|
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
|
|
