|
OMIM |
Link |
Information gain |
01 |
|
cavitary optic disc anomalies
|
[NCBI]
|
0.00209383
|
|
|
short rib-polydactyly syndrome, type ii
|
[NCBI]
|
0.000650784
|
|
|
PPR
|
[NCBI]
|
0.000486439
|
|
|
leber optic atrophy
|
[NCBI]
|
0.000316592
|
|
|
papillorenal syndrome
|
[NCBI]
|
0.000239403
|
|
|
CMTX5
|
[NCBI]
|
0.000201868
|
|
|
POAG
|
[NCBI]
|
0.000200892
|
|
|
dystonia, familial, with visual failure and striatal lucencies
|
[NCBI]
|
0.00018492
|
|
|
GFAP
|
[NCBI]
|
0.000177467
|
|
|
temporal arteritis
|
[NCBI]
|
0.00017521
|
|
|
XFS
|
[NCBI]
|
0.000147098
|
|
|
MBP
|
[NCBI]
|
0.000132228
|
|
|
NF1
|
[NCBI]
|
9.00849e-05
|
|
|
nonarteritic anterior ischemic optic neuropathy, susceptibility to
|
[NCBI]
|
7.94318e-05
|
|
|
RCDP2
|
[NCBI]
|
7.94318e-05
|
|
|
MYOC
|
[NCBI]
|
7.58244e-05
|
|
|
hyperpipecolatemia
|
[NCBI]
|
7.44097e-05
|
|
|
NDUFA1
|
[NCBI]
|
7.2176e-05
|
|
|
cherubism
|
[NCBI]
|
7.05892e-05
|
|
|
MTS
|
[NCBI]
|
6.26967e-05
|
|
|
infantile spasm syndrome, x-linked
|
[NCBI]
|
6.16909e-05
|
|
|
septooptic dysplasia
|
[NCBI]
|
6.07448e-05
|
|
|
PRPS1
|
[NCBI]
|
5.60041e-05
|
|
|
GNPAT
|
[NCBI]
|
5.476e-05
|
|
|
KAL2
|
[NCBI]
|
5.40892e-05
|
|
|
mitochondrial complex i deficiency
|
[NCBI]
|
5.34967e-05
|
|
|
cerebrotendinous xanthomatosis
|
[NCBI]
|
5.18422e-05
|
|
|
SOD2
|
[NCBI]
|
4.89357e-05
|
|
|
GLC1A
|
[NCBI]
|
4.85487e-05
|
|
|
PAX2
|
[NCBI]
|
4.51022e-05
|
|
|
EDN1
|
[NCBI]
|
4.51022e-05
|
|
|
EDNRB
|
[NCBI]
|
4.24212e-05
|
|
|
CMT1B
|
[NCBI]
|
4.20561e-05
|
|
|
OPTN
|
[NCBI]
|
4.08732e-05
|
|
|
NS1
|
[NCBI]
|
3.35402e-05
|
|
|
VHL
|
[NCBI]
|
2.93137e-05
|
|
|
RB1
|
[NCBI]
|
2.24117e-05
|
|
|
AS
|
[NCBI]
|
1.56645e-05
|
|
|
ALD
|
[NCBI]
|
1.22924e-05
|
|
|
MUC1
|
[NCBI]
|
1.15218e-05
|
|
|
BDNF
|
[NCBI]
|
7.99943e-06
|
|
|
FMF
|
[NCBI]
|
7.60621e-06
|
|
|
EPO
|
[NCBI]
|
3.14225e-06
|
|
|
MPO
|
[NCBI]
|
3.13959e-06
|
|
|
AD
|
[NCBI]
|
3.10809e-07
|
|
|
SLE
|
[NCBI]
|
2.94733e-07
|
|