|
OMIM |
Link |
Information gain |
01 |
|
MYP2
|
[NCBI]
|
0.00903571
|
|
|
MYP1
|
[NCBI]
|
0.00215012
|
|
|
OPEM
|
[NCBI]
|
0.00166522
|
|
|
knobloch syndrome, type ii
|
[NCBI]
|
0.00166522
|
|
|
myopia 6
|
[NCBI]
|
0.00136577
|
|
|
MYP3
|
[NCBI]
|
0.00123085
|
|
|
ectopia lentis with ectopia of pupil
|
[NCBI]
|
0.00123085
|
|
|
MACOM
|
[NCBI]
|
0.00123085
|
|
|
STL1
|
[NCBI]
|
0.000841793
|
|
|
myopia 12
|
[NCBI]
|
0.000830911
|
|
|
CORDX2
|
[NCBI]
|
0.000830911
|
|
|
microcoria, congenital
|
[NCBI]
|
0.000830911
|
|
|
myopia 13
|
[NCBI]
|
0.000830911
|
|
|
myopia 5
|
[NCBI]
|
0.000613741
|
|
|
myopia 8
|
[NCBI]
|
0.000613741
|
|
|
myopia 10
|
[NCBI]
|
0.000613741
|
|
|
myopia 9
|
[NCBI]
|
0.000613741
|
|
|
myopia 14
|
[NCBI]
|
0.000613741
|
|
|
CACD
|
[NCBI]
|
0.000613741
|
|
|
myopia 7
|
[NCBI]
|
0.000613741
|
|
|
myopia 4
|
[NCBI]
|
0.000613741
|
|
|
vitreoretinal degeneration, snowflake type
|
[NCBI]
|
0.000532264
|
|
|
chorioretinal atrophy, progressive bifocal
|
[NCBI]
|
0.00047963
|
|
|
ophthalmoplegia, familial static
|
[NCBI]
|
0.00047963
|
|
|
KNO
|
[NCBI]
|
0.000438584
|
|
|
alport syndrome, autosomal dominant
|
[NCBI]
|
0.000418599
|
|
|
CTPP1
|
[NCBI]
|
0.000409827
|
|
|
AIED
|
[NCBI]
|
0.000368808
|
|
|
oculocerebral syndrome with hypopigmentation
|
[NCBI]
|
0.000362544
|
|
|
CSNB1A
|
[NCBI]
|
0.0003521
|
|
|
kenny-caffey syndrome, type 2
|
[NCBI]
|
0.000311958
|
|
|
WZS
|
[NCBI]
|
0.000310444
|
|
|
marshall syndrome
|
[NCBI]
|
0.000294722
|
|
|
CBBM
|
[NCBI]
|
0.000274795
|
|
|
lymphedema, microcephaly, chorioretinopathy syndrome
|
[NCBI]
|
0.000254649
|
|
|
donnai-barrow syndrome
|
[NCBI]
|
0.000252606
|
|
|
COL2A1
|
[NCBI]
|
0.000223035
|
|
|
deafness, cochlear, with myopia and intellectual impairment
|
[NCBI]
|
0.000219856
|
|
|
fundus dystrophy, pseudoinflammatory, recessive form
|
[NCBI]
|
0.000188919
|
|
|
MEB
|
[NCBI]
|
0.000160523
|
|
|
COH1
|
[NCBI]
|
0.000154367
|
|
|
SLE
|
[NCBI]
|
0.000153107
|
|
|
CSNB1B
|
[NCBI]
|
0.000152059
|
|
|
cataract-microcornea syndrome
|
[NCBI]
|
0.000147039
|
|
|
SFD
|
[NCBI]
|
0.000124611
|
|
|
WGN1
|
[NCBI]
|
0.000124611
|
|
|
papillorenal syndrome
|
[NCBI]
|
0.000118362
|
|
|
microspherophakia with hernia
|
[NCBI]
|
0.000109848
|
|
|
spondyloepiphyseal dysplasia, myopia, and sensorineural deafness
|
[NCBI]
|
0.000109848
|
|
|
dandy-walker malformation with mental retardation, macrocephaly, myopia, and brachytelephalangy
|
[NCBI]
|
0.000109848
|
|
|
gastrocutaneous syndrome
|
[NCBI]
|
0.000109848
|
|
|
blepharoptosis, myopia, and ectopia lentis
|
[NCBI]
|
0.000109848
|
|
|
epiphyseal dysplasia of femoral head, myopia, and deafness
|
[NCBI]
|
0.000109848
|
|
|
lattice degeneration of retina leading to retinal detachment
|
[NCBI]
|
0.000109848
|
|
|
polydactyly, postaxial, with progressive myopia
|
[NCBI]
|
0.000109848
|
|
|
sinus node disease and myopia
|
[NCBI]
|
0.000109848
|
|
|
myopia, infantile severe
|
[NCBI]
|
0.000109848
|
|
|
COL18A1
|
[NCBI]
|
0.000108271
|
|
|
COL11A1
|
