|
OMIM |
Link |
Information gain |
01 |
|
VRNI
|
[NCBI]
|
0.0448703
|
|
|
RP
|
[NCBI]
|
0.00553022
|
|
|
MCDR1
|
[NCBI]
|
0.00272227
|
|
|
NNO1
|
[NCBI]
|
0.00141565
|
|
|
OPA2
|
[NCBI]
|
0.0011036
|
|
|
cavitary optic disc anomalies
|
[NCBI]
|
0.0011036
|
|
|
RA
|
[NCBI]
|
0.00104808
|
|
|
RP6
|
[NCBI]
|
0.000942672
|
|
|
RP24
|
[NCBI]
|
0.000942672
|
|
|
CBBM
|
[NCBI]
|
0.000896893
|
|
|
leber optic atrophy
|
[NCBI]
|
0.000889194
|
|
|
arteriosclerosis, severe juvenile
|
[NCBI]
|
0.0007318
|
|
|
CORDX2
|
[NCBI]
|
0.0007318
|
|
|
behcet syndrome
|
[NCBI]
|
0.000664045
|
|
|
CF
|
[NCBI]
|
0.000606797
|
|
|
CDB2
|
[NCBI]
|
0.000581967
|
|
|
corneal dystrophy, crystalline, of schnyder
|
[NCBI]
|
0.000540875
|
|
|
STGD1
|
[NCBI]
|
0.00048361
|
|
|
retinoschisis of fovea
|
[NCBI]
|
0.00047079
|
|
|
dilution, pigmentary
|
[NCBI]
|
0.00047079
|
|
|
VMD1
|
[NCBI]
|
0.00047079
|
|
|
retinal cone dystrophy 2
|
[NCBI]
|
0.00047079
|
|
|
temporal arteritis
|
[NCBI]
|
0.000463935
|
|
|
OPA1
|
[NCBI]
|
0.000444593
|
|
|
VMD
|
[NCBI]
|
0.000413567
|
|
|
CORD2
|
[NCBI]
|
0.000397408
|
|
|
macular dystrophy, butterfly-shaped pigmentary, 2
|
[NCBI]
|
0.000374894
|
|
|
astigmatism
|
[NCBI]
|
0.000374894
|
|
|
AN2
|
[NCBI]
|
0.000319658
|
|
|
CORD5
|
[NCBI]
|
0.000314095
|
|
|
VRCP
|
[NCBI]
|
0.000314095
|
|
|
ectopia lentis with ectopia of pupil
|
[NCBI]
|
0.000314095
|
|
|
MYP1
|
[NCBI]
|
0.000314095
|
|
|
macular dystrophy, vitelliform, adult-onset
|
[NCBI]
|
0.00028803
|
|
|
CDB1
|
[NCBI]
|
0.00027718
|
|
|
chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism
|
[NCBI]
|
0.000269964
|
|
|
CORD7
|
[NCBI]
|
0.000269964
|
|
|
chorioretinal atrophy, progressive bifocal
|
[NCBI]
|
0.000269964
|
|
|
OPA4
|
[NCBI]
|
0.000269964
|
|
|
pars planitis
|
[NCBI]
|
0.000263464
|
|
|
CDA
|
[NCBI]
|
0.000259223
|
|
|
CDGG1
|
[NCBI]
|
0.000251609
|
|
|
CHM
|
[NCBI]
|
0.000245492
|
|
|
STGD3
|
[NCBI]
|
0.000244682
|
|
|
PPCRA
|
[NCBI]
|
0.000241229
|
|
|
macular edema, cystoid
|
[NCBI]
|
0.000235652
|
|
|
ESCS
|
[NCBI]
|
0.000217171
|
|
|
foveal hypoplasia and presenile cataract syndrome
|
[NCBI]
|
0.00021311
|
|
|
CSNB1B
|
[NCBI]
|
0.00021311
|
|
|
ocular motor apraxia
