|
OMIM |
Link |
Information gain |
01 |
|
centralopathic epilepsy
|
[NCBI]
|
0.00194777
|
|
|
SPS
|
[NCBI]
|
0.0011791
|
|
|
myoclonic epilepsy of unverricht and lundborg
|
[NCBI]
|
0.000342861
|
|
|
EIG
|
[NCBI]
|
0.000279446
|
|
|
SMEI
|
[NCBI]
|
0.000209099
|
|
|
encephalopathy, neonatal severe, due to mecp2 mutations
|
[NCBI]
|
0.000116971
|
|
|
hyperekplexia, hereditary
|
[NCBI]
|
0.000100626
|
|
|
GTS
|
[NCBI]
|
5.03651e-05
|
|
|
AS
|
[NCBI]
|
4.9094e-05
|
|
|
RTT
|
[NCBI]
|
4.72705e-05
|
|
|
FTD
|
[NCBI]
|
3.89536e-05
|
|
|
NPY
|
[NCBI]
|
3.6175e-05
|
|
|
PD
|
[NCBI]
|
2.57952e-05
|
|
|
BDNF
|
[NCBI]
|
2.40463e-05
|
|
|
MECP2
|
[NCBI]
|
2.39889e-05
|
|
|
HD
|
[NCBI]
|
1.79523e-05
|
|
|
CHAT
|
[NCBI]
|
9.89031e-06
|
|
|
GFAP
|
[NCBI]
|
7.55401e-06
|
|
|
AD
|
[NCBI]
|
7.38128e-06
|
|
|
PRL
|
[NCBI]
|
4.72131e-06
|
|