|
OMIM |
Link |
Information gain |
01 |
|
behr syndrome
|
[NCBI]
|
0.00152161
|
|
|
cavitary optic disc anomalies
|
[NCBI]
|
0.00138638
|
|
|
strabismus, susceptibility to
|
[NCBI]
|
0.00107507
|
|
|
acroosteolysis with osteoporosis and changes in skull and mandible
|
[NCBI]
|
0.000924208
|
|
|
unique green phenomenon
|
[NCBI]
|
0.000907885
|
|
|
GLC1F
|
[NCBI]
|
0.000907885
|
|
|
temporal arteritis
|
[NCBI]
|
0.000903688
|
|
|
leber optic atrophy, susceptibility to
|
[NCBI]
|
0.000901326
|
|
|
blepharophimosis with ptosis, syndactyly, and short stature
|
[NCBI]
|
0.000690406
|
|
|
retinal cone dystrophy 2
|
[NCBI]
|
0.000690406
|
|
|
mental retardation with optic atrophy, deafness, and seizures
|
[NCBI]
|
0.000608619
|
|
|
CORD5
|
[NCBI]
|
0.000555675
|
|
|
VRCP
|
[NCBI]
|
0.000555675
|
|
|
ectopia lentis with ectopia of pupil
|
[NCBI]
|
0.000555675
|
|
|
RP
|
[NCBI]
|
0.000527786
|
|
|
ichthyosis follicularis, atrichia, and photophobia syndrome
|
[NCBI]
|
0.000459406
|
|
|
CMM
|
[NCBI]
|
0.000450915
|
|
|
ocular motor apraxia
|
[NCBI]
|
0.000437349
|
|
|
CDB2
|
[NCBI]
|
0.000418126
|
|
|
leber optic atrophy
|
[NCBI]
|
0.000377128
|
|
|
VRNI
|
[NCBI]
|
0.000362511
|
|
|
PPR
|
[NCBI]
|
0.000175114
|
|
|
CF
|
[NCBI]
|
0.000166694
|
|
|
CMTX5
|
[NCBI]
|
0.000155007
|
|
|
kabuki syndrome
|
[NCBI]
|
0.000150501
|
|
|
STGD1
|
[NCBI]
|
0.000144479
|
|
|
foveal hypoplasia and presenile cataract syndrome
|
[NCBI]
|
0.000132166
|
|
|
POAG
|
[NCBI]
|
0.000131004
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
0.000128081
|
|
|
PRL
|
[NCBI]
|
0.000117911
|
|
|
neuraminidase deficiency
|
[NCBI]
|
0.000114761
|
|
|
CJD
|
[NCBI]
|
0.000114621
|
|
|
CBP
|
[NCBI]
|
0.000102103
|
|
|
PERRS
|
[NCBI]
|
9.98991e-05
|
|
|
fourth cranial nerve palsy, familial congenital
|
[NCBI]
|
9.98991e-05
|
|
|
OOCH
|
[NCBI]
|
9.98991e-05
|
|
|
cholestasis with gallstone, ataxia, and visual disturbance
|
[NCBI]
|
9.98991e-05
|
|
|
reese retinal dysplasia
|
[NCBI]
|
9.98991e-05
|
|
|
CLN1
|
[NCBI]
|
8.6399e-05
|
|
|
RGS9BP
|
[NCBI]
|
8.08766e-05
|
|
|
RGS9
|
[NCBI]
|
8.08766e-05
|
|
|
gaucher disease, type iii
|
[NCBI]
|
8.06549e-05
|
|
|
SLE
|
[NCBI]
|
7.9879e-05
|
|
|
OPA1
|
