|
OMIM |
Link |
Information gain |
01 |
|
MG
|
[NCBI]
|
0.00282514
|
|
|
MEAX
|
[NCBI]
|
0.00194777
|
|
|
pena-shokeir syndrome, type i
|
[NCBI]
|
0.00183065
|
|
|
myasthenic syndrome, congenital, fast-channel
|
[NCBI]
|
0.00037431
|
|
|
ACHE
|
[NCBI]
|
0.000370031
|
|
|
myasthenic syndrome, congenital, associated with episodic apnea
|
[NCBI]
|
0.000192242
|
|
|
myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency
|
[NCBI]
|
0.000183971
|
|
|
CHAT
|
[NCBI]
|
0.000123526
|
|
|
myotonia congenita, autosomal recessive
|
[NCBI]
|
9.30365e-05
|
|
|
CHRNA1
|
[NCBI]
|
8.55445e-05
|
|
|
AMC
|
[NCBI]
|
8.43071e-05
|
|
|
danon disease
|
[NCBI]
|
7.67194e-05
|
|
|
SCCMS
|
[NCBI]
|
7.67194e-05
|
|
|
SLC18A3
|
[NCBI]
|
4.98976e-05
|
|
|
CHRNE
|
[NCBI]
|
4.97907e-05
|
|
|
LYNX1
|
[NCBI]
|
3.69016e-05
|
|
|
SMAX1
|
[NCBI]
|
3.6264e-05
|
|
|
CHRNA9
|
[NCBI]
|
3.22827e-05
|
|
|
RIC3
|
[NCBI]
|
3.09311e-05
|
|
|
ABL2
|
[NCBI]
|
3.09311e-05
|
|
|
CHRNG
|
[NCBI]
|
2.81926e-05
|
|
|
MUSK
|
[NCBI]
|
2.81926e-05
|
|
|
COLQ
|
[NCBI]
|
2.75228e-05
|
|
|
CHRNA7
|
[NCBI]
|
2.75228e-05
|
|
|
CHRND
|
[NCBI]
|
2.75228e-05
|
|
|
AGRN
|
[NCBI]
|
2.69279e-05
|
|
|
ITPR1
|
[NCBI]
|
2.59068e-05
|
|
|
RAPSN
|
[NCBI]
|
2.4313e-05
|
|
|
UTRN
|
[NCBI]
|
2.33693e-05
|
|
|
BCHE
|
[NCBI]
|
2.28223e-05
|
|
|
DAG1
|
[NCBI]
|
2.12584e-05
|
|
|
CALCA
|
[NCBI]
|
2.07079e-05
|
|
|
ABL1
|
[NCBI]
|
1.82483e-05
|
|
|
AANAT
|
[NCBI]
|
1.77296e-05
|
|
|
CNTF
|
[NCBI]
|
1.45601e-05
|
|
|
DMD
|
[NCBI]
|
1.09563e-05
|
|
|
JAK2
|
[NCBI]
|
1.03033e-05
|
|
|
CDK5
|
[NCBI]
|
9.19964e-06
|
|
|
SDC2
|
[NCBI]
|
8.80583e-06
|
|
|
EGF
|
[NCBI]
|
4.5305e-06
|
|
|
AR
|
[NCBI]
|
4.31752e-06
|
|
|
VIP
|
[NCBI]
|
2.8087e-06
|
|
|
NGFB
|
[NCBI]
|
2.58059e-06
|
|
|
TH
|
[NCBI]
|
1.93313e-06
|
|
|
GFAP
|
[NCBI]
|
2.52522e-08
|
|