|
OMIM |
Link |
Information gain |
01 |
|
pulmonary disease, chronic obstructive
|
[NCBI]
|
0.00111789
|
|
|
PI
|
[NCBI]
|
0.000318425
|
|
|
cutis laxa, autosomal recessive, type i
|
[NCBI]
|
0.000210476
|
|
|
emphysema, congenital, with deafness, penoscrotal web, and mental retardation
|
[NCBI]
|
0.000157129
|
|
|
FUT8
|
[NCBI]
|
6.94637e-05
|
|
|
LOXL1
|
[NCBI]
|
6.42646e-05
|
|
|
FBLN5
|
[NCBI]
|
5.63802e-05
|
|
|
NFE2L2
|
[NCBI]
|
5.47179e-05
|
|
|
SFTPD
|
[NCBI]
|
5.47179e-05
|
|
|
PRTN3
|
[NCBI]
|
5.32952e-05
|
|
|
MFS
|
[NCBI]
|
5.15443e-05
|
|
|
SFTPC
|
[NCBI]
|
4.82238e-05
|
|
|
VEGF
|
[NCBI]
|
4.73241e-05
|
|
|
KL
|
[NCBI]
|
4.54718e-05
|
|
|
TGFBR2
|
[NCBI]
|
4.11639e-05
|
|
|
IL13
|
[NCBI]
|
3.87683e-05
|
|
|
TGFB1
|
[NCBI]
|
3.38607e-05
|
|
|
ELN
|
[NCBI]
|
3.28175e-05
|
|
|
SLPI
|
[NCBI]
|
2.91591e-05
|
|
|
PLTP
|
[NCBI]
|
2.76033e-05
|
|
|
FBN1
|
[NCBI]
|
2.69562e-05
|
|
|
CP
|
[NCBI]
|
1.99905e-05
|
|
|
ABCC1
|
[NCBI]
|
1.82418e-05
|
|
|
HP
|
[NCBI]
|
1.68727e-05
|
|
|
GAPDH
|
[NCBI]
|
1.6442e-05
|
|
|
ADA
|
[NCBI]
|
8.54837e-06
|
|
|
CF
|
[NCBI]
|
4.9598e-06
|
|
|
TNF
|
[NCBI]
|
1.35508e-06
|
|
|
SLE
|
[NCBI]
|
8.98124e-07
|
|