|
OMIM |
Link |
Information gain |
01 |
|
PI
|
[NCBI]
|
0.00164565
|
|
|
IGAD1
|
[NCBI]
|
0.000952205
|
|
|
emphysema, hereditary pulmonary
|
[NCBI]
|
0.000402845
|
|
|
cutis laxa, autosomal recessive, type i
|
[NCBI]
|
0.000372931
|
|
|
MMP12
|
[NCBI]
|
0.000154447
|
|
|
hemolytic anemia, congenital, with emphysema and cutis laxa
|
[NCBI]
|
0.000133566
|
|
|
CLE
|
[NCBI]
|
0.000133566
|
|
|
heterotopia, periventricular, ehlers-danlos variant
|
[NCBI]
|
9.71155e-05
|
|
|
HMOX1
|
[NCBI]
|
9.39817e-05
|
|
|
cutis laxa, autosomal dominant
|
[NCBI]
|
7.40678e-05
|
|
|
lung cancer
|
[NCBI]
|
6.49604e-05
|
|
|
pheochromocytoma
|
[NCBI]
|
6.10572e-05
|
|
|
LTBP4
|
[NCBI]
|
5.64589e-05
|
|
|
PCTT
|
[NCBI]
|
5.63773e-05
|
|
|
PGL1
|
[NCBI]
|
5.63773e-05
|
|
|
CSA
|
[NCBI]
|
5.33665e-05
|
|
|
ITGB6
|
[NCBI]
|
5.30861e-05
|
|
|
HGF
|
[NCBI]
|
5.17621e-05
|
|
|
CCR6
|
[NCBI]
|
5.05794e-05
|
|
|
ARMD1
|
[NCBI]
|
5.00797e-05
|
|
|
ITGAV
|
[NCBI]
|
4.69232e-05
|
|
|
SFTPD
|
[NCBI]
|
4.69232e-05
|
|
|
LAMB1
|
[NCBI]
|
4.69232e-05
|
|
|
menkes disease
|
[NCBI]
|
4.54145e-05
|
|
|
LAM
|
[NCBI]
|
3.33796e-05
|
|
|
PXE
|
[NCBI]
|
3.0197e-05
|
|
|
UGB
|
[NCBI]
|
2.82018e-05
|
|
|
MMP9
|
[NCBI]
|
2.73473e-05
|
|
|
TGFB1
|
[NCBI]
|
2.61948e-05
|
|
|
ELN
|
[NCBI]
|
2.51682e-05
|
|
|
SLPI
|
[NCBI]
|
2.15837e-05
|
|
|
RNASE3
|
[NCBI]
|
1.49014e-05
|
|
|
SLE
|
[NCBI]
|
1.4722e-05
|
|
|
FGF7
|
[NCBI]
|
1.28332e-05
|
|
|
VEGF
|
[NCBI]
|
1.04818e-05
|
|
|
MPO
|
[NCBI]
|
1.04015e-05
|
|
|
TLR4
|
[NCBI]
|
8.88111e-06
|
|
|
CF
|
[NCBI]
|
6.97748e-06
|
|
|
EGF
|
[NCBI]
|
4.07075e-06
|
|
|
TNF
|
[NCBI]
|
3.0387e-06
|
|
|
PCNA
|
[NCBI]
|
1.40922e-06
|
|
|
CEACAM5
|
[NCBI]
|
1.1944e-08
|
|