|
OMIM |
Link |
Information
gain |
01 |
|
|
pierre robin sequence with pectus excavatum and rib and scapular anomalies
|
[NCBI]
|
0.00270288
|
|
|
|
TARPS
|
[NCBI]
|
0.00221606
|
|
|
|
ear malformation
|
[NCBI]
|
0.000880362
|
|
|
|
catel-manzke syndrome
|
[NCBI]
|
0.000543957
|
|
|
|
mohr syndrome
|
[NCBI]
|
0.000533572
|
|
|
|
pierre robin syndrome
|
[NCBI]
|
0.000514281
|
|
|
|
cerebrocostomandibular syndrome
|
[NCBI]
|
0.00037333
|
|
|
|
STL1
|
[NCBI]
|
0.000305412
|
|
|
|
arthrogryposis multiplex congenita with whistling face
|
[NCBI]
|
0.000225178
|
|
|
|
CPI
|
[NCBI]
|
0.000196541
|
|
|
|
pierre robin sequence with facial and digital anomalies
|
[NCBI]
|
0.000127818
|
|
|
|
ventricular extrasystoles with syncope, perodactyly, and robin sequence
|
[NCBI]
|
0.000127818
|
|
|
|
robin sequence with distinctive facial appearance and brachydactyly
|
[NCBI]
|
0.000127818
|
|
|
|
ectodermal dysplasia, hypohidrotic, with hypothyroidism and agenesis of the corpus callosum
|
[NCBI]
|
0.000105351
|
|
|
|
pierre robin syndrome and oligodactyly
|
[NCBI]
|
0.000105351
|
|
|
|
myopathy, congenital nonprogressive, with moebius sequence and robin sequence
|
[NCBI]
|
9.68753e-05
|
|
|
|
robin sequence with cleft mandible and limb anomalies
|
[NCBI]
|
9.13729e-05
|
|
|
|
COL11A2
|
[NCBI]
|
7.32984e-05
|
|
|
|
WZS
|
[NCBI]
|
7.07404e-05
|
|
|
|
WGN1
|
[NCBI]
|
6.83453e-05
|
|
|
|
marshall syndrome
|
[NCBI]
|
6.72698e-05
|
|
|
|
OPD2
|
[NCBI]
|
6.6262e-05
|
|
|
|
SOX9
|
[NCBI]
|
6.62258e-05
|
|
|
|
apnea, obstructive sleep
|
[NCBI]
|
6.61063e-05
|
|
|
|
campomelic dysplasia
|
[NCBI]
|
5.10787e-05
|
|
|
|
phenylketonuria
|
[NCBI]
|
4.53799e-05
|
|
|
|
AMC
|
[NCBI]
|
4.34971e-05
|
|
|
|
velocardiofacial syndrome
|
[NCBI]
|
4.32681e-05
|
|
