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01 Hemiplegia [NCBI]

Gene


 Gene Link Information
Gain		 01
CACNA1A [NCBI] 0.000290589
ATP1A2 [NCBI] 0.000239356
MS [NCBI] 0.000187091
TEC [NCBI] 0.000154258
NEWENTRY [NCBI] 9.5351e-05
SLC1A3 [NCBI] 3.0733e-05
GER [NCBI] 2.37246e-05
NEFM [NCBI] 1.66041e-05
PTH [NCBI] 1.14635e-05
F2 [NCBI] 1.00692e-05
PRKCSH [NCBI] 9.20907e-06
CACNA1C [NCBI] 9.13452e-06
CACNA1F [NCBI] 8.47657e-06
TRH [NCBI] 7.83908e-06
SCN1A [NCBI] 7.13704e-06
MARCKS [NCBI] 6.80908e-06
MB [NCBI] 6.19154e-06
NOTCH3 [NCBI] 5.40203e-06
SCN5A [NCBI] 5.14132e-06
MBL2 [NCBI] 4.97742e-06
PAX6 [NCBI] 4.80011e-06
F5 [NCBI] 3.51919e-06
ADA [NCBI] 3.13187e-06
VIP [NCBI] 2.90054e-06
NPY [NCBI] 2.12403e-06
GFAP [NCBI] 1.62976e-06
APOE [NCBI] 1.28204e-06
EGF [NCBI] 7.40689e-07
TNF [NCBI] 1.45826e-07



OMIM


 OMIM Link Information
gain		 01
migraine with or without aura, susceptibility to, 6 [NCBI] 0.00182258
MYMY1 [NCBI] 0.00138193
FHM1 [NCBI] 0.00135806
alternating hemiplegia of childhood [NCBI] 0.000679551
sneddon syndrome [NCBI] 0.000644828
ATP1A2 [NCBI] 0.000588349
porencephaly, familial [NCBI] 0.000504073
CACNA1A [NCBI] 0.000466666
FHM2 [NCBI] 0.000426875
AOS [NCBI] 0.000383542
behcet syndrome [NCBI] 0.000353076
HFM [NCBI] 0.000282209
CADASIL [NCBI] 0.000275801
hhhh syndrome [NCBI] 0.000120229
BGLAP [NCBI] 0.000113558
SCA6 [NCBI] 0.000107115
ataxic diplegia with defective cellular immunity [NCBI] 9.77659e-05
RA [NCBI] 9.65736e-05
FHM3 [NCBI] 8.92934e-05
papilloma of choroid plexus [NCBI] 7.97084e-05
sulfocysteinuria [NCBI] 7.37493e-05
cerebral palsy, spastic, symmetric, autosomal recessive [NCBI] 6.94132e-05
hypoparathyroidism, sensorineural deafness, and renal disease [NCBI] 6.60038e-05
MCCC1 [NCBI] 6.51968e-05
3-@methylcrotonyl-coa carboxylase 1 deficiency [NCBI] 6.3195e-05
enchondromatosis, multiple [NCBI] 5.87312e-05
SLC1A3 [NCBI] 5.29826e-05
COL4A1 [NCBI] 5.29826e-05
EA2 [NCBI] 5.23988e-05
AIMAH [NCBI] 4.44048e-05
SCN1A [NCBI] 4.33297e-05
DYT1 [NCBI] 4.03137e-05
ornithine transcarbamylase deficiency, hyperammonemia due to [NCBI] 3.83523e-05
KAL1 [NCBI] 3.535e-05
PTH [NCBI] 3.30243e-05
krabbe disease [NCBI] 2.72549e-05
MB [NCBI] 2.67685e-05
WBS [NCBI] 2.01657e-05
AT [NCBI] 1.32191e-05
ADA [NCBI] 9.31392e-06
VIP [NCBI] 8.03805e-06
panencephalitis, subacute sclerosing [NCBI] 5.73481e-06
NPY [NCBI] 4.37015e-06
GFAP [NCBI] 2.35333e-06
CJD [NCBI] 1.15606e-06
TNF [NCBI] 8.4838e-07
SLE [NCBI] 3.53714e-07
EGF [NCBI] 4.17001e-08



Database Center for Life Science