Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Paresis [NCBI]

Gene


 Gene Link Information
Gain		 01
MS [NCBI] 0.00022669
HFM [NCBI] 0.000141293
WG [NCBI] 0.000133008
PMP22 [NCBI] 3.28295e-05
IGAN [NCBI] 3.02222e-05
CACNA1A [NCBI] 1.57259e-05
ATP13A2 [NCBI] 1.26217e-05
ALG3 [NCBI] 1.24066e-05
ARHGDIB [NCBI] 1.22155e-05
MYH1 [NCBI] 1.14891e-05
ATP6 [NCBI] 1.09805e-05
RTN4R [NCBI] 1.07349e-05
AMPD1 [NCBI] 9.8133e-06
CTSA [NCBI] 9.0102e-06
NOTCH4 [NCBI] 8.85067e-06
ATP1A2 [NCBI] 8.59201e-06
KRIT1 [NCBI] 8.46585e-06
PLP1 [NCBI] 8.32955e-06
MPZ [NCBI] 7.94572e-06
CD40LG [NCBI] 7.54772e-06
SPN [NCBI] 7.3366e-06
CYP3A4 [NCBI] 5.70813e-06
ADAMTS13 [NCBI] 5.39991e-06
BMP2 [NCBI] 5.24815e-06
BDNF [NCBI] 3.97102e-06
ACHE [NCBI] 3.85788e-06
MBP [NCBI] 3.48152e-06
PTH [NCBI] 2.05926e-06
PTGS2 [NCBI] 2.05586e-06



OMIM


 OMIM Link Information
gain		 01
polymicrogyria, unilateral [NCBI] 0.00266538
HFM [NCBI] 0.000449081
brain small vessel disease with hemorrhage [NCBI] 0.000114976
IP [NCBI] 0.000106987
adie pupil [NCBI] 0.000100992
LBSL [NCBI] 0.000100992
CDG1D [NCBI] 9.68989e-05
KRS [NCBI] 9.68989e-05
charcot-marie-tooth disease, axonal, type 2j [NCBI] 9.36381e-05
SPMM [NCBI] 9.09269e-05
PLSJ [NCBI] 8.3156e-05
sturge-weber syndrome [NCBI] 8.3156e-05
STXBP1 [NCBI] 7.06867e-05
ALG3 [NCBI] 6.81758e-05
GRIA3 [NCBI] 6.30871e-05
CADASIL [NCBI] 6.26034e-05
meningioma, familial [NCBI] 6.0217e-05
AMPD1 [NCBI] 5.58717e-05
NF2 [NCBI] 5.41503e-05
HGPS [NCBI] 5.13836e-05
MTATP6 [NCBI] 4.65908e-05
CSF3 [NCBI] 4.4764e-05
CACNA1A [NCBI] 4.45577e-05
CJD [NCBI] 4.21138e-05
MPZ [NCBI] 3.86117e-05
PMP22 [NCBI] 3.23347e-05
ALD [NCBI] 2.45041e-05
lymphoma, non-hodgkin, familial [NCBI] 1.56856e-05
BDNF [NCBI] 1.40694e-05
ACHE [NCBI] 1.2993e-05
MBP [NCBI] 1.11911e-05
AVP [NCBI] 1.03266e-05
SLE [NCBI] 8.21474e-06
PTH [NCBI] 4.23734e-06



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