|
OMIM |
Link |
Information gain |
01 |
|
cdags syndrome
|
[NCBI]
|
0.00156953
|
|
|
dandy-walker-like malformation with atrioventricular septal defect
|
[NCBI]
|
0.00105678
|
|
|
CCD
|
[NCBI]
|
0.000328122
|
|
|
PFM
|
[NCBI]
|
0.000255003
|
|
|
SCS
|
[NCBI]
|
0.000228812
|
|
|
osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones, but without fractures
|
[NCBI]
|
0.000222912
|
|
|
lambdoid synostosis
|
[NCBI]
|
0.000222912
|
|
|
CLSD
|
[NCBI]
|
0.000183645
|
|
|
carpenter syndrome
|
[NCBI]
|
0.000168831
|
|
|
trigonocephaly, nonsyndromic
|
[NCBI]
|
0.000168831
|
|
|
CRS2
|
[NCBI]
|
0.000159214
|
|
|
FGFR2
|
[NCBI]
|
0.000139276
|
|
|
KNO
|
[NCBI]
|
0.000134047
|
|
|
crouzon syndrome
|
[NCBI]
|
0.000134047
|
|
|
RNS
|
[NCBI]
|
0.000134047
|
|
|
potocki-shaffer syndrome
|
[NCBI]
|
0.000120983
|
|
|
apert syndrome
|
[NCBI]
|
0.000118968
|
|
|
ACP5
|
[NCBI]
|
0.00011847
|
|
|
MADA
|
[NCBI]
|
0.000110624
|
|
|
CFNS
|
[NCBI]
|
0.000105379
|
|
|
SCDO1
|
[NCBI]
|
9.54385e-05
|
|
|
MSX2
|
[NCBI]
|
9.19206e-05
|
|
|
osteogenesis imperfecta, type i
|
[NCBI]
|
8.0872e-05
|
|
|
CPI
|
[NCBI]
|
6.69918e-05
|
|
|
RAB23
|
[NCBI]
|
4.83963e-05
|
|
|
FAM20C
|
[NCBI]
|
4.51283e-05
|
|
|
SEC23A
|
[NCBI]
|
4.51283e-05
|
|
|
GJA1
|
[NCBI]
|
4.10618e-05
|
|
|
EFNB1
|
[NCBI]
|
3.92142e-05
|
|
|
DCN
|
[NCBI]
|
3.25734e-05
|
|
|
BGN
|
[NCBI]
|
3.09506e-05
|
|
|
PCNA
|
[NCBI]
|
2.88642e-05
|
|
|
FGF2
|
[NCBI]
|
2.15591e-05
|
|
|
IHH
|
[NCBI]
|
2.01739e-05
|
|
|
SPP1
|
[NCBI]
|
9.49258e-06
|
|
|
SHH
|
[NCBI]
|
9.19476e-06
|
|
|
PTK2
|
[NCBI]
|
7.48101e-06
|
|
|
EGF
|
[NCBI]
|
3.02938e-07
|
|