|
OMIM |
Link |
Information gain |
01 |
|
MCDR1
|
[NCBI]
|
0.0161811
|
|
|
ARMD1
|
[NCBI]
|
0.00511957
|
|
|
macular edema, cystoid
|
[NCBI]
|
0.00301024
|
|
|
CFH
|
[NCBI]
|
0.00295925
|
|
|
VMD
|
[NCBI]
|
0.0029293
|
|
|
VMD1
|
[NCBI]
|
0.00169383
|
|
|
STGD1
|
[NCBI]
|
0.00144266
|
|
|
macular dystrophy, butterfly-shaped pigmentary, 2
|
[NCBI]
|
0.00139431
|
|
|
ARMD4
|
[NCBI]
|
0.00136233
|
|
|
ABCA4
|
[NCBI]
|
0.00132937
|
|
|
chorioretinal atrophy, progressive bifocal
|
[NCBI]
|
0.00125932
|
|
|
CORD7
|
[NCBI]
|
0.00116688
|
|
|
STGD3
|
[NCBI]
|
0.00110971
|
|
|
S EYE
|
[NCBI]
|
0.000845054
|
|
|
STGD4
|
[NCBI]
|
0.000845054
|
|
|
macular dystrophy, vitelliform, adult-onset
|
[NCBI]
|
0.000789658
|
|
|
loc387715 gene
|
[NCBI]
|
0.000738596
|
|
|
SFD
|
[NCBI]
|
0.000710715
|
|
|
ARMD7
|
[NCBI]
|
0.000679364
|
|
|
BEST1
|
[NCBI]
|
0.000664041
|
|
|
ELOVL4
|
[NCBI]
|
0.000615161
|
|
|
RP
|
[NCBI]
|
0.000597201
|
|
|
VEGF
|
[NCBI]
|
0.000562422
|
|
|
cone-rod dystrophy and amelogenesis imperfecta
|
[NCBI]
|
0.000546269
|
|
|
TIMP3
|
[NCBI]
|
0.000512582
|
|
|
VRNI
|
[NCBI]
|
0.000461932
|
|
|
SPG15
|
[NCBI]
|
0.000423625
|
|
|
patterned dystrophy of retinal pigment epithelium
|
[NCBI]
|
0.000399224
|
|
|
RCD1
|
[NCBI]
|
0.00039802
|
|
|
PRPH2
|
[NCBI]
|
0.000350004
|
|
|
DHRD
|
[NCBI]
|
0.000313022
|
|
|
ARMD10
|
[NCBI]
|
0.000290722
|
|
|
SCA7
|
[NCBI]
|
0.000273227
|
|
|
eem syndrome
|
[NCBI]
|
0.0002543
|
|
|
ARMD2
|
[NCBI]
|
0.0002543
|
|
|
PEDF
|
[NCBI]
|
0.000249488
|
|
|
HTRA1
|
[NCBI]
|
0.000245786
|
|
|
HMCN1
|
[NCBI]
|
0.000207742
|
|
|
APOE
|
[NCBI]
|
0.000196842
|
|
|
ARMD3
|
[NCBI]
|
0.000193743
|
|
|
ARMD9
|
[NCBI]
|
0.000193743
|
|
|
PLEKHA1
|
[NCBI]
|
0.0001842
|
|
|
macular dystrophy, concentric annular
|
[NCBI]
|
0.000162829
|
|
|
drusen of bruch membrane
|
[NCBI]
|
0.000162829
|
|
|
RS1
|
[NCBI]
|
0.00015939
|
|
|
ATD1
|
[NCBI]
|
0.000151911
|
|
|
HJMD
|
[NCBI]
|
0.00014888
|
|
|
macular dystrophy, fenestrated sheen type
|
[NCBI]
|