|
[NCBI]
|
0.000207827
|
|
|
NYS2
|
[NCBI]
|
0.000207827
|
|
|
MCOP1
|
[NCBI]
|
0.000207827
|
|
|
CSNB1A
|
[NCBI]
|
0.000200645
|
|
|
HPS
|
[NCBI]
|
0.000188577
|
|
|
RCD1
|
[NCBI]
|
0.000184614
|
|
|
MCOPS1
|
[NCBI]
|
0.000184614
|
|
|
AD
|
[NCBI]
|
0.000184176
|
|
|
RHO
|
[NCBI]
|
0.000176874
|
|
|
XFS
|
[NCBI]
|
0.000168897
|
|
|
coloboma of optic nerve
|
[NCBI]
|
0.000167421
|
|
|
pseudopapilledema
|
[NCBI]
|
0.000167421
|
|
|
LORD
|
[NCBI]
|
0.000167421
|
|
|
WGN1
|
[NCBI]
|
0.000163977
|
|
|
OCA1A
|
[NCBI]
|
0.000161283
|
|
|
CORD6
|
[NCBI]
|
0.000150249
|
|
|
hereditary motor and sensory neuropathy vi
|
[NCBI]
|
0.000150249
|
|
|
ZLS
|
[NCBI]
|
0.000147759
|
|
|
WM1
|
[NCBI]
|
0.000147759
|
|
|
RCD3A
|
[NCBI]
|
0.000138498
|
|
|
mucopolysaccharidosis type vi
|
[NCBI]
|
0.0001351
|
|
|
sjogren syndrome
|
[NCBI]
|
0.000132808
|
|
|
nonarteritic anterior ischemic optic neuropathy, susceptibility to
|
[NCBI]
|
0.00012952
|
|
|
patterned dystrophy of retinal pigment epithelium
|
[NCBI]
|
0.00012952
|
|
|
RP2
|
[NCBI]
|
0.000126824
|
|
|
AN1
|
[NCBI]
|
0.00012225
|
|
|
MTND4
|
[NCBI]
|
0.000120884
|
|
|
RP1
|
[NCBI]
|
0.000118248
|
|
|
TGFBI
|
[NCBI]
|
0.000114265
|
|
|
fundus albipunctatus
|
[NCBI]
|
0.000110878
|
|
|
trichomegaly
|
[NCBI]
|
0.000102757
|
|
|
ophthalmoplegia, progressive, with scrotal tongue and mental deficiency
|
[NCBI]
|
0.000102757
|
|
|
PERRS
|
[NCBI]
|
0.000102757
|
|
|
CSNB2B
|
[NCBI]
|
0.000102757
|
|
|
RP30
|
[NCBI]
|
0.000102757
|
|
|
retinal degeneration with nanophthalmos, cystic macular degeneration, and angle closure glaucoma
|
[NCBI]
|
0.000102757
|
|
|
grouped pigmentation of the macula
|
[NCBI]
|
0.000102757
|
|
|
choroidal osteoma, bilateral
|
[NCBI]
|
0.000102757
|
|
|
CDL1
|
[NCBI]
|
0.000102136
|
|
|
melanoma, uveal
|
[NCBI]
|
0.000100776
|
|
|
ELOVL4
|
[NCBI]
|
9.83049e-05
|
|
|
MYP2
|
[NCBI]
|
9.73407e-05
|
|
|
CORDX1
|
[NCBI]
|
9.19516e-05
|
|
|
ACHM2
|
[NCBI]
|
9.19516e-05
|
|
|
OCP
|
[NCBI]
|
8.66121e-05
|
|
|
CRX
|
[NCBI]
|
8.64223e-05
|
|
|
GUCY2D
|
[NCBI]
|
8.43815e-05
|
|
|
EVR1
|
[NCBI]
|
8.3974e-05
|
|
|
VEGF
|
[NCBI]
|
8.24903e-05
|
|
|
SLS
|
[NCBI]
|
8.13051e-05
|
|
|
AIED
|
[NCBI]
