|
OMIM |
Link |
Information gain |
01 |
|
VRNI
|
[NCBI]
|
0.0271464
|
|
|
palatopharyngeal incompetence
|
[NCBI]
|
0.00181123
|
|
|
APC
|
[NCBI]
|
0.00128253
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
0.000830895
|
|
|
IS1
|
[NCBI]
|
0.000576886
|
|
|
PTH
|
[NCBI]
|
0.000399053
|
|
|
thrombasthenia-thrombocytopenia, hereditary
|
[NCBI]
|
0.00035739
|
|
|
AVSD
|
[NCBI]
|
0.000284331
|
|
|
MG
|
[NCBI]
|
0.000249515
|
|
|
LAM
|
[NCBI]
|
0.000224877
|
|
|
CHED1
|
[NCBI]
|
0.000216207
|
|
|
apnea, obstructive sleep
|
[NCBI]
|
0.000203642
|
|
|
AVP
|
[NCBI]
|
0.00019708
|
|
|
nephrolithiasis, calcium oxalate
|
[NCBI]
|
0.000163927
|
|
|
TNF
|
[NCBI]
|
0.000156767
|
|
|
ehlers-danlos syndrome, type vib
|
[NCBI]
|
0.000150668
|
|
|
porokeratosis of mibelli
|
[NCBI]
|
0.000150668
|
|
|
jejunal atresia
|
[NCBI]
|
0.000150668
|
|
|
OCP
|
[NCBI]
|
0.000149783
|
|
|
urogenital adysplasia, hereditary
|
[NCBI]
|
0.000126424
|
|
|
aortic valve disease
|
[NCBI]
|
0.00012081
|
|
|
gastroesophageal reflux
|
[NCBI]
|
0.000101855
|
|
|
hyperoxaluria, primary, type i
|
[NCBI]
|
0.000101778
|
|
|
KLK3
|
[NCBI]
|
9.95498e-05
|
|
|
ALB
|
[NCBI]
|
9.45891e-05
|
|
|
TFPI
|
[NCBI]
|
8.97192e-05
|
|
|
MFS
|
[NCBI]
|
8.86395e-05
|
|
|
PLG
|
[NCBI]
|
8.06214e-05
|
|
|
SLE
|
[NCBI]
|
7.227e-05
|
|
|
HGF
|
[NCBI]
|
7.09711e-05
|
|
|
deafness, conductive, with stapes fixation
|
[NCBI]
|
6.82777e-05
|
|
|
CF
|
[NCBI]
|
6.17055e-05
|
|
|
EGFR
|
[NCBI]
|
6.14746e-05
|
|
|
OD
|
[NCBI]
|
6.06931e-05
|
|
|
CRC
|
[NCBI]
|
5.82284e-05
|
|
|
IS
|
[NCBI]
|
5.76529e-05
|
|
|
LBP
|
[NCBI]
|
5.6141e-05
|
|
|
MPO
|
[NCBI]
|
5.38025e-05
|
|
|
tricuspid atresia
|
[NCBI]
|
5.22137e-05
|
|
|
WAS
|
[NCBI]
|
4.9562e-05
|
|
|
tuftsin deficiency
|
[NCBI]
|
4.81869e-05
|
|
|
HP
|
[NCBI]
|
4.63575e-05
|
|
|
peters anomaly
|
[NCBI]
|
4.4992e-05
|
|
|
RA
|
[NCBI]
|
4.40399e-05
|
|
|
young syndrome
|
[NCBI]
|
4.23468e-05
|
|
|
OPMD
|
[NCBI]
|
4.17111e-05
|
|
|
CHED2
|
[NCBI]
|
4.00923e-05
|
|
|
LUM
|
[NCBI]
|
3.96253e-05
|
|
|
CCK
|
[NCBI]
|
3.89325e-05
|
|
|
colloid cysts of third ventricle
|
[NCBI]
|
3.81298e-05
|
|
|
PVOD
|
[NCBI]
|
3.81298e-05
|
|
|
klippel-trenaunay-weber syndrome
|
[NCBI]
|
3.75083e-05
|
|
|
NF2
|
[NCBI]
|
3.69882e-05
|
|
|
NGFB
|
[NCBI]
|
3.53594e-05
|
|
|
sea-blue histiocyte disease
|
[NCBI]
|
3.48395e-05
|
|
|
corneal dystrophy, gelatinous drop-like
|
[NCBI]
