Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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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