|
OMIM |
Link |
Information gain |
01 |
|
VRNI
|
[NCBI]
|
0.0509132
|
|
|
EVR1
|
[NCBI]
|
0.00181714
|
|
|
EVR3
|
[NCBI]
|
0.00151824
|
|
|
VRCP
|
[NCBI]
|
0.00151824
|
|
|
retinoschisis of fovea
|
[NCBI]
|
0.00124505
|
|
|
AIC
|
[NCBI]
|
0.00115038
|
|
|
vasculopathy, retinal, with cerebral leukodystrophy
|
[NCBI]
|
0.000671045
|
|
|
CORDX2
|
[NCBI]
|
0.000622084
|
|
|
EVR2
|
[NCBI]
|
0.00059385
|
|
|
arima syndrome
|
[NCBI]
|
0.000555816
|
|
|
coats disease
|
[NCBI]
|
0.000478981
|
|
|
RA
|
[NCBI]
|
0.000456802
|
|
|
RP
|
[NCBI]
|
0.000450475
|
|
|
ornithine aminotransferase deficiency
|
[NCBI]
|
0.000379632
|
|
|
GFAP
|
[NCBI]
|
0.000337878
|
|
|
NDP
|
[NCBI]
|
0.000333869
|
|
|
FSHMD1A
|
[NCBI]
|
0.000301722
|
|
|
CORD5
|
[NCBI]
|
0.000277517
|
|
|
RS1
|
[NCBI]
|
0.000275483
|
|
|
FZD4
|
[NCBI]
|
0.000273969
|
|
|
APC
|
[NCBI]
|
0.000273819
|
|
|
STGD1
|
[NCBI]
|
0.000263922
|
|
|
VEGF
|
[NCBI]
|
0.000251251
|
|
|
PEDF
|
[NCBI]
|
0.000249173
|
|
|
ND
|
[NCBI]
|
0.000248699
|
|
|
microcephaly with chorioretinopathy, autosomal recessive
|
[NCBI]
|
0.00024082
|
|
|
USH2B
|
[NCBI]
|
0.00024082
|
|
|
EVR4
|
[NCBI]
|
0.000219902
|
|
|
LRP5
|
[NCBI]
|
0.000212179
|
|
|
PPCRA
|
[NCBI]
|
0.000209871
|
|
|
ACHM3
|
[NCBI]
|
0.000194587
|
|
|
prepapillary vascular loops
|
[NCBI]
|
0.000191392
|
|
|
fleck retina, familial benign
|
[NCBI]
|
0.000191392
|
|
|
RCD1
|
[NCBI]
|
0.000188894
|
|
|
RNANC
|
[NCBI]
|
0.000188894
|
|
|
HYPX
|
[NCBI]
|
0.000152712
|
|
|
hypertension with brachydactyly
|
[NCBI]
|
0.000152712
|
|
|
ESCS
|
[NCBI]
|
0.000150888
|
|
|
CMM
|
[NCBI]
|
0.000148229
|
|
|
PRD
|
[NCBI]
|
0.000146535
|
|
|
roifman syndrome
|
[NCBI]
|
0.000146535
|
|
|
CNGB3
|
[NCBI]
|
0.000138914
|
|
|
DA5
|
[NCBI]
|
0.000138237
|
|
|
TREX1
|
[NCBI]
|
0.00013515
|
|
|
leber optic atrophy
|
[NCBI]
|
0.000113813
|
|
|
SCA7
|
[NCBI]
|
9.90398e-05
|
|
|
RCV1
|
[NCBI]
|
9.70601e-05
|
|
|
WGN1
|
[NCBI]
|
9.64832e-05
|
|
|
IP
|
[NCBI]
|
9.58581e-05
|
|
|
LCA12
|
[NCBI]
|
9.56626e-05
|
|
|
HRX
|
[NCBI]
|
9.56626e-05
|
|
|
retinal nonattachment and falciform detachment
|
[NCBI]
|
9.56626e-05
|
|
|
microphthalmia, posterior, with retinitis pigmentosa, foveoschisis, and optic disc drusen
|
[NCBI]
|
9.56626e-05
|
|
|
retinoschisis, autosomal dominant
|
[NCBI]
|
