565e-07
APOE [NCBI] 5.9287e-07
VWF [NCBI] 4.13046e-07
EPO [NCBI] 2.68689e-07
MPO [NCBI] 2.51647e-07
CFTR [NCBI] 1.8001e-07
GFAP [NCBI] 9.28984e-08
PTGS2 [NCBI] 8.36492e-08
TH [NCBI] 5.11754e-08
EGF [NCBI] 4.11517e-09



OMIM


 OMIM Link Information
gain		 01
IS1 [NCBI] 0.0203953
spondylometaphyseal dysplasia, corner fracture type [NCBI] 0.00278544
SCDO1 [NCBI] 0.00205983
AIC [NCBI] 0.00191663
spondyloepimetaphyseal dysplasia, sponastrime type [NCBI] 0.00186312
GO [NCBI] 0.00172726
spondyloenchondrodysplasia [NCBI] 0.00172726
spondylometaphyseal dysplasia, kozlowski type [NCBI] 0.00143002
costovertebral segmentation anomalies [NCBI] 0.00123999
hemifacial microsomia with radial defects [NCBI] 0.00111067
HFM [NCBI] 0.00106942
klippel-feil syndrome, autosomal dominant [NCBI] 0.00101241
acrodysostosis [NCBI] 0.000933263
arthrogryposis-like disorder [NCBI] 0.000926331
bone size quantitative trait locus 3 [NCBI] 0.000926331
vertebral ossification, defect in, with nephrogenic rests [NCBI] 0.000926331
SPOAN [NCBI] 0.000926331
SEMDIT [NCBI] 0.000926331
DBQD [NCBI] 0.00076095
spondylocarpotarsal synostosis syndrome [NCBI] 0.000634493
acropectorovertebral dysplasia, f-form of [NCBI] 0.00061896
otoonychoperoneal syndrome [NCBI] 0.00061896
scheuermann disease [NCBI] 0.00061896
BMND2 [NCBI] 0.00061896
three m syndrome [NCBI] 0.000603335
OPLL [NCBI] 0.000578253
spondyloepimetaphyseal dysplasia, strudwick type [NCBI] 0.000557176
microcephalic osteodysplastic primordial dwarfism, type iii [NCBI] 0.000505201
bone size quantitative trait locus 1 [NCBI] 0.000505201
spondylometaphyseal dysplasia, sedaghatian type [NCBI] 0.000505201
spondyloepiphyseal dysplasia tarda, autosomal dominant [NCBI] 0.000505201
proteus syndrome [NCBI] 0.000441493
HCH [NCBI] 0.000436298
hypertrichotic osteochondrodysplasia [NCBI] 0.000432597
klippel-feil syndrome, autosomal recessive [NCBI] 0.000432597
SGM1 [NCBI] 0.000432597
spondyloepiphyseal dysplasia tarda, toledo type [NCBI] 0.000432597
dyssegmental dysplasia, rolland-desbuquois type [NCBI] 0.000432597
AOI [NCBI] 0.000427595
vater association [NCBI] 0.000412223
VDR [NCBI] 0.000401519
ALGS1 [NCBI] 0.000397179
SLE [NCBI] 0.000394488
microcephalic osteodysplastic primordial dwarfism, type i [NCBI] 0.000379538
opsismodysplasia [NCBI] 0.000379538
epiphyseal dysplasia, microcephaly, and nystagmus [NCBI] 0.000379538
lateral meningocele syndrome [NCBI] 0.000379538
spondyloperipheral dysplasia [NCBI] 0.000356322
PPAC [NCBI] 0.000341089
fibrochondrogenesis [NCBI] 0.000337993
short rib-polydactyly syndrome, type i [NCBI] 0.000337993
neuropathy, hereditary motor and sensory, russe type [NCBI] 0.000337993
DLL3 [NCBI] 0.000332569
spondyloocular syndrome, autosomal recessive [NCBI] 0.000300811
acroosteolysis with osteoporosis and changes in skull and mandible [NCBI] 0.000251035
LRS1 [NCBI] 0.000228887
CF [NCBI] 0.000226876
mucolipidosis iiia [NCBI] 0.000223696
