|
OMIM |
Link |
Information gain |
01 |
|
ETL2
|
[NCBI]
|
0.00158697
|
|
|
heterotopia, periventricular, associated with chromosome 5p anomalies
|
[NCBI]
|
0.00119841
|
|
|
epilepsy, myoclonic, benign adult familial, type 2
|
[NCBI]
|
0.00098052
|
|
|
alopecia, psychomotor epilepsy, pyorrhea, and mental subnormality
|
[NCBI]
|
0.00098052
|
|
|
amyloidosis vii
|
[NCBI]
|
0.000100104
|
|
|
heterotopia, periventricular, x-linked dominant
|
[NCBI]
|
9.27799e-05
|
|
|
SCA10
|
[NCBI]
|
8.92647e-05
|
|
|
myoclonic dystonia
|
[NCBI]
|
7.99294e-05
|
|
|
SGCE
|
[NCBI]
|
5.63183e-05
|
|
|
FLNA
|
[NCBI]
|
5.00962e-05
|
|
|
CACNA1A
|
[NCBI]
|
4.72778e-05
|
|
|
GTS
|
[NCBI]
|
4.11849e-05
|
|
|
TS
|
[NCBI]
|
3.70827e-05
|
|
|
CP
|
[NCBI]
|
3.2154e-05
|
|
|
CJD
|
[NCBI]
|
2.58282e-05
|
|
|
TTR
|
[NCBI]
|
2.29303e-05
|
|
|
NPY
|
[NCBI]
|
1.37146e-05
|
|
|
APOE
|
[NCBI]
|
1.17302e-05
|
|
|
GFAP
|
[NCBI]
|
1.08059e-05
|
|
|
PRL
|
[NCBI]
|
8.94895e-06
|
|
|
VEGF
|
[NCBI]
|
1.76921e-06
|
|