9.56626e-05
|
|
|
ophthalmoplegia, progressive, with scrotal tongue and mental deficiency
|
[NCBI]
|
9.56626e-05
|
|
|
ARB
|
[NCBI]
|
9.56626e-05
|
|
|
rod-cone dystrophy, sensorineural deafness, and fanconi-type renal dysfunction
|
[NCBI]
|
9.56626e-05
|
|
|
cone-rod dystrophy 11
|
[NCBI]
|
9.56626e-05
|
|
|
GUCY2E
|
[NCBI]
|
9.56626e-05
|
|
|
iris pigment layer, cleavage of
|
[NCBI]
|
9.56626e-05
|
|
|
CSNBAD3
|
[NCBI]
|
9.56626e-05
|
|
|
birdshot chorioretinopathy
|
[NCBI]
|
9.56626e-05
|
|
|
guanylyl cyclase, membrane, type d, murine
|
[NCBI]
|
9.56626e-05
|
|
|
CBBM
|
[NCBI]
|
9.50777e-05
|
|
|
branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging
|
[NCBI]
|
9.50777e-05
|
|
|
ACHM2
|
[NCBI]
|
9.4287e-05
|
|
|
ABCA4
|
[NCBI]
|
8.88865e-05
|
|
|
RDH5
|
[NCBI]
|
8.58331e-05
|
|
|
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency
|
[NCBI]
|
8.21661e-05
|
|
|
CRB1
|
[NCBI]
|
8.08376e-05
|
|
|
CRX
|
[NCBI]
|
7.35612e-05
|
|
|
revesz syndrome
|
[NCBI]
|
7.32343e-05
|
|
|
aplasia cutis congenita, high myopia, and cone-rod dysfunction
|
[NCBI]
|
7.32343e-05
|
|
|
brain small vessel disease with hemorrhage
|
[NCBI]
|
7.32343e-05
|
|
|
WM1
|
[NCBI]
|
7.26133e-05
|
|
|
RLBP1
|
[NCBI]
|
6.71519e-05
|
|
|
PXE
|
[NCBI]
|
6.5954e-05
|
|
|
LBX2
|
[NCBI]
|
6.52104e-05
|
|
|
GPR75
|
[NCBI]
|
6.52104e-05
|
|
|
FAM46A
|
[NCBI]
|
6.52104e-05
|
|
|
EDG5
|
[NCBI]
|
6.52104e-05
|
|
|
USP11
|
[NCBI]
|
6.52104e-05
|
|
|
RDH8
|
[NCBI]
|
6.52104e-05
|
|
|
RAXL1
|
[NCBI]
|
6.52104e-05
|
|
|
STL1
|
[NCBI]
|
6.51455e-05
|
|
|
laurence-moon syndrome
|
[NCBI]
|
6.47964e-05
|
|
|
albinism, ocular, with sensorineural deafness
|
[NCBI]
|
6.47964e-05
|
|
|
BBS
|
[NCBI]
|
6.20934e-05
|
|
|
VHL
|
[NCBI]
|
6.17545e-05
|
|
|
AD
|
[NCBI]
|
6.04952e-05
|
|
|
HANAC
|
[NCBI]
|
5.93324e-05
|
|
|
pars planitis
|
[NCBI]
|
5.93324e-05
|
|
|
glutamate monosodium sensitivity
|
[NCBI]
|
5.93324e-05
|
|
|
CHM
|
[NCBI]
|
5.50194e-05
|
|
|
KSS
|
[NCBI]
|
5.44233e-05
|
|
|
PRPH2
|
[NCBI]
|
5.36152e-05
|
|
|
CCM
|
[NCBI]
|
5.28369e-05
|
|
|
OA1
|
[NCBI]
|
5.2568e-05
|
|
|
ramon syndrome
|
[NCBI]
|
5.2061e-05
|
|
|
ADAM15
|
[NCBI]
|
5.14437e-05
|
|
|
DR1
|
[NCBI]
|
5.14437e-05
|
|
|
GUCY2F
|
[NCBI]
|
5.14437e-05
|
|
|
NF2
|
[NCBI]
|
4.98568e-05
|
|
|
ARMD1
|
[NCBI]
|
