|
OMIM |
Link |
Information
gain |
01 |
|
|
HHF7
|
[NCBI]
|
0.00222949
|
|
|
|
neuropathy, hereditary sensory and autonomic, type i, with cough and gastroesophageal reflux
|
[NCBI]
|
0.00102023
|
|
|
|
LQT1
|
[NCBI]
|
0.000966384
|
|
|
|
JLNS1
|
[NCBI]
|
0.000650278
|
|
|
|
MVP
|
[NCBI]
|
0.00053523
|
|
|
|
cardiac conduction defect
|
[NCBI]
|
0.000280726
|
|
|
|
VF
|
[NCBI]
|
0.000189453
|
|
|
|
orthostatic intolerance
|
[NCBI]
|
0.000182101
|
|
|
|
breath-holding spells
|
[NCBI]
|
0.000176131
|
|
|
|
brugada syndrome 1
|
[NCBI]
|
0.000135505
|
|
|
|
tachycardia, hypertension, microphthalmia, and hyperglycinuria
|
[NCBI]
|
0.00012182
|
|
|
|
cardioauditory syndrome of sanchez cascos
|
[NCBI]
|
0.00012182
|
|
|
|
SCN5A
|
[NCBI]
|
9.96218e-05
|
|
|
|
syncope, familial neurocardiogenic
|
[NCBI]
|
9.93556e-05
|
|
|
|
brugada syndrome 2
|
[NCBI]
|
9.08822e-05
|
|
|
|
atrial standstill
|
[NCBI]
|
8.53826e-05
|
|
|
|
KCNH2
|
[NCBI]
|
8.33408e-05
|
|
|
|
SSS1
|
[NCBI]
|
8.12954e-05
|
|
|
|
SLC6A2
|
[NCBI]
|
7.77884e-05
|
|
|
|
sick sinus syndrome, autosomal dominant
|
[NCBI]
|
7.53344e-05
|
|
|
|
CMD1E
|
[NCBI]
|
7.53344e-05
|
|
|
|
SQT1
|
[NCBI]
|
7.53344e-05
|
|
|
|
CPVT
|
[NCBI]
|
7.30194e-05
|
|
|
|
CMH
|
[NCBI]
|
7.26477e-05
|
|
|
|
GPD1L
|
[NCBI]
|
7.25879e-05
|
|
|
|
gitelman syndrome
|
[NCBI]
|
6.75853e-05
|
|
|
|
LQT3
|
[NCBI]
|
6.47746e-05
|
|
|
|
KCNJ8
|
[NCBI]
|
6.46996e-05
|
|
|
|
HCHWAD
|
[NCBI]
|
6.35352e-05
|
|
|
|
CASQ2
|
[NCBI]
|
6.1612e-05
|
|
|
|
infantile spasm syndrome, x-linked
|
[NCBI]
|
6.03072e-05
|
|
|
|
KCNE1
|
[NCBI]
|
5.65341e-05
|
|
|
|
EDMD2
|
[NCBI]
|
5.60591e-05
|
|
|
|
GJA5
|
[NCBI]
|
5.57696e-05
|
|
|
|
andersen cardiodysrhythmic periodic paralysis
|
[NCBI]
|
5.15507e-05
|
|
|
|
HHF1
|
[NCBI]
|
4.4467e-05
|
|
|
|
KCNQ1
|
[NCBI]
|
4.24944e-05
|
|
|
|
CLS
|
[NCBI]
|
3.86249e-05
|
|
|
|
LMNA
|
[NCBI]
|
3.65014e-05
|
|
|
|
AVP
|
[NCBI]
|
3.08722e-05
|
|
|
|
GIP
|
[NCBI]
|
2.65437e-05
|
|
|
|
KSS
|
[NCBI]
|
2.54461e-05
|
|
|
|
PRL
|
[NCBI]
|
2.30439e-05
|
|