9.68358e-05
|
|
|
myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders
|
[NCBI]
|
9.68358e-05
|
|
|
EFEMP1
|
[NCBI]
|
8.93777e-05
|
|
|
TNF
|
[NCBI]
|
8.56323e-05
|
|
|
FBLN5
|
[NCBI]
|
8.4885e-05
|
|
|
C3
|
[NCBI]
|
8.3087e-05
|
|
|
spinocerebellar degeneration with macular corneal dystrophy, congenital cataracts, and myopia
|
[NCBI]
|
7.44043e-05
|
|
|
reticular dystrophy of retinal pigment epithelium
|
[NCBI]
|
7.44043e-05
|
|
|
LORD
|
[NCBI]
|
6.59634e-05
|
|
|
fundus dystrophy, pseudoinflammatory, recessive form
|
[NCBI]
|
6.59634e-05
|
|
|
CRP
|
[NCBI]
|
6.18657e-05
|
|
|
FADS3
|
[NCBI]
|
6.1367e-05
|
|
|
C1QTNF5
|
[NCBI]
|
6.1367e-05
|
|
|
C11ORF9
|
[NCBI]
|
6.1367e-05
|
|
|
IMPG1
|
[NCBI]
|
6.1367e-05
|
|
|
FADS2
|
[NCBI]
|
6.1367e-05
|
|
|
CFB
|
[NCBI]
|
6.06796e-05
|
|
|
LCA5
|
[NCBI]
|
6.04963e-05
|
|
|
RP19
|
[NCBI]
|
6.04963e-05
|
|
|
RP7
|
[NCBI]
|
5.64415e-05
|
|
|
complement component 2 deficiency
|
[NCBI]
|
5.16814e-05
|
|
|
foveal hypoplasia and presenile cataract syndrome
|
[NCBI]
|
5.05455e-05
|
|
|
CORD3
|
[NCBI]
|
5.05455e-05
|
|
|
young-simpson syndrome
|
[NCBI]
|
5.05455e-05
|
|
|
CFHR3
|
[NCBI]
|
4.76069e-05
|
|
|
CFHR1
|
[NCBI]
|
4.76069e-05
|
|
|
BEST2
|
[NCBI]
|
4.76069e-05
|
|
|
BEST3
|
[NCBI]
|
4.76069e-05
|
|
|
IMPG2
|
[NCBI]
|
4.76069e-05
|
|
|
OPTC
|
[NCBI]
|
4.76069e-05
|
|
|
DR1
|
[NCBI]
|
4.76069e-05
|
|
|
BEST4
|
[NCBI]
|
4.76069e-05
|
|
|
glutathione synthetase deficiency
|
[NCBI]
|
4.45089e-05
|
|
|
fundus albipunctatus
|
[NCBI]
|
4.45089e-05
|
|
|
UGB
|
[NCBI]
|
4.27569e-05
|
|
|
LCA5
|
[NCBI]
|
4.24262e-05
|
|
|
FADS1
|
[NCBI]
|
4.24262e-05
|
|
|
aceruloplasminemia
|
[NCBI]
|
3.68157e-05
|
|
|
MCDC1
|
[NCBI]
|
3.58431e-05
|
|
|
diabetes-deafness syndrome, maternally transmitted
|
[NCBI]
|
3.58431e-05
|
|
|
PPCD1
|
[NCBI]
|
3.49302e-05
|
|
|
CORD2
|
[NCBI]
|
3.49302e-05
|
|
|
MFRP
|
[NCBI]
|
3.45971e-05
|
|
|
ESCS
|
[NCBI]
|
3.3258e-05
|
|
|
danon disease
|
[NCBI]
|
3.3258e-05
|
|
|
DDB1
|
[NCBI]
|
3.29533e-05
|
|
