|
OMIM |
Link |
Information gain |
01 |
|
corneal dystrophy, crystalline, of schnyder
|
[NCBI]
|
0.00272372
|
|
|
cutis laxa, corneal clouding, and mental retardation
|
[NCBI]
|
0.0013128
|
|
|
spondyloepiphyseal dysplasia tarda, toledo type
|
[NCBI]
|
0.0013128
|
|
|
FED
|
[NCBI]
|
0.00121967
|
|
|
LCAT
|
[NCBI]
|
0.00105704
|
|
|
acromegaloid changes, cutis verticis gyrata, and corneal leukoma
|
[NCBI]
|
0.000952205
|
|
|
CND
|
[NCBI]
|
0.000652698
|
|
|
persistent hyperplastic primary vitreous, autosomal recessive
|
[NCBI]
|
0.000599634
|
|
|
CNA1
|
[NCBI]
|
0.000599634
|
|
|
dermochondrocorneal dystrophy
|
[NCBI]
|
0.000560268
|
|
|
mucolipidosis iv
|
[NCBI]
|
0.000524531
|
|
|
RNANC
|
[NCBI]
|
0.000503004
|
|
|
CHED1
|
[NCBI]
|
0.000503004
|
|
|
CDB2
|
[NCBI]
|
0.000461483
|
|
|
MCOP1
|
[NCBI]
|
0.000444338
|
|
|
MCOPS1
|
[NCBI]
|
0.00042895
|
|
|
osteolysis, hereditary, of carpal bones with nephropathy
|
[NCBI]
|
0.000390496
|
|
|
microcephalic osteodysplastic primordial dwarfism, type i
|
[NCBI]
|
0.000360016
|
|
|
CSCD
|
[NCBI]
|
0.00030377
|
|
|
FRNS
|
[NCBI]
|
0.000273342
|
|
|
peters anomaly
|
[NCBI]
|
0.000272844
|
|
|
lecithin:cholesterol acyltransferase deficiency
|
[NCBI]
|
0.000268221
|
|
|
mucopolysaccharidoses, unclassified types
|
[NCBI]
|
0.000195673
|
|
|
ichthyosis, x-linked
|
[NCBI]
|
0.000165304
|
|
|
WARBM
|
[NCBI]
|
0.000153775
|
|
|
winchester syndrome
|
[NCBI]
|
0.000149435
|
|
|
CDB1
|
[NCBI]
|
0.000139114
|
|
|
CDGG1
|
[NCBI]
|
0.000129097
|
|
|
SLE
|
[NCBI]
|
0.000116966
|
|
|
brachymesomelia-renal syndrome
|
[NCBI]
|
0.000113208
|
|
|
kyrle disease
|
[NCBI]
|
0.000113208
|
|
|
peters anomaly with cataract
|
[NCBI]
|
0.000113208
|
|
|
sclerocornea
|
[NCBI]
|
0.000113208
|
|
|
congenital corneal opacities, cornea guttata, and corectopia
|
[NCBI]
|
0.000113208
|
|
|
MCOPS7
|
[NCBI]
|
0.000104764
|
|
|
mucopolysaccharidosis type vi
|
[NCBI]
|
0.000103781
|
|
|
TGD
|
[NCBI]
|
0.000102827
|
|
|
tyrosine transaminase deficiency
|
[NCBI]
|
9.96173e-05
|
|
|
DCN
|
[NCBI]
|
9.84825e-05
|
|
|
subaortic stenosis--short stature syndrome
|
[NCBI]
|
9.075e-05
|
|
|
mental retardation syndrome, mietens-weber type
|
[NCBI]
|
9.075e-05
|
|
|
coloboma, uveal, with cleft lip and palate and mental retardation
|
[NCBI]
|
8.22828e-05
|
|
|
corneal degeneration, band-shaped spheroid
|
[NCBI]
|
8.22828e-05
|
|
|
moved to 310600
|
[NCBI]
|
8.22828e-05
|
|
|
hurler syndrome
|
[NCBI]
|
8.22721e-05
|
|
|
OCP
|
[NCBI]
|
7.82004e-05
|
|
|
APOA1
|
[NCBI]
|
7.78607e-05
|
|
|
PAX6
|
[NCBI]
|
7.5323e-05
|
|
|
corneal fleck dystrophy
|
[NCBI]
|
7.27084e-05
|
|
|
CNA2
|
[NCBI]
|
6.94592e-05
|
|
|
GBA
|
[NCBI]
|
6.77995e-05
|
|
|
short syndrome
|
[NCBI]
|
6.4451e-05
|
|
|
gaucher disease, type iiic
|
[NCBI]
|
6.4451e-05
|
|
|
hypoalphalipoproteinemia, primary
|
[NCBI]
|
6.4451e-05
|
|
|
bietti crystalline corneoretinal dystrophy
|
[NCBI]
|
6.4451e-05
|
|
|
cataract-microcornea syndrome
|
[NCBI]
|
6.4451e-05
|
|
|
corneal dystrophy, epithelial basement membrane
|
[NCBI]
|
6.4451e-05
|
|
|
fabry disease
|
[NCBI]
|
6.37216e-05
|
|
|
PIP5K3
|
[NCBI]
|
6.19002e-05
|
|
|
ASMD
|
[NCBI]
|
6.06443e-05
|
|
|
HRD
|
[NCBI]
|
5.90355e-05
|
|
|
KCS
|
[NCBI]
|
5.90355e-05
|
|
|
SLC4A4
|
[NCBI]
|
5.85252e-05
|
|
|
corneal dystrophy, gelatinous drop-like
|
[NCBI]
|
5.75747e-05
|
|
|
wagr syndrome
|
[NCBI]
|
5.75747e-05
|
|
|
CDA
|
[NCBI]
|
5.50039e-05
|
|
|
MCDC1
|
[NCBI]
|
5.17945e-05
|
|
|
CIPA
|
[NCBI]
|
4.91306e-05
|
|
|
MAN2B1
|
[NCBI]
|
4.6692e-05
|
|
|
FOXC1
|
[NCBI]
|
4.25339e-05
|
|
|
gm1-gangliosidosis, type i
|
[NCBI]
|
4.1043e-05
|
|
|
TGFBI
|
[NCBI]
|
3.962e-05
|
|
|
mannosidosis, alpha b, lysosomal
|
[NCBI]
|
3.92211e-05
|
|
|
CSTB
|
[NCBI]
|
3.77166e-05
|
|
|
walker-warburg syndrome
|
[NCBI]
|
3.75951e-05
|
|
|
FDH
|
[NCBI]
|
3.6128e-05
|
|
|
AN2
|
[NCBI]
|
3.41672e-05
|
|
|
CSA
|
[NCBI]
|
3.35675e-05
|
|
|
myoclonic epilepsy of unverricht and lundborg
|
[NCBI]
|
3.32765e-05
|
|
|
HP
|
[NCBI]
|
1.47003e-05
|
|
|
VRNI
|
[NCBI]
|
5.97617e-06
|
|
|
TNFSF6
|
[NCBI]
|
5.83454e-06
|
|
|
EGF
|
[NCBI]
|
3.07512e-07
|
|