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MeSH keywords -> Related genes, diseases (OMIM)


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01 Paralysis [NCBI]

Gene


 Gene Link Information
Gain		 01
MS [NCBI] 0.00076066
PMP22 [NCBI] 0.000303357
MBS1 [NCBI] 0.000233856
HFM [NCBI] 0.000110639
SCN4A [NCBI] 5.16805e-05
ACHE [NCBI] 3.70975e-05
PVR [NCBI] 3.12629e-05
MBP [NCBI] 2.81745e-05
CACNA1S [NCBI] 2.71154e-05
CNTF [NCBI] 2.27938e-05
CS [NCBI] 2.08842e-05
MUSK [NCBI] 2.05525e-05
ALS2 [NCBI] 1.65327e-05
SLC12A3 [NCBI] 1.36892e-05
KCNJ8 [NCBI] 1.2689e-05
MOG [NCBI] 1.237e-05
GAS8 [NCBI] 1.11207e-05
DNAJC5 [NCBI] 1.00543e-05
NBEA [NCBI] 9.80847e-06
NEFH [NCBI] 9.78332e-06
SOD1 [NCBI] 9.64122e-06
PXMP2 [NCBI] 9.59354e-06
PPP1R12A [NCBI] 8.93187e-06
ATP6V1B1 [NCBI] 8.79993e-06
NIPA1 [NCBI] 8.45605e-06
KLC1 [NCBI] 8.16995e-06
KIF21A [NCBI] 8.08433e-06
SCN8A [NCBI] 8.00281e-06
TPI1 [NCBI] 7.8506e-06
SEPT9 [NCBI] 7.5207e-06
PARK2 [NCBI] 7.00201e-06
MCOLN1 [NCBI] 6.87897e-06
LIF [NCBI] 6.76968e-06
IL3 [NCBI] 6.75995e-06
OLIG2 [NCBI] 6.75995e-06
LGALS1 [NCBI] 6.44615e-06
PPT2 [NCBI] 5.97704e-06
NR1I3 [NCBI] 5.97704e-06
NEFM [NCBI] 5.81643e-06
KRIT1 [NCBI] 5.66989e-06
PLP1 [NCBI] 5.53517e-06
TRH [NCBI] 5.40092e-06
MB [NCBI] 4.92352e-06
SST [NCBI] 4.80044e-06
TIMP1 [NCBI] 4.67494e-06
PARK7 [NCBI] 4.39327e-06
NEFL [NCBI] 4.35675e-06
SMN2 [NCBI] 4.31222e-06
CD22 [NCBI] 4.23504e-06
CDK5 [NCBI] 4.21012e-06
CD83 [NCBI] 4.18558e-06
CIITA [NCBI] 4.14549e-06
JAK3 [NCBI] 4.09867e-06
GER [NCBI] 3.85086e-06
KCNH6 [NCBI] 3.77923e-06
ERG [NCBI] 3.75428e-06
HSPB1 [NCBI] 3.58433e-06
CD99 [NCBI] 3.55137e-06
SLC2A4 [NCBI] 3.48226e-06
GJB1 [NCBI] 3.08991e-06
SLC2A1 [NCBI] 2.91914e-06
TROVE2 [NCBI] 2.6217e-06
IFNGR1 [NCBI] 2.57852e-06
MMP9 [NCBI] 2.56722e-06
ACP5 [NCBI] 2.42803e-06
APOE [NCBI] 2.4233e-06
NME1 [NCBI] 2.34638e-06
TNFRSF11A [NCBI] 2.30379e-06
TNFSF11 [NCBI] 2.09083e-06
SNCA [NCBI] 1.82395e-06
BDNF [NCBI] 1.42573e-06
EGF [NCBI] 1.36224e-06
LPL [NCBI] 1.31595e-06
AVP [NCBI] 1.30247e-06
VEGFA [NCBI] 5.40907e-07