|
7.94863e-05
|
|
|
KTCN1
|
[NCBI]
|
7.74364e-05
|
|
|
PROS1
|
[NCBI]
|
7.60756e-05
|
|
|
hyperoxaluria, primary, type i
|
[NCBI]
|
7.54979e-05
|
|
|
fibrosis of extraocular muscles, congenital, with synergistic divergence
|
[NCBI]
|
7.51015e-05
|
|
|
retinopathy, pericentral pigmentary, dominant
|
[NCBI]
|
7.51015e-05
|
|
|
bothnia retinal dystrophy
|
[NCBI]
|
7.51015e-05
|
|
|
MCOPCB4
|
[NCBI]
|
7.51015e-05
|
|
|
reticular dystrophy of retinal pigment epithelium
|
[NCBI]
|
7.51015e-05
|
|
|
retinopathy, pericentral pigmentary, autosomal recessive
|
[NCBI]
|
7.51015e-05
|
|
|
RS1
|
[NCBI]
|
7.1348e-05
|
|
|
ABCA4
|
[NCBI]
|
6.95955e-05
|
|
|
LCA1
|
[NCBI]
|
6.71439e-05
|
|
|
GRM6
|
[NCBI]
|
6.69955e-05
|
|
|
SLE
|
[NCBI]
|
6.55181e-05
|
|
|
coats disease
|
[NCBI]
|
6.47373e-05
|
|
|
HJMD
|
[NCBI]
|
6.47373e-05
|
|
|
angioid streaks
|
[NCBI]
|
6.47373e-05
|
|
|
moved to 310600
|
[NCBI]
|
6.47373e-05
|
|
|
fundus dystrophy, pseudoinflammatory, recessive form
|
[NCBI]
|
6.47373e-05
|
|
|
yemenite deaf-blind hypopigmentation syndrome
|
[NCBI]
|
6.47373e-05
|
|
|
drusen of bruch membrane
|
[NCBI]
|
6.47373e-05
|
|
|
keratitis, hereditary
|
[NCBI]
|
6.47373e-05
|
|
|
chromosome xp11.3 deletion syndrome
|
[NCBI]
|
6.47373e-05
|
|
|
RP3
|
[NCBI]
|
6.16686e-05
|
|
|
PAX6
|
[NCBI]
|
5.94397e-05
|
|
|
corneal dystrophy and perceptive deafness
|
[NCBI]
|
5.80484e-05
|
|
|
amyloidosis, familial visceral
|
[NCBI]
|
5.80484e-05
|
|
|
CORDX3
|
[NCBI]
|
5.80484e-05
|
|
|
RDH5
|
[NCBI]
|
5.75688e-05
|
|
|
tritanopia
|
[NCBI]
|
5.75688e-05
|
|
|
NF1
|
[NCBI]
|
5.64727e-05
|
|
|
WFS1
|
[NCBI]
|
5.48429e-05
|
|
|
COH1
|
[NCBI]
|
5.38324e-05
|
|
|
CSCD
|
[NCBI]
|
5.31051e-05
|
|
|
optic nerve hypoplasia, bilateral
|
[NCBI]
|
5.31051e-05
|
|
|
LCA2
|
[NCBI]
|
5.31051e-05
|
|
|
3-@methylglutaconic aciduria, type iii
|
[NCBI]
|
5.31051e-05
|
|
|
chorioretinal dysplasia-microcephaly-mental retardation syndrome
|
[NCBI]
|
5.31051e-05
|
|
|
NRL
|
[NCBI]
|
4.98942e-05
|
|
|
RP14
|
[NCBI]
|
4.91899e-05
|
|
|
corneal dystrophy, epithelial basement membrane
|
[NCBI]
|
4.91899e-05
|
|
|
peters anomaly
|
[NCBI]
|
4.91899e-05
|
|
|
oguchi disease
|
[NCBI]
|
4.91899e-05
|