4.93904e-05
|
|
|
bietti crystalline corneoretinal dystrophy
|
[NCBI]
|
4.71115e-05
|
|
|
TNF
|
[NCBI]
|
4.67279e-05
|
|
|
VSX1
|
[NCBI]
|
4.62563e-05
|
|
|
GNAT1
|
[NCBI]
|
4.62563e-05
|
|
|
C1ORF36
|
[NCBI]
|
4.62563e-05
|
|
|
PDE6A
|
[NCBI]
|
4.62563e-05
|
|
|
RPGR
|
[NCBI]
|
4.54534e-05
|
|
|
RP12
|
[NCBI]
|
4.51242e-05
|
|
|
KNO
|
[NCBI]
|
4.33636e-05
|
|
|
cherubism
|
[NCBI]
|
4.33636e-05
|
|
|
fundus albipunctatus
|
[NCBI]
|
4.33636e-05
|
|
|
DLG4
|
[NCBI]
|
4.28925e-05
|
|
|
EFEMP2
|
[NCBI]
|
4.28925e-05
|
|
|
HRD
|
[NCBI]
|
4.17842e-05
|
|
|
KCS
|
[NCBI]
|
4.17842e-05
|
|
|
ROM1
|
[NCBI]
|
4.03949e-05
|
|
|
CNGA3
|
[NCBI]
|
4.03949e-05
|
|
|
antiphospholipid syndrome
|
[NCBI]
|
4.03528e-05
|
|
|
COL2A1
|
[NCBI]
|
3.9317e-05
|
|
|
WZS
|
[NCBI]
|
3.90446e-05
|
|
|
IFNA2
|
[NCBI]
|
3.84073e-05
|
|
|
MFRP
|
[NCBI]
|
3.84073e-05
|
|
|
GNAT2
|
[NCBI]
|
3.84073e-05
|
|
|
COL9A1
|
[NCBI]
|
3.84073e-05
|
|
|
CORDX1
|
[NCBI]
|
3.78408e-05
|
|
|
WS2A
|
[NCBI]
|
3.78408e-05
|
|
|
complement factor h deficiency
|
[NCBI]
|
3.5689e-05
|
|
|
sarcoidosis
|
[NCBI]
|
3.5689e-05
|
|
|
coenzyme q10 deficiency
|
[NCBI]
|
3.5689e-05
|
|
|
AIPL1
|
[NCBI]
|
3.53459e-05
|
|
|
GUCA1A
|
[NCBI]
|
3.53459e-05
|
|
|
DLL4
|
[NCBI]
|
3.53459e-05
|
|
|
EPAS1
|
[NCBI]
|
3.53459e-05
|
|
|
synovitis, granulomatous, with uveitis and cranial neuropathies
|
[NCBI]
|
3.47195e-05
|
|
|
MCDC1
|
[NCBI]
|
3.47195e-05
|
|
|
MERTK
|
[NCBI]
|
3.41141e-05
|
|
|
MKKS
|
[NCBI]
|
3.41141e-05
|
|
|
papillorenal syndrome
|
[NCBI]
|
3.38098e-05
|
|
|
DHRD
|
[NCBI]
|
3.38098e-05
|
|
|
mulibrey nanism
|
[NCBI]
|
3.38098e-05
|
|
|
NRL
|
[NCBI]
|
3.30213e-05
|
|
|
RBP3
|
[NCBI]
|
3.30213e-05
|
|
|
RPGRIP1
|
[NCBI]
|
3.30213e-05
|
|
|
AIED
|
[NCBI]
|
3.21438e-05
|
|
|
danon disease
|
[NCBI]
|
3.21438e-05
|
|
|
CACNA1F
|
[NCBI]
|
3.03335e-05
|
|
|
SLSN1
|
[NCBI]
|
2.99566e-05
|
|
|
HADHA
|
[NCBI]
|
2.88855e-05
|
|
|
BEST1
|
[NCBI]
|
2.88855e-05
|
|
|
JBTS1
|
[NCBI]
|
2.84561e-05
|
|
|
PLG
|
[NCBI]
|
2.75624e-05
|
|
|
ALMS
|
[NCBI]
|
2.7481e-05
|
|
|
MELAS
|
[NCBI]
|
2.7481e-05
|
|
|
RPE65
|
[NCBI]
|
2.70576e-05
|
|
|
MKKS
|
[NCBI]
|
2.53792e-05
|
|
|
cerebrotendinous xanthomatosis
|
[NCBI]
|
2.53792e-05
|
|
|
LCA1
|
[NCBI]
|
2.53792e-05
|
|
|
TS
|
[NCBI]
|
2.46119e-05
|
|
|
graves disease