pseudodiastrophic dysplasia [NCBI] 0.000222536
vacterl association with hydrocephalus [NCBI] 0.000222536
gracile bone dysplasia [NCBI] 0.000222536
ACG1A [NCBI] 0.000210841
TD1 [NCBI] 0.000209199
PTH [NCBI] 0.000201976
OSCS [NCBI] 0.000194048
BMND1 [NCBI] 0.000182857
acromesomelic dysplasia, hunter-thompson type [NCBI] 0.000182857
ACH [NCBI] 0.000179947
immunoosseous dysplasia, schimke type [NCBI] 0.000166719
FOP [NCBI] 0.000165785
rokitansky-kuster-hauser syndrome [NCBI] 0.000160154
neural tube defects [NCBI] 0.000154301
PAX1 [NCBI] 0.000150865
lethal short-limb skeletal dysplasia, al gazali type [NCBI] 0.000150349
rod-cone dystrophy, sensorineural deafness, and fanconi-type renal dysfunction [NCBI] 0.000150349
cholesterol pneumonia [NCBI] 0.000150349
polydactyly, postaxial, with dental and vertebral anomalies [NCBI] 0.000150349
SCDO2 [NCBI] 0.000150349
vertebral fusion, posterior lumbosacral, with blepharoptosis [NCBI] 0.000150349
cervical vertebral bridge [NCBI] 0.000150349
dwarfism with tall vertebrae [NCBI] 0.000150349
spinal dysplasia, anhalt type [NCBI] 0.000150349
brachyrachia [NCBI] 0.000150349
spondyloepiphyseal dysplasia tarda with characteristic facies [NCBI] 0.000150349
osteochondrodysplasia, rhizomelic, with callosal agenesis, thrombocytopenia, hydrocephalus, and hypertension [NCBI] 0.000150349
aphalangy with hemivertebrae [NCBI] 0.000150349
spondyloepiphyseal dysplasia, myopia, and sensorineural deafness [NCBI] 0.000150349
polydactyly, imperforate anus, and vertebral anomalies [NCBI] 0.000150349
spondyloepimetaphyseal dysplasia, micromelic [NCBI] 0.000150349
dextrocardia with unusual facies and microphthalmia [NCBI] 0.000150349
dyssegmental dysplasia with glaucoma [NCBI] 0.000150349
FFS [NCBI] 0.000149024
FMD [NCBI] 0.000139816
robinow syndrome, autosomal dominant [NCBI] 0.000131175
chiari malformation type i [NCBI] 0.000121604
robinow syndrome, autosomal recessive [NCBI] 0.000116354
mucopolysaccharidosis type vii [NCBI] 0.000111229
neurofibromatosis, familial spinal [NCBI] 0.000111213
SCDO3 [NCBI] 0.000111213
platyspondyly with amelogenesis imperfecta [NCBI] 0.000111213
second metatarsal-metacarpal syndrome [NCBI] 0.000111213
hydrocephalus, skeletal anomalies, and mental disturbance [NCBI] 0.000111213
ulna metaphyseal dysplasia syndrome [NCBI] 0.000111213
roifman syndrome [NCBI] 0.000111213
larsen-like syndrome, lethal type [NCBI] 0.000111213
spondylometaphyseal dysplasia, east african type [NCBI] 0.000111213
chondrodysplasia punctata, tibia-metacarpal type [NCBI] 0.000111213
BGLAP [NCBI] 0.000103065
RSMD1 [NCBI] 0.000102317
vitamin d-dependent rickets, type ii [NCBI] 9.83963e-05
alopecia-contractures-dwarfism mental retardation syndrome [NCBI] 9.65283e-05
osteomesopyknosis [NCBI] 9.65283e-05
camptodactyly, tall stature, and hearing loss syndrome [NCBI] 9.65283e-05
ankylosing vertebral hyperostosis with tylosis [NCBI] 9.65283e-05