|
3.3433e-05
|
|
|
SMDP1
|
[NCBI]
|
3.3433e-05
|
|
|
CRS1
|
[NCBI]
|
3.21497e-05
|
|
|
NSHPT
|
[NCBI]
|
3.21497e-05
|
|
|
NAGS
|
[NCBI]
|
3.01796e-05
|
|
|
WGN1
|
[NCBI]
|
2.9881e-05
|
|
|
wolff-parkinson-white syndrome
|
[NCBI]
|
2.88687e-05
|
|
|
EPO
|
[NCBI]
|
2.81116e-05
|
|
|
GIST
|
[NCBI]
|
2.78296e-05
|
|
|
sacral defect with anterior meningocele
|
[NCBI]
|
2.70391e-05
|
|
|
AFP
|
[NCBI]
|
2.59707e-05
|
|
|
EGF
|
[NCBI]
|
2.57558e-05
|
|
|
aneurysm, intracranial berry, 1
|
[NCBI]
|
2.55477e-05
|
|
|
NCSTN
|
[NCBI]
|
2.30991e-05
|
|
|
CEACAM5
|
[NCBI]
|
2.28557e-05
|
|
|
ehlers-danlos syndrome, type vi
|
[NCBI]
|
2.2068e-05
|
|
|
GIP
|
[NCBI]
|
1.98787e-05
|
|
|
polycystic kidneys
|
[NCBI]
|
1.9804e-05
|
|
|
HGFAC
|
[NCBI]
|
1.96075e-05
|
|
|
RNASE3
|
[NCBI]
|
1.95423e-05
|
|
|
IL2RG
|
[NCBI]
|
1.91378e-05
|
|
|
MBP
|
[NCBI]
|
1.90897e-05
|
|
|
CASR
|
[NCBI]
|
1.89759e-05
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
1.894e-05
|
|
|
HRPT1
|
[NCBI]
|
1.89319e-05
|
|
|
GAS
|
[NCBI]
|
1.86917e-05
|
|
|
PTX3
|
[NCBI]
|
1.86917e-05
|
|
|
pfeiffer syndrome
|
[NCBI]
|
1.80406e-05
|
|
|
EFE
|
[NCBI]
|
1.80406e-05
|
|
|
IL2
|
[NCBI]
|
1.73756e-05
|
|
|
EVA
|
[NCBI]
|
1.68168e-05
|
|
|
ehlers-danlos syndrome, type i
|
[NCBI]
|
1.60667e-05
|
|
|
AIMAH
|
[NCBI]
|
1.50267e-05
|
|
|
SPINK1
|
[NCBI]
|
1.49862e-05
|
|
|
pta deficiency
|
[NCBI]
|
1.48864e-05
|
|
|
BCL6
|
[NCBI]
|
1.48864e-05
|
|
|
VEGF
|
[NCBI]
|
1.47257e-05
|
|
|
HHC1
|
[NCBI]
|
1.47005e-05
|
|
|
obesity
|
[NCBI]
|
1.43837e-05
|
|
|
EIG
|
[NCBI]
|
1.4295e-05
|
|
|
F3
|
[NCBI]
|
1.36313e-05
|
|
|
WFS1
|
[NCBI]
|
1.34856e-05
|
|
|
BCPM
|
[NCBI]
|
1.32024e-05
|
|
|
DWS
|
[NCBI]
|
1.31918e-05
|
|
|
TG
|
[NCBI]
|
1.27129e-05
|
|
|
TTR
|
[NCBI]
|
1.25586e-05
|
|
|
AN2
|
[NCBI]
|
1.21415e-05
|
|
|
PRL
|
[NCBI]
|
1.1621e-05
|
|
|
CSF3
|
[NCBI]
|
1.15265e-05
|
|
|
PCI
|
[NCBI]
|
1.15265e-05
|
|
|
LPL
|
[NCBI]
|
1.11927e-05
|
|
|
protoporphyria, erythropoietic
|
[NCBI]
|
1.08328e-05
|
|
|
TGFB1
|
[NCBI]
|
1.05091e-05
|
|
|
hla-d histocompatibility type
|
[NCBI]
|
1.03259e-05
|
|
|
B2M
|
[NCBI]
|
1.00493e-05
|
|
|
OXT
|
[NCBI]
|
9.61753e-06
|
|
|
CP
|
[NCBI]
|
9.56094e-06
|
|
|
PCNA
|
[NCBI]
|
9.06129e-06
|
|
|
CPI
|
[NCBI]
|
8.81714e-06
|
|
|
CPB2
|
[NCBI]
|
8.70446e-06
|
|
|
tyrosinemia, type i
|
[NCBI]
|
8.70446e-06
|
|
|
LSA
|
[NCBI]
|
8.44554e-06
|
|
|
TSC2
|
[NCBI]
|
8.34837e-06
