|
OMIM |
Link |
Information gain |
01 |
|
apert syndrome
|
[NCBI]
|
0.00358812
|
|
|
SCS
|
[NCBI]
|
0.00348419
|
|
|
FGFR2
|
[NCBI]
|
0.00333857
|
|
|
pfeiffer syndrome
|
[NCBI]
|
0.00257874
|
|
|
TWIST1
|
[NCBI]
|
0.000951674
|
|
|
carpenter syndrome
|
[NCBI]
|
0.000603003
|
|
|
robinow-sorauf syndrome
|
[NCBI]
|
0.000391895
|
|
|
acrocephalopolysyndactyly type iv
|
[NCBI]
|
0.00032411
|
|
|
FGFR3
|
[NCBI]
|
0.000254007
|
|
|
crouzon syndrome
|
[NCBI]
|
0.00018741
|
|
|
TWISTNB
|
[NCBI]
|
0.000148687
|
|
|
FGFR1
|
[NCBI]
|
0.00013749
|
|
|
muenke syndrome
|
[NCBI]
|
0.000134977
|
|
|
JWS
|
[NCBI]
|
0.000131569
|
|
|
acrocephalopolysyndactyly type iii
|
[NCBI]
|
0.000107894
|
|
|
craniosynostosis, philadelphia type
|
[NCBI]
|
0.000107894
|
|
|
summitt syndrome
|
[NCBI]
|
8.54423e-05
|
|
|
CRS2
|
[NCBI]
|
7.14934e-05
|
|
|
FGF2
|
[NCBI]
|
6.46947e-05
|
|
|
RAB23
|
[NCBI]
|
6.05077e-05
|
|
|
HDAC9
|
[NCBI]
|
5.53119e-05
|
|
|
RTD
|
[NCBI]
|
4.31379e-05
|
|
|
MSX2
|
[NCBI]
|
4.10277e-05
|
|
|
RUNX2
|
[NCBI]
|
3.26806e-05
|
|
|
FGF8
|
[NCBI]
|
2.96207e-05
|
|
|
NS1
|
[NCBI]
|
1.94581e-05
|
|
|
HPS
|
[NCBI]
|
1.32662e-05
|
|
|
CHS
|
[NCBI]
|
9.91459e-06
|
|
|
SPP1
|
[NCBI]
|
3.97165e-06
|
|