|
OMIM |
Link |
Information gain |
01 |
|
kenny-caffey syndrome, type 2
|
[NCBI]
|
0.00106493
|
|
|
brugada syndrome 1
|
[NCBI]
|
0.000163797
|
|
|
AVP
|
[NCBI]
|
0.000134801
|
|
|
LQT1
|
[NCBI]
|
0.000125385
|
|
|
paroxysmal extreme pain disorder
|
[NCBI]
|
9.52359e-05
|
|
|
SSS1
|
[NCBI]
|
9.52359e-05
|
|
|
cardiomyopathy, infantile histiocytoid
|
[NCBI]
|
9.19754e-05
|
|
|
AQP4
|
[NCBI]
|
9.00769e-05
|
|
|
SQT1
|
[NCBI]
|
8.92647e-05
|
|
|
acyl-coa dehydrogenase, long-chain, deficiency of
|
[NCBI]
|
8.92647e-05
|
|
|
leiomyomatosis, esophageal and vulval, with nephropathy
|
[NCBI]
|
8.14952e-05
|
|
|
KCNQ1
|
[NCBI]
|
8.14623e-05
|
|
|
LQT3
|
[NCBI]
|
7.86743e-05
|
|
|
ARVD1
|
[NCBI]
|
7.06814e-05
|
|
|
sudden infant death syndrome
|
[NCBI]
|
6.65411e-05
|
|
|
KCNH2
|
[NCBI]
|
6.52749e-05
|
|
|
FCER1A
|
[NCBI]
|
6.36884e-05
|
|
|
FCER1G
|
[NCBI]
|
6.36884e-05
|
|
|
CDSP
|
[NCBI]
|
6.27664e-05
|
|
|
LGMD2A
|
[NCBI]
|
6.13869e-05
|
|
|
BMD
|
[NCBI]
|
5.7498e-05
|
|
|
KCNJ8
|
[NCBI]
|
5.58044e-05
|
|
|
IGKC
|
[NCBI]
|
4.48975e-05
|
|
|
BDNF
|
[NCBI]
|
4.44828e-05
|
|
|
KSS
|
[NCBI]
|
3.86308e-05
|
|
|
SCN5A
|
[NCBI]
|
3.36654e-05
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
3.19549e-05
|
|
|
ACADM
|
[NCBI]
|
2.83719e-05
|
|
|
MB
|
[NCBI]
|
2.53008e-05
|
|
|
TS
|
[NCBI]
|
1.98042e-05
|
|
|
TFPI
|
[NCBI]
|
1.41136e-05
|
|
|
XDH
|
[NCBI]
|
1.39362e-05
|
|
|
APOE
|
[NCBI]
|
1.34639e-05
|
|
|
GDNF
|
[NCBI]
|
1.18641e-05
|
|
|
EPO
|
[NCBI]
|
1.12776e-05
|
|
|
MPO
|
[NCBI]
|
1.12712e-05
|
|
|
SLE
|
[NCBI]
|
1.07046e-05
|
|
|
CJD
|
[NCBI]
|
1.00272e-05
|
|
|
TNFSF6
|
[NCBI]
|
7.18636e-06
|
|
|
MG
|
[NCBI]
|
6.17165e-06
|
|
|
ACHE
|
[NCBI]
|
4.64986e-06
|
|
|
TNF
|
[NCBI]
|
4.29539e-06
|
|
|
VEGF
|
[NCBI]
|
2.70024e-06
|
|
|
NGFB
|
[NCBI]
|
1.3396e-06
|
|
|
PTH
|
[NCBI]
|
1.03097e-08
|
|