|
OMIM |
Link |
Information gain |
01 |
|
klippel-feil syndrome, autosomal dominant
|
[NCBI]
|
0.00800204
|
|
|
klippel-feil syndrome, autosomal recessive
|
[NCBI]
|
0.00593937
|
|
|
SGM1
|
[NCBI]
|
0.0039217
|
|
|
sprengel deformity
|
[NCBI]
|
0.00164346
|
|
|
wildervanck syndrome
|
[NCBI]
|
0.00121496
|
|
|
poland syndrome
|
[NCBI]
|
0.000757362
|
|
|
hemifacial microsomia with radial defects
|
[NCBI]
|
0.000575485
|
|
|
gordon syndrome
|
[NCBI]
|
0.000459383
|
|
|
pena-shokeir syndrome, type i
|
[NCBI]
|
0.000245071
|
|
|
DWS
|
[NCBI]
|
0.000241468
|
|
|
murcs association
|
[NCBI]
|
0.000211037
|
|
|
PAX1
|
[NCBI]
|
0.000176026
|
|
|
muenke syndrome
|
[NCBI]
|
8.87204e-05
|
|
|
SCDO1
|
[NCBI]
|
6.88341e-05
|
|
|
AMC
|
[NCBI]
|
5.68389e-05
|
|
|
FOP
|
[NCBI]
|
5.48607e-05
|
|
|
FGFR3
|
[NCBI]
|
4.52049e-05
|
|
|
FA
|
[NCBI]
|
2.36081e-05
|
|