|
OMIM |
Link |
Information gain |
01 |
|
megalocornea-mental retardation syndrome
|
[NCBI]
|
0.00095223
|
|
|
marden-walker syndrome
|
[NCBI]
|
0.00081137
|
|
|
SPS
|
[NCBI]
|
0.000626166
|
|
|
IS1
|
[NCBI]
|
0.000303583
|
|
|
dystonia with ringbinden
|
[NCBI]
|
0.000162613
|
|
|
muscular dystrophy, congenital, megaconial type
|
[NCBI]
|
0.000162613
|
|
|
muscular hypertonia, lethal
|
[NCBI]
|
0.000162613
|
|
|
aniridia, partial, with unilateral renal agenesis and psychomotor retardation
|
[NCBI]
|
0.000134845
|
|
|
axenfeld-rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities
|
[NCBI]
|
0.000124368
|
|
|
nevo syndrome
|
[NCBI]
|
0.000117566
|
|
|
mulibrey nanism
|
[NCBI]
|
9.20518e-05
|
|
|
weaver syndrome
|
[NCBI]
|
8.53373e-05
|
|
|
glycogen storage disease iv
|
[NCBI]
|
8.53373e-05
|
|
|
RIEG1
|
[NCBI]
|
8.21841e-05
|
|
|
MDC1A
|
[NCBI]
|
8.12356e-05
|
|
|
CLN1
|
[NCBI]
|
8.03304e-05
|
|
|
VIP
|
[NCBI]
|
7.82916e-05
|
|
|
SJS1
|
[NCBI]
|
7.18359e-05
|
|
|
AMC
|
[NCBI]
|
6.46905e-05
|
|
|
PWS
|
[NCBI]
|
5.84367e-05
|
|
|
HCRT
|
[NCBI]
|
5.37863e-05
|
|
|
ZS
|
[NCBI]
|
5.32777e-05
|
|
|
krabbe disease
|
[NCBI]
|
5.19985e-05
|
|
|
NPY
|
[NCBI]
|
4.72473e-05
|
|
|
DMD
|
[NCBI]
|
4.00705e-05
|
|
|
ADM
|
[NCBI]
|
3.3711e-05
|
|
|
AS
|
[NCBI]
|
2.87984e-05
|
|
|
PLOD1
|
[NCBI]
|
2.7442e-05
|
|
|
SPG4
|
[NCBI]
|
2.47411e-05
|
|
|
PTHLH
|
[NCBI]
|
2.29748e-05
|
|
|
CCK
|
[NCBI]
|
1.77594e-05
|
|
|
OXT
|
[NCBI]
|
1.48035e-05
|
|
|
FAAH
|
[NCBI]
|
1.42916e-05
|
|
|
NPPA
|
[NCBI]
|
1.30603e-05
|
|
|
MG
|
[NCBI]
|
9.32541e-06
|
|
|
POMC
|
[NCBI]
|
7.15642e-06
|
|
|
ACHE
|
[NCBI]
|
6.37897e-06
|
|
|
RA
|
[NCBI]
|
6.20514e-06
|
|
|
AD
|
[NCBI]
|
1.72682e-06
|
|
|
AR
|
[NCBI]
|
1.68778e-06
|
|
|
CRH
|
[NCBI]
|
1.40144e-06
|
|
|
BDNF
|
[NCBI]
|
1.36286e-06
|
|
|
GFAP
|
[NCBI]
|
1.05372e-06
|
|
|
AVP
|
[NCBI]
|
8.11925e-07
|
|
|
TH
|
[NCBI]
|
7.96845e-07
|
|
|
TNF
|
[NCBI]
|
4.14243e-07
|
|
|
EGFR
|
[NCBI]
|
3.40085e-07
|
|