[NCBI]
|
7.96253e-05
|
|
|
retinopathy, pericentral pigmentary, autosomal recessive
|
[NCBI]
|
7.74605e-05
|
|
|
COH1
|
[NCBI]
|
7.01502e-05
|
|
|
OCA1A
|
[NCBI]
|
7.01502e-05
|
|
|
optic atrophy, hearing loss, and peripheral neuropathy, autosomal recessive
|
[NCBI]
|
6.90124e-05
|
|
|
ARTS
|
[NCBI]
|
6.90124e-05
|
|
|
arhinia, choanal atresia, and microphthalmia
|
[NCBI]
|
6.90124e-05
|
|
|
coloboma of optic nerve
|
[NCBI]
|
6.90124e-05
|
|
|
AN2
|
[NCBI]
|
6.47681e-05
|
|
|
PRD
|
[NCBI]
|
6.35382e-05
|
|
|
pseudopapilledema
|
[NCBI]
|
5.94763e-05
|
|
|
DLAT
|
[NCBI]
|
5.85252e-05
|
|
|
dystonia, familial, with visual failure and striatal lucencies
|
[NCBI]
|
5.62463e-05
|
|
|
nonarteritic anterior ischemic optic neuropathy, susceptibility to
|
[NCBI]
|
5.62463e-05
|
|
|
oguchi disease
|
[NCBI]
|
5.62463e-05
|
|
|
IFNA2
|
[NCBI]
|
5.40176e-05
|
|
|
NTF3
|
[NCBI]
|
5.40176e-05
|
|
|
PPCRA
|
[NCBI]
|
5.3566e-05
|
|
|
tritanopia
|
[NCBI]
|
5.2356e-05
|
|
|
rheumatoid arthritis, systemic juvenile
|
[NCBI]
|
5.12764e-05
|
|
|
TUB
|
[NCBI]
|
5.09339e-05
|
|
|
EPAS1
|
[NCBI]
|
5.09339e-05
|
|
|
PRPS1
|
[NCBI]
|
5.09339e-05
|
|
|
NYS1
|
[NCBI]
|
4.92788e-05
|
|
|
ELOVL4
|
[NCBI]
|
4.8587e-05
|
|
|
PXE
|
[NCBI]
|
4.82751e-05
|
|
|
TIMM8A
|
[NCBI]
|
4.75941e-05
|
|
|
pierson syndrome
|
[NCBI]
|
4.7508e-05
|
|
|
CLCN7
|
[NCBI]
|
4.6692e-05
|
|
|
amyloidosis vii
|
[NCBI]
|
4.59184e-05
|
|
|
macular dystrophy, vitelliform, adult-onset
|
[NCBI]
|
4.59184e-05
|
|
|
CACNA1F
|
[NCBI]
|
4.58656e-05
|
|
|
CRX
|
[NCBI]
|
4.5103e-05
|
|
|
schwannomatosis
|
[NCBI]
|
4.44767e-05
|
|
|
antiphospholipid syndrome
|
[NCBI]
|
4.44767e-05
|
|
|
CDA
|
[NCBI]
|
4.19443e-05
|
|
|
NF1
|
[NCBI]
|
4.18096e-05
|
|
|
MTND5
|
[NCBI]
|
4.09693e-05
|
|
|
SFD
|
[NCBI]
|
4.08195e-05
|
|
|
MTS
|
[NCBI]
|
3.97721e-05
|
|
|
FRDA
|
[NCBI]
|
3.97222e-05
|
|
|
XPC
|
[NCBI]
|
3.84342e-05
|
|
|
krabbe disease
|
[NCBI]
|
3.82909e-05
|
|
|
CORD2
|
[NCBI]
|
3.78724e-05
|
|
|
DHRD
|
[NCBI]
|
3.78724e-05
|
|
|
CPE
|
[NCBI]
|
3.70481e-05
|
|
|
ESCS
|
[NCBI]
|
3.61859e-05
|
|
|
PDHA1
|
[NCBI]
|
3.6124e-05
|
|
|
OPTN
|
[NCBI]
|
3.58345e-05
|
|
|
DLB
|
[NCBI]
|
3.54092e-05
|
|
|
PRPH2
|
[NCBI]
|
3.528e-05