|
|
RPE65
|
[NCBI]
|
4.88173e-05
|
|
|
IP
|
[NCBI]
|
4.66462e-05
|
|
|
CORD3
|
[NCBI]
|
4.59541e-05
|
|
|
sturge-weber syndrome
|
[NCBI]
|
4.59541e-05
|
|
|
retinal arteries, tortuosity of
|
[NCBI]
|
4.48291e-05
|
|
|
MTND6
|
[NCBI]
|
4.45511e-05
|
|
|
EVR2
|
[NCBI]
|
4.3201e-05
|
|
|
short syndrome
|
[NCBI]
|
4.3201e-05
|
|
|
rheumatoid arthritis, systemic juvenile
|
[NCBI]
|
4.3201e-05
|
|
|
antiphospholipid syndrome
|
[NCBI]
|
4.3201e-05
|
|
|
ornithine aminotransferase deficiency
|
[NCBI]
|
4.28877e-05
|
|
|
MTND1
|
[NCBI]
|
3.89754e-05
|
|
|
RLBP1
|
[NCBI]
|
3.87561e-05
|
|
|
CZP1
|
[NCBI]
|
3.86972e-05
|
|
|
schwannomatosis
|
[NCBI]
|
3.86972e-05
|
|
|
CSNB2A
|
[NCBI]
|
3.86972e-05
|
|
|
NYS1
|
[NCBI]
|
3.86972e-05
|
|
|
keratitis-ichthyosis-deafness syndrome, autosomal dominant
|
[NCBI]
|
3.86972e-05
|
|
|
ARMD1
|
[NCBI]
|
3.84989e-05
|
|
|
RPGR
|
[NCBI]
|
3.7718e-05
|
|
|
coloboma, ocular
|
[NCBI]
|
3.68093e-05
|
|
|
ASMD
|
[NCBI]
|
3.68093e-05
|
|
|
HSS
|
[NCBI]
|
3.68093e-05
|
|
|
kniest dysplasia
|
[NCBI]
|
3.68093e-05
|
|
|
SFD
|
[NCBI]
|
3.51044e-05
|
|
|
sarcoidosis
|
[NCBI]
|
3.51044e-05
|
|
|
SNDI
|
[NCBI]
|
3.51044e-05
|
|
|
homocystinuria
|
[NCBI]
|
3.20414e-05
|
|
|
RGS9BP
|
[NCBI]
|
3.14563e-05
|
|
|
PPCD1
|
[NCBI]
|
3.08146e-05
|
|
|
danon disease
|
[NCBI]
|
3.08146e-05
|
|
|
CCT
|
[NCBI]
|
2.99563e-05
|
|
|
CABP4
|
[NCBI]
|
2.99563e-05
|
|
|
PWS
|
[NCBI]
|
2.98519e-05
|
|
|
GRK1
|
[NCBI]
|
2.87615e-05
|
|
|
DHRD
|
[NCBI]
|
2.84628e-05
|
|
|
FSCN2
|
[NCBI]
|
2.69188e-05
|
|
|
RCV1
|
[NCBI]
|
2.61763e-05
|
|
|
GUCA1A
|
[NCBI]
|
2.55171e-05
|
|
|
IMPDH1
|
[NCBI]
|
2.55171e-05
|
|
|
RGS9
|
[NCBI]
|
2.49243e-05
|
|
|
GLC3A
|
[NCBI]
|
2.45886e-05
|
|
|
HPS1
|
[NCBI]
|
2.43859e-05
|
|
|
APS1
|
[NCBI]
|
2.41858e-05
|
|
|
CRYGC
|
[NCBI]
|
2.38927e-05
|
|
|
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency
|
[NCBI]
|
2.37531e-05
|
|
|
CACNA1F
|
[NCBI]
|
2.30156e-05
|
|
|
CDLS1
|
[NCBI]
|
2.28795e-05
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
2.26875e-05
|
|
|
TULP1
|
[NCBI]
|
2.26218e-05
|
|
|
FDH
|
[NCBI]
|
2.14925e-05
|
|
|
SEDC
|
[NCBI]
|
2.14925e-05
|
|
|
gaucher disease, type iii
|
[NCBI]
|
2.14925e-05
|
