|
OMIM |
Link |
Information gain |
01 |
|
spatial visualization, aptitude for
|
[NCBI]
|
0.0025497
|
|
|
CGF1
|
[NCBI]
|
0.00237459
|
|
|
gonadal dysgenesis, xx type, with deafness
|
[NCBI]
|
0.00200421
|
|
|
NS1
|
[NCBI]
|
0.00159415
|
|
|
GBY
|
[NCBI]
|
0.00132809
|
|
|
gordon syndrome
|
[NCBI]
|
0.00114309
|
|
|
GDXY
|
[NCBI]
|
0.0008283
|
|
|
brachydactyly-mental retardation syndrome
|
[NCBI]
|
0.000607072
|
|
|
noonan syndrome 2
|
[NCBI]
|
0.000607072
|
|
|
immunoglobulin m, level of
|
[NCBI]
|
0.000567689
|
|
|
prognathism, mandibular
|
[NCBI]
|
0.000536375
|
|
|
ASD1
|
[NCBI]
|
0.000510391
|
|
|
GCY
|
[NCBI]
|
0.000510391
|
|
|
SHOX
|
[NCBI]
|
0.000472609
|
|
|
XIST
|
[NCBI]
|
0.000467078
|
|
|
DA5
|
[NCBI]
|
0.000451673
|
|
|
gonadal dysgenesis, xy type
|
[NCBI]
|
0.000436268
|
|
|
ODG1
|
[NCBI]
|
0.000370157
|
|
|
LWD
|
[NCBI]
|
0.000330824
|
|
|
SRY
|
[NCBI]
|
0.000249327
|
|
|
ISS
|
[NCBI]
|
0.000243069
|
|
|
nuchal bleb, familial
|
[NCBI]
|
0.000189726
|
|
|
ODG2
|
[NCBI]
|
0.000161791
|
|
|
BDE
|
[NCBI]
|
0.000161791
|
|
|
aortic valve disease
|
[NCBI]
|
0.000160745
|
|
|
SHOXY
|
[NCBI]
|
0.000149428
|
|
|
RA
|
[NCBI]
|
0.000124134
|
|
|
SHOX2
|
[NCBI]
|
0.000121877
|
|
|
POF1
|
[NCBI]
|
0.000119364
|
|
|
RPS4X
|
[NCBI]
|
0.000107824
|
|
|
sjogren-larsson-like ichthyosis without cns or eye involvement
|
[NCBI]
|
9.47367e-05
|
|
|
SRS
|
[NCBI]
|
8.68047e-05
|
|
|
genitopalatocardiac syndrome
|
[NCBI]
|
8.62662e-05
|
|
|
DSS
|
[NCBI]
|
8.07696e-05
|
|
|
WT1
|
[NCBI]
|
7.74856e-05
|
|
|
frasier syndrome
|
[NCBI]
|
7.34328e-05
|
|
|
HYR
|
[NCBI]
|
7.07301e-05
|
|
|
MAOA
|
[NCBI]
|
6.66149e-05
|
|
|
NYS1
|
[NCBI]
|
6.6398e-05
|
|
|
WT1
|
[NCBI]
|
6.46713e-05
|
|
|
GH1
|
[NCBI]
|
6.39455e-05
|
|
|
lymphedema, hereditary, i
|
[NCBI]
|
6.01878e-05
|
|
|
TPO
|
[NCBI]
|
5.92733e-05
|
|
|
nondisjunction
|
[NCBI]
|
5.67342e-05
|
|
|
denys-drash syndrome
|
[NCBI]
|
5.67342e-05
|
|
|
CDPX1
|
[NCBI]
|
5.39002e-05
|
|
|
lymphedema-distichiasis syndrome
|
[NCBI]
|
5.14985e-05
|
|
|
UCMD
|
[NCBI]
|
5.00797e-05
|
|
|
faciogenital dysplasia
|
[NCBI]
|
4.59344e-05
|
|
|
growth hormone insensitivity syndrome
|
[NCBI]
|
4.26665e-05
|
|
|
FGD1
|
[NCBI]
|
4.23842e-05
|
|
|
HEMB
|
[NCBI]
|
4.14666e-05
|
|
|
campomelic dysplasia
|
[NCBI]
|
4.06957e-05
|
|
|
SHBG
|
[NCBI]
|
3.87736e-05
|
|
|
SSX1
|
[NCBI]
|
3.82052e-05
|
|
|
BGN
|
[NCBI]
|
3.75474e-05
|
|
|
GHRH
|
[NCBI]
|
3.70963e-05
|
|
|
DCN
|
[NCBI]
|
3.58043e-05
|
|
|
TBG
|
[NCBI]
|
3.43263e-05
|
|
|
hurler syndrome
|
[NCBI]
|
3.3952e-05
|
|
|
CHM
|
[NCBI]
|
3.34528e-05
|
|
|
PAEP
|
[NCBI]
|
3.05833e-05
|
|
|
DAZ
|
[NCBI]
|
3.0278e-05
|
|
|
GNRH1
|
[NCBI]
|
2.93065e-05
|
|
|
AHO
|
[NCBI]
|
2.7571e-05
|
|
|
AR
|
[NCBI]
|
2.62205e-05
|
|
|
KAL1
|
[NCBI]
|
2.5994e-05
|
|
|
TG
|
[NCBI]
|
2.54697e-05
|
|
|
IGFALS
|
[NCBI]
|
2.164e-05
|
|
|
CD
|
[NCBI]
|
2.13984e-05
|
|
|
ichthyosis, x-linked
|
[NCBI]
|
2.11737e-05
|
|
|
PCD
|
[NCBI]
|
1.97532e-05
|
|
|
DMD
|
[NCBI]
|
1.8478e-05
|
|
|
VEGF
|
[NCBI]
|
1.84507e-05
|
|
|
GHR
|
[NCBI]
|
1.7651e-05
|
|
|
RTT
|
[NCBI]
|
1.43681e-05
|
|
|
GIP
|
[NCBI]
|
1.079e-05
|
|
|
CVID
|
[NCBI]
|
1.03737e-05
|
|
|
AFP
|
[NCBI]
|
8.41619e-06
|
|
|
TNFRSF11B
|
[NCBI]
|
4.19194e-06
|
|
|
G6PD
|
[NCBI]
|
1.47326e-06
|
|
|
PCNA
|
[NCBI]
|
8.0422e-07
|
|
|
PRL
|
[NCBI]
|
7.90303e-07
|
|