|
OMIM |
Link |
Information gain |
01 |
|
VRNI
|
[NCBI]
|
0.00839858
|
|
|
MCDR1
|
[NCBI]
|
0.00666552
|
|
|
EVR3
|
[NCBI]
|
0.00266033
|
|
|
macular dystrophy, butterfly-shaped pigmentary, 2
|
[NCBI]
|
0.00167847
|
|
|
microcephaly with chorioretinopathy, autosomal recessive
|
[NCBI]
|
0.00148689
|
|
|
RP
|
[NCBI]
|
0.00136676
|
|
|
SFD
|
[NCBI]
|
0.00119572
|
|
|
STGD1
|
[NCBI]
|
0.00105236
|
|
|
dilution, pigmentary
|
[NCBI]
|
0.000741598
|
|
|
CACD
|
[NCBI]
|
0.000741598
|
|
|
retinal cone dystrophy 2
|
[NCBI]
|
0.000741598
|
|
|
CORD5
|
[NCBI]
|
0.000626283
|
|
|
vitreoretinal degeneration, snowflake type
|
[NCBI]
|
0.000626283
|
|
|
AIC
|
[NCBI]
|
0.000588219
|
|
|
RP6
|
[NCBI]
|
0.000552124
|
|
|
trichomegaly with mental retardation, dwarfism, and pigmentary degeneration of retina
|
[NCBI]
|
0.000552124
|
|
|
RP24
|
[NCBI]
|
0.000552124
|
|
|
APC
|
[NCBI]
|
0.000541842
|
|
|
WGN1
|
[NCBI]
|
0.00053897
|
|
|
PXE
|
[NCBI]
|
0.000534285
|
|
|
chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism
|
[NCBI]
|
0.00049751
|
|
|
chorioretinal atrophy, progressive bifocal
|
[NCBI]
|
0.00049751
|
|
|
fundus dystrophy, pseudoinflammatory, recessive form
|
[NCBI]
|
0.000461037
|
|
|
macular edema, cystoid
|
[NCBI]
|
0.000454408
|
|
|
CHM
|
[NCBI]
|
0.000427353
|
|
|
CFEOM3
|
[NCBI]
|
0.000388826
|
|
|
CORD2
|
[NCBI]
|
0.000369873
|
|
|
fundus albipunctatus
|
[NCBI]
|
0.000365945
|
|
|
macular dystrophy, vitelliform, adult-onset
|
[NCBI]
|
0.000326095
|
|
|
bietti crystalline corneoretinal dystrophy
|
[NCBI]
|
0.000311709
|
|
|
prepapillary vascular loops
|
[NCBI]
|
0.000307233
|
|
|
CBBM
|
[NCBI]
|
0.000301124
|
|
|
RHO
|
[NCBI]
|
0.000288093
|
|
|
VMD
|
[NCBI]
|
0.000284424
|
|
|
DHRD
|
[NCBI]
|
0.000270968
|
|
|
leber optic atrophy
|
[NCBI]
|
0.000236974
|
|
|
ESCS
|
[NCBI]
|
0.000219264
|
|
|
EVR1
|
[NCBI]
|
0.000203876
|
|
|
PRPH2
|
[NCBI]
|
0.000190177
|
|
|
RS1
|
[NCBI]
|
0.00017014
|
|
|
ACHM2
|
[NCBI]
|
0.000155295
|
|
|
HRX
|
[NCBI]
|
0.000153554
|
|
|
microphthalmia, posterior, with retinitis pigmentosa, foveoschisis, and optic disc drusen
|
[NCBI]
|
0.000153554
|
|
|
optic atrophy with negative electroretinograms
|
[NCBI]
|
0.000153554
|
|
|
angioid streaks
|
[NCBI]
|
0.000153554
|
|
|
ophthalmoplegia, progressive, with scrotal tongue and mental deficiency
|
[NCBI]
|
0.000153554
|
|
|
retinal degeneration with nanophthalmos, cystic macular degeneration, and angle closure glaucoma
|
[NCBI]
|
0.000153554
|
|
|
cone dystrophy, x-linked, with tapetal-like sheen
|
[NCBI]
|
0.000153554
|
|
|
retinopathy, pericentral pigmentary, dominant
|
[NCBI]
|