|
|
|
ABCA4
|
[NCBI]
|
3.40181e-05
|
|
|
deafness, conductive, with stapes fixation
|
[NCBI]
|
3.39681e-05
|
|
|
CSNB1A
|
[NCBI]
|
3.32971e-05
|
|
|
USH2A
|
[NCBI]
|
3.32971e-05
|
|
|
refsum disease
|
[NCBI]
|
3.26556e-05
|
|
|
PSNP1
|
[NCBI]
|
3.20411e-05
|
|
|
ALMS
|
[NCBI]
|
3.14516e-05
|
|
|
MTND4
|
[NCBI]
|
3.13465e-05
|
|
|
RPGR
|
[NCBI]
|
3.11686e-05
|
|
|
PAX6
|
[NCBI]
|
3.06539e-05
|
|
|
alzheimer disease 3
|
[NCBI]
|
3.03402e-05
|
|
|
camurati-engelmann disease
|
[NCBI]
|
2.98152e-05
|
|
|
ABCD1
|
[NCBI]
|
2.97006e-05
|
|
|
MTHFR
|
[NCBI]
|
2.94028e-05
|
|
|
RP3
|
[NCBI]
|
2.93089e-05
|
|
|
DYX1
|
[NCBI]
|
2.93089e-05
|
|
|
mucolipidosis iv
|
[NCBI]
|
2.882e-05
|
|
|
factor v deficiency
|
[NCBI]
|
2.8039e-05
|
|
|
OCRL
|
[NCBI]
|
2.78902e-05
|
|
|
mucopolysaccharidosis type vi
|
[NCBI]
|
2.78902e-05
|
|
|
TGD
|
[NCBI]
|
2.74475e-05
|
|
|
usher syndrome, type i
|
[NCBI]
|
2.70184e-05
|
|
|
ODDD
|
[NCBI]
|
2.70184e-05
|
|
|
CADASIL
|
[NCBI]
|
2.61981e-05
|
|
|
MEB
|
[NCBI]
|
2.61981e-05
|
|
|
RHO
|
[NCBI]
|
2.56882e-05
|
|
|
walker-warburg syndrome
|
[NCBI]
|
2.50527e-05
|
|
|
ALD
|
[NCBI]
|
2.47895e-05
|
|
|
GCPS
|
[NCBI]
|
2.36623e-05
|
|
|
WFS1
|
[NCBI]
|
2.33361e-05
|
|
|
melanoma, uveal
|
[NCBI]
|
2.2707e-05
|
|
|
CDG1A
|
[NCBI]
|
2.24034e-05
|
|
|
PSEN1
|
[NCBI]
|
2.19787e-05
|
|
|
CLN3
|
[NCBI]
|
2.15328e-05
|
|
|
CSA
|
[NCBI]
|
2.12551e-05
|
|
|
CHM
|
[NCBI]
|
2.09834e-05
|
|
|
BPES
|
[NCBI]
|
2.04566e-05
|
|
|
SCA7
|
[NCBI]
|
2.02013e-05
|
|
|
NF2
|
[NCBI]
|
1.85467e-05
|
|
|
TS
|
[NCBI]
|
1.76019e-05
|
|
|
OCP
|
[NCBI]
|
1.63322e-05
|
|
|
APOE
|
[NCBI]
|
1.07798e-05
|
|
|
CDLS1
|
[NCBI]
|
1.05181e-05
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
1.02393e-05
|
|
|
BBS
|
[NCBI]
|
9.43112e-06
|
|
|
SMAX1
|
[NCBI]
|
7.90505e-06
|
|
|
VIP
|
[NCBI]
|
5.52252e-06
|
|
|
PD
|
[NCBI]
|
3.41118e-06
|
|
|
MFS
|
[NCBI]
|
2.65594e-06
|
|
|
NPY
|
[NCBI]
|
2.3605e-06
|
|
|
AD
|
[NCBI]
|
1.91842e-06
|
|
|
PWS
|
[NCBI]
|
1.2357e-06
|
|
|
amyloidosis vi
|
[NCBI]
|
1.16997e-06
|
|
|
FMF
|
[NCBI]
|
7.27525e-07
|
|
|
NGFB
|
[NCBI]
|
6.60907e-07
|
|
|
EGF
|
[NCBI]
|
3.07512e-07
|
|
|
VEGF
|
[NCBI]
|
1.79554e-07
|
|
|
GTS
|
[NCBI]
|
1.66276e-07
|
|