|
OMIM |
Link |
Information gain |
01 |
|
AVSD
|
[NCBI]
|
0.00261483
|
|
|
FRNS
|
[NCBI]
|
0.00110591
|
|
|
patent ductus arteriosus
|
[NCBI]
|
0.000764597
|
|
|
acanthosis nigricans
|
[NCBI]
|
0.000693453
|
|
|
tibia, hypoplasia of, with polydactyly
|
[NCBI]
|
0.000607858
|
|
|
cayler cardiofacial syndrome
|
[NCBI]
|
0.000480827
|
|
|
AOS
|
[NCBI]
|
0.000383542
|
|
|
kabuki syndrome
|
[NCBI]
|
0.00034134
|
|
|
asplenia with cardiovascular anomalies
|
[NCBI]
|
0.000293635
|
|
|
HEY2
|
[NCBI]
|
0.000252393
|
|
|
aneurysm of interventricular septum
|
[NCBI]
|
0.000196473
|
|
|
AVSD2
|
[NCBI]
|
0.000172907
|
|
|
EVC
|
[NCBI]
|
0.000170489
|
|
|
CRELD1
|
[NCBI]
|
0.000163492
|
|
|
CMH
|
[NCBI]
|
0.000157874
|
|
|
heart, malformation of
|
[NCBI]
|
0.000113606
|
|
|
cardiac septal defects with coarctation of the aorta
|
[NCBI]
|
0.000113606
|
|
|
cranioacrofacial syndrome
|
[NCBI]
|
0.000113606
|
|
|
distichiasis with congenital anomalies of the heart and peripheral vasculature
|
[NCBI]
|
0.000113606
|
|
|
gonadal dysgenesis, xy type, with associated anomalies
|
[NCBI]
|
0.000113606
|
|
|
pulmonary atresia with ventricular septal defect
|
[NCBI]
|
0.000113606
|
|
|
aortic arch interruption, facial palsy, and retinal coloboma
|
[NCBI]
|
9.11475e-05
|
|
|
craniosynostosis-mental retardation syndrome of lin and gettig
|
[NCBI]
|
9.11475e-05
|
|
|
stratton-parker syndrome
|
[NCBI]
|
9.11475e-05
|
|
|
HOS
|
[NCBI]
|
8.55726e-05
|
|
|
mental retardation, buenos aires type
|
[NCBI]
|
8.26799e-05
|
|
|
heterotaxy, visceral, 2, autosomal
|
[NCBI]
|
7.71861e-05
|
|
|
right ventricular hypoplasia, isolated
|
[NCBI]
|
7.31047e-05
|
|
|
weyers acrofacial dysostosis
|
[NCBI]
|
6.98552e-05
|
|
|
lujan-fryns syndrome
|
[NCBI]
|
6.48462e-05
|
|
|
emanuel syndrome
|
[NCBI]
|
6.28292e-05
|
|
|
atrial septal defect with atrioventricular conduction defects
|
[NCBI]
|
6.28292e-05
|
|
|
RXRA
|
[NCBI]
|
6.23732e-05
|
|
|
MCOPS9
|
[NCBI]
|
5.94297e-05
|
|
|
HTX1
|
[NCBI]
|
5.79685e-05
|
|
|
CTHM
|
[NCBI]
|
5.42527e-05
|
|
|
cerebrocostomandibular syndrome
|
[NCBI]
|
5.42527e-05
|
|
|
PFM
|
[NCBI]
|
5.42527e-05
|
|
|
tetralogy of fallot
|
[NCBI]
|
5.31858e-05
|
|
|
DGS
|
[NCBI]
|
5.15176e-05
|
|
|
seckel syndrome 1
|
[NCBI]
|
5.1247e-05
|
|
|
papillorenal syndrome
|
[NCBI]
|
5.1247e-05
|
|
|
DRRS
|
[NCBI]
|
5.1247e-05
|
|
|
PTPN11
|
[NCBI]
|
5.04881e-05
|
|
|
EDN1
|
[NCBI]
|
5.00371e-05
|
|
|
PAX2
|
[NCBI]
|
5.00371e-05
|
|
|
contractural arachnodactyly, congenital
|
[NCBI]
|
4.52417e-05
|
|
|
andersen cardiodysrhythmic periodic paralysis
|
[NCBI]
|
4.35001e-05
|
|
|
MKKS
|
[NCBI]
|
4.24297e-05
|
|
|
ODDD
|
[NCBI]
|
4.00416e-05
|
|
|
TBS
|
[NCBI]
|
3.96058e-05
|
|
|
charge syndrome
|
[NCBI]
|
3.91822e-05
|
|
|
cardiofaciocutaneous syndrome
|
[NCBI]
|
3.79783e-05
|
|
|
SERPINA6
|
[NCBI]
|
3.5045e-05
|
|
|
CES
|
[NCBI]
|
3.42435e-05
|
|
|
costello syndrome
|
[NCBI]
|
3.3655e-05
|
|
|
BPES
|
[NCBI]
|
3.30892e-05
|
|
|
ADM
|
[NCBI]
|
3.07695e-05
|
|
|
GJA1
|
[NCBI]
|
3.02297e-05
|
|
|
AMC
|
[NCBI]
|
2.98673e-05
|
|
|
SVAS
|
[NCBI]
|
2.70569e-05
|
|
|
NS1
|
[NCBI]
|
2.45677e-05
|
|
|
TFPI
|
[NCBI]
|
2.1804e-05
|
|
|
TNF
|
[NCBI]
|
7.53248e-06
|
|
|
PWS
|
[NCBI]
|
1.59835e-06
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
8.60451e-08
|
|