|
|
|
LQT1
|
[NCBI]
|
8.27983e-06
|
|
|
ALGS1
|
[NCBI]
|
8.27983e-06
|
|
|
CHH
|
[NCBI]
|
7.95839e-06
|
|
|
CJD
|
[NCBI]
|
7.92632e-06
|
|
|
NPY
|
[NCBI]
|
7.84202e-06
|
|
|
MCP
|
[NCBI]
|
7.19047e-06
|
|
|
GCK
|
[NCBI]
|
7.19047e-06
|
|
|
lynch syndrome i
|
[NCBI]
|
7.06755e-06
|
|
|
SLPI
|
[NCBI]
|
6.64097e-06
|
|
|
APOE
|
[NCBI]
|
6.44663e-06
|
|
|
MEN2A
|
[NCBI]
|
5.67769e-06
|
|
|
thrombasthenia of glanzmann and naegeli
|
[NCBI]
|
5.5648e-06
|
|
|
homocystinuria
|
[NCBI]
|
5.05836e-06
|
|
|
temporal arteritis
|
[NCBI]
|
4.89473e-06
|
|
|
HFM
|
[NCBI]
|
4.78637e-06
|
|
|
ABP1
|
[NCBI]
|
4.68361e-06
|
|
|
SST
|
[NCBI]
|
4.33669e-06
|
|
|
MB
|
[NCBI]
|
4.22675e-06
|
|
|
BGLAP
|
[NCBI]
|
4.17279e-06
|
|
|
PF4
|
[NCBI]
|
4.12267e-06
|
|
|
ACHE
|
[NCBI]
|
4.10505e-06
|
|
|
danubian endemic familial nephropathy
|
[NCBI]
|
4.09183e-06
|
|
|
IL6
|
[NCBI]
|
4.06686e-06
|
|
|
PD
|
[NCBI]
|
3.86111e-06
|
|
|
LEP
|
[NCBI]
|
3.81309e-06
|
|
|
FRAP1
|
[NCBI]
|
3.1007e-06
|
|
|
GTS
|
[NCBI]
|
3.08399e-06
|
|
|
VIP
|
[NCBI]
|
3.08002e-06
|
|
|
ACH
|
[NCBI]
|
2.89072e-06
|
|
|
DBA
|
[NCBI]
|
2.82602e-06
|
|
|
XDH
|
[NCBI]
|
2.69885e-06
|
|
|
PWS
|
[NCBI]
|
2.63156e-06
|
|
|
BBS
|
[NCBI]
|
2.46031e-06
|
|
|
VHL
|
[NCBI]
|
2.40294e-06
|
|
|
OSM
|
[NCBI]
|
2.39861e-06
|
|
|
SHBG
|
[NCBI]
|
1.78898e-06
|
|
|
SPP1
|
[NCBI]
|
1.70822e-06
|
|
|
HBB
|
[NCBI]
|
1.65133e-06
|
|
|
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency
|
[NCBI]
|
1.42272e-06
|
|
|
VDR
|
[NCBI]
|
1.38334e-06
|
|
|
CVID
|
[NCBI]
|
1.35524e-06
|
|
|
EV
|
[NCBI]
|
1.25344e-06
|
|
|
HPS
|
[NCBI]
|
1.25344e-06
|
|
|
ALK
|
[NCBI]
|
1.17541e-06
|
|
|
ADA
|
[NCBI]
|
1.13696e-06
|
|
|
FGF7
|
[NCBI]
|
9.76715e-07
|
|
|
amyloidosis vi
|
[NCBI]
|
8.11485e-07
|
|
|
BWS
|
[NCBI]
|
7.9352e-07
|
|
|
GFAP
|
[NCBI]
|
7.7354e-07
|
|
|
FA
|
[NCBI]
|
7.64081e-07
|
|
|
MBL2
|
[NCBI]
|
7.30172e-07
|
|
|
NPPA
|
[NCBI]
|
6.45426e-07
|
|
|
TNFSF6
|
[NCBI]
|
5.80511e-07
|
|
|
APOB
|
[NCBI]
|
5.55931e-07
|
|
|
MDD
|
[NCBI]
|
4.98957e-07
|
|
|
PI
|
[NCBI]
|
4.22037e-07
|
|
|
FMF
|
[NCBI]
|
2.90527e-07
|
|
|
TNFRSF11B
|
[NCBI]
|
2.35042e-07
|
|
|
WBS
|
[NCBI]
|
2.05232e-07
|
|
|
CAT
|
[NCBI]
|
5.36879e-08
|
|
|
BL
|
[NCBI]
|
4.63146e-08
|
|
|
SHH
|
[NCBI]
|
4.17933e-08
|
|
|
PJS
|
[NCBI]
|
3.12851e-08
|
|
|
RP
|
[NCBI]
|
2.37661e-08
|
|
|
CTGF
|
[NCBI]
|
1.914e-09
|
|
|
CRH
|
[NCBI]
|
3.55806e-11
|
|