|
OMIM |
Link |
Information gain |
01 |
|
apnea, obstructive sleep
|
[NCBI]
|
0.0153174
|
|
|
CPI
|
[NCBI]
|
0.00319081
|
|
|
palatopharyngeal incompetence
|
[NCBI]
|
0.00250724
|
|
|
torus palatinus and torus mandibularis
|
[NCBI]
|
0.00159766
|
|
|
cleft palate-lateral synechia syndrome
|
[NCBI]
|
0.000796446
|
|
|
prognathism, mandibular
|
[NCBI]
|
0.000796446
|
|
|
OPD2
|
[NCBI]
|
0.000695953
|
|
|
OPD1
|
[NCBI]
|
0.000388754
|
|
|
OFC1
|
[NCBI]
|
0.000304209
|
|
|
EGF
|
[NCBI]
|
0.000302727
|
|
|
c syndrome
|
[NCBI]
|
0.000222518
|
|
|
suprabulbar paresis, congenital
|
[NCBI]
|
0.000189909
|
|
|
pena-shokeir syndrome, type i
|
[NCBI]
|
0.000175204
|
|
|
keratosis palmoplantaris striata i
|
[NCBI]
|
0.000126283
|
|
|
c-like syndrome
|
[NCBI]
|
0.000126283
|
|
|
arhinia, choanal atresia, and microphthalmia
|
[NCBI]
|
0.000126283
|
|
|
focal epithelial hyperplasia, oral
|
[NCBI]
|
0.000126283
|
|
|
holzgreve syndrome
|
[NCBI]
|
0.000119159
|
|
|
ODG2
|
[NCBI]
|
0.000113488
|
|
|
lymphedema, hereditary, ii
|
[NCBI]
|
0.000113488
|
|
|
hyperostosis corticalis generalisata, benign form of worth, with torus palatinus
|
[NCBI]
|
0.000108778
|
|
|
BMND1
|
[NCBI]
|
0.000108778
|
|
|
LDS
|
[NCBI]
|
0.000108778
|
|
|
PCNA
|
[NCBI]
|
9.29733e-05
|
|
|
cerebrocostomandibular syndrome
|
[NCBI]
|
8.82907e-05
|
|
|
heterotopia, periventricular, x-linked dominant
|
[NCBI]
|
8.62997e-05
|
|
|
SLE
|
[NCBI]
|
8.42131e-05
|
|
|
SATB2
|
[NCBI]
|
8.3529e-05
|
|
|
SMMCI
|
[NCBI]
|
7.95333e-05
|
|
|
TGFB3
|
[NCBI]
|
7.67095e-05
|
|
|
HFM
|
[NCBI]
|
7.19067e-05
|
|
|
COH1
|
[NCBI]
|
7.06812e-05
|
|
|
SJS1
|
[NCBI]
|
6.76332e-05
|
|
|
LWD
|
[NCBI]
|
6.57805e-05
|
|
|
RTS
|
[NCBI]
|
6.32257e-05
|
|
|
sotos syndrome
|
[NCBI]
|
6.16518e-05
|
|
|
RSTS
|
[NCBI]
|
5.87648e-05
|
|
|
AMC
|
[NCBI]
|
5.80909e-05
|
|
|
TCOF
|
[NCBI]
|
5.67943e-05
|
|
|
VWS
|
[NCBI]
|
5.67943e-05
|
|
|
CF
|
[NCBI]
|
5.61754e-05
|
|
|
FGF10
|
[NCBI]
|
5.47079e-05
|
|
|
MKS1
|
[NCBI]
|
5.38156e-05
|
|
|
CD
|
[NCBI]
|
5.32598e-05
|
|
|
FLNA
|
[NCBI]
|
5.06996e-05
|
|
|
DLX6
|
[NCBI]
|
4.54896e-05
|
|
|
OSR2
|
[NCBI]
|
4.17246e-05
|
|
|
PJS
|
[NCBI]
|
3.93834e-05
|
|
|
BCNS
|
[NCBI]
|
3.87739e-05
|
|
|
PDGFC
|
[NCBI]
|
3.74643e-05
|
|
|
PLUNC
|
[NCBI]
|
3.74643e-05
|
|
|
TBX22
|
[NCBI]
|
3.60174e-05
|
|
|
INHBB
|
[NCBI]
|
3.60174e-05
|
|
|
DLX5
|
[NCBI]
|
3.60174e-05
|
|
|
fragile x mental retardation syndrome
|
[NCBI]
|
3.54265e-05
|
|
|
IRF6
|
[NCBI]
|
3.48148e-05
|
|
|
TAS2R16
|
[NCBI]
|
3.48148e-05
|
|
|
LHX8
|
[NCBI]
|
3.48148e-05
|
|
|
IP
|
[NCBI]
|
3.3925e-05
|
|
|
SUMO1
|
[NCBI]
|
3.20877e-05
|
|
|
DSC1
|
[NCBI]
|
3.13696e-05
|
|
|
DSC2
|
[NCBI]
|
3.07172e-05
|
|
|
MFS
|
[NCBI]
|
2.76894e-05
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
2.7511e-05
|
|
|
LRP5
|
[NCBI]
|
2.73146e-05
|
|
|
EYA1
|
[NCBI]
|
2.73146e-05
|
|
|
AHR
|
[NCBI]
|
2.7168e-05
|
|
|
SFRP1
|
[NCBI]
|
2.62418e-05
|
|
|
TGFBR2
|
[NCBI]
|
2.56076e-05
|
|
|
mucopolysaccharidosis type iva
|
[NCBI]
|
2.50258e-05
|
|
|
SHOX
|
[NCBI]
|
2.50258e-05
|
|
|
SHH
|
[NCBI]
|
2.46335e-05
|
|
|
DLG1
|
[NCBI]
|
2.44884e-05
|
|
|
CDH1
|
[NCBI]
|
2.35232e-05
|
|
|
INHBA
|
[NCBI]
|
2.24784e-05
|
|
|
GSC
|
[NCBI]
|
1.95217e-05
|
|
|
TRPV1
|
[NCBI]
|
1.65882e-05
|
|
|
FGFR2
|
[NCBI]
|
1.54599e-05
|
|
|
SRS
|
[NCBI]
|
1.51402e-05
|
|
|
MAP3K5
|
[NCBI]
|
1.36592e-05
|
|
|
NGFR
|
[NCBI]
|
1.2214e-05
|
|
|
INS
|
[NCBI]
|
1.00335e-05
|
|
|
CHAT
|
[NCBI]
|
9.75087e-06
|
|
|
CEACAM5
|
[NCBI]
|
4.0678e-06
|
|
|
NPY
|
[NCBI]
|
1.76543e-06
|
|
|
PTK2
|
[NCBI]
|
1.13882e-06
|
|
|
ACHE
|
[NCBI]
|
9.38286e-07
|
|
|
EGFR
|
[NCBI]
|
2.71087e-07
|
|
|
PTH
|
[NCBI]
|
1.56641e-07
|
|
|
TH
|
[NCBI]
|
1.20486e-07
|
|
|
MBP
|
[NCBI]
|
4.37169e-09
|
|