|
OMIM |
Link |
Information gain |
01 |
|
necrotizing encephalopathy, acute, autosomal dominant
|
[NCBI]
|
0.00107364
|
|
|
autism
|
[NCBI]
|
0.000553779
|
|
|
AGS1
|
[NCBI]
|
0.000155665
|
|
|
MBP
|
[NCBI]
|
0.000155125
|
|
|
GFAP
|
[NCBI]
|
0.000133927
|
|
|
senile plaque formation
|
[NCBI]
|
0.000131018
|
|
|
reese retinal dysplasia
|
[NCBI]
|
0.000131018
|
|
|
craniofacial dyssynostosis with short stature
|
[NCBI]
|
0.000100073
|
|
|
pyridoxamine 5-prime-phosphate oxidase deficiency
|
[NCBI]
|
0.000100073
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
8.96266e-05
|
|
|
ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant
|
[NCBI]
|
8.72191e-05
|
|
|
cerebral palsy, spastic, symmetric, autosomal recessive
|
[NCBI]
|
8.0164e-05
|
|
|
apnea, obstructive sleep
|
[NCBI]
|
7.89651e-05
|
|
|
glutathione synthetase deficiency
|
[NCBI]
|
7.8364e-05
|
|
|
MAP2
|
[NCBI]
|
6.74993e-05
|
|
|
GALR2
|
[NCBI]
|
6.55281e-05
|
|
|
PNPO
|
[NCBI]
|
6.55281e-05
|
|
|
crigler-najjar syndrome
|
[NCBI]
|
6.30739e-05
|
|
|
alzheimer disease 3
|
[NCBI]
|
6.06417e-05
|
|
|
autonomic control, congenital failure of
|
[NCBI]
|
5.90339e-05
|
|
|
MTHFD1
|
[NCBI]
|
5.45574e-05
|
|
|
ADHD
|
[NCBI]
|
5.17951e-05
|
|
|
HHF2
|
[NCBI]
|
4.88614e-05
|
|
|
PTGS2
|
[NCBI]
|
3.32733e-05
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
2.7491e-05
|
|
|
RTT
|
[NCBI]
|
2.64999e-05
|
|
|
ADCYAP1
|
[NCBI]
|
2.62519e-05
|
|
|
BDNF
|
[NCBI]
|
2.55071e-05
|
|
|
GTS
|
[NCBI]
|
1.93524e-05
|
|
|
TLR4
|
[NCBI]
|
1.68847e-05
|
|
|
COMT
|
[NCBI]
|
1.6479e-05
|
|
|
APOE
|
[NCBI]
|
1.63969e-05
|
|
|
GDNF
|
[NCBI]
|
1.34922e-05
|
|
|
AD
|
[NCBI]
|
1.20038e-05
|
|
|
NPPA
|
[NCBI]
|
8.98163e-06
|
|
|
G6PD
|
[NCBI]
|
7.89409e-06
|
|
|
CCK
|
[NCBI]
|
7.22422e-06
|
|
|
CAT
|
[NCBI]
|
6.81096e-06
|
|
|
CJD
|
[NCBI]
|
6.6813e-06
|
|
|
SLE
|
[NCBI]
|
6.47722e-06
|
|
|
ACHE
|
[NCBI]
|
5.95947e-06
|
|
|
EPO
|
[NCBI]
|
2.31752e-06
|
|
|
NGFB
|
[NCBI]
|
2.22843e-06
|
|