[NCBI]
|
0.000104948
|
|
|
LRP2
|
[NCBI]
|
0.000102103
|
|
|
SEDC
|
[NCBI]
|
9.43677e-05
|
|
|
GLC1A
|
[NCBI]
|
9.34974e-05
|
|
|
spinocerebellar degeneration with macular corneal dystrophy, congenital cataracts, and myopia
|
[NCBI]
|
8.73936e-05
|
|
|
growth retardation, deafness, femoral epiphyseal dysplasia, and lacrimal duct obstruction
|
[NCBI]
|
8.73936e-05
|
|
|
epiphyseal dysplasia, multiple, with myopia and conductive deafness
|
[NCBI]
|
8.73936e-05
|
|
|
camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye
|
[NCBI]
|
8.73936e-05
|
|
|
limb deficiencies, distal, with micrognathia
|
[NCBI]
|
8.73936e-05
|
|
|
CHM
|
[NCBI]
|
8.21358e-05
|
|
|
oculocerebral hypopigmentation syndrome of preus
|
[NCBI]
|
7.89299e-05
|
|
|
cataract, autosomal dominant, multiple types 1
|
[NCBI]
|
7.34399e-05
|
|
|
CORD6
|
[NCBI]
|
7.34399e-05
|
|
|
VIPR2
|
[NCBI]
|
6.70987e-05
|
|
|
chorioretinal dysplasia-microcephaly-mental retardation syndrome
|
[NCBI]
|
6.61167e-05
|
|
|
SCRA
|
[NCBI]
|
6.61167e-05
|
|
|
MYOC
|
[NCBI]
|
6.56162e-05
|
|
|
RCD3A
|
[NCBI]
|
6.34207e-05
|
|
|
STL2
|
[NCBI]
|
6.34207e-05
|
|
|
SMS
|
[NCBI]
|
6.09176e-05
|
|
|
COH1
|
[NCBI]
|
5.85252e-05
|
|
|
weill-marchesani syndrome, autosomal recessive
|
[NCBI]
|
5.73156e-05
|
|
|
NYX
|
[NCBI]
|
5.60164e-05
|
|
|
IRID1
|
[NCBI]
|
5.57103e-05
|
|
|
WSS
|
[NCBI]
|
5.4253e-05
|
|
|
COL9A1
|
[NCBI]
|
5.40176e-05
|
|
|
TGIF
|
[NCBI]
|
5.2356e-05
|
|
|
CORDX1
|
[NCBI]
|
5.16891e-05
|
|
|
LPIN2
|
[NCBI]
|
5.09339e-05
|
|
|
kniest dysplasia
|
[NCBI]
|
5.05486e-05
|
|
|
BFSP2
|
[NCBI]
|
4.96909e-05
|
|
|
POMGNT1
|
[NCBI]
|
4.96909e-05
|
|
|
CORD2
|
[NCBI]
|
4.75544e-05
|
|
|
DHRD
|
[NCBI]
|
4.75544e-05
|
|
|
immunoosseous dysplasia, schimke type
|
[NCBI]
|
4.66718e-05
|
|
|
CACNA1F
|
[NCBI]
|
4.58656e-05
|
|
|
danon disease
|
[NCBI]
|
4.58366e-05
|
|
|
KTCN1
|
[NCBI]
|
4.50442e-05
|
|
|
VIP
|
[NCBI]
|
4.44627e-05
|
|
|
ehlers-danlos syndrome, type vi
|
[NCBI]
|
4.22278e-05
|
|
|
SLC6A3
|
[NCBI]
|
4.21038e-05
|
|
|
GJA8
|
[NCBI]
|
4.19842e-05
|
|
|
GUCY2D
|
[NCBI]
|
4.19842e-05
|
|
|
OPA1
|
[NCBI]
|
4.04986e-05
|
|
|
biotinidase deficiency
|
[NCBI]
|
4.04103e-05
|
|
|
TIMP3
|
[NCBI]
|
3.962e-05
|
|
|
EGR1
|
[NCBI]
|
3.84342e-05
|
|
|
NRCLP1
|
[NCBI]
|
3.73212e-05
|
|
|
OPTN
|
[NCBI]
|
3.58345e-05
|
|
|
POAG
|
[NCBI]
|
3.55662e-05
|
|
|
ehlers-danlos syndrome, type i
|
[NCBI]
|
3.55662e-05
|
|
|
contractural arachnodactyly, congenital
|
[NCBI]
|
3.528e-05
|
|
|
TGFB1
|
[NCBI]
|
3.15277e-05
|
|
|
PAX6
|
[NCBI]
|
3.06539e-05
|
|
|
RP
|
[NCBI]
|
2.99567e-05
|
|
|
TNC
|
[NCBI]
|
2.60931e-05
|
|
|
RHO
|
[NCBI]
|
2.56882e-05
|
|
|
homocystinuria
|
[NCBI]
|
2.47463e-05
|
|
|
SLS
|
[NCBI]
|
2.39743e-05
|
|
|
VRNI
|
[NCBI]
|
1.93588e-05
|
|
|
CDLS1
|
[NCBI]
|
1.86457e-05
|
|
|
FGF7
|
[NCBI]
|
1.78047e-05
|
|
|
EGF
|
[NCBI]
|
8.86234e-06
|
|
|
MFS
|
[NCBI]
|
8.66093e-06
|
|
|
CHAT
|
[NCBI]
|
8.65674e-06
|
|
|
GTS
|
[NCBI]
|
3.69872e-06
|
|
|
NGFB
|
[NCBI]
|
6.60907e-07
|
|
|
PWS
|
[NCBI]
|
4.58286e-07
|
|