|
OMIM |
Link |
Information gain |
01 |
|
VRNI
|
[NCBI]
|
0.138436
|
|
|
RNANC
|
[NCBI]
|
0.00201654
|
|
|
STL1
|
[NCBI]
|
0.000790283
|
|
|
vitreoretinal degeneration, snowflake type
|
[NCBI]
|
0.000769415
|
|
|
cavitary optic disc anomalies
|
[NCBI]
|
0.000639129
|
|
|
WGN1
|
[NCBI]
|
0.000634652
|
|
|
EVR1
|
[NCBI]
|
0.000557294
|
|
|
GFAP
|
[NCBI]
|
0.000529818
|
|
|
stickler syndrome, type i, nonsyndromic ocular
|
[NCBI]
|
0.000395428
|
|
|
COL2A1
|
[NCBI]
|
0.000390747
|
|
|
KNO
|
[NCBI]
|
0.000348293
|
|
|
persistent hyperplastic primary vitreous, autosomal dominant
|
[NCBI]
|
0.000319337
|
|
|
knobloch syndrome, type ii
|
[NCBI]
|
0.000319337
|
|
|
ND
|
[NCBI]
|
0.000283469
|
|
|
RS1
|
[NCBI]
|
0.000276974
|
|
|
walker-warburg syndrome
|
[NCBI]
|
0.000245339
|
|
|
spondyloocular syndrome, autosomal recessive
|
[NCBI]
|
0.000228234
|
|
|
MYP2
|
[NCBI]
|
0.000208476
|
|
|
coloboma of optic nerve
|
[NCBI]
|
0.000197294
|
|
|
persistent hyperplastic primary vitreous, autosomal recessive
|
[NCBI]
|
0.000194491
|
|
|
ectopia lentis with ectopia of pupil
|
[NCBI]
|
0.000194491
|
|
|
FSHMD1A
|
[NCBI]
|
0.000175644
|
|
|
SEDC
|
[NCBI]
|
0.000174354
|
|
|
NDP
|
[NCBI]
|
0.000170374
|
|
|
COL18A1
|
[NCBI]
|
0.000154068
|
|
|
EVR2
|
[NCBI]
|
0.000151051
|
|
|
VEGF
|
[NCBI]
|
0.000134451
|
|
|
microspherophakia with hernia
|
[NCBI]
|
0.000114013
|
|
|
lattice degeneration of retina leading to retinal detachment
|
[NCBI]
|
0.000114013
|
|
|
retinal nonattachment and falciform detachment
|
[NCBI]
|
0.000114013
|
|
|
revesz syndrome
|
[NCBI]
|
9.15549e-05
|
|
|
RLBP1
|
[NCBI]
|
8.3829e-05
|
|
|
craniosynostosis with ectopia lentis
|
[NCBI]
|
7.75929e-05
|
|
|
coats disease
|
[NCBI]
|
7.35111e-05
|
|
|
donnai-barrow syndrome
|
[NCBI]
|
6.7561e-05
|
|
|
STL2
|
[NCBI]
|
6.7561e-05
|
|
|
WZS
|
[NCBI]
|
5.70341e-05
|
|
|
kniest dysplasia
|
[NCBI]
|
5.46555e-05
|
|
|
VAMP2
|
[NCBI]
|
5.46148e-05
|
|
|
marshall syndrome
|
[NCBI]
|
5.35882e-05
|
|
|
papillorenal syndrome
|
[NCBI]
|
5.16487e-05
|
|
|
ehlers-danlos syndrome, type vi
|
[NCBI]
|
4.62927e-05
|
|
|
HGF
|
[NCBI]
|
4.38659e-05
|
|
|
BCL10
|
[NCBI]
|
4.36643e-05
|
|
|
PDCD8
|
[NCBI]
|
4.33608e-05
|
|
|
SLC1A3
|
[NCBI]
|
4.24244e-05
|
|
|
PEDF
|
[NCBI]
|
4.1953e-05
|
|
|
RBP3
|
[NCBI]
|
4.13237e-05
|
|
|
ehlers-danlos syndrome, type i
|
[NCBI]
|
3.95765e-05
|
|
|
COL11A1
|
[NCBI]
|
3.78523e-05
|
|
|
COH1
|
[NCBI]
|
3.76186e-05
|
|
|
CMTC
|
[NCBI]
|
3.65555e-05
|
|
|
melanoma, uveal
|
[NCBI]
|
3.58866e-05
|
|
|
CES
|
[NCBI]
|
3.46327e-05
|
|
|
LRP5
|
[NCBI]
|
3.37407e-05
|
|
|
FCMD
|
[NCBI]
|
3.32018e-05
|
|
|
ornithine aminotransferase deficiency
|
[NCBI]
|
2.75835e-05
|
|
|
TF
|
[NCBI]
|
2.54849e-05
|
|
|
SMS
|
[NCBI]
|
2.37757e-05
|
|
|
protein c deficiency, congenital thrombotic disease due to
|
[NCBI]
|
2.26107e-05
|
|
|
TS
|
[NCBI]
|
2.23566e-05
|
|
|
VHL
|
[NCBI]
|
2.0906e-05
|
|
|
VIM
|
[NCBI]
|
2.07424e-05
|
|
|
IP
|
[NCBI]
|
2.00408e-05
|
|
|
CFH
|
[NCBI]
|
1.87024e-05
|
|
|
TNF
|
[NCBI]
|
1.80923e-05
|
|
|
RB1
|
[NCBI]
|
1.10267e-05
|
|
|
CTGF
|
[NCBI]
|
7.44431e-06
|
|
|
EGF
|
[NCBI]
|
6.68111e-06
|
|
|
SLE
|
[NCBI]
|
6.59852e-06
|
|
|
GDNF
|
[NCBI]
|
4.66063e-06
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
2.36833e-06
|
|
|
RP
|
[NCBI]
|
1.76641e-06
|
|
|
RNASE3
|
[NCBI]
|
1.69812e-06
|
|
|
TNFSF6
|
[NCBI]
|
1.41724e-06
|
|
|
NGFB
|
[NCBI]
|
6.67807e-07
|
|
|
BDNF
|
[NCBI]
|
5.70101e-07
|
|
|
PCNA
|
[NCBI]
|
4.27337e-07
|
|
|
AVP
|
[NCBI]
|
2.52823e-08
|
|
|
APC
|
[NCBI]
|
8.88894e-09
|
|