|
OMIM |
Link |
Information gain |
01 |
|
renal hamartomas, nephroblastomatosis, and fetal gigantism
|
[NCBI]
|
0.00441265
|
|
|
sotos syndrome
|
[NCBI]
|
0.00292948
|
|
|
proteus syndrome
|
[NCBI]
|
0.00149567
|
|
|
BWS
|
[NCBI]
|
0.00084353
|
|
|
SGBS1
|
[NCBI]
|
0.000825233
|
|
|
megalencephaly
|
[NCBI]
|
0.000765046
|
|
|
acrodysostosis
|
[NCBI]
|
0.000572697
|
|
|
PRL
|
[NCBI]
|
0.000259863
|
|
|
klippel-trenaunay-weber syndrome
|
[NCBI]
|
0.000242681
|
|
|
NSD1
|
[NCBI]
|
0.00024264
|
|
|
GNAS
|
[NCBI]
|
0.000176097
|
|
|
SOST
|
[NCBI]
|
0.000124785
|
|
|
acromegaly
|
[NCBI]
|
0.000118639
|
|
|
hydrocephalus, tall stature, joint laxity, and kyphoscoliosis
|
[NCBI]
|
0.000114861
|
|
|
momo syndrome
|
[NCBI]
|
0.000114861
|
|
|
SLE
|
[NCBI]
|
0.000101991
|
|
|
GPC3
|
[NCBI]
|
9.31317e-05
|
|
|
puerto rican infant hypotonia syndrome
|
[NCBI]
|
9.2402e-05
|
|
|
macrocephaly
|
[NCBI]
|
8.39333e-05
|
|
|
macrocephaly, benign familial
|
[NCBI]
|
7.84385e-05
|
|
|
nevo syndrome
|
[NCBI]
|
7.84385e-05
|
|
|
macrocephaly/autism syndrome
|
[NCBI]
|
7.11054e-05
|
|
|
ABAT
|
[NCBI]
|
6.94637e-05
|
|
|
AGGF1
|
[NCBI]
|
6.94637e-05
|
|
|
MAS
|
[NCBI]
|
6.6361e-05
|
|
|
ANXA7
|
[NCBI]
|
6.0889e-05
|
|
|
BCNS
|
[NCBI]
|
5.57344e-05
|
|
|
GHRH
|
[NCBI]
|
5.3757e-05
|
|
|
SOCS2
|
[NCBI]
|
5.20516e-05
|
|
|
crouzon syndrome
|
[NCBI]
|
5.07564e-05
|
|
|
weaver syndrome
|
[NCBI]
|
4.77851e-05
|
|
|
CDKN1B
|
[NCBI]
|
4.67522e-05
|
|
|
CGL2
|
[NCBI]
|
4.47251e-05
|
|
|
TCOF1
|
[NCBI]
|
4.28513e-05
|
|
|
ODDD
|
[NCBI]
|
4.12589e-05
|
|
|
IGF2
|
[NCBI]
|
3.97243e-05
|
|
|
HRG
|
[NCBI]
|
3.90767e-05
|
|
|
BRRS
|
[NCBI]
|
3.32105e-05
|
|
|
WS1
|
[NCBI]
|
3.29538e-05
|
|
|
TCOF
|
[NCBI]
|
3.15019e-05
|
|
|
IGFALS
|
[NCBI]
|
2.99821e-05
|
|
|
HGPS
|
[NCBI]
|
2.95657e-05
|
|
|
NS1
|
[NCBI]
|
2.57172e-05
|
|
|
BDNF
|
[NCBI]
|
5.91395e-06
|
|
|
TS
|
[NCBI]
|
4.11647e-06
|
|
|
PWS
|
[NCBI]
|
2.10624e-06
|
|
|
NGFB
|
[NCBI]
|
1.59882e-06
|
|