|
OMIM |
Link |
Information gain |
01 |
|
NF1
|
[NCBI]
|
0.0167534
|
|
|
NFNS
|
[NCBI]
|
0.00132492
|
|
|
NF2
|
[NCBI]
|
0.00101862
|
|
|
proteus syndrome
|
[NCBI]
|
0.00092109
|
|
|
polymicrogyria, unilateral
|
[NCBI]
|
0.000880362
|
|
|
dyschromatosis universalis hereditaria
|
[NCBI]
|
0.000798231
|
|
|
noonan syndrome 2
|
[NCBI]
|
0.000744944
|
|
|
horner syndrome, congenital
|
[NCBI]
|
0.000744944
|
|
|
MYMY1
|
[NCBI]
|
0.000545541
|
|
|
FEB1
|
[NCBI]
|
0.000545541
|
|
|
RASA1
|
[NCBI]
|
0.000476591
|
|
|
JMML
|
[NCBI]
|
0.000449539
|
|
|
cafe-au-lait spots, multiple
|
[NCBI]
|
0.000402465
|
|
|
watson syndrome
|
[NCBI]
|
0.000381132
|
|
|
NF3B
|
[NCBI]
|
0.000295556
|
|
|
neurofibromatosis, familial spinal
|
[NCBI]
|
0.000277487
|
|
|
leopard syndrome 1
|
[NCBI]
|
0.000250226
|
|
|
mismatch repair cancer syndrome
|
[NCBI]
|
0.000248042
|
|
|
GIST
|
[NCBI]
|
0.000237674
|
|
|
SRS
|
[NCBI]
|
0.000199582
|
|
|
meningioma, familial
|
[NCBI]
|
0.000155172
|
|
|
CMT1A
|
[NCBI]
|
0.000133101
|
|
|
MLH1
|
[NCBI]
|
0.00012363
|
|
|
EVI2A
|
[NCBI]
|
0.000121246
|
|
|
EVI2B
|
[NCBI]
|
0.000121246
|
|
|
NS1
|
[NCBI]
|
0.00011622
|
|
|
NF4
|
[NCBI]
|
0.0001105
|
|
|
NFLS
|
[NCBI]
|
0.0001105
|
|
|
MEN2B
|
[NCBI]
|
9.94021e-05
|
|
|
VEGF
|
[NCBI]
|
9.3173e-05
|
|
|
NF3A
|
[NCBI]
|
8.80447e-05
|
|
|
neuroblastoma
|
[NCBI]
|
8.40082e-05
|
|
|
SUZ12
|
[NCBI]
|
7.97273e-05
|
|
|
TS
|
[NCBI]
|
7.04849e-05
|
|
|
MSH2
|
[NCBI]
|
6.95623e-05
|
|
|
CF
|
[NCBI]
|
6.89576e-05
|
|
|
NF2
|
[NCBI]
|
6.68029e-05
|
|
|
AK3L1
|
[NCBI]
|
6.0608e-05
|
|
|
RNF135
|
[NCBI]
|
6.0608e-05
|
|
|
ACH
|
[NCBI]
|
5.80852e-05
|
|
|
VHL
|
[NCBI]
|
5.61329e-05
|
|
|
PGL4
|
[NCBI]
|
5.23314e-05
|
|
|
fibromuscular dysplasia of arteries
|
[NCBI]
|
5.11902e-05
|
|
|
CORD2
|
[NCBI]
|
4.81938e-05
|
|
|
OMG
|
[NCBI]
|
4.68496e-05
|
|
|
C17ORF41
|
[NCBI]
|
4.68496e-05
|
|
|
SPRED1
|
[NCBI]
|
4.68496e-05
|
|
|
dyschromatosis symmetrica hereditaria 1
|
[NCBI]
|
4.10424e-05
|
|
|
pheochromocytoma
|
[NCBI]
|
3.84225e-05
|
|
|
UNC119
|
[NCBI]
|
3.83151e-05
|
|
|
exostoses, multiple, type i
|
[NCBI]
|
3.5384e-05
|
|
|
cardiofaciocutaneous syndrome
|
[NCBI]
|
3.49964e-05
|
|
|
PGL1
|
[NCBI]
|
3.3891e-05
|
|
|
LWD
|
[NCBI]
|
3.28629e-05
|
|
|
costello syndrome
|
[NCBI]
|
3.07135e-05
|
|
|
HTLVR
|
[NCBI]
|
2.95781e-05
|
|
|
EGFR
|
[NCBI]
|
2.95057e-05
|
|
|
glioma of brain, familial
|
[NCBI]
|
2.85959e-05
|
|
|
MMP13
|
[NCBI]
|
2.84937e-05
|
|
|
METAP2
|
[NCBI]
|
2.75203e-05
|
|
|
TNXB
|
[NCBI]
|
2.66377e-05
|
|
|
DLK1
|
[NCBI]
|
2.58307e-05
|
|
|
lynch syndrome i
|
[NCBI]
|
2.51303e-05
|
|
|
MEN2A
|
[NCBI]
|
2.31734e-05
|
|
|
EGF
|
[NCBI]
|
2.15354e-05
|
|
|
EYA1
|
[NCBI]
|
2.10903e-05
|
|
|
DCT
|
[NCBI]
|
2.10903e-05
|
|
|
PTPN11
|
[NCBI]
|
2.06391e-05
|
|
|
EV
|
[NCBI]
|
1.53968e-05
|
|
|
STK11
|
[NCBI]
|
1.47683e-05
|
|
|
NGFB
|
[NCBI]
|
1.17247e-05
|
|
|
KRAS
|
[NCBI]
|
1.12258e-05
|
|
|
PTN
|
[NCBI]
|
1.10852e-05
|
|
|
PJS
|
[NCBI]
|
1.07683e-05
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
9.96255e-06
|
|
|
NGFR
|
[NCBI]
|
9.25105e-06
|
|
|
TNC
|
[NCBI]
|
7.63647e-06
|
|
|
CDK4
|
[NCBI]
|
6.22254e-06
|
|
|
SDC2
|
[NCBI]
|
4.22382e-06
|
|
|
MUC1
|
[NCBI]
|
4.16601e-06
|
|
|
PEDF
|
[NCBI]
|
4.00869e-06
|
|
|
HGF
|
[NCBI]
|
3.57346e-06
|
|
|
PMP22
|
[NCBI]
|
3.49652e-06
|
|
|
TP53
|
[NCBI]
|
1.86089e-06
|
|
|
GFAP
|
[NCBI]
|
1.18016e-06
|
|
|
APC
|
[NCBI]
|
5.5065e-07
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
1.51933e-07
|
|
|
GDNF
|
[NCBI]
|
1.22569e-07
|
|
|
FRAP1
|
[NCBI]
|
7.69404e-08
|
|