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MeSH keywords -> Related genes, diseases (OMIM)


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01 Paraplegia [NCBI]

Gene


 Gene Link Information
Gain		 01
SPG26 [NCBI] 0.000352784
SPOAN [NCBI] 0.000352784
SPG25 [NCBI] 0.000352784
LOC647275 [NCBI] 0.000352784
SPG12 [NCBI] 0.000292051
SPAST [NCBI] 0.00014321
PLP1 [NCBI] 0.000115187
L1CAM [NCBI] 8.51369e-05
SPG7 [NCBI] 5.45369e-05
ATL1 [NCBI] 5.27065e-05
KIF5A [NCBI] 3.64635e-05
MS [NCBI] 2.56455e-05
GER [NCBI] 2.37246e-05
NIPA1 [NCBI] 2.07118e-05
MBP [NCBI] 2.04616e-05
STAC [NCBI] 1.56321e-05
ZFP90 [NCBI] 1.56321e-05
YME1L1 [NCBI] 1.32518e-05
OPALIN [NCBI] 1.32518e-05
TH [NCBI] 1.09553e-05
ATRN [NCBI] 9.4485e-06
SPG20 [NCBI] 9.32593e-06
LIG1 [NCBI] 8.73229e-06
SCN8A [NCBI] 8.65068e-06
MYT1 [NCBI] 8.42692e-06
NAGS [NCBI] 8.3584e-06
CNTN2 [NCBI] 8.22911e-06
SLC16A2 [NCBI] 8.05186e-06
NUMA1 [NCBI] 7.65337e-06
BSCL2 [NCBI] 7.48439e-06
RFC1 [NCBI] 6.96815e-06
ATRX [NCBI] 6.82592e-06
TRH [NCBI] 6.61622e-06
HSPD1 [NCBI] 6.59661e-06
SLC19A2 [NCBI] 6.25288e-06
BDNF [NCBI] 6.11001e-06
GJA1 [NCBI] 6.05163e-06
ABCA4 [NCBI] 5.33359e-06
FXN [NCBI] 4.3807e-06
NEFH [NCBI] 4.35578e-06
GFAP [NCBI] 4.22241e-06
AMBP [NCBI] 4.20257e-06
PARP1 [NCBI] 4.18025e-06
XRCC5 [NCBI] 4.01201e-06
PRKDC [NCBI] 3.85082e-06
FOLR1 [NCBI] 3.61668e-06
PLN [NCBI] 3.60122e-06
UMOD [NCBI] 3.50432e-06
CHAT [NCBI] 2.94982e-06
VHL [NCBI] 2.78621e-06
PTH [NCBI] 2.51342e-06
CALCA [NCBI] 2.25471e-06
ACHE [NCBI] 1.86859e-06
AVP [NCBI] 1.83686e-06
MTHFR [NCBI] 1.83239e-06
VWF [NCBI] 1.12109e-06
NGF [NCBI] 1.05696e-06
PRL [NCBI] 8.87497e-07
CASP3 [NCBI] 6.94602e-07
TNF [NCBI] 4.24663e-09