|
|
ALMS
|
[NCBI]
|
2.08098e-05
|
|
|
VHL
|
[NCBI]
|
2.07724e-05
|
|
|
CYP1B1
|
[NCBI]
|
2.01707e-05
|
|
|
MFN2
|
[NCBI]
|
1.99259e-05
|
|
|
LRP5
|
[NCBI]
|
1.9691e-05
|
|
|
usher syndrome, type i
|
[NCBI]
|
1.95347e-05
|
|
|
OPA1
|
[NCBI]
|
1.9248e-05
|
|
|
RBP4
|
[NCBI]
|
1.84527e-05
|
|
|
STL1
|
[NCBI]
|
1.83659e-05
|
|
|
neuraminidase deficiency with beta-galactosidase deficiency
|
[NCBI]
|
1.82699e-05
|
|
|
SOX10
|
[NCBI]
|
1.79209e-05
|
|
|
NDP
|
[NCBI]
|
1.74343e-05
|
|
|
PRPH2
|
[NCBI]
|
1.74343e-05
|
|
|
EGR1
|
[NCBI]
|
1.67055e-05
|
|
|
APC
|
[NCBI]
|
1.63273e-05
|
|
|
OCA2
|
[NCBI]
|
1.58234e-05
|
|
|
CLN3
|
[NCBI]
|
1.53699e-05
|
|
|
GCPS
|
[NCBI]
|
1.53699e-05
|
|
|
CDG1A
|
[NCBI]
|
1.49322e-05
|
|
|
neuraminidase deficiency
|
[NCBI]
|
1.49322e-05
|
|
|
ATS
|
[NCBI]
|
1.49322e-05
|
|
|
FMF
|
[NCBI]
|
1.47218e-05
|
|
|
CTNS
|
[NCBI]
|
1.45096e-05
|
|
|
GLC1A
|
[NCBI]
|
1.45096e-05
|
|
|
TNF
|
[NCBI]
|
1.44197e-05
|
|
|
POAG
|
[NCBI]
|
1.37064e-05
|
|
|
MTTL1
|
[NCBI]
|
1.30255e-05
|
|
|
RTS
|
[NCBI]
|
1.25966e-05
|
|
|
COL2A1
|
[NCBI]
|
1.2176e-05
|
|
|
ALGS1
|
[NCBI]
|
1.19131e-05
|
|
|
PXE
|
[NCBI]
|
1.17576e-05
|
|
|
TS
|
[NCBI]
|
1.16144e-05
|
|
|
CSA
|
[NCBI]
|
1.12702e-05
|
|
|
HHT
|
[NCBI]
|
1.06644e-05
|
|
|
NF2
|
[NCBI]
|
1.06644e-05
|
|
|
SCA7
|
[NCBI]
|
1.00927e-05
|
|
|
KDR
|
[NCBI]
|
9.90198e-06
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
9.72268e-06
|
|
|
NPC1
|
[NCBI]
|
9.04131e-06
|
|
|
FGFR2
|
[NCBI]
|
8.9742e-06
|
|
|
BPES
|
[NCBI]
|
8.79599e-06
|
|
|
HOS
|
[NCBI]
|
8.32465e-06
|
|
|
ND
|
[NCBI]
|
7.04991e-06
|
|
|
RB1
|
[NCBI]
|
7.02091e-06
|
|
|
CP
|
[NCBI]
|
5.5201e-06
|
|
|
GTS
|
[NCBI]
|
4.74556e-06
|
|
|
NGFB
|
[NCBI]
|
3.54798e-06
|
|
|
PTH
|
[NCBI]
|
3.42663e-06
|
|
|
MFS
|
[NCBI]
|
3.03351e-06
|
|
|
CHAT
|
[NCBI]
|
2.76545e-06
|
|
|
FRDA
|
[NCBI]
|
1.94915e-06
|
|
|
TTR
|
[NCBI]
|
1.82588e-06
|
|
|
CMM
|
[NCBI]
|
1.71162e-06
|
|
|
MS
|
[NCBI]
|
1.54495e-06
|
|
|
BBS
|
[NCBI]
|
1.19998e-06
|
|
|
G6PD
|
[NCBI]
|
4.16994e-07
|
|
|
BDNF
|
[NCBI]
|
4.03529e-07
|
|
|
GFAP
|
[NCBI]
|
1.62832e-07
|
|
|
DRPLA
|
[NCBI]
|
1.48694e-07
|
|
|
PRL
|
[NCBI]
|
1.4853e-07
|
|
|
TSD
|
[NCBI]
|
1.11661e-07
|
|