|
OMIM |
Link |
Information gain |
01 |
|
CF
|
[NCBI]
|
0.0040173
|
|
|
CPL
|
[NCBI]
|
0.00334721
|
|
|
DIP
|
[NCBI]
|
0.00115219
|
|
|
MPO
|
[NCBI]
|
0.00110331
|
|
|
pulmonary alveolar proteinosis, acquired
|
[NCBI]
|
0.00107356
|
|
|
histiocytosis, familial lipochrome
|
[NCBI]
|
0.000925375
|
|
|
pulmonary alveolar microlithiasis
|
[NCBI]
|
0.000815659
|
|
|
pulmonary function
|
[NCBI]
|
0.000707844
|
|
|
mucoepithelial dysplasia, hereditary
|
[NCBI]
|
0.000626005
|
|
|
testicular microlithiasis
|
[NCBI]
|
0.000626005
|
|
|
behcet syndrome
|
[NCBI]
|
0.000556594
|
|
|
eosinophilia, familial
|
[NCBI]
|
0.000533713
|
|
|
letterer-siwe disease
|
[NCBI]
|
0.000454478
|
|
|
dermatitis, atopic
|
[NCBI]
|
0.000418126
|
|
|
achalasia, familial esophageal
|
[NCBI]
|
0.000353749
|
|
|
LAM
|
[NCBI]
|
0.000310987
|
|
|
OD
|
[NCBI]
|
0.00028809
|
|
|
SLE
|
[NCBI]
|
0.000221585
|
|
|
TNF
|
[NCBI]
|
0.000199306
|
|
|
urogenital adysplasia, hereditary
|
[NCBI]
|
0.000190329
|
|
|
CEACAM5
|
[NCBI]
|
0.000184136
|
|
|
UGB
|
[NCBI]
|
0.000182455
|
|
|
young syndrome
|
[NCBI]
|
0.000176991
|
|
|
PI
|
[NCBI]
|
0.00017615
|
|
|
IS1
|
[NCBI]
|
0.000173924
|
|
|
pulmonary hemosiderosis
|
[NCBI]
|
0.000169389
|
|
|
CFTR
|
[NCBI]
|
0.000164119
|
|
|
sarcoidosis
|
[NCBI]
|
0.000130101
|
|
|
LIP
|
[NCBI]
|
0.000129654
|
|
|
TLR4
|
[NCBI]
|
0.000125308
|
|
|
XDH
|
[NCBI]
|
0.00011408
|
|
|
SFTPB
|
[NCBI]
|
0.000110884
|
|
|
choreoathetosis, hypothyroidism, and neonatal respiratory distress
|
[NCBI]
|
0.000107829
|
|
|
NKX2-1
|
[NCBI]
|
0.000103425
|
|
|
CVID
|
[NCBI]
|
9.17507e-05
|
|
|
SLC34A2
|
[NCBI]
|
9.09523e-05
|
|
|
ACE2
|
[NCBI]
|
9.09523e-05
|
|
|
HES
|
[NCBI]
|
8.89696e-05
|
|
|
MG
|
[NCBI]
|
8.62577e-05
|
|
|
bowen syndrome of multiple malformations
|
[NCBI]
|
8.46778e-05
|
|
|
hemosiderosis, pulmonary, with deficiency of gamma-a globulin
|
[NCBI]
|
8.46778e-05
|
|
|
pulmonary nodular lymphoid hyperplasia, familial
|
[NCBI]
|
8.46778e-05
|
|
|
cyanosis and hepatic disease
|
[NCBI]
|
8.46778e-05
|
|
|
pulmonary bullae causing pneumothorax
|
[NCBI]
|
8.46778e-05
|
|
|
cystic disease of lung
|
[NCBI]
|
8.46778e-05
|
|
|
granulomatous disease due to combined cellular and humoral immune defects
|
[NCBI]
|
8.46778e-05
|
|
|
SMDP1
|
[NCBI]
|
8.2616e-05
|
|
|
SCNN1A
|
[NCBI]
|
6.89242e-05
|
|
|
FGF7
|
[NCBI]
|
6.38041e-05
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
6.02784e-05
|
|
|
tracheal antimicrobial peptide
|
[NCBI]
|
5.9218e-05
|
|
|
EGFR
|
[NCBI]
|
5.60641e-05
|
|
|
hydrops fetalis, idiopathic
|
[NCBI]
|
5.3898e-05
|
|
|
pulmonary fibrosis, idiopathic
