|
OMIM |
Link |
Information gain |
01 |
|
MG
|
[NCBI]
|
0.110514
|
|
|
myasthenia, limb-girdle, with tubular aggregates
|
[NCBI]
|
0.00369413
|
|
|
RA
|
[NCBI]
|
0.00299852
|
|
|
myasthenia gravis with thymus hyperplasia
|
[NCBI]
|
0.00181547
|
|
|
SLE
|
[NCBI]
|
0.00166834
|
|
|
pena-shokeir syndrome, type i
|
[NCBI]
|
0.00152661
|
|
|
myasthenia, familial infantile, 1
|
[NCBI]
|
0.00105062
|
|
|
myasthenic syndrome, congenital, associated with episodic apnea
|
[NCBI]
|
0.000626519
|
|
|
CHRNE
|
[NCBI]
|
0.000578927
|
|
|
APS2
|
[NCBI]
|
0.00051152
|
|
|
SCCMS
|
[NCBI]
|
0.000461734
|
|
|
CHRNA1
|
[NCBI]
|
0.000427922
|
|
|
DWS
|
[NCBI]
|
0.000319021
|
|
|
myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency
|
[NCBI]
|
0.000278567
|
|
|
CJD
|
[NCBI]
|
0.000246807
|
|
|
ACHE
|
[NCBI]
|
0.000232516
|
|
|
myasthenia, limb-girdle, familial
|
[NCBI]
|
0.000223578
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
0.000143539
|
|
|
CHRNB1
|
[NCBI]
|
0.000130201
|
|
|
AKAP12
|
[NCBI]
|
0.000121627
|
|
|
CHRND
|
[NCBI]
|
0.000115743
|
|
|
myasthenic syndrome, congenital, fast-channel
|
[NCBI]
|
0.000113479
|
|
|
MBP
|
[NCBI]
|
0.000107967
|
|
|
myasthenia, limb-girdle, autoimmune
|
[NCBI]
|
0.000101232
|
|
|
AIRE
|
[NCBI]
|
9.5731e-05
|
|
|
complement component 2 deficiency
|
[NCBI]
|
7.76965e-05
|
|
|
myasthenia, congenital, refractory to acetylcholinesterase inhibitors
|
[NCBI]
|
6.59487e-05
|
|
|
EAD
|
[NCBI]
|
6.54169e-05
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
6.38258e-05
|
|
|
CHRNG
|
[NCBI]
|
5.55556e-05
|
|
|
VAMP2
|
[NCBI]
|
5.55556e-05
|
|
|
RMD
|
[NCBI]
|
5.53202e-05
|
|
|
COLQ
|
[NCBI]
|
5.21832e-05
|
|
|
DAP3
|
[NCBI]
|
5.21832e-05
|
|
|
ICSBP1
|
[NCBI]
|
4.76808e-05
|
|
|
CXCL10
|
[NCBI]
|
4.60218e-05
|
|
|
CXCR3
|
[NCBI]
|
4.60218e-05
|
|
|
CNTFR
|
[NCBI]
|
4.60218e-05
|
|
|
RAPSN
|
[NCBI]
|
4.12703e-05
|
|
|
TCRA
|
[NCBI]
|
3.46715e-05
|
|
|
IL2
|
[NCBI]
|
3.17919e-05
|
|
|
ADA
|
[NCBI]
|
3.14927e-05
|
|
|
thymoma, familial
|
[NCBI]
|
3.03244e-05
|
|
|
CACNA1A
|
[NCBI]
|
2.62639e-05
|
|
|
FOXP3
|
[NCBI]
|
2.62639e-05
|
|
|
MB
|
[NCBI]
|
1.75351e-05
|
|
|
IFNA1
|
[NCBI]
|
1.70166e-05
|
|
|
OSM
|
[NCBI]
|
1.4759e-05
|
|
|
MAG
|
[NCBI]
|
1.28148e-05
|
|
|
TNF
|
[NCBI]
|
1.12325e-05
|
|
|
TG
|
[NCBI]
|
1.05237e-05
|
|
|
TPO
|
[NCBI]
|
9.65528e-06
|
|
|
GAPDH
|
[NCBI]
|
8.78414e-06
|
|
|
autoimmune disease
|
[NCBI]
|
8.77088e-06
|
|
|
epidermolysis bullosa simplex and limb-girdle muscular dystrophy
|
[NCBI]
|
8.77088e-06
|
|
|
AFP
|
[NCBI]
|
8.19963e-06
|
|
|
OPMD
|
[NCBI]
|
7.62062e-06
|
|
|
CD
|
[NCBI]
|
5.06826e-06
|
|
|
CEACAM5
|
[NCBI]
|
4.54938e-06
|
|
|
AMC
|
[NCBI]
|
3.88904e-06
|
|
|
APS1
|
[NCBI]
|
3.34659e-06
|
|
|
NGFB
|
[NCBI]
|
1.73455e-06
|
|
|
VIP
|
[NCBI]
|
1.65194e-06
|
|
|
PRL
|
[NCBI]
|
9.94577e-07
|
|
|
PTH
|
[NCBI]
|
5.50286e-08
|
|
|
EGFR
|
[NCBI]
|
3.98443e-08
|
|