|
OMIM |
Link |
Information gain |
01 |
|
JBTS1
|
[NCBI]
|
0.00430599
|
|
|
immotile cilia syndrome due to defective radial spokes
|
[NCBI]
|
0.00105062
|
|
|
varadi-papp syndrome
|
[NCBI]
|
0.000475624
|
|
|
apnea, obstructive sleep
|
[NCBI]
|
0.0003163
|
|
|
klippel-trenaunay-weber syndrome
|
[NCBI]
|
0.000229643
|
|
|
autonomic control, congenital failure of
|
[NCBI]
|
0.000131337
|
|
|
PWS
|
[NCBI]
|
0.000112991
|
|
|
dandy-walker malformation with postaxial polydactyly
|
[NCBI]
|
0.000103524
|
|
|
ACH
|
[NCBI]
|
8.80335e-05
|
|
|
MECP2
|
[NCBI]
|
8.61734e-05
|
|
|
CF
|
[NCBI]
|
8.26587e-05
|
|
|
MUC7
|
[NCBI]
|
8.00936e-05
|
|
|
marshall-smith syndrome
|
[NCBI]
|
7.94923e-05
|
|
|
breath-holding spells
|
[NCBI]
|
7.94923e-05
|
|
|
GBS
|
[NCBI]
|
7.17352e-05
|
|
|
encephalopathy, neonatal severe, due to mecp2 mutations
|
[NCBI]
|
7.02662e-05
|
|
|
RTT
|
[NCBI]
|
6.50915e-05
|
|
|
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency
|
[NCBI]
|
5.94566e-05
|
|
|
sudden infant death syndrome
|
[NCBI]
|
5.68306e-05
|
|
|
OKS
|
[NCBI]
|
5.51122e-05
|
|
|
ECM1
|
[NCBI]
|
5.49429e-05
|
|
|
kartagener syndrome
|
[NCBI]
|
4.65387e-05
|
|
|
FOXP3
|
[NCBI]
|
4.53837e-05
|
|
|
BDNF
|
[NCBI]
|
4.33937e-05
|
|
|
asthma, susceptibility to
|
[NCBI]
|
4.14898e-05
|
|
|
MPZ
|
[NCBI]
|
3.9435e-05
|
|
|
IL6
|
[NCBI]
|
3.60694e-05
|
|
|
SMS
|
[NCBI]
|
3.49666e-05
|
|
|
PI
|
[NCBI]
|
2.86475e-05
|
|
|
GDNF
|
[NCBI]
|
2.2222e-05
|
|
|
RNASE3
|
[NCBI]
|
1.74625e-05
|
|
|
RA
|
[NCBI]
|
1.70167e-05
|
|
|
MG
|
[NCBI]
|
1.45367e-05
|
|
|
MPO
|
[NCBI]
|
8.87366e-06
|
|
|
SLE
|
[NCBI]
|
5.56922e-06
|
|
|
TNF
|
[NCBI]
|
1.43151e-06
|
|