OMIM


 OMIM Link Information
gain		 01
SPG15 [NCBI] 0.00242373
SPG23 [NCBI] 0.00232623
SPG12 [NCBI] 0.00151113
SPG5A [NCBI] 0.00129155
SPOAN [NCBI] 0.00101415
SPAX3 [NCBI] 0.00101415
SPG3A [NCBI] 0.000933486
SPG4 [NCBI] 0.000864637
SPG26 [NCBI] 0.000796434
SPG19 [NCBI] 0.000714407
angioma, hereditary neurocutaneous [NCBI] 0.000590318
L1CAM [NCBI] 0.000563861
SPG2 [NCBI] 0.000555918
masa syndrome [NCBI] 0.000555918
SPG6 [NCBI] 0.000428103
ALD [NCBI] 0.000344498
SPG10 [NCBI] 0.000340225
PMD [NCBI] 0.00032999
neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive [NCBI] 0.000293581
DWS [NCBI] 0.000284621
PLP1 [NCBI] 0.000279667
SPG4 [NCBI] 0.000242974
AHDS [NCBI] 0.000198827
limb defects, distal transverse, with mental retardation and spasticity [NCBI] 0.000188919
SPG20 [NCBI] 0.000174947
homocarnosinosis [NCBI] 0.000165361
SPG13 [NCBI] 0.000158019
SPG17 [NCBI] 0.000135473
ALS2 [NCBI] 0.000124611
SLE [NCBI] 0.000116877
kallmann syndrome with spastic paraplegia [NCBI] 0.000109848
mental retardation with spastic paraplegia and palmoplantar hyperkeratosis [NCBI] 0.000109848
SPERM [NCBI] 0.000109848
spastic paraplegia, sensorineural deafness, mental retardation, and progressive nephropathy [NCBI] 0.000109848
spastic paraplegia with precocious puberty [NCBI] 0.000109848
amyotrophic dystonic paraplegia [NCBI] 0.000109848
HSAS [NCBI] 9.9126e-05
SLC16A2 [NCBI] 9.78704e-05
alsin [NCBI] 9.63983e-05
SPG7 [NCBI] 9.25449e-05
spastic paresis, glaucoma, and mental retardation [NCBI] 8.73936e-05
fitzsimmons-guilbert syndrome [NCBI] 7.89299e-05
YME1L1 [NCBI] 7.7366e-05
SPG25 [NCBI] 7.7366e-05
SPG8 [NCBI] 7.34399e-05
SPG7 [NCBI] 7.34399e-05
branchial myoclonus with spastic paraparesis and cerebellar ataxia [NCBI] 6.93624e-05
SLS [NCBI] 6.92782e-05
ABCD1 [NCBI] 6.63681e-05
syndactyly, type iii [NCBI] 6.61167e-05
PTGFR [NCBI] 6.35894e-05
3-@methylglutaconic aciduria, type iii [NCBI] 6.34207e-05
SCA1 [NCBI] 6.27158e-05
MBP [NCBI] 5.88575e-05
HAM [NCBI] 5.73156e-05
PLSJ [NCBI] 5.57103e-05
KIF5A [NCBI] 5.50183e-05
SPG20 [NCBI] 5.50183e-05
HSPD1 [NCBI] 5.25107e-05
ADLTE [NCBI] 5.05486e-05
NIPA1 [NCBI] 5.05132e-05
sitosterolemia [NCBI] 4.94855e-05
ATRN [NCBI] 4.50875e-05
lymphedema-distichiasis syndrome [NCBI] 4.42903e-05
SCN8A [NCBI] 4.40959e-05
SPG3A [NCBI] 4.09019e-05
alzheimer disease 3 [NCBI] 3.98496e-05
ATRX [NCBI] 3.98496e-05
exostoses, multiple, type i [NCBI] 3.47607e-05
ATRX [NCBI] 3.10409e-05
CMT1B [NCBI] 2.92712e-05
CMT1A [NCBI] 2.63701e-05
PSEN1 [NCBI] 1.86446e-05
fabry disease [NCBI] 1.84066e-05
krabbe disease [NCBI] 1.79422e-05
KSS [NCBI] 1.49443e-05
DRPLA [NCBI] 1.48568e-05
BDNF [NCBI] 1.34782e-05
leber optic atrophy [NCBI] 1.23774e-05
TH [NCBI] 1.17459e-05
TNF [NCBI] 8.43491e-06
GDNF [NCBI] 7.44983e-06
CHAT [NCBI] 5.92612e-06
GFAP [NCBI] 4.88684e-06
KLK3 [NCBI] 1.81342e-06
ACHE [NCBI] 1.56282e-06
CD [NCBI] 5.1243e-07
AVP [NCBI] 4.31846e-07
PTH [NCBI] 4.2555e-07
PRL [NCBI] 8.86295e-08
NGFB [NCBI] 6.02081e-09



Database Center for Life Science