|
OMIM |
Link |
Information gain |
01 |
|
callosities, hereditary painful
|
[NCBI]
|
0.00211895
|
|
|
MSSE
|
[NCBI]
|
0.00162298
|
|
|
isotretinoin embryopathy-like syndrome
|
[NCBI]
|
0.000905179
|
|
|
VRNI
|
[NCBI]
|
0.000648341
|
|
|
TCOF
|
[NCBI]
|
0.000414779
|
|
|
STGD1
|
[NCBI]
|
0.00020649
|
|
|
perifolliculitis capitis abscedens et suffodiens, familial
|
[NCBI]
|
0.00017905
|
|
|
JMML
|
[NCBI]
|
0.000158206
|
|
|
BCNS
|
[NCBI]
|
0.000143282
|
|
|
vohwinkel syndrome, variant form
|
[NCBI]
|
0.000122069
|
|
|
deafness, congenital, with keratopachydermia and constrictions of fingers and toes
|
[NCBI]
|
0.000110424
|
|
|
KFSD
|
[NCBI]
|
0.000105048
|
|
|
EPS
|
[NCBI]
|
0.000100708
|
|
|
XPA
|
[NCBI]
|
8.01673e-05
|
|
|
MTS
|
[NCBI]
|
7.72087e-05
|
|
|
GNMT
|
[NCBI]
|
5.46862e-05
|
|
|
ABCA4
|
[NCBI]
|
5.42003e-05
|
|
|
DGS
|
[NCBI]
|
5.3421e-05
|
|
|
PXE
|
[NCBI]
|
4.75729e-05
|
|
|
TG
|
[NCBI]
|
3.35997e-05
|
|
|
CVID
|
[NCBI]
|
3.12085e-05
|
|
|
RARB
|
[NCBI]
|
3.05942e-05
|
|
|
APOC3
|
[NCBI]
|
2.93539e-05
|
|
|
KLK3
|
[NCBI]
|
2.92515e-05
|
|
|
EGF
|
[NCBI]
|
1.9171e-05
|
|
|
NPM1
|
[NCBI]
|
1.79858e-05
|
|
|
EGFR
|
[NCBI]
|
1.61923e-05
|
|
|
ACP5
|
[NCBI]
|
9.50328e-06
|
|
|
VEGF
|
[NCBI]
|
6.0702e-06
|
|
|
F3
|
[NCBI]
|
4.54017e-06
|
|
|
PCNA
|
[NCBI]
|
1.6932e-06
|
|
|
PTH
|
[NCBI]
|
4.91755e-07
|
|
|
SLE
|
[NCBI]
|
4.26637e-07
|
|
|
NGFB
|
[NCBI]
|
3.57862e-07
|
|