Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Spasm [NCBI]

Gene


 Gene Link Information
Gain		 01
AIC [NCBI] 0.000596739
MS [NCBI] 0.000460155
SPG21 [NCBI] 1.5697e-05
HSPB6 [NCBI] 1.43838e-05
GABARAP [NCBI] 1.43838e-05
MOCS1 [NCBI] 1.38054e-05
MTNR1A [NCBI] 1.33737e-05
SNAP25 [NCBI] 1.06622e-05
SLC12A3 [NCBI] 1.0205e-05
PANK2 [NCBI] 1.01458e-05
CNN1 [NCBI] 9.24665e-06
GFAP [NCBI] 4.67282e-06



OMIM


 OMIM Link Information
gain		 01
AIC [NCBI] 0.00395097
SPS [NCBI] 0.00189863
dwarfism, familial, with muscle spasms [NCBI] 0.00100366
GSM1 [NCBI] 0.000611315
SPG15 [NCBI] 0.000579915
AMCN [NCBI] 0.000440615
achalasia, familial esophageal [NCBI] 0.000429633
hemifacial spasm, familial [NCBI] 0.000398698
satoyoshi syndrome [NCBI] 0.000220196
EKD1 [NCBI] 0.0002057
gamstorp-wohlfart syndrome [NCBI] 0.000132242
SLS [NCBI] 0.000113459
mast syndrome [NCBI] 0.000109774
paralysis agitans, juvenile, of hunt [NCBI] 0.000109774
torticollis [NCBI] 9.57923e-05
acidic cluster protein, 33-kd [NCBI] 8.7436e-05
3-@methylglutaconic aciduria, type iii [NCBI] 8.57315e-05
MTS [NCBI] 7.16717e-05
EA1 [NCBI] 7.16717e-05
GAD2 [NCBI] 6.28306e-05
biotinidase deficiency [NCBI] 6.24302e-05
central core disease of muscle [NCBI] 6.18557e-05
citrullinemia, classic [NCBI] 6.13011e-05
GCDH [NCBI] 5.83402e-05
SPG3A [NCBI] 5.66143e-05
NOS3 [NCBI] 5.25043e-05
MHS1 [NCBI] 4.97985e-05
LNS [NCBI] 4.82929e-05
HPRT1 [NCBI] 4.51904e-05
SMS [NCBI] 4.09893e-05
CDLS1 [NCBI] 3.94317e-05
fabry disease [NCBI] 3.91649e-05
TS [NCBI] 1.67499e-05
GFAP [NCBI] 1.56487e-05
panencephalitis, subacute sclerosing [NCBI] 1.45577e-05
PD [NCBI] 1.06107e-05
MG [NCBI] 4.05845e-06



Database Center for Life Science