|
[NCBI]
|
2.39913e-05
|
|
|
hyperoxaluria, primary, type i
|
[NCBI]
|
2.35587e-05
|
|
|
SMPD1
|
[NCBI]
|
2.34269e-05
|
|
|
BDNF
|
[NCBI]
|
2.27559e-05
|
|
|
FIH
|
[NCBI]
|
2.27338e-05
|
|
|
EGFR
|
[NCBI]
|
2.23557e-05
|
|
|
HLA-A
|
[NCBI]
|
2.20345e-05
|
|
|
PDE6B
|
[NCBI]
|
2.14105e-05
|
|
|
walker-warburg syndrome
|
[NCBI]
|
2.12254e-05
|
|
|
AQP4
|
[NCBI]
|
2.08266e-05
|
|
|
COH1
|
[NCBI]
|
2.05326e-05
|
|
|
OCA1A
|
[NCBI]
|
2.05326e-05
|
|
|
ATS
|
[NCBI]
|
2.05326e-05
|
|
|
VMD
|
[NCBI]
|
1.98759e-05
|
|
|
MTATP6
|
[NCBI]
|
1.9273e-05
|
|
|
neuraminidase deficiency with beta-galactosidase deficiency
|
[NCBI]
|
1.85875e-05
|
|
|
MMP2
|
[NCBI]
|
1.79516e-05
|
|
|
RP2
|
[NCBI]
|
1.7552e-05
|
|
|
CTNS
|
[NCBI]
|
1.7289e-05
|
|
|
sickle cell anemia
|
[NCBI]
|
1.65376e-05
|
|
|
NF2
|
[NCBI]
|
1.61171e-05
|
|
|
MKS1
|
[NCBI]
|
1.5832e-05
|
|
|
ABL
|
[NCBI]
|
1.56061e-05
|
|
|
CLS
|
[NCBI]
|
1.47457e-05
|
|
|
TYR
|
[NCBI]
|
1.43399e-05
|
|
|
CNTF
|
[NCBI]
|
1.3588e-05
|
|
|
MITF
|
[NCBI]
|
1.2882e-05
|
|
|
MTTL1
|
[NCBI]
|
1.27718e-05
|
|
|
MCP
|
[NCBI]
|
1.27718e-05
|
|
|
gaucher disease, type i
|
[NCBI]
|
1.21823e-05
|
|
|
TF
|
[NCBI]
|
1.16916e-05
|
|
|
NGFB
|
[NCBI]
|
1.08676e-05
|
|
|
MPO
|
[NCBI]
|
1.05007e-05
|
|
|
KDR
|
[NCBI]
|
1.04348e-05
|
|
|
homocystinuria
|
[NCBI]
|
1.02762e-05
|
|
|
HHT
|
[NCBI]
|
1.02749e-05
|
|
|
APOE
|
[NCBI]
|
7.55601e-06
|
|
|
ZS
|
[NCBI]
|
7.18956e-06
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
6.49293e-06
|
|
|
PRNP
|
[NCBI]
|
5.35273e-06
|
|
|
CHAT
|
[NCBI]
|
5.01553e-06
|
|
|
HPS
|
[NCBI]
|
4.63995e-06
|
|
|
RB1
|
[NCBI]
|
4.48267e-06
|
|
|
NPY
|
[NCBI]
|
4.20937e-06
|
|
|
EGF
|
[NCBI]
|
4.08307e-06
|
|
|
ACE
|
[NCBI]
|
3.28482e-06
|
|
|
DGS
|
[NCBI]
|
3.16715e-06
|
|
|
DMD
|
[NCBI]
|
2.99143e-06
|
|
|
temporal arteritis
|
[NCBI]
|
2.87135e-06
|
|
|
TH
|
[NCBI]
|
2.20969e-06
|
|
|
CTGF
|
[NCBI]
|
1.90503e-06
|
|
|
TNFSF6
|
[NCBI]
|
1.66604e-06
|
|
|
GDNF
|
[NCBI]
|
4.32881e-07
|
|
|
APOB
|
[NCBI]
|
2.26493e-07
|
|
|
TTR
|
[NCBI]
|
1.74371e-07
|
|
|
SPS
|
[NCBI]
|
1.39177e-07
|
|
|
SLE
|
[NCBI]
|
1.35743e-07
|
|
|
kabuki syndrome
|
[NCBI]
|
1.00596e-07
|
|
|
HBB
|
[NCBI]
|
9.89416e-08
|
|
|
HGF
|
[NCBI]
|
6.67984e-08
|
|
|
VDR
|
[NCBI]
|
6.36624e-08
|
|
|
CJD
|
[NCBI]
|
2.37813e-09
|
|