MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Walking
[NCBI]
Gene
Gene
Link
Information
Gain
01
MS
[NCBI]
0.00222101
AIS
[NCBI]
8.25524e-05
FOP
[NCBI]
5.44576e-05
PTH
[NCBI]
7.2114e-06
NPPB
[NCBI]
5.23573e-06
TOR1A
[NCBI]
4.88608e-06
BDNF
[NCBI]
4.19073e-06
SLC6A3
[NCBI]
3.8035e-06
CST3
[NCBI]
3.49218e-06
EDIL3
[NCBI]
3.40171e-06
ARHGEF5
[NCBI]
3.23741e-06
CTDSP1
[NCBI]
3.18535e-06
SPG11
[NCBI]
3.1614e-06
CD3EAP
[NCBI]
3.13865e-06
ERC1
[NCBI]
3.05756e-06
SIM1
[NCBI]
2.98877e-06
VDR
[NCBI]
2.96141e-06
ITM2B
[NCBI]
2.82896e-06
NOS3
[NCBI]
2.73594e-06
BSCL2
[NCBI]
2.72862e-06
LPL
[NCBI]
2.71243e-06
CEACAM8
[NCBI]
2.67758e-06
MFN2
[NCBI]
2.60351e-06
EDNRA
[NCBI]
2.52237e-06
GRID2
[NCBI]
2.47364e-06
VWF
[NCBI]
2.46314e-06
FOXP2
[NCBI]
2.44868e-06
ATF3
[NCBI]
2.32229e-06
COMP
[NCBI]
2.1162e-06
TNFRSF1B
[NCBI]
2.0957e-06
NCK1
[NCBI]
2.02758e-06
RAB7A
[NCBI]
2.02758e-06
TNFRSF1A
[NCBI]
2.01998e-06
PDE5A
[NCBI]
1.8928e-06
MATN1
[NCBI]
1.85339e-06
CS
[NCBI]
1.84056e-06
HSPB1
[NCBI]
1.73311e-06
MECP2
[NCBI]
1.69406e-06
ITPR1
[NCBI]
1.68059e-06
IL4
[NCBI]
1.60431e-06
IFNG
[NCBI]
1.58391e-06
MOG
[NCBI]
1.56919e-06
GJB1
[NCBI]
1.56303e-06
IGF1
[NCBI]
1.55763e-06
IL2
[NCBI]
1.50038e-06
SHBG
[NCBI]
1.4992e-06
CCL2
[NCBI]
1.43674e-06
PAX6
[NCBI]
1.39625e-06
PLN
[NCBI]
1.33827e-06
ESR1
[NCBI]
1.32778e-06
ACE
[NCBI]
1.27632e-06
SOD1
[NCBI]
1.26617e-06
IL6
[NCBI]
1.1793e-06
NOS2
[NCBI]
1.10112e-06
GFAP
[NCBI]
9.52009e-07
VEGFA
[NCBI]
9.50031e-07
TGFB1
[NCBI]
9.34069e-07
EPO
[NCBI]
8.94021e-07
TNF
[NCBI]
3.76256e-07
OMIM
OMIM
Link
Information
gain
01
cerebellar hypoplasia, mental retardation, and quadrupedal locomotion
[NCBI]
0.00110387
spondyloenchondrodysplasia
[NCBI]
0.00103894
IS1
[NCBI]
0.000920544
RA
[NCBI]
0.000436137
AMC
[NCBI]
0.000206368
d-2-@hydroxyglutaric aciduria
[NCBI]
9.39095e-05
PD
[NCBI]
8.82564e-05
spinal muscular atrophy, proximal, adult, autosomal dominant
[NCBI]
8.36939e-05
congenital cataracts, facial dysmorphism, and neuropathy
[NCBI]
7.51818e-05
myoclonic epilepsy of unverricht and lundborg
[NCBI]
5.18861e-05
FOP
[NCBI]
5.08751e-05
AS
[NCBI]
4.95015e-05
PTH
[NCBI]
4.03189e-05
EFNB3
[NCBI]
4.02501e-05
EPHA4
[NCBI]
3.37009e-05
RP
[NCBI]
2.74651e-05
XPA
[NCBI]
2.59888e-05
DRPLA
[NCBI]
2.59834e-05
SLC6A3
[NCBI]
2.53484e-05
ATF3
[NCBI]
2.32185e-05
BDNF
[NCBI]
2.32131e-05
GPT
[NCBI]
2.25821e-05
GJB1
[NCBI]
1.91146e-05
VDR
[NCBI]
1.88819e-05
RTT
[NCBI]
1.76424e-05
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency
[NCBI]
1.63741e-05
COMP
[NCBI]
1.59492e-05
LPL
[NCBI]
1.47728e-05
CRH
[NCBI]
1.12607e-05
AD
[NCBI]
9.86547e-06
HD
[NCBI]
9.70747e-06
XDH
[NCBI]
9.10787e-06
SHBG
[NCBI]
7.69814e-06
NPPA
[NCBI]
4.49707e-06
EPO
[NCBI]
2.09818e-06
GFAP
[NCBI]
2.01253e-06
VEGF
[NCBI]
1.64918e-06
CF
[NCBI]
1.17663e-06
MDD
[NCBI]
2.38446e-08
Database Center for Life Science