|
OMIM |
Link |
Information gain |
01 |
|
SVAS
|
[NCBI]
|
0.00395889
|
|
|
aortic aneurysm, familial thoracic 1
|
[NCBI]
|
0.00335645
|
|
|
WBS
|
[NCBI]
|
0.00219108
|
|
|
aortic valve disease
|
[NCBI]
|
0.00142678
|
|
|
ELN
|
[NCBI]
|
0.00064613
|
|
|
calcific aortic disease with immunologic abnormalities, familial
|
[NCBI]
|
0.000528872
|
|
|
RA
|
[NCBI]
|
0.00030167
|
|
|
EFE
|
[NCBI]
|
0.000154697
|
|
|
hypercalcemia, idiopathic, of infancy
|
[NCBI]
|
0.000143409
|
|
|
CMH
|
[NCBI]
|
0.00012648
|
|
|
ARH
|
[NCBI]
|
0.000120965
|
|
|
SLE
|
[NCBI]
|
0.000114321
|
|
|
scheie syndrome
|
[NCBI]
|
0.000109773
|
|
|
AVSD
|
[NCBI]
|
0.000108505
|
|
|
pfeiffer-palm-teller syndrome
|
[NCBI]
|
0.000105527
|
|
|
alkaptonuria
|
[NCBI]
|
9.38464e-05
|
|
|
mucopolysaccharidosis type vi
|
[NCBI]
|
8.8637e-05
|
|
|
subaortic stenosis, membranous
|
[NCBI]
|
8.30787e-05
|
|
|
OBSCN
|
[NCBI]
|
8.29498e-05
|
|
|
mental retardation, fra12a type
|
[NCBI]
|
6.18244e-05
|
|
|
CDK9
|
[NCBI]
|
6.05968e-05
|
|
|
ectopia lentis, isolated
|
[NCBI]
|
5.68344e-05
|
|
|
NPPA
|
[NCBI]
|
5.26549e-05
|
|
|
fibromuscular dysplasia of arteries
|
[NCBI]
|
4.63073e-05
|
|
|
PTPN11
|
[NCBI]
|
4.25603e-05
|
|
|
AFD1
|
[NCBI]
|
3.93755e-05
|
|
|
dyschromatosis symmetrica hereditaria 1
|
[NCBI]
|
3.62424e-05
|
|
|
CALCRL
|
[NCBI]
|
3.51634e-05
|
|
|
SPP1
|
[NCBI]
|
3.38414e-05
|
|
|
TNFRSF11B
|
[NCBI]
|
3.37813e-05
|
|
|
BSG
|
[NCBI]
|
3.28644e-05
|
|
|
MFS
|
[NCBI]
|
2.80653e-05
|
|
|
FBN1
|
[NCBI]
|
2.66712e-05
|
|
|
von willebrand disease
|
[NCBI]
|
2.54189e-05
|
|
|
bullous erythroderma ichthyosiformis congenita of brocq
|
[NCBI]
|
2.35425e-05
|
|
|
ADM
|
[NCBI]
|
2.30201e-05
|
|
|
GJA1
|
[NCBI]
|
2.24921e-05
|
|
|
osteogenesis imperfecta, type i
|
[NCBI]
|
1.94165e-05
|
|
|
AVP
|
[NCBI]
|
1.56254e-05
|
|
|
CTGF
|
[NCBI]
|
1.55014e-05
|
|
|
FRDA
|
[NCBI]
|
1.49815e-05
|
|
|
APOE
|
[NCBI]
|
1.39059e-05
|
|
|
VEGF
|
[NCBI]
|
3.18362e-06
|
|
|
EPO
|
[NCBI]
|
1.5409e-06
|
|
|
PCNA
|
[NCBI]
|
9.0011e-07
|
|
|
EGFR
|
[NCBI]
|
2.08268e-07
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
1.49013e-07
|
|
|
FMF
|
[NCBI]
|
3.06713e-08
|
|