spondylolisthesis [NCBI] 9.65283e-05
gombo syndrome [NCBI] 9.65283e-05
spondylocostal dysostosis with anal atresia and urogenital anomalies [NCBI] 9.65283e-05
myeloma, multiple [NCBI] 9.65283e-05
spondyloepimetaphyseal dysplasia, type ii [NCBI] 9.65283e-05
AOIII [NCBI] 9.65283e-05
ENPP1 [NCBI] 9.35143e-05
isotretinoin embryopathy-like syndrome [NCBI] 8.70415e-05
CMT4H [NCBI] 8.70415e-05
humerospinal dysostosis [NCBI] 8.70415e-05
LFNG [NCBI] 8.66093e-05
MBS [NCBI] 8.33817e-05
campomelic dysplasia [NCBI] 8.24872e-05
SMC [NCBI] 8.00232e-05
HCA2 [NCBI] 8.00232e-05
encephalopathy, ethylmalonic [NCBI] 8.00232e-05
MLRD [NCBI] 8.00232e-05
SMAX1 [NCBI] 7.7645e-05
MESP2 [NCBI] 7.53419e-05
enchondromatosis, multiple [NCBI] 7.44589e-05
chromosome 18p deletion syndrome [NCBI] 7.44589e-05
fibromatosis, gingival, with hypertrichosis [NCBI] 7.44589e-05
cleft lip/palate with abnormal thumbs and microcephaly [NCBI] 7.44589e-05
OSMED [NCBI] 7.44589e-05
keutel syndrome [NCBI] 7.44589e-05
avascular necrosis of femoral head, primary [NCBI] 7.44589e-05
MCDS [NCBI] 7.44589e-05
vacterl association with hydrocephalus, x-linked [NCBI] 7.44589e-05
boomerang dysplasia [NCBI] 7.44589e-05
oeis complex [NCBI] 7.44589e-05
FGFR3 [NCBI] 7.3077e-05
COL2A1 [NCBI] 7.11505e-05
ACP5 [NCBI] 7.06647e-05
CMT4B2 [NCBI] 6.98553e-05
TD2 [NCBI] 6.59345e-05
CMT4B1 [NCBI] 6.59345e-05
CMT4C [NCBI] 6.59345e-05
FLNB [NCBI] 6.53135e-05
HMN2A [NCBI] 6.25242e-05
multiple pterygium syndrome, lethal type [NCBI] 6.25242e-05
wildervanck syndrome [NCBI] 6.25242e-05
RNS [NCBI] 6.25242e-05
morquio syndrome b [NCBI] 6.25242e-05
AMDM [NCBI] 6.25242e-05
CMT4D [NCBI] 6.25242e-05
multiple pterygium syndrome, escobar variant [NCBI] 5.95102e-05
osteoporosis [NCBI] 5.95102e-05
DLL1 [NCBI] 5.76947e-05
SYNS1 [NCBI] 5.68128e-05
CMT4A [NCBI] 5.43742e-05
DMC [NCBI] 5.43742e-05
mucopolysaccharidosis type iva [NCBI] 5.21808e-05
osteogenesis imperfecta, type iii [NCBI] 5.2151e-05
osteogenesis imperfecta, type iv [NCBI] 5.2151e-05
currarino syndrome [NCBI] 5.011e-05
OPD2 [NCBI] 5.011e-05
diabetes insipidus, neurohypophyseal type [NCBI] 5.011e-05
cerebrocostomandibular syndrome [NCBI] 5.011e-05
TNFRSF1B [NCBI] 4.9582e-05
trichodentoosseous syndrome [NCBI] 4.82251e-05
camurati-engelmann disease [NCBI] 4.82251e-05
feingold syndrome [NCBI] 4.82251e-05
neuropathy, congenital hypomyelinating [NCBI] 4.82251e-05
GACI [NCBI] 4.64755e-05
pfeiffer syndrome [NCBI] 4.48442e-05
poland syndrome [NCBI] 4.42278e-05
ATD1 [NCBI] 4.42278e-05
BCNS [NCBI] 4.39816e-05
asplenia with cardiovascular anomalies [NCBI] 4.33172e-05
STL1 [NCBI] 4.1883e-05
mesoderm posterior 1 [NCBI] 4.14109e-05
MNS [NCBI] 4.05317e-05
SEDC [NCBI] 4.05317e-05
ESR1 [NCBI] 3.93059e-05
MKKS [NCBI] 3.8046e-05
lymphedema-distichiasis syndrome [NCBI] 3.8046e-05
mucopolysaccharidosis type vi [NCBI] 3.8046e-05
SH3TC2 [NCBI] 3.76484e-05
PFM [NCBI] 3.68984e-05
