|
OMIM |
Link |
Information gain |
01 |
|
hypertelorism with esophageal abnormality and hypospadias
|
[NCBI]
|
0.00953533
|
|
|
cleft larynx, posterior
|
[NCBI]
|
0.0011521
|
|
|
DIP
|
[NCBI]
|
0.000924992
|
|
|
SGM1
|
[NCBI]
|
0.000849287
|
|
|
mohr syndrome
|
[NCBI]
|
0.000627765
|
|
|
varadi-papp syndrome
|
[NCBI]
|
0.00056773
|
|
|
short rib-polydactyly syndrome, type ii
|
[NCBI]
|
0.000535469
|
|
|
subglottic bar
|
[NCBI]
|
0.000495394
|
|
|
laryngeal web, familial
|
[NCBI]
|
0.000408019
|
|
|
ATD1
|
[NCBI]
|
0.000377037
|
|
|
tracheobronchial stenosis, congenital
|
[NCBI]
|
0.000203637
|
|
|
nasal bones, absence of
|
[NCBI]
|
0.000203637
|
|
|
laryngeal atresia, encephalocele, and limb deformities
|
[NCBI]
|
0.000203637
|
|
|
hirschsprung disease with heart defects, laryngeal anomalies, and preaxial polydactyly
|
[NCBI]
|
0.000203637
|
|
|
PHS
|
[NCBI]
|
0.000200411
|
|
|
thoracopelvic dysostosis
|
[NCBI]
|
0.000164381
|
|
|
PC1
|
[NCBI]
|
0.000164381
|
|
|
larynx, congenital partial atresia of
|
[NCBI]
|
0.000149577
|
|
|
TLPD
|
[NCBI]
|
0.000139971
|
|
|
LOCS
|
[NCBI]
|
0.000139971
|
|
|
robin sequence with cleft mandible and limb anomalies
|
[NCBI]
|
0.000139971
|
|
|
marshall-smith syndrome
|
[NCBI]
|
0.000122426
|
|
|
PCNA
|
[NCBI]
|
0.000107163
|
|
|
biotinidase deficiency
|
[NCBI]
|
0.000104005
|
|
|
EGFR
|
[NCBI]
|
0.000102617
|
|
|
lipoid proteinosis of urbach and wiethe
|
[NCBI]
|
9.98404e-05
|
|
|
epidermolysis bullosa letalis
|
[NCBI]
|
9.79714e-05
|
|
|
AFD1
|
[NCBI]
|
9.30205e-05
|
|
|
apnea, obstructive sleep
|
[NCBI]
|
9.16192e-05
|
|
|
HAE
|
[NCBI]
|
9.15498e-05
|
|
|
UMS
|
[NCBI]
|
9.15498e-05
|
|
|
fraser syndrome
|
[NCBI]
|
8.6347e-05
|
|
|
NPY
|
[NCBI]
|
8.06933e-05
|
|
|
MSD
|
[NCBI]
|
7.91072e-05
|
|
|
RTS
|
[NCBI]
|
7.65123e-05
|
|
|
GCPS
|
[NCBI]
|
7.3401e-05
|
|
|
AMC
|
[NCBI]
|
7.12839e-05
|
|
|
TCOF
|
[NCBI]
|
6.99605e-05
|
|
|
TRPV2
|
[NCBI]
|
5.12785e-05
|
|
|
RA
|
[NCBI]
|
4.54529e-05
|
|
|
GTS
|
[NCBI]
|
3.94586e-05
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
3.94586e-05
|
|
|
C1NH
|
[NCBI]
|
3.86626e-05
|
|
|
SLE
|
[NCBI]
|
3.5736e-05
|
|
|
ANXA1
|
[NCBI]
|
3.53356e-05
|
|
|
DGS
|
[NCBI]
|
3.37518e-05
|
|
|
VIP
|
[NCBI]
|
2.9809e-05
|
|
|
temporal arteritis
|
[NCBI]
|
2.73037e-05
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
2.5345e-05
|
|
|
PGR
|
[NCBI]
|
1.59682e-05
|
|
|
TH
|
[NCBI]
|
1.33502e-05
|
|
|
HD
|
[NCBI]
|
1.17304e-05
|
|
|
CYP1A1
|
[NCBI]
|
9.71336e-06
|
|
|
XDH
|
[NCBI]
|
8.56064e-06
|
|
|
G6PD
|
[NCBI]
|
6.34386e-06
|
|
|
ADA
|
[NCBI]
|
5.84845e-06
|
|
|
ACHE
|
[NCBI]
|
5.66269e-06
|
|
|
VEGF
|
[NCBI]
|
3.53112e-06
|
|
|
CAT
|
[NCBI]
|
3.06527e-06
|
|
|
EGF
|
[NCBI]
|
2.55872e-06
|
|
|
AR
|
[NCBI]
|
2.01246e-06
|
|
|
PTH
|
[NCBI]
|
2.1798e-07
|
|