|
OMIM |
Link |
Information gain |
01 |
|
cayler cardiofacial syndrome
|
[NCBI]
|
0.00288467
|
|
|
tetralogy of fallot
|
[NCBI]
|
0.00153152
|
|
|
patent ductus arteriosus
|
[NCBI]
|
0.000744944
|
|
|
corpus callosum, agenesis of, with facial anomalies and robin sequence
|
[NCBI]
|
0.000647644
|
|
|
cleidocranial dysplasia with micrognathia, absent thumbs, and distal aphalangia
|
[NCBI]
|
0.000625244
|
|
|
AVSD
|
[NCBI]
|
0.000490584
|
|
|
dandy-walker-like malformation with atrioventricular septal defect
|
[NCBI]
|
0.000476563
|
|
|
DWS
|
[NCBI]
|
0.000364525
|
|
|
CTHM
|
[NCBI]
|
0.000253857
|
|
|
velocardiofacial syndrome
|
[NCBI]
|
0.00025334
|
|
|
ZFPM2
|
[NCBI]
|
0.000140847
|
|
|
tetralogy of fallot syndrome, autosomal recessive
|
[NCBI]
|
0.000124742
|
|
|
hypertelorism and tetralogy of fallot
|
[NCBI]
|
0.000124742
|
|
|
tetralogy of fallot and glaucoma
|
[NCBI]
|
0.000124742
|
|
|
JAG1
|
[NCBI]
|
0.000108783
|
|
|
fibromatosis, gingival, with hypertrichosis and mental retardation
|
[NCBI]
|
0.000102276
|
|
|
ASD2
|
[NCBI]
|
0.000102276
|
|
|
SLC7A4
|
[NCBI]
|
9.09049e-05
|
|
|
recombinant chromosome 8 syndrome
|
[NCBI]
|
8.42118e-05
|
|
|
frontonasal dysplasia
|
[NCBI]
|
7.59315e-05
|
|
|
DGS
|
[NCBI]
|
7.26791e-05
|
|
|
MCOPS9
|
[NCBI]
|
7.0493e-05
|
|
|
c syndrome
|
[NCBI]
|
6.52869e-05
|
|
|
AFD1
|
[NCBI]
|
5.82209e-05
|
|
|
GATA4
|
[NCBI]
|
5.51073e-05
|
|
|
MKKS
|
[NCBI]
|
5.33472e-05
|
|
|
NKX2E
|
[NCBI]
|
5.14568e-05
|
|
|
charge syndrome
|
[NCBI]
|
5.00486e-05
|
|
|
HMI
|
[NCBI]
|
4.30599e-05
|
|
|
FGA
|
[NCBI]
|
3.91617e-05
|
|
|
NS1
|
[NCBI]
|
3.49964e-05
|
|
|
VEGF
|
[NCBI]
|
3.39459e-05
|
|
|
BBS
|
[NCBI]
|
3.08666e-05
|
|
|
GJA1
|
[NCBI]
|
3.02297e-05
|
|
|
PTH
|
[NCBI]
|
2.90036e-06
|
|
|
TNF
|
[NCBI]
|
3.81825e-07
|
|