0.000153554
|
|
|
retinitis pigmentosa inversa with deafness
|
[NCBI]
|
0.000153554
|
|
|
amaurosis congenita, cone-rod type, with congenital hypertrichosis
|
[NCBI]
|
0.000153554
|
|
|
LCA1
|
[NCBI]
|
0.000150477
|
|
|
CORDX1
|
[NCBI]
|
0.000146057
|
|
|
TIMP3
|
[NCBI]
|
0.000144876
|
|
|
AIED
|
[NCBI]
|
0.000141974
|
|
|
papillorenal syndrome
|
[NCBI]
|
0.000141974
|
|
|
SLS
|
[NCBI]
|
0.000140627
|
|
|
CMM
|
[NCBI]
|
0.000138667
|
|
|
septooptic dysplasia
|
[NCBI]
|
0.000134646
|
|
|
RDH5
|
[NCBI]
|
0.000125657
|
|
|
OPA1
|
[NCBI]
|
0.000114938
|
|
|
macular dystrophy, concentric annular
|
[NCBI]
|
0.000114402
|
|
|
NNO2
|
[NCBI]
|
0.000114402
|
|
|
optic atrophy 1 and deafness
|
[NCBI]
|
0.000114402
|
|
|
nonarteritic anterior ischemic optic neuropathy, susceptibility to
|
[NCBI]
|
0.000114402
|
|
|
retinopathy, pericentral pigmentary, autosomal recessive
|
[NCBI]
|
0.000114402
|
|
|
choroidal osteoma, bilateral
|
[NCBI]
|
0.000114402
|
|
|
pseudopapilledema
|
[NCBI]
|
0.000114402
|
|
|
albinism, ocular, with sensorineural deafness
|
[NCBI]
|
0.000114402
|
|
|
RP26
|
[NCBI]
|
0.000114402
|
|
|
melanoma, uveal
|
[NCBI]
|
0.00011046
|
|
|
NF2
|
[NCBI]
|
0.00010441
|
|
|
RP3
|
[NCBI]
|
0.000102546
|
|
|
retinal dystrophy, reticular pigmentary, of posterior pole
|
[NCBI]
|
9.97023e-05
|
|
|
LCA5
|
[NCBI]
|
9.97023e-05
|
|
|
mydriatic response to pharmacologic agents
|
[NCBI]
|
9.97023e-05
|
|
|
grouped pigmentation of the macula
|
[NCBI]
|
9.97023e-05
|
|
|
keratitis, hereditary
|
[NCBI]
|
9.97023e-05
|
|
|
antiphospholipid syndrome
|
[NCBI]
|
9.97023e-05
|
|
|
reese retinal dysplasia
|
[NCBI]
|
9.97023e-05
|
|
|
retinal arteries, tortuosity of
|
[NCBI]
|
9.12201e-05
|
|
|
CLN3
|
[NCBI]
|
9.11648e-05
|
|
|
CORD3
|
[NCBI]
|
9.02004e-05
|
|
|
CSNB1B
|
[NCBI]
|
9.02004e-05
|
|
|
WS1
|
[NCBI]
|
8.97369e-05
|
|
|
ARMD1
|
[NCBI]
|
8.70032e-05
|
|
|
MFRP
|
[NCBI]
|
8.69564e-05
|
|
|
RP2
|
[NCBI]
|
8.53133e-05
|
|
|
KSS
|
[NCBI]
|
8.50417e-05
|
|
|
RP14
|
[NCBI]
|
8.3167e-05
|
|
|
SCRA
|
[NCBI]
|
8.3167e-05
|
|
|
foveal hypoplasia and presenile cataract syndrome
|
[NCBI]
|
7.75876e-05
|
|
|
chorioretinal dysplasia-microcephaly-mental retardation syndrome
|
[NCBI]
|
7.75876e-05
|
|
|
oguchi disease
|
[NCBI]
|
7.75876e-05
|
|
|
PPCRA
|
[NCBI]
|
7.75876e-05
|
|
|
TULP1
|
[NCBI]
|
7.51689e-05
|
|
|
ND
|
[NCBI]
|
7.42969e-05
|
|
|
neuraminidase deficiency
|
[NCBI]
|
7.42969e-05
|
|
|
RCD3A
|
[NCBI]
|
7.29689e-05
|
|
|
patterned dystrophy of retinal pigment epithelium
|
[NCBI]
|
7.29689e-05
|
|
|
SLE
|
[NCBI]
|
7.08491e-05
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
