|
OMIM |
Link |
Information gain |
01 |
|
spatial visualization, aptitude for
|
[NCBI]
|
0.000912577
|
|
|
migraine with or without aura, susceptibility to, 1
|
[NCBI]
|
0.000732018
|
|
|
MDD
|
[NCBI]
|
0.000571915
|
|
|
RA
|
[NCBI]
|
0.000150913
|
|
|
apnea, obstructive sleep
|
[NCBI]
|
9.52893e-05
|
|
|
GTS
|
[NCBI]
|
8.58032e-05
|
|
|
ADHD
|
[NCBI]
|
8.48848e-05
|
|
|
AD
|
[NCBI]
|
7.82107e-05
|
|
|
OCD1
|
[NCBI]
|
7.24489e-05
|
|
|
CMT4A
|
[NCBI]
|
7.0644e-05
|
|
|
WS2A
|
[NCBI]
|
6.89914e-05
|
|
|
disorganization, mouse, homolog of
|
[NCBI]
|
6.74677e-05
|
|
|
CMTX1
|
[NCBI]
|
4.851e-05
|
|
|
CMT1B
|
[NCBI]
|
4.33103e-05
|
|
|
WS1
|
[NCBI]
|
4.17327e-05
|
|
|
A1BG
|
[NCBI]
|
4.09124e-05
|
|
|
XRCC9
|
[NCBI]
|
3.21843e-05
|
|
|
SLE
|
[NCBI]
|
3.0985e-05
|
|
|
WT1
|
[NCBI]
|
3.06014e-05
|
|
|
CBD
|
[NCBI]
|
2.86273e-05
|
|
|
PAX3
|
[NCBI]
|
2.44793e-05
|
|
|
MPZ
|
[NCBI]
|
2.27691e-05
|
|
|
MECP2
|
[NCBI]
|
2.00125e-05
|
|
|
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency
|
[NCBI]
|
1.84962e-05
|
|
|
AKR1B1
|
[NCBI]
|
1.70848e-05
|
|
|
INS
|
[NCBI]
|
1.54115e-05
|
|
|
RTT
|
[NCBI]
|
1.40029e-05
|
|
|
ALB
|
[NCBI]
|
1.26333e-05
|
|
|
KLK3
|
[NCBI]
|
1.21923e-05
|
|
|
HD
|
[NCBI]
|
1.17321e-05
|
|
|
COMT
|
[NCBI]
|
1.13655e-05
|
|
|
APOB
|
[NCBI]
|
9.79716e-06
|
|
|
CHAT
|
[NCBI]
|
6.32111e-06
|
|
|
LPL
|
[NCBI]
|
5.6196e-06
|
|
|
APOE
|
[NCBI]
|
4.78929e-06
|
|
|
CCK
|
[NCBI]
|
3.69817e-06
|
|
|
CRC
|
[NCBI]
|
3.68061e-06
|
|
|
GFAP
|
[NCBI]
|
3.47804e-06
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
2.12185e-06
|
|
|
PWS
|
[NCBI]
|
2.03606e-06
|
|
|
PRL
|
[NCBI]
|
1.71514e-06
|
|
|
CF
|
[NCBI]
|
7.10237e-07
|
|
|
CJD
|
[NCBI]
|
5.94662e-07
|
|
|
EGF
|
[NCBI]
|
4.79133e-08
|
|