|
OMIM |
Link |
Information gain |
01 |
|
EMWX
|
[NCBI]
|
0.00137383
|
|
|
myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency
|
[NCBI]
|
0.0012178
|
|
|
myasthenia, limb-girdle, with tubular aggregates
|
[NCBI]
|
0.000948879
|
|
|
CHRNE
|
[NCBI]
|
0.000730648
|
|
|
RAPSN
|
[NCBI]
|
0.000687457
|
|
|
SCCMS
|
[NCBI]
|
0.000495623
|
|
|
myasthenic syndrome, congenital, fast-channel
|
[NCBI]
|
0.000312924
|
|
|
myasthenic syndrome, congenital, associated with episodic apnea
|
[NCBI]
|
0.000270336
|
|
|
CHRNA1
|
[NCBI]
|
0.000171793
|
|
|
MUSK
|
[NCBI]
|
0.000162469
|
|
|
CHAT
|
[NCBI]
|
0.000154858
|
|
|
COLQ
|
[NCBI]
|
0.000134913
|
|
|
CHRND
|
[NCBI]
|
0.000129026
|
|
|
ACHE
|
[NCBI]
|
0.000113922
|
|
|
myasthenia, limb-girdle, familial
|
[NCBI]
|
9.17009e-05
|
|
|
MG
|
[NCBI]
|
8.79425e-05
|
|
|
EAD
|
[NCBI]
|
8.57315e-05
|
|
|
PRPS2
|
[NCBI]
|
8.11133e-05
|
|
|
DOK7
|
[NCBI]
|
8.11133e-05
|
|
|
opitz syndrome
|
[NCBI]
|
7.95849e-05
|
|
|
multiple pterygium syndrome, lethal type
|
[NCBI]
|
7.51466e-05
|
|
|
amelogenesis imperfecta, hypoplastic/hypomaturation, x-linked 1
|
[NCBI]
|
7.27487e-05
|
|
|
multiple pterygium syndrome, escobar variant
|
[NCBI]
|
7.27487e-05
|
|
|
CHRNG
|
[NCBI]
|
6.21367e-05
|
|
|
MCOPS7
|
[NCBI]
|
5.97447e-05
|
|
|
OA1
|
[NCBI]
|
3.49895e-05
|
|
|
SCN4A
|
[NCBI]
|
3.47374e-05
|
|
|
CACNA1A
|
[NCBI]
|
3.27221e-05
|
|