|
OMIM |
Link |
Information gain |
01 |
|
ASD1
|
[NCBI]
|
0.00727658
|
|
|
AVSD
|
[NCBI]
|
0.00248322
|
|
|
axenfeld-rieger anomaly with cardiac defects and sensorineural hearing loss
|
[NCBI]
|
0.00171781
|
|
|
atrial septal defect with atrioventricular conduction defects
|
[NCBI]
|
0.000858821
|
|
|
TARPS
|
[NCBI]
|
0.000785962
|
|
|
HOS
|
[NCBI]
|
0.000526206
|
|
|
NKX2E
|
[NCBI]
|
0.000512938
|
|
|
lymphedema, microcephaly, chorioretinopathy syndrome
|
[NCBI]
|
0.000419401
|
|
|
DURS1
|
[NCBI]
|
0.000419401
|
|
|
dandy-walker-like malformation with atrioventricular septal defect
|
[NCBI]
|
0.000384327
|
|
|
asplenia with cardiovascular anomalies
|
[NCBI]
|
0.000291227
|
|
|
AOS
|
[NCBI]
|
0.00027482
|
|
|
right ventricular hypoplasia, isolated
|
[NCBI]
|
0.000171715
|
|
|
cardiofaciocutaneous syndrome
|
[NCBI]
|
0.000166208
|
|
|
DRRS
|
[NCBI]
|
0.000124673
|
|
|
lymphedema, atrial septal defect, and facial changes
|
[NCBI]
|
0.000113012
|
|
|
brachydactyly, type e, with atrial septal defect, type ii
|
[NCBI]
|
0.000113012
|
|
|
cardiac septal defects with coarctation of the aorta
|
[NCBI]
|
0.000113012
|
|
|
pulmonic stenosis, atrial septal defect, and unique electrocardiographic abnormalities
|
[NCBI]
|
0.000113012
|
|
|
atrial septal defect, secundum, with various cardiac and noncardiac defects
|
[NCBI]
|
0.000113012
|
|
|
cardiac malformation, cleft lip-palate, microcephaly and digital anomalies
|
[NCBI]
|
0.000113012
|
|
|
EVC
|
[NCBI]
|
9.88932e-05
|
|
|
TLL1
|
[NCBI]
|
8.96982e-05
|
|
|
rapadilino syndrome
|
[NCBI]
|
8.20878e-05
|
|
|
heterotaxy, visceral, 2, autosomal
|
[NCBI]
|
7.65946e-05
|
|
|
AVSD2
|
[NCBI]
|
7.25138e-05
|
|
|
CRELD1
|
[NCBI]
|
7.07183e-05
|
|
|
emanuel syndrome
|
[NCBI]
|
6.22404e-05
|
|
|
MYH6
|
[NCBI]
|
5.97434e-05
|
|
|
megalencephaly-cutis marmorata telangiectatica congenita
|
[NCBI]
|
5.8842e-05
|
|
|
WSS
|
[NCBI]
|
5.73814e-05
|
|
|
CRS1
|
[NCBI]
|
5.60441e-05
|
|
|
ACG2
|
[NCBI]
|
5.4811e-05
|
|
|
SALL4
|
[NCBI]
|
5.25308e-05
|
|
|
PQBP1
|
[NCBI]
|
5.19102e-05
|
|
|
seckel syndrome 1
|
[NCBI]
|
5.06632e-05
|
|
|
TRPS1
|
[NCBI]
|
4.6664e-05
|
|
|
weaver syndrome
|
[NCBI]
|
4.59741e-05
|
|
|
contractural arachnodactyly, congenital
|
[NCBI]
|
4.40399e-05
|
|
|
MKKS
|
[NCBI]
|
4.1853e-05
|
|
|
fraser syndrome
|
[NCBI]
|
4.13451e-05
|
|
|
MCOPS7
|
[NCBI]
|
4.08535e-05
|
|
|
TBS
|
[NCBI]
|
3.90323e-05
|
|
|
charge syndrome
|
[NCBI]
|
3.86093e-05
|
|
|
CES
|
[NCBI]
|
3.36783e-05
|
|
|
costello syndrome
|
[NCBI]
|
3.30909e-05
|
|
|
TH
|
[NCBI]
|
3.30448e-05
|
|
|
CF
|
[NCBI]
|
3.09147e-05
|
|
|
CLS
|
[NCBI]
|
3.02262e-05
|
|
|
ADM
|
[NCBI]
|
2.95844e-05
|
|
|
AMC
|
[NCBI]
|
2.93114e-05
|
|
|
velocardiofacial syndrome
|
[NCBI]
|
2.90915e-05
|
|
|
AVP
|
[NCBI]
|
7.58292e-06
|
|
|
KLK3
|
[NCBI]
|
1.91382e-06
|
|
|
apnea, obstructive sleep
|
[NCBI]
|
1.38274e-06
|
|
|
PWS
|
[NCBI]
|
1.37912e-06
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
1.61473e-07
|
|