|
FSCN2
|
[NCBI]
|
3.29533e-05
|
|
|
SAG
|
[NCBI]
|
3.29533e-05
|
|
|
cutis laxa, autosomal recessive, type i
|
[NCBI]
|
3.24883e-05
|
|
|
GUCA1A
|
[NCBI]
|
3.1549e-05
|
|
|
MTTE
|
[NCBI]
|
3.1549e-05
|
|
|
CX3CR1
|
[NCBI]
|
3.1549e-05
|
|
|
OLR1
|
[NCBI]
|
3.1549e-05
|
|
|
RDH5
|
[NCBI]
|
3.1549e-05
|
|
|
CNGB3
|
[NCBI]
|
3.03239e-05
|
|
|
HLA-C
|
[NCBI]
|
3.03239e-05
|
|
|
PCNA
|
[NCBI]
|
2.82079e-05
|
|
|
HEPH
|
[NCBI]
|
2.73785e-05
|
|
|
CCR2
|
[NCBI]
|
2.73785e-05
|
|
|
PON1
|
[NCBI]
|
2.69759e-05
|
|
|
homocysteinemia
|
[NCBI]
|
2.69585e-05
|
|
|
RP3
|
[NCBI]
|
2.64593e-05
|
|
|
ERCC6
|
[NCBI]
|
2.44927e-05
|
|
|
IGF1R
|
[NCBI]
|
2.38917e-05
|
|
|
VLDLR
|
[NCBI]
|
2.33274e-05
|
|
|
HLA-B
|
[NCBI]
|
2.18163e-05
|
|
|
HLA-DRB1
|
[NCBI]
|
1.97499e-05
|
|
|
CLN3
|
[NCBI]
|
1.88328e-05
|
|
|
neuraminidase deficiency
|
[NCBI]
|
1.85622e-05
|
|
|
CHM
|
[NCBI]
|
1.82976e-05
|
|
|
IGF1
|
[NCBI]
|
1.74834e-05
|
|
|
ENG
|
[NCBI]
|
1.61643e-05
|
|
|
A2M
|
[NCBI]
|
1.50236e-05
|
|
|
CP
|
[NCBI]
|
1.3681e-05
|
|
|
CCL2
|
[NCBI]
|
1.27999e-05
|
|
|
SLS
|
[NCBI]
|
1.27879e-05
|
|
|
RPGR
|
[NCBI]
|
1.26398e-05
|
|
|
PAX6
|
[NCBI]
|
1.21786e-05
|
|
|
NPY
|
[NCBI]
|
1.07984e-05
|
|
|
ESR1
|
[NCBI]
|
1.06937e-05
|
|
|
MTTL1
|
[NCBI]
|
9.46099e-06
|
|
|
SLPI
|
[NCBI]
|
8.87069e-06
|
|
|
RHO
|
[NCBI]
|
7.90862e-06
|
|
|
TLR4
|
[NCBI]
|
7.2352e-06
|
|
|
IL6
|
[NCBI]
|
6.03808e-06
|
|
|
AGER
|
[NCBI]
|
5.69455e-06
|
|
|
CAT
|
[NCBI]
|
5.24847e-06
|
|
|
BDNF
|
[NCBI]
|
5.15098e-06
|
|
|
SDC2
|
[NCBI]
|
4.73719e-06
|
|
|
F3
|
[NCBI]
|
3.70824e-06
|
|
|
TNFSF6
|
[NCBI]
|
2.58342e-06
|
|
|
APOB
|
[NCBI]
|
2.35854e-06
|
|
|
GFAP
|
[NCBI]
|
2.17523e-06
|
|
|
PXE
|
[NCBI]
|
1.95709e-06
|
|
|
SOD1
|
[NCBI]
|
1.83701e-06
|
|
|
ACE
|
[NCBI]
|
1.27344e-06
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
7.93004e-07
|
|
|
CNTF
|
[NCBI]
|
5.86855e-07
|
|
|
CTGF
|
[NCBI]
|
4.13931e-07
|
|
|
SOD2
|
[NCBI]
|
2.6479e-07
|
|
|
TF
|
[NCBI]
|
2.59183e-07
|
|
|
XDH
|
[NCBI]
|
1.18316e-07
|
|