|
OMIM |
Link |
Information
gain |
01 |
|
|
apnea, obstructive sleep
|
[NCBI]
|
0.00146507
|
|
|
|
fatty metamorphosis of viscera
|
[NCBI]
|
0.00138193
|
|
|
|
JBTS1
|
[NCBI]
|
0.000971903
|
|
|
|
JBTS2
|
[NCBI]
|
0.000613493
|
|
|
|
breath-holding spells
|
[NCBI]
|
0.000611213
|
|
|
|
mohr syndrome
|
[NCBI]
|
0.000473781
|
|
|
|
varadi-papp syndrome
|
[NCBI]
|
0.000462747
|
|
|
|
BCHE
|
[NCBI]
|
0.000428876
|
|
|
|
myasthenic syndrome, congenital, associated with episodic apnea
|
[NCBI]
|
0.00027669
|
|
|
|
sudden infant death syndrome
|
[NCBI]
|
0.000153803
|
|
|
|
dandy-walker malformation with postaxial polydactyly
|
[NCBI]
|
0.000111802
|
|
|
|
ACH
|
[NCBI]
|
0.00010457
|
|
|
|
JBTS5
|
[NCBI]
|
0.000103324
|
|
|
|
SLC5A3
|
[NCBI]
|
8.76514e-05
|
|
|
|
JBTS3
|
[NCBI]
|
8.54378e-05
|
|
|
|
corpus callosum, agenesis of
|
[NCBI]
|
8.34102e-05
|
|
|
|
CHAT
|
[NCBI]
|
7.59109e-05
|
|
|
|
MUSK
|
[NCBI]
|
7.38721e-05
|
|
|
|
septooptic dysplasia
|
[NCBI]
|
7.17329e-05
|
|
|
|
myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency
|
[NCBI]
|
6.63054e-05
|
|
|
|
TLX3
|
[NCBI]
|
6.27854e-05
|
|
|
|
autonomic control, congenital failure of
|
[NCBI]
|
6.22591e-05
|
|
|
|
AHI1
|
[NCBI]
|
5.76986e-05
|
|
|
|
ADK
|
[NCBI]
|
5.76986e-05
|
|
|
|
hurler syndrome
|
[NCBI]
|
5.05277e-05
|
|
|
|
AVP
|
[NCBI]
|
4.69751e-05
|
|
|
|
MB
|
[NCBI]
|
3.01703e-05
|
|
|
|
RTT
|
[NCBI]
|
2.95253e-05
|
|
|
|
ADCYAP1
|
[NCBI]
|
2.93246e-05
|
|
|
|
PWS
|
[NCBI]
|
1.50375e-05
|
|
|
|
SLE
|
[NCBI]
|
1.33498e-05
|
|
|
|
PD
|
[NCBI]
|
1.21748e-05
|
|
|
|
CAT
|
[NCBI]
|
9.32432e-06
|
|
|
|
ACHE
|
[NCBI]
|
8.39656e-06
|
|
