|
OMIM |
Link |
Information
gain |
01 |
|
|
SVAS
|
[NCBI]
|
0.00127301
|
|
|
|
AOS
|
[NCBI]
|
0.0011114
|
|
|
|
splenic hypoplasia
|
[NCBI]
|
0.000773718
|
|
|
|
osteolysis, hereditary, of carpal bones with nephropathy
|
[NCBI]
|
0.000601472
|
|
|
|
pulmonic stenosis
|
[NCBI]
|
0.000595323
|
|
|
|
cayler cardiofacial syndrome
|
[NCBI]
|
0.000528971
|
|
|
|
MVP
|
[NCBI]
|
0.000464945
|
|
|
|
leopard syndrome 1
|
[NCBI]
|
0.000373565
|
|
|
|
NS1
|
[NCBI]
|
0.000350256
|
|
|
|
WBS
|
[NCBI]
|
0.000346037
|
|
|
|
watson syndrome
|
[NCBI]
|
0.000288959
|
|
|
|
keutel syndrome
|
[NCBI]
|
0.000278895
|
|
|
|
ALGS1
|
[NCBI]
|
0.000156283
|
|
|
|
AVSD
|
[NCBI]
|
0.000146808
|
|
|
|
pulmonic stenosis and congenital nephrosis
|
[NCBI]
|
0.000118506
|
|
|
|
disproportionate short stature with ptosis and valvular heart lesions
|
[NCBI]
|
0.000118506
|
|
|
|
prune belly syndrome with pulmonic stenosis, mental retardation, and deafness
|
[NCBI]
|
0.000118506
|
|
|
|
cranioacrofacial syndrome
|
[NCBI]
|
0.000118506
|
|
|
|
pulmonic stenosis and deafness
|
[NCBI]
|
0.000118506
|
|
|
|
cardiofaciocutaneous syndrome
|
[NCBI]
|
0.000108155
|
|
|
|
NF1
|
[NCBI]
|
8.79231e-05
|
|
|
|
mental retardation, fra12a type
|
[NCBI]
|
7.47363e-05
|
|
|
|
VLDLRCH
|
[NCBI]
|
6.76988e-05
|
|
|
|
noonan-like/multiple giant cell lesion syndrome
|
[NCBI]
|
6.42916e-05
|
|
|
|
PTPN11
|
[NCBI]
|
6.27854e-05
|
|
|
|
BMP2
|
[NCBI]
|
6.14875e-05
|
|
|
|
ATS
|
[NCBI]
|
6.14849e-05
|
|
|
|
asplenia with cardiovascular anomalies
|
[NCBI]
|
5.4349e-05
|
|
|
|
NPHS1
|
[NCBI]
|
5.13668e-05
|
|
|
|
SGBS1
|
[NCBI]
|
4.57264e-05
|
|
|
|
charge syndrome
|
[NCBI]
|
4.39408e-05
|
|
|
|
bullous erythroderma ichthyosiformis congenita of brocq
|
[NCBI]
|
3.5682e-05
|
|
|
|
NPPA
|
[NCBI]
|
2.61937e-05
|
|
|
|
CMH
|
[NCBI]
|
2.25332e-05
|
|
