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MeSH keywords -> Related genes, diseases (OMIM)


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01 Stiff-Person Syndrome [NCBI]

Gene


 Gene Link Information
Gain		 01
GLRA1 [NCBI] 9.80828e-05
AMPH [NCBI] 7.95913e-05
GAD2 [NCBI] 4.92536e-05
PTPRN [NCBI] 4.8849e-05
GABARAP [NCBI] 2.75606e-05
GAD1 [NCBI] 2.36181e-05
TOR1A [NCBI] 1.60983e-05
GPHN [NCBI] 1.29712e-05
CALB1 [NCBI] 1.24376e-05
HSD17B4 [NCBI] 9.8175e-06
CLN3 [NCBI] 7.57834e-06
ATXN3 [NCBI] 6.79683e-06



OMIM


 OMIM Link Information
gain		 01
SPS [NCBI] 0.0398197
cerebral palsy, ataxic, autosomal recessive [NCBI] 0.000454561
AMPH [NCBI] 0.000356436
hyperekplexia, hereditary [NCBI] 0.000337652
GLRA1 [NCBI] 0.00020768
DYT1 [NCBI] 0.000117048
cerebral palsy, spastic, symmetric, autosomal recessive [NCBI] 0.000106243
RSMD1 [NCBI] 8.3549e-05
GPHN [NCBI] 6.90048e-05
GAD1 [NCBI] 6.05698e-05
GAD2 [NCBI] 5.54947e-05
MG [NCBI] 2.32447e-05



Database Center for Life Science