|
[NCBI]
|
5.37712e-05
|
|
|
NSIAD
|
[NCBI]
|
4.84771e-05
|
|
|
PCD
|
[NCBI]
|
4.61586e-05
|
|
|
PTHLH
|
[NCBI]
|
4.47115e-05
|
|
|
DKC
|
[NCBI]
|
4.39855e-05
|
|
|
EGF
|
[NCBI]
|
4.22274e-05
|
|
|
STRA6
|
[NCBI]
|
4.02873e-05
|
|
|
TLR2
|
[NCBI]
|
3.89056e-05
|
|
|
HSAN3
|
[NCBI]
|
3.86338e-05
|
|
|
TRAF1
|
[NCBI]
|
3.69351e-05
|
|
|
pulmonary edema of mountaineers
|
[NCBI]
|
3.44848e-05
|
|
|
SDC1
|
[NCBI]
|
3.44491e-05
|
|
|
BPI
|
[NCBI]
|
3.44491e-05
|
|
|
sickle cell anemia
|
[NCBI]
|
3.37389e-05
|
|
|
RNASE3
|
[NCBI]
|
3.28837e-05
|
|
|
AFP
|
[NCBI]
|
3.26549e-05
|
|
|
BCL2A1
|
[NCBI]
|
3.24732e-05
|
|
|
CXCL1
|
[NCBI]
|
3.24732e-05
|
|
|
CCL19
|
[NCBI]
|
3.24732e-05
|
|
|
MIRN155
|
[NCBI]
|
3.24732e-05
|
|
|
CPM
|
[NCBI]
|
3.24732e-05
|
|
|
NGFB
|
[NCBI]
|
3.18904e-05
|
|
|
MCOPS9
|
[NCBI]
|
3.12311e-05
|
|
|
FIP1L1
|
[NCBI]
|
3.08344e-05
|
|
|
SEPN1
|
[NCBI]
|
3.08344e-05
|
|
|
PRDX5
|
[NCBI]
|
3.08344e-05
|
|
|
TSC2
|
[NCBI]
|
2.99271e-05
|
|
|
pneumothorax, primary spontaneous
|
[NCBI]
|
2.98428e-05
|
|
|
AQP5
|
[NCBI]
|
2.94352e-05
|
|
|
SFTPA1
|
[NCBI]
|
2.94352e-05
|
|
|
GFAP
|
[NCBI]
|
2.91597e-05
|
|
|
RA
|
[NCBI]
|
2.89548e-05
|
|
|
apnea, obstructive sleep
|
[NCBI]
|
2.89258e-05
|
|
|
KEAP1
|
[NCBI]
|
2.8215e-05
|
|
|
ALB
|
[NCBI]
|
2.64915e-05
|
|
|
cutis laxa, autosomal dominant
|
[NCBI]
|
2.63458e-05
|
|
|
stuve-wiedemann syndrome
|
[NCBI]
|
2.63458e-05
|
|
|
MMP7
|
[NCBI]
|
2.61639e-05
|
|
|
SLPI
|
[NCBI]
|
2.59845e-05
|
|
|
FLCN
|
[NCBI]
|
2.52847e-05
|
|
|
SFTPC
|
[NCBI]
|
2.44811e-05
|
|
|
afibrinogenemia, congenital
|
[NCBI]
|
2.44255e-05
|
|
|
hurler-scheie syndrome
|
[NCBI]
|
2.44255e-05
|
|
|
ADA
|
[NCBI]
|
2.4075e-05
|
|
|
TLR7
|
[NCBI]
|
2.37414e-05
|
|
|
MMP12
|
[NCBI]
|
2.37414e-05
|
|
|
PTH
|
[NCBI]
|
2.36352e-05
|
|
|
cirrhosis, familial
|
[NCBI]
|
2.35588e-05
|
|
|
SERPINA6
|
[NCBI]
|
2.30028e-05
|
|
|
PWS
|
[NCBI]
|
2.25118e-05
|
|
|
SCN1
|
[NCBI]
|
2.19792e-05
|
|
|
IL1RN
|
[NCBI]
|
2.12636e-05
|
|
|
C4A
|
[NCBI]
|
2.12636e-05
|
|
|
OPTB3
|
[NCBI]
|
2.12558e-05
|
|
|
cutis laxa, autosomal recessive, type i
|
[NCBI]
|
2.12558e-05
|
|
|
C4B
|
[NCBI]
|
2.07368e-05
|
|
|
ACE
|
[NCBI]
|
2.02152e-05
|
|
|
methylmalonic aciduria and homocystinuria, cblc type
|
[NCBI]
|
1.99215e-05
|
|
|
AGTR1
|
[NCBI]
|
1.93197e-05
|
|
|
AACT
|
[NCBI]
|
1.93197e-05
|
|
|
PTX3
|
[NCBI]
|
1.93197e-05
|
|
|
AAA
|
[NCBI]
|
1.9304e-05
|
|
|
VIP
|
[NCBI]
|
1.82042e-05
|
|
|
lung cancer
|
[NCBI]
|
1.81548e-05
|
|
|
TLR5
|
[NCBI]
|
1.80982e-05
|
|
|
BTC
|
[NCBI]
|
1.7027e-05
|
|
|
CSF2
|
[NCBI]
|
1.7027e-05
|
|
|
PARP1
|
[NCBI]
