|
OMIM |
Link |
Information gain |
01 |
|
aortic aneurysm, familial thoracic 1
|
[NCBI]
|
0.00750153
|
|
|
MFS
|
[NCBI]
|
0.00145186
|
|
|
aortic aneurysm, abdominal
|
[NCBI]
|
0.0010809
|
|
|
CVD1
|
[NCBI]
|
0.000744944
|
|
|
aortic valve disease
|
[NCBI]
|
0.000721878
|
|
|
temporal arteritis
|
[NCBI]
|
0.000435042
|
|
|
behcet syndrome
|
[NCBI]
|
0.000334214
|
|
|
COL3A1
|
[NCBI]
|
0.000207785
|
|
|
aortic aneurysm, giant congenital
|
[NCBI]
|
0.000198565
|
|
|
FBN1
|
[NCBI]
|
0.00017599
|
|
|
LDS
|
[NCBI]
|
0.00013918
|
|
|
TGFBR2
|
[NCBI]
|
0.000102256
|
|
|
heterotopia, periventricular, ehlers-danlos variant
|
[NCBI]
|
7.82229e-05
|
|
|
furlong syndrome: fs
|
[NCBI]
|
7.82229e-05
|
|
|
aortic aneurysm, familial thoracic 4
|
[NCBI]
|
7.82229e-05
|
|
|
menkes disease
|
[NCBI]
|
7.62897e-05
|
|
|
TMBIM1
|
[NCBI]
|
7.2176e-05
|
|
|
phace association
|
[NCBI]
|
6.58794e-05
|
|
|
ectopia lentis, isolated
|
[NCBI]
|
6.58794e-05
|
|
|
MFS2
|
[NCBI]
|
6.38614e-05
|
|
|
shprintzen-goldberg craniosynostosis syndrome
|
[NCBI]
|
6.04601e-05
|
|
|
fibromuscular dysplasia of arteries
|
[NCBI]
|
5.52795e-05
|
|
|
cutis laxa, autosomal dominant
|
[NCBI]
|
5.52795e-05
|
|
|
TGFBR1
|
[NCBI]
|
5.476e-05
|
|
|
ORW2
|
[NCBI]
|
4.8988e-05
|
|
|
MYH11
|
[NCBI]
|
4.31157e-05
|
|
|
contractural arachnodactyly, congenital
|
[NCBI]
|
4.03164e-05
|
|
|
ehlers-danlos syndrome, type iv, autosomal dominant
|
[NCBI]
|
3.9775e-05
|
|
|
APOE
|
[NCBI]
|
3.91793e-05
|
|
|
MMP9
|
[NCBI]
|
3.77166e-05
|
|
|
ELN
|
[NCBI]
|
3.5498e-05
|
|
|
TNC
|
[NCBI]
|
3.10631e-05
|
|
|
ALGS1
|
[NCBI]
|
3.06235e-05
|
|
|
ABP1
|
[NCBI]
|
2.91704e-05
|
|
|
HHT
|
[NCBI]
|
2.64663e-05
|
|
|
OSM
|
[NCBI]
|
2.55688e-05
|
|
|
TS
|
[NCBI]
|
2.33381e-05
|
|
|
TFPI
|
[NCBI]
|
1.71284e-05
|
|
|
XDH
|
[NCBI]
|
1.69456e-05
|
|
|
SPP1
|
[NCBI]
|
1.32406e-05
|
|
|
SLE
|
[NCBI]
|
1.11427e-05
|
|
|
GFAP
|
[NCBI]
|
3.38411e-06
|
|
|
PTH
|
[NCBI]
|
6.24883e-07
|
|
|
VEGF
|
[NCBI]
|
5.89348e-07
|
|