|
OMIM |
Link |
Information gain |
01 |
|
corneal dystrophy, crystalline, of schnyder
|
[NCBI]
|
0.00987787
|
|
|
CDB2
|
[NCBI]
|
0.0080335
|
|
|
CHED1
|
[NCBI]
|
0.00485916
|
|
|
dermochondrocorneal dystrophy
|
[NCBI]
|
0.00210568
|
|
|
FECD2
|
[NCBI]
|
0.00198143
|
|
|
PPCD1
|
[NCBI]
|
0.00170196
|
|
|
TGFBI
|
[NCBI]
|
0.00161897
|
|
|
CDGG1
|
[NCBI]
|
0.00149466
|
|
|
MCDC1
|
[NCBI]
|
0.00145551
|
|
|
CDA
|
[NCBI]
|
0.00145081
|
|
|
CDL1
|
[NCBI]
|
0.00134647
|
|
|
CDB1
|
[NCBI]
|
0.00124224
|
|
|
corneal erosions, recurring hereditary
|
[NCBI]
|
0.000873351
|
|
|
CHED2
|
[NCBI]
|
0.000826423
|
|
|
corneal dystrophy, gelatinous drop-like
|
[NCBI]
|
0.000820901
|
|
|
amyloidosis v
|
[NCBI]
|
0.000728197
|
|
|
corneal dystrophy, juvenile epithelial, of meesmann
|
[NCBI]
|
0.000722745
|
|
|
corneal dystrophy, epithelial basement membrane
|
[NCBI]
|
0.000673911
|
|
|
cone-rod dystrophy and amelogenesis imperfecta
|
[NCBI]
|
0.000574326
|
|
|
bietti crystalline corneoretinal dystrophy
|
[NCBI]
|
0.000546304
|
|
|
CHST6
|
[NCBI]
|
0.000528996
|
|
|
CNA1
|
[NCBI]
|
0.000521502
|
|
|
corneal fleck dystrophy
|
[NCBI]
|
0.000515714
|
|
|
RCD1
|
[NCBI]
|
0.000425595
|
|
|
CSCD
|
[NCBI]
|
0.00041236
|
|
|
corneal dystrophy and perceptive deafness
|
[NCBI]
|
0.000371828
|
|
|
KRT12
|
[NCBI]
|
0.000350296
|
|
|
MCDR1
|
[NCBI]
|
0.00026055
|
|
|
TACSTD2
|
[NCBI]
|
0.000253954
|
|
|
PIP5K3
|
[NCBI]
|
0.000225892
|
|
|
PPCD3
|
[NCBI]
|
0.00020597
|
|
|
CDL3A
|
[NCBI]
|
0.00020597
|
|
|
SLC4A11
|
[NCBI]
|
0.000203537
|
|
|
CDH3
|
[NCBI]
|
0.000184565
|
|
|
GSN
|
[NCBI]
|
0.000180445
|
|
|
FECD1
|
[NCBI]
|
0.000175043
|
|
|
corneal degeneration, band-shaped spheroid
|
[NCBI]
|
0.000175043
|
|
|
HJMD
|
[NCBI]
|
0.00016108
|
|
|
cytochrome p450, family 4, subfamily v, polypeptide 2
|
[NCBI]
|
0.000150461
|
|
|
CNA2
|
[NCBI]
|
0.000144172
|
|
|
COL8A2
|
[NCBI]
|
0.000131484
|
|
|
KRT3
|
[NCBI]
|
0.00012291
|
|
|
TCF8
|
[NCBI]
|
0.00012291
|
|
|
DHRD
|
[NCBI]
|
0.000104633
|
|
|
endothelial dystrophy, congenital hereditary, with nail hypoplasia
|
[NCBI]
|
0.000102933
|
|
|
spondyloepiphyseal dysplasia with punctate corneal dystrophy
|
[NCBI]
|
0.000102933
|
|
|
spinocerebellar degeneration and corneal dystrophy
|
[NCBI]
|
0.000102933
|
|
|
KFSD
|
[NCBI]
|
0.000102806
|
|
|
STGD1
|
[NCBI]
|
8.8752e-05
|
|
|
DCN
|
[NCBI]
|
8.6992e-05
|
|
|
spinocerebellar degeneration with macular corneal dystrophy, congenital cataracts, and myopia
|
[NCBI]
|
8.04882e-05
|
|
|
PPCD2
|
[NCBI]
|
8.04882e-05
|
|
|
CHST5
|
[NCBI]
|
7.51642e-05
|
|
|
ARID1A
|
[NCBI]
|
7.51642e-05
|
|
|
COD3
|
[NCBI]
|
7.20343e-05
|
|
|
fundus dystrophy, pseudoinflammatory, recessive form
|
[NCBI]
|
7.20343e-05
|
|
|
ABCA4
|
[NCBI]
|
7.0734e-05
|
|
|
RP19
|
[NCBI]
|
6.65542e-05
|
|
|
eem syndrome
|
[NCBI]
|
6.65542e-05
|
|
|
jejunal atresia with microcephaly and ocular anomalies
|
[NCBI]
|
6.24865e-05
|
|
|
CLK2
|
[NCBI]
|
6.13886e-05
|
|
|
PRKAA2
|
[NCBI]
|
5.61923e-05
|
|
|
ALDH3A1
|
[NCBI]
|
5.61923e-05
|
|
|
EFEMP2
|
[NCBI]
|
5.28196e-05
|
|
|
ASMD
|
[NCBI]
|
5.0489e-05
|
|
|
EFEMP1
|
[NCBI]
|
5.0313e-05
|
|
|
macular dystrophy, vitelliform, adult-onset
|
[NCBI]
|
4.88935e-05
|
|
|
GUCA1A
|
[NCBI]
|
4.52373e-05
|
|
|
NBIA1
|
[NCBI]
|
3.68731e-05
|
|
|
tyrosine transaminase deficiency
|
[NCBI]
|
3.68599e-05
|
|
|
GUCY2D
|
[NCBI]
|
3.63125e-05
|
|
|
COL4A3
|
[NCBI]
|
3.20675e-05
|
|
|
CLU
|
[NCBI]
|
2.70869e-05
|
|
|
VMD
|
[NCBI]
|
2.64388e-05
|
|
|
ichthyosis, x-linked
|
[NCBI]
|
2.16641e-05
|
|
|
APRT
|
[NCBI]
|
1.71189e-05
|
|
|
FGF7
|
[NCBI]
|
1.25969e-05
|
|
|
HP
|
[NCBI]
|
9.69643e-06
|
|
|
TTR
|
[NCBI]
|
4.94827e-06
|
|
|
RP
|
[NCBI]
|
3.70351e-06
|
|
|
APOE
|
[NCBI]
|
3.6903e-06
|
|
|
HGF
|
[NCBI]
|
2.33742e-07
|
|
|
EGF
|
[NCBI]
|
1.33427e-07
|
|