|
1.66976e-05
|
|
|
CYBB
|
[NCBI]
|
1.66976e-05
|
|
|
LTA
|
[NCBI]
|
1.60748e-05
|
|
|
CPE
|
[NCBI]
|
1.60748e-05
|
|
|
faciogenital dysplasia
|
[NCBI]
|
1.56896e-05
|
|
|
cerebrotendinous xanthomatosis
|
[NCBI]
|
1.56896e-05
|
|
|
IL13
|
[NCBI]
|
1.54948e-05
|
|
|
fabry disease
|
[NCBI]
|
1.49911e-05
|
|
|
TNFRSF6
|
[NCBI]
|
1.49526e-05
|
|
|
FLNA
|
[NCBI]
|
1.44438e-05
|
|
|
RSMD1
|
[NCBI]
|
1.40418e-05
|
|
|
SOD2
|
[NCBI]
|
1.34612e-05
|
|
|
A2M
|
[NCBI]
|
1.30852e-05
|
|
|
MMP9
|
[NCBI]
|
1.21081e-05
|
|
|
MLL
|
[NCBI]
|
1.21081e-05
|
|
|
TGFB1
|
[NCBI]
|
1.108e-05
|
|
|
TS
|
[NCBI]
|
1.06876e-05
|
|
|
STAT3
|
[NCBI]
|
1.06862e-05
|
|
|
WFS1
|
[NCBI]
|
1.0518e-05
|
|
|
IL4
|
[NCBI]
|
1.03204e-05
|
|
|
ELN
|
[NCBI]
|
1.01777e-05
|
|
|
HPS
|
[NCBI]
|
9.62965e-06
|
|
|
HGF
|
[NCBI]
|
9.60476e-06
|
|
|
MBL2
|
[NCBI]
|
9.5919e-06
|
|
|
MVP
|
[NCBI]
|
9.009e-06
|
|
|
AVP
|
[NCBI]
|
9.00654e-06
|
|
|
BDNF
|
[NCBI]
|
8.73817e-06
|
|
|
EPO
|
[NCBI]
|
8.56739e-06
|
|
|
MUC1
|
[NCBI]
|
8.40204e-06
|
|
|
GBA
|
[NCBI]
|
7.24274e-06
|
|
|
TG
|
[NCBI]
|
7.15726e-06
|
|
|
PCNA
|
[NCBI]
|
6.98879e-06
|
|
|
ACADM
|
[NCBI]
|
6.97712e-06
|
|
|
TNC
|
[NCBI]
|
6.55946e-06
|
|
|
G6PD
|
[NCBI]
|
6.39667e-06
|
|
|
hurler syndrome
|
[NCBI]
|
6.36248e-06
|
|
|
ABCG2
|
[NCBI]
|
6.17028e-06
|
|
|
CAT
|
[NCBI]
|
5.73617e-06
|
|
|
SHH
|
[NCBI]
|
5.58577e-06
|
|
|
PF4
|
[NCBI]
|
4.8297e-06
|
|
|
LPI
|
[NCBI]
|
4.809e-06
|
|
|
von willebrand disease
|
[NCBI]
|
4.56529e-06
|
|
|
AGER
|
[NCBI]
|
4.19743e-06
|
|
|
CGD
|
[NCBI]
|
4.11034e-06
|
|
|
VDR
|
[NCBI]
|
3.26696e-06
|
|
|
JMML
|
[NCBI]
|
3.22e-06
|
|
|
HHT
|
[NCBI]
|
3.22e-06
|
|
|
SPINK1
|
[NCBI]
|
3.0987e-06
|
|
|
ADM
|
[NCBI]
|
2.98598e-06
|
|
|
danubian endemic familial nephropathy
|
[NCBI]
|
2.20499e-06
|
|
|
MFS
|
[NCBI]
|
2.15566e-06
|
|
|
CYP1A1
|
[NCBI]
|
1.75481e-06
|
|
|
CHAT
|
[NCBI]
|
1.44285e-06
|
|
|
ZS
|
[NCBI]
|
1.34459e-06
|
|
|
SHBG
|
[NCBI]
|
1.34322e-06
|
|
|
CP
|
[NCBI]
|
1.22511e-06
|
|
|
NPPA
|
[NCBI]
|
1.08715e-06
|
|
|
VEGF
|
[NCBI]
|
9.63646e-07
|
|
|
VHL
|
[NCBI]
|
9.55961e-07
|
|
|
temporal arteritis
|
[NCBI]
|
9.05578e-07
|
|
|
ABCC1
|
[NCBI]
|
5.57292e-07
|
|
|
SPP1
|
[NCBI]
|
4.80418e-07
|
|
|
FMF
|
[NCBI]
|
3.87726e-07
|
|
|
TNFSF6
|
[NCBI]
|
2.86785e-07
|
|
|
F3
|
[NCBI]
|
2.43116e-07
|
|
|
AT
|
[NCBI]
|
2.14188e-07
|
|
|
HP
|
[NCBI]
|
1.98915e-07
|
|
|
GAPDH
|
[NCBI]
|
1.20953e-07
|
|
|
CRH
|
[NCBI]
|
8.46337e-08
|
|
|
BCNS
|
[NCBI]
|
5.20467e-08
|
|
|
TFPI
|
[NCBI]
|
7.37172e-09
|
|
|
TF
|
[NCBI]
|
2.16776e-09
|
|
|
FRAP1
|
[NCBI]
|
8.3657e-10
|
|
|
ACP5
|
[NCBI]
|
3.45561e-11
|
|