|
OMIM |
Link |
Information gain |
01 |
|
ECA1
|
[NCBI]
|
0.00138221
|
|
|
EIG4
|
[NCBI]
|
0.00101415
|
|
|
FEB9
|
[NCBI]
|
0.00101415
|
|
|
EIG
|
[NCBI]
|
0.000939698
|
|
|
CPD2
|
[NCBI]
|
0.000796434
|
|
|
epilepsy, myoclonic, benign adult familial, type 2
|
[NCBI]
|
0.000796434
|
|
|
EFMR
|
[NCBI]
|
0.000621736
|
|
|
CLN4B
|
[NCBI]
|
0.000564232
|
|
|
kohlschutter-tonz syndrome
|
[NCBI]
|
0.000541934
|
|
|
folic acid, transport defect involving
|
[NCBI]
|
0.00052247
|
|
|
ETL2
|
[NCBI]
|
0.000475624
|
|
|
epilepsy, myoclonic, benign adult familial, type 1
|
[NCBI]
|
0.000462747
|
|
|
AOS
|
[NCBI]
|
0.000284621
|
|
|
PPR
|
[NCBI]
|
0.000270777
|
|
|
EKD1
|
[NCBI]
|
0.00021507
|
|
|
epilepsy, benign neonatal, autosomal recessive
|
[NCBI]
|
0.000125147
|
|
|
mental retardation syndrome, belgian type
|
[NCBI]
|
0.000125147
|
|
|
SMEI
|
[NCBI]
|
0.000121437
|
|
|
split-foot deformity with mandibulofacial dysostosis
|
[NCBI]
|
9.42065e-05
|
|
|
schizencephaly
|
[NCBI]
|
9.42065e-05
|
|
|
epilepsy, reading
|
[NCBI]
|
8.87053e-05
|
|
|
JRKL
|
[NCBI]
|
8.86222e-05
|
|
|
CVG/MR
|
[NCBI]
|
8.46164e-05
|
|
|
ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant
|
[NCBI]
|
8.13594e-05
|
|
|
basal ganglia disease, adult-onset
|
[NCBI]
|
8.13594e-05
|
|
|
hypotension, orthostatic
|
[NCBI]
|
7.86521e-05
|
|
|
valproate embryopathy, susceptibility to
|
[NCBI]
|
7.86521e-05
|
|
|
breath-holding spells
|
[NCBI]
|
7.86521e-05
|
|
|
radioulnar synostosis
|
[NCBI]
|
7.63355e-05
|
|
|
porencephaly, familial
|
[NCBI]
|
7.4311e-05
|
|
|
corpus callosum, agenesis of
|
[NCBI]
|
7.4311e-05
|
|
|
encephalopathy, neonatal severe, due to mecp2 mutations
|
[NCBI]
|
6.94279e-05
|
|
|
ACCPN
|
[NCBI]
|
6.80825e-05
|
|
|
JRK
|
[NCBI]
|
6.6266e-05
|
|
|
ADLTE
|
[NCBI]
|
6.56897e-05
|
|
|
COL4A1
|
[NCBI]
|
5.74238e-05
|
|
|
lipoid proteinosis of urbach and wiethe
|
[NCBI]
|
5.72558e-05
|
|
|
myoclonic epilepsy of lafora
|
[NCBI]
|
5.27316e-05
|
|
|
PKS
|
[NCBI]
|
5.27316e-05
|
|
|
CADASIL
|
[NCBI]
|
5.04472e-05
|
|
|
SPG3A
|
[NCBI]
|
4.96191e-05
|
|
|
SCN1A
|
[NCBI]
|
4.77604e-05
|
|
|
SLC18A2
|
[NCBI]
|
4.65199e-05
|
|
|
myoclonic epilepsy of unverricht and lundborg
|
[NCBI]
|
4.48004e-05
|
|
|
ornithine transcarbamylase deficiency, hyperammonemia due to
|
[NCBI]
|
4.31199e-05
|
|
|
ASPA
|
[NCBI]
|
4.29688e-05
|
|
|
CACNA1A
|
[NCBI]
|
4.01586e-05
|
|
|
NPC1
|
[NCBI]
|
3.9582e-05
|
|
|
SCA1
|
[NCBI]
|
3.50691e-05
|
|
|
SLC6A4
|
[NCBI]
|
3.44565e-05
|
|
|
HPRT1
|
[NCBI]
|
3.2695e-05
|
|
|
FRDA
|
[NCBI]
|
3.2633e-05
|
|
|
TH
|
[NCBI]
|
3.10072e-05
|
|
|
MECP2
|
[NCBI]
|
3.05768e-05
|
|
|
DRPLA
|
[NCBI]
|
2.84253e-05
|
|
|
INS
|
[NCBI]
|
2.59161e-05
|
|
|
MJD
|
[NCBI]
|
2.06135e-05
|
|
|
PRL
|
[NCBI]
|
1.79004e-05
|
|
|
CAT
|
[NCBI]
|
1.01372e-05
|
|
|
ACHE
|
[NCBI]
|
9.19037e-06
|
|
|
CRH
|
[NCBI]
|
8.24088e-06
|
|
|
MBP
|
[NCBI]
|
7.53087e-06
|
|
|
AVP
|
[NCBI]
|
6.74788e-06
|
|
|
GFAP
|
[NCBI]
|
5.1522e-06
|
|
|
NGFB
|
[NCBI]
|
4.75806e-06
|
|
|
PTH
|
[NCBI]
|
1.68736e-06
|
|
|
SLE
|
[NCBI]
|
1.32416e-06
|
|