HOXB8 [NCBI] 3.5207e-05
NFIX [NCBI] 3.5207e-05
TBX18 [NCBI] 3.5207e-05
BGS [NCBI] 3.47665e-05
OKS [NCBI] 3.47665e-05
COH1 [NCBI] 3.37736e-05
CHX10 [NCBI] 3.3393e-05
NPR2 [NCBI] 3.3393e-05
GUSB [NCBI] 3.33465e-05
FGFR2 [NCBI] 3.27752e-05
FAM20C [NCBI] 3.19486e-05
FDH [NCBI] 3.10438e-05
SJS1 [NCBI] 3.10438e-05
SEPN1 [NCBI] 3.07485e-05
frank-ter haar syndrome [NCBI] 3.07485e-05
NCSTN [NCBI] 3.07485e-05
FANCB [NCBI] 3.07485e-05
PHS [NCBI] 3.02073e-05
XPA [NCBI] 3.02073e-05
SIM2 [NCBI] 2.97218e-05
NOTCH2 [NCBI] 2.97218e-05
MSD [NCBI] 2.94033e-05
LWD [NCBI] 2.94033e-05
RCDP1 [NCBI] 2.86299e-05
NCOR1 [NCBI] 2.80289e-05
CALCR [NCBI] 2.80289e-05
NDRG1 [NCBI] 2.73132e-05
TLX1 [NCBI] 2.73132e-05
hypophosphatemic rickets, x-linked dominant [NCBI] 2.7167e-05
COL11A2 [NCBI] 2.66633e-05
AEBP1 [NCBI] 2.66633e-05
BMI1 [NCBI] 2.66633e-05
CDX2 [NCBI] 2.60682e-05
GDAP1 [NCBI] 2.60682e-05
SHH [NCBI] 2.60241e-05
SCS [NCBI] 2.58052e-05
ETS2 [NCBI] 2.55194e-05
MTMR2 [NCBI] 2.55194e-05
ROR2 [NCBI] 2.50103e-05
COL10A1 [NCBI] 2.50103e-05
MMP13 [NCBI] 2.50103e-05
NF1 [NCBI] 2.46993e-05
EGF [NCBI] 2.44699e-05
FOXC2 [NCBI] 2.40908e-05
PDGFRA [NCBI] 2.36727e-05
EGR2 [NCBI] 2.36727e-05
PRX [NCBI] 2.36727e-05
TRPS2 [NCBI] 2.33427e-05
CRMO [NCBI] 2.33427e-05
hypertrophic neuropathy of dejerine-sottas [NCBI] 2.33427e-05
HIP1 [NCBI] 2.32781e-05
contractural arachnodactyly, congenital [NCBI] 2.29046e-05
SRS [NCBI] 2.20976e-05
adenylyl cyclase, soluble [NCBI] 2.10066e-05
PTHR1 [NCBI] 2.07353e-05
JAG1 [NCBI] 2.04742e-05
COL6A1 [NCBI] 1.998e-05
GDF5 [NCBI] 1.9519e-05
IGF1 [NCBI] 1.86809e-05
TNFRSF11B [NCBI] 1.86597e-05
CLS [NCBI] 1.83555e-05
BPES [NCBI] 1.83555e-05
neuraminidase deficiency [NCBI] 1.79295e-05
CHH [NCBI] 1.75146e-05
PSACH [NCBI] 1.71104e-05
PAX3 [NCBI] 1.62284e-05
mucolipidosis ii [NCBI] 1.59581e-05
osteogenesis imperfecta, type i [NCBI] 1.55928e-05
COL1A1 [NCBI] 1.52151e-05
NOTCH1 [NCBI] 1.45462e-05
PD [NCBI] 1.3228e-05
MAS [NCBI] 1.26715e-05
FMF [NCBI] 1.21449e-05
CASR [NCBI] 1.11749e-05
PTHLH [NCBI] 1.00489e-05
STAT1 [NCBI] 9.51242e-06
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency [NCBI] 8.73159e-06
RA [NCBI] 8.72816e-06
VEGF [NCBI] 8.13017e-06
IHH [NCBI] 7.83315e-06
GHR [NCBI] 7.69732e-06
TH [NCBI] 7.00768e-06
CD [NCBI] 5.68123e-06
TNF [NCBI] 5.42169e-06
GFAP [NCBI] 5.19013e-06
ALB [NCBI] 5.17663e-06
FA [NCBI] 4.39644e-06
AVP [NCBI] 4.26424e-06
COMT [NCBI] 2.90548e-06
CTGF [NCBI] 2.16031e-06
MFS [NCBI] 2.14641e-06
MPO [NCBI] 1.99328e-06
EPO [NCBI] 1.68651e-06
ACHE [NCBI] 9.40852e-07
CEACAM5 [NCBI] 6.86843e-07
AHR [NCBI] 6.62428e-07
GNRH1 [NCBI] 6.39043e-07
SPP1 [NCBI] 4.47319e-07
DGS [NCBI] 4.39577e-07
AT [NCBI] 3.22001e-07
CAT [NCBI] 3.15169e-07
CFTR [NCBI] 1.65763e-07
KLK3 [NCBI] 1.56154e-07
temporal arteritis [NCBI] 1.0488e-07
HGF [NCBI] 8.45813e-08
AFP [NCBI] 2.59754e-08
APOE [NCBI] 6.44393e-09
CVID [NCBI] 4.86298e-09



Database Center for Life Science