7.06249e-05
|
|
|
phace association
|
[NCBI]
|
6.9033e-05
|
|
|
VEGF
|
[NCBI]
|
6.75899e-05
|
|
|
EVR2
|
[NCBI]
|
6.56076e-05
|
|
|
CSNB2A
|
[NCBI]
|
6.56076e-05
|
|
|
LRP5
|
[NCBI]
|
6.51914e-05
|
|
|
diabetes-deafness syndrome, maternally transmitted
|
[NCBI]
|
6.25785e-05
|
|
|
STGD3
|
[NCBI]
|
5.9866e-05
|
|
|
amyloidosis vii
|
[NCBI]
|
5.9866e-05
|
|
|
CERKL
|
[NCBI]
|
5.55501e-05
|
|
|
ornithine aminotransferase deficiency
|
[NCBI]
|
5.44865e-05
|
|
|
ALMS
|
[NCBI]
|
5.31179e-05
|
|
|
camurati-engelmann disease
|
[NCBI]
|
5.12179e-05
|
|
|
mulibrey nanism
|
[NCBI]
|
5.12179e-05
|
|
|
RLBP1
|
[NCBI]
|
5.11527e-05
|
|
|
COL2A1
|
[NCBI]
|
4.97411e-05
|
|
|
RPGR
|
[NCBI]
|
4.92138e-05
|
|
|
SLSN1
|
[NCBI]
|
4.78068e-05
|
|
|
niemann-pick disease, type a
|
[NCBI]
|
4.62647e-05
|
|
|
usher syndrome, type i
|
[NCBI]
|
4.62647e-05
|
|
|
MPP4
|
[NCBI]
|
4.55696e-05
|
|
|
IFNA2
|
[NCBI]
|
4.55696e-05
|
|
|
STL1
|
[NCBI]
|
4.48154e-05
|
|
|
OCRL
|
[NCBI]
|
4.3449e-05
|
|
|
TTR
|
[NCBI]
|
4.22788e-05
|
|
|
CSNB1A
|
[NCBI]
|
4.21573e-05
|
|
|
RP1
|
[NCBI]
|
4.21573e-05
|
|
|
hyperoxaluria, primary, type i
|
[NCBI]
|
4.21573e-05
|
|
|
LCA5
|
[NCBI]
|
4.18046e-05
|
|
|
mucopolysaccharidosis type vi
|
[NCBI]
|
4.09332e-05
|
|
|
GRK1
|
[NCBI]
|
3.93606e-05
|
|
|
HMCN1
|
[NCBI]
|
3.75442e-05
|
|
|
COH1
|
[NCBI]
|
3.66003e-05
|
|
|
ELOVL4
|
[NCBI]
|
3.60973e-05
|
|
|
GLC1A
|
[NCBI]
|
3.56358e-05
|
|
|
tritanopia
|
[NCBI]
|
3.48946e-05
|
|
|
RCV1
|
[NCBI]
|
3.38654e-05
|
|
|
MTTE
|
[NCBI]
|
3.38654e-05
|
|
|
NR2E3
|
[NCBI]
|
3.21674e-05
|
|
|
CMTX1
|
[NCBI]
|
3.21545e-05
|
|
|
MEB
|
[NCBI]
|
3.1366e-05
|
|
|
LRAT
|
[NCBI]
|
3.07968e-05
|
|
|
CACNA1F
|
[NCBI]
|
3.01992e-05
|
|
|
CRX
|
[NCBI]
|
2.96479e-05
|
|
|
MTHFR
|
[NCBI]
|
2.96479e-05
|
|
|
factor v deficiency
|
[NCBI]
|
2.91362e-05
|
|
|
ATS
|
[NCBI]
|
2.84809e-05
|
|
|
SCA7
|
[NCBI]
|
2.71791e-05
|
|
|
glycogen storage disease i
|
[NCBI]
|
2.4831e-05
|
|
|
PAX2
|
[NCBI]
|
2.43134e-05
|
|
|
OA1
|
[NCBI]
|
2.38313e-05
|
|
|
AN2
|
[NCBI]
|
2.32088e-05
|
|
|
ALGS1
|
[NCBI]
|
2.1737e-05
|
|
|
MTTL1
|
[NCBI]
|
2.04045e-05
|
|
|
gaucher disease, type i
|
[NCBI]
|
1.99486e-05
|
|
|
PAX6
|
[NCBI]
|
1.82284e-05
|
|
|
BSG
|
[NCBI]
|
1.73559e-05
|
|
|
apc gene
|
[NCBI]
|
1.69159e-05
|
|
|
ichthyosis, x-linked
|
[NCBI]
|
1.65031e-05
|
|
|
VHL
|
[NCBI]
|
1.55213e-05
|
|
|
PLG
|
[NCBI]
|
1.50692e-05
|
|
|
temporal arteritis
|
[NCBI]
|
1.18965e-05
|
|
|
NF1
|
[NCBI]
|
1.15434e-05
|
|
|
GFAP
|
[NCBI]
|
1.02415e-05
|
|
|
FSHMD1A
|
[NCBI]
|
8.23025e-06
|
|
|
HPS
|
[NCBI]
|
5.73285e-06
|
|
|
TS
|
[NCBI]
|
7.02327e-07
|
|