|
OMIM |
Link |
Information gain |
01 |
|
RTT
|
[NCBI]
|
0.0222386
|
|
|
MECP2
|
[NCBI]
|
0.00565351
|
|
|
autism
|
[NCBI]
|
0.00179948
|
|
|
encephalopathy, neonatal severe, due to mecp2 mutations
|
[NCBI]
|
0.00112559
|
|
|
MRXS13
|
[NCBI]
|
0.00108088
|
|
|
MRXSL
|
[NCBI]
|
0.000603661
|
|
|
rett syndrome, atypical, cdkl5-related
|
[NCBI]
|
0.000347558
|
|
|
autism, x-linked, susceptibility to, 3
|
[NCBI]
|
0.000265711
|
|
|
AS
|
[NCBI]
|
0.000257021
|
|
|
infantile spasm syndrome, x-linked
|
[NCBI]
|
0.000143168
|
|
|
CDKL5
|
[NCBI]
|
0.000123645
|
|
|
DNMT1
|
[NCBI]
|
9.8313e-05
|
|
|
MBD1
|
[NCBI]
|
9.41121e-05
|
|
|
DLX5
|
[NCBI]
|
5.73542e-05
|
|
|
UBE3A
|
[NCBI]
|
4.34424e-05
|
|
|
XIST
|
[NCBI]
|
3.197e-05
|
|
|
CRC
|
[NCBI]
|
3.00566e-05
|
|
|
DLX6
|
[NCBI]
|
2.9646e-05
|
|
|
NTNG1
|
[NCBI]
|
2.78295e-05
|
|
|
SIN3A
|
[NCBI]
|
2.64796e-05
|
|
|
RCOR
|
[NCBI]
|
2.64796e-05
|
|
|
HIST1H3C
|
[NCBI]
|
2.30785e-05
|
|
|
SMARCA2
|
[NCBI]
|
2.30785e-05
|
|
|
GABRB3
|
[NCBI]
|
1.92372e-05
|
|
|
TSIX
|
[NCBI]
|
1.89427e-05
|
|
|
VEGF
|
[NCBI]
|
1.82037e-05
|
|
|
H3F3A
|
[NCBI]
|
1.7677e-05
|
|
|
HDAC2
|
[NCBI]
|
1.63025e-05
|
|
|
ATRX
|
[NCBI]
|
1.48151e-05
|
|
|
REST
|
[NCBI]
|
1.39832e-05
|
|
|
OPRM1
|
[NCBI]
|
1.00362e-05
|
|
|
TYR
|
[NCBI]
|
9.9873e-06
|
|
|
HDAC1
|
[NCBI]
|
9.48078e-06
|
|
|
ILK
|
[NCBI]
|
6.11653e-06
|
|
|
BDNF
|
[NCBI]
|
5.22771e-06
|
|
|
TH
|
[NCBI]
|
2.73756e-06
|
|
|
CRH
|
[NCBI]
|
2.06055e-06
|
|
|
GFAP
|
[NCBI]
|
1.87133e-06
|
|
|
CHAT
|
[NCBI]
|
8.85634e-07
|
|
|
PWS
|
[NCBI]
|
7.16934e-08
|
|