|
OMIM |
Link |
Information gain |
01 |
|
MVP
|
[NCBI]
|
0.0101939
|
|
|
aortic valve disease
|
[NCBI]
|
0.000999533
|
|
|
AVSD
|
[NCBI]
|
0.000880791
|
|
|
AOS
|
[NCBI]
|
0.000465939
|
|
|
CMH
|
[NCBI]
|
0.00039947
|
|
|
SLE
|
[NCBI]
|
0.00032501
|
|
|
gaucher disease, type iiic
|
[NCBI]
|
0.000295733
|
|
|
calcific aortic disease with immunologic abnormalities, familial
|
[NCBI]
|
0.000278985
|
|
|
scheie syndrome
|
[NCBI]
|
0.000226783
|
|
|
MFS
|
[NCBI]
|
0.000160475
|
|
|
marfanoid hypermobility syndrome
|
[NCBI]
|
0.000132876
|
|
|
ebstein anomaly
|
[NCBI]
|
0.000123287
|
|
|
heart block, congenital
|
[NCBI]
|
0.0001105
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
0.000103534
|
|
|
chondrodysplasia punctata, autosomal dominant
|
[NCBI]
|
8.33465e-05
|
|
|
andersen cardiodysrhythmic periodic paralysis
|
[NCBI]
|
7.8132e-05
|
|
|
EFE
|
[NCBI]
|
7.51422e-05
|
|
|
NPY
|
[NCBI]
|
6.79203e-05
|
|
|
costello syndrome
|
[NCBI]
|
6.37958e-05
|
|
|
NPPA
|
[NCBI]
|
6.1869e-05
|
|
|
FOP
|
[NCBI]
|
5.95516e-05
|
|
|
GUSB
|
[NCBI]
|
5.95439e-05
|
|
|
LECT1
|
[NCBI]
|
4.51283e-05
|
|
|
AVP
|
[NCBI]
|
4.19102e-05
|
|
|
ARSB
|
[NCBI]
|
3.43772e-05
|
|
|
TNNT2
|
[NCBI]
|
3.43772e-05
|
|
|
FBN1
|
[NCBI]
|
2.86458e-05
|
|
|
TGFB1
|
[NCBI]
|
2.8388e-05
|
|
|
RA
|
[NCBI]
|
2.69782e-05
|
|
|
DMD
|
[NCBI]
|
2.53731e-05
|
|
|
SERPINA6
|
[NCBI]
|
2.05777e-05
|
|
|
CHAT
|
[NCBI]
|
1.63221e-05
|
|
|
GFAP
|
[NCBI]
|
1.09305e-05
|
|
|
ACHE
|
[NCBI]
|
1.05248e-05
|
|
|
TH
|
[NCBI]
|
9.46095e-06
|
|
|
HGF
|
[NCBI]
|
3.85156e-06
|
|
|
EPO
|
[NCBI]
|
3.70718e-06
|
|
|
PCNA
|
[NCBI]
|
3.06311e-06
|
|
|
TNF
|
[NCBI]
|
5.29443e-08
|
|