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01 Myotonia [NCBI]

Gene


 Gene Link Information
Gain		 01
CLCN1 [NCBI] 0.00021955
SCN4A [NCBI] 0.000109734
DMPK [NCBI] 2.36631e-05
CNBP [NCBI] 9.8175e-06
KCNA1 [NCBI] 9.5425e-06
CDC42 [NCBI] 9.06523e-06



OMIM


 OMIM Link Information
gain		 01
DM2 [NCBI] 0.00109739
marden-walker syndrome [NCBI] 0.000984578
HYPP [NCBI] 0.000720266
SJS1 [NCBI] 0.000716702
CLCN1 [NCBI] 0.000697924
myotonia, potassium-aggravated [NCBI] 0.000627678
myotonia congenita, autosomal recessive [NCBI] 0.000467614
SCN4A [NCBI] 0.000362399
myotonia congenita, autosomal dominant [NCBI] 0.000313543
PMC [NCBI] 0.000307051
DMPK [NCBI] 0.000282463
myotonia with skeletal abnormalities and mental retardation [NCBI] 0.000119344
myotonic myopathy with cylindrical spirals [NCBI] 0.000119344
brody myopathy [NCBI] 6.67384e-05
stuve-wiedemann syndrome [NCBI] 5.99304e-05
EA1 [NCBI] 5.88591e-05
CDC42 [NCBI] 5.86705e-05
ATP2A1 [NCBI] 5.86705e-05
dystrophia myotonica 1 [NCBI] 5.44998e-05
HOKPP [NCBI] 5.02757e-05
FFI [NCBI] 2.82615e-05
MG [NCBI] 2.97266e-10



Database Center for Life Science