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MeSH keywords -> Related genes, diseases (OMIM)


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01 Muscle Hypertonia [NCBI]


Gene


Gene Link Information
Gain
01
MS [NCBI] 0.000117314
GLRA1 [NCBI] 5.56696e-05
GER [NCBI] 5.38017e-05
TRAK1 [NCBI] 3.40503e-05
TRAK2 [NCBI] 1.5332e-05
GCHFR [NCBI] 1.43147e-05
SLC6A5 [NCBI] 1.3969e-05
ALG12 [NCBI] 1.36815e-05
NSF [NCBI] 1.27007e-05
KCNMA1 [NCBI] 1.14735e-05
HGS [NCBI] 1.1402e-05
SCN4A [NCBI] 9.08612e-06
PTGER1 [NCBI] 8.9302e-06
MSTN [NCBI] 8.75712e-06
TRPV1 [NCBI] 8.59996e-06
PMP22 [NCBI] 6.54143e-06
NGF [NCBI] 3.67239e-06




OMIM


OMIM Link Information
gain
01
microcephaly, hiatus hernia, and nephrotic syndrome [NCBI] 0.000880362
hyperekplexia, hereditary [NCBI] 0.000672013
SPS [NCBI] 0.000603963
GLRA1 [NCBI] 0.000291873
yemenite deaf-blind hypopigmentation syndrome [NCBI] 0.000112852
CDG1G [NCBI] 0.000107346
stuve-wiedemann syndrome [NCBI] 8.42761e-05
TRAK1 [NCBI] 8.00936e-05
weaver syndrome [NCBI] 7.64665e-05
infantile sialic acid storage disorder [NCBI] 7.45252e-05
ALG12 [NCBI] 7.15158e-05
COH1 [NCBI] 6.69024e-05
SLC1A3 [NCBI] 6.26709e-05
NSF [NCBI] 6.15648e-05
SOX10 [NCBI] 5.21546e-05
DPYD [NCBI] 4.93514e-05
tyrosinemia, type i [NCBI] 4.22596e-05
NGFB [NCBI] 8.74059e-06
AD [NCBI] 6.80853e-06




Database Center for Life Science