|
OMIM |
Link |
Information
gain |
01 |
|
|
PCA
|
[NCBI]
|
0.00782859
|
|
|
|
oculootofacial dysplasia
|
[NCBI]
|
0.00206288
|
|
|
|
burn-mckeown syndrome
|
[NCBI]
|
0.00206288
|
|
|
|
charge syndrome
|
[NCBI]
|
0.00203562
|
|
|
|
ACC
|
[NCBI]
|
0.000431005
|
|
|
|
coffin-siris syndrome
|
[NCBI]
|
0.000358734
|
|
|
|
holoprosencephaly
|
[NCBI]
|
0.000323443
|
|
|
|
EEC1
|
[NCBI]
|
0.000319041
|
|
|
|
CHD7
|
[NCBI]
|
0.000257554
|
|
|
|
carbimazole sensitivity
|
[NCBI]
|
0.000216521
|
|
|
|
hypothyroidism, athyroidal, with spiky hair and cleft palate
|
[NCBI]
|
0.000206921
|
|
|
|
SEMA3E
|
[NCBI]
|
0.000178697
|
|
|
|
radial ray hypoplasia with choanal atresia
|
[NCBI]
|
0.000130439
|
|
|
|
breasts and nipples, absence of
|
[NCBI]
|
0.000107971
|
|
|
|
monosomy 9p syndrome
|
[NCBI]
|
9.39907e-05
|
|
|
|
charge-like syndrome, x-linked
|
[NCBI]
|
9.39907e-05
|
|
|
|
SMMCI
|
[NCBI]
|
6.7023e-05
|
|
|
|
FOXE1
|
[NCBI]
|
6.58157e-05
|
|
|
|
PPS
|
[NCBI]
|
6.24992e-05
|
|
|
|
KAL2
|
[NCBI]
|
6.12371e-05
|
|
|
|
CHNG2
|
[NCBI]
|
5.89784e-05
|
|
|
|
PITX2
|
[NCBI]
|
5.60041e-05
|
|
|
|
PHS
|
[NCBI]
|
5.3289e-05
|
|
|
|
SHH
|
[NCBI]
|
3.07419e-05
|
|
|
|
PWS
|
[NCBI]
|
1.19524e-05
|
|