OMIM


 OMIM Link Information
gain		 01
MBS [NCBI] 0.00208685
HNPP [NCBI] 0.00143388
SPG23 [NCBI] 0.00132132
brachial palsy, familial congenital [NCBI] 0.000766909
ALS3 [NCBI] 0.000684933
ALS5 [NCBI] 0.000684933
saccharopinuria [NCBI] 0.0006318
ophthalmoplegia, familial static [NCBI] 0.0006318
bulbar palsy, progressive, with sensorineural deafness [NCBI] 0.000592366
PSNP2 [NCBI] 0.000592366
HCFP1 [NCBI] 0.000592366
HYPP [NCBI] 0.00053999
thyrotoxic periodic paralysis [NCBI] 0.000504737
microtia with meatal atresia and conductive deafness [NCBI] 0.000493306
HNA [NCBI] 0.000441121
PMP22 [NCBI] 0.000437686
CGF [NCBI] 0.000382327
palatopharyngeal incompetence [NCBI] 0.000268332
PMC [NCBI] 0.000267154
pena-shokeir syndrome, type i [NCBI] 0.000260747
HOKPP [NCBI] 0.000255893
normokalemic periodic paralysis [NCBI] 0.00021922
ALD [NCBI] 0.000198753
SCN4A [NCBI] 0.000174575
HFM [NCBI] 0.000162511
CACNA1S [NCBI] 0.000152979
ACHE [NCBI] 0.000131993
ALS2 [NCBI] 0.00012398
SLS [NCBI] 0.000122502
SPG2 [NCBI] 0.000112513
spastic paraparesis and deafness [NCBI] 0.000109532
fourth cranial nerve palsy, familial congenital [NCBI] 0.000109532
PNPLA6 [NCBI] 9.52709e-05
MBP [NCBI] 9.34222e-05
alsin [NCBI] 9.30611e-05
SPG3A [NCBI] 9.12048e-05
CNTF [NCBI] 8.98555e-05
spastic paresis, glaucoma, and mental retardation [NCBI] 8.70777e-05
spinal muscular atrophy, scapuloperoneal [NCBI] 8.70777e-05
laryngeal abductor paralysis [NCBI] 8.70777e-05
PVR [NCBI] 8.59901e-05
limb defects, distal transverse, with mental retardation and spasticity [NCBI] 7.86143e-05
CMT1A [NCBI] 7.37174e-05
FBD [NCBI] 7.31247e-05
IAHSP [NCBI] 7.31247e-05
SPG13 [NCBI] 6.58022e-05
encephalopathy, ethylmalonic [NCBI] 6.58022e-05
NN [NCBI] 6.31066e-05
ALS4 [NCBI] 6.31066e-05
NR1I3 [NCBI] 6.19295e-05
spinal muscular atrophy, proximal, adult, autosomal dominant [NCBI] 5.87887e-05
myotonia, potassium-aggravated [NCBI] 5.87887e-05
BPP [NCBI] 5.70026e-05
HAM [NCBI] 5.70026e-05
UCHL3 [NCBI] 5.67329e-05
PLSJ [NCBI] 5.53976e-05
sc phocomelia syndrome [NCBI] 5.53976e-05
ESCO2 [NCBI] 5.08531e-05
HSPD1 [NCBI] 5.08531e-05
CYP1A2 [NCBI] 5.08531e-05
DSMA1 [NCBI] 5.02374e-05
pituitary dwarfism iii [NCBI] 4.91747e-05
alpers diffuse degeneration of cerebral gray matter with hepatic cirrhosis [NCBI] 4.81797e-05
amyloidosis v [NCBI] 4.72443e-05
PPARBP [NCBI] 4.71966e-05
glutaric acidemia i [NCBI] 4.6362e-05
VED [NCBI] 4.6362e-05
PHA2 [NCBI] 4.55272e-05
SCN8A [NCBI] 4.24427e-05
PSNP1 [NCBI] 4.12904e-05
SMA2 [NCBI] 4.12904e-05
UCHL1 [NCBI] 4.07182e-05
KCNJ2 [NCBI] 3.99576e-05
andersen cardiodysrhythmic periodic paralysis [NCBI] 3.95435e-05
TNFRSF11A [NCBI] 3.92518e-05
SPG3A [NCBI] 3.92518e-05
MCOLN1 [NCBI] 3.92518e-05
SLC12A3 [NCBI] 3.79766e-05
SLE [NCBI] 3.77326e-05
megaloblastic anemia 1 [NCBI] 3.74894e-05
SPG7 [NCBI] 3.73964e-05
TPI1 [NCBI] 3.68487e-05
SPG4 [NCBI] 3.65588e-05
DDIT3 [NCBI] 3.63302e-05
ODDD [NCBI] 3.61144e-05
RBS [NCBI] 3.52634e-05
ALPL [NCBI] 3.36922e-05
IL3 [NCBI] 3.2263e-05
EDMD [NCBI] 3.03834e-05
SPG4 [NCBI] 3.01803e-05
L1CAM [NCBI] 2.99165e-05
JAK3 [NCBI] 2.96597e-05
CMT1B [NCBI] 2.89753e-05
SCA7 [NCBI] 2.89753e-05
CCM [NCBI] 2.87096e-05
ANG [NCBI] 2.86965e-05
factor x deficiency [NCBI] 2.84702e-05
AMC [NCBI] 2.60786e-05
TNFSF11 [NCBI] 2.52735e-05
SMA1 [NCBI] 2.35059e-05
ALS1 [NCBI] 2.35059e-05
GJB1 [NCBI] 2.2069e-05
CDK5 [NCBI] 2.00546e-05
SST [NCBI] 1.87942e-05
MB [NCBI] 1.8639e-05
MS [NCBI] 1.78997e-05
PMD [NCBI] 1.65863e-05
VEGF [NCBI] 1.51835e-05
DRPLA [NCBI] 1.45963e-05
SOD1 [NCBI] 1.23224e-05
RTT [NCBI] 8.48204e-06
CVID [NCBI] 5.14397e-06
HD [NCBI] 4.49889e-06
MG [NCBI] 3.59469e-06
TNFSF6 [NCBI] 2.4753e-06
BDNF [NCBI] 1.35711e-06
LPL [NCBI] 1.15523e-06
AVP [NCBI] 9.68106e-08
EGF [NCBI] 3.50923e-08
APOE [NCBI] 5.14251e-09
PD [NCBI] 6.74402e-10



Database Center for Life Science