|
OMIM |
Link |
Information gain |
01 |
|
ND
|
[NCBI]
|
0.00435073
|
|
|
LCA1
|
[NCBI]
|
0.00216552
|
|
|
persistent hyperplastic primary vitreous, autosomal dominant
|
[NCBI]
|
0.00189724
|
|
|
NDP
|
[NCBI]
|
0.00150973
|
|
|
persistent hyperplastic primary vitreous, autosomal recessive
|
[NCBI]
|
0.00146205
|
|
|
arima syndrome
|
[NCBI]
|
0.0011921
|
|
|
oculocerebral syndrome with hypopigmentation
|
[NCBI]
|
0.0011921
|
|
|
MCOPS10
|
[NCBI]
|
0.000945056
|
|
|
SLSN3
|
[NCBI]
|
0.000945056
|
|
|
RP
|
[NCBI]
|
0.000837497
|
|
|
temporal arteritis
|
[NCBI]
|
0.000800602
|
|
|
HHG
|
[NCBI]
|
0.000727474
|
|
|
SCAR3
|
[NCBI]
|
0.000645584
|
|
|
iris pigment epithelium anomalies
|
[NCBI]
|
0.000645584
|
|
|
CND
|
[NCBI]
|
0.000645584
|
|
|
cavitary optic disc anomalies
|
[NCBI]
|
0.000592537
|
|
|
cataract, congenital or juvenile
|
[NCBI]
|
0.000521908
|
|
|
RNANC
|
[NCBI]
|
0.000495958
|
|
|
ichthyosis follicularis, atrichia, and photophobia syndrome
|
[NCBI]
|
0.000495958
|
|
|
MCOP1
|
[NCBI]
|
0.000437344
|
|
|
ehlers-danlos syndrome, type vib
|
[NCBI]
|
0.000421973
|
|
|
ALMS
|
[NCBI]
|
0.00042143
|
|
|
leber optic atrophy, susceptibility to
|
[NCBI]
|
0.000372708
|
|
|
lymphedema, microcephaly, chorioretinopathy syndrome
|
[NCBI]
|
0.000362597
|
|
|
LCA2
|
[NCBI]
|
0.000321229
|
|
|
OPPG
|
[NCBI]
|
0.000312558
|
|
|
GUCY2D
|
[NCBI]
|
0.000311392
|
|
|
SLSN1
|
[NCBI]
|
0.00028455
|
|
|
JBTS1
|
[NCBI]
|
0.00028242
|
|
|
RPE65
|
[NCBI]
|
0.000251719
|
|
|
SLE
|
[NCBI]
|
0.00024433
|
|
|
leber optic atrophy
|
[NCBI]
|
0.000239966
|
|
|
MTS
|
[NCBI]
|
0.000162593
|
|
|
LCA4
|
[NCBI]
|
0.000160481
|
|
|
CRB1
|
[NCBI]
|
0.000153463
|
|
|
PRD
|
[NCBI]
|
0.000146535
|
|
|
klippel-trenaunay-weber syndrome
|
[NCBI]
|
0.000138113
|
|
|
glaucoma, normal tension, susceptibility to
|
[NCBI]
|
0.000123724
|
|
|
RDH12
|
[NCBI]
|
0.000123692
|
|
|
usher syndrome, type i
|
[NCBI]
|
0.000121246
|
|
|
STL1
|
[NCBI]
|
0.000117321
|
|
|
EVR2
|
[NCBI]
|
0.000114419
|
|
|
NPHP4
|
[NCBI]
|
0.000104732
|
|
|
USH3
|
[NCBI]
|
0.000101403
|
|
|
SCA7
|
[NCBI]
|
9.90398e-05
|
|
|
cortical blindness, retardation, and postaxial polydactyly
|
[NCBI]
|
9.56626e-05
|
|
|
aicar transformylase/imp cyclohydrolase, deficiency of
|
[NCBI]
|
9.56626e-05
|
|
|
RP35
|
[NCBI]
|
9.56626e-05
|
|
|
CORD10
|
[NCBI]
|
9.56626e-05
|
|
|
pseudoglaucoma
|
[NCBI]
|
9.56626e-05
|
|
|
rodrigues blindness
|
[NCBI]
|
9.56626e-05
|
|
|
amaurosis congenita, cone-rod type, with congenital hypertrichosis
|
[NCBI]
|
9.56626e-05
|
|
|
RPGRIP1
|
[NCBI]
|
9.29831e-05
|
|
|
septooptic dysplasia
|
[NCBI]
|
9.0312e-05
|
|
|
CRX
|
[NCBI]
|
8.56809e-05
|
|
|
PRL
|
[NCBI]
|
8.00068e-05
|
|
|
ehlers-danlos syndrome, type vi
|
[NCBI]
|
7.94316e-05
|
|
|
NPHP1
|
[NCBI]
|
7.3514e-05
|
|
|
amish infantile epilepsy syndrome
|
[NCBI]
|
7.32343e-05
|
|
|
NFRCD
|
[NCBI]
|
7.32343e-05
|
|
|
MSS
|
[NCBI]
|
7.14392e-05
|
|
|
ATIC
|
[NCBI]
|
7.12884e-05
|
|
|
SEDC
|
[NCBI]
|
6.68106e-05
|
|
|
MYO7A
|
[NCBI]
|
6.67082e-05
|
|
|
GLC1A
|
[NCBI]
|
6.59662e-05
|
|
|
retinohepatoendocrinologic syndrome
|
[NCBI]
|
6.47964e-05
|
|
|
LCA10
|
[NCBI]
|
6.47964e-05
|
|
|
ARTS
|
[NCBI]
|
6.47964e-05
|
|
|
oculocerebral hypopigmentation syndrome of preus
|
[NCBI]
|
6.47964e-05
|
|
|
osteopetrosis and infantile neuroaxonal dystrophy
|
[NCBI]
|
6.47964e-05
|
|
|
coloboma of optic nerve
|
[NCBI]
|
6.47964e-05
|
|
|
yemenite deaf-blind hypopigmentation syndrome
|
[NCBI]
|
6.47964e-05
|
|
|
MAOA
|
[NCBI]
|
5.99564e-05
|
|
|
CSNBAD1
|
[NCBI]
|
5.93324e-05
|
|
|
LCA5
|
[NCBI]
|
5.93324e-05
|
|
|
internal carotid artery, spontaneous dissection of
|
[NCBI]
|
5.93324e-05
|
|
|
spastic ataxia
|
[NCBI]
|
5.93324e-05
|
|
|
USH1G
|
[NCBI]
|
5.93324e-05
|
|
|
CLN10
|
[NCBI]
|
5.93324e-05
|
|
|
leber congenital amaurosis, type iii
|
[NCBI]
|
5.93324e-05
|
|
|
ST3GAL5
|
[NCBI]
|
5.75153e-05
|
|
|
OPN4
|
[NCBI]
|
5.75153e-05
|
|
|
CNGA1
|
[NCBI]
|
5.75153e-05
|
|
|
RPGR
|
[NCBI]
|
5.73024e-05
|
|
|
OPTB2
|
[NCBI]
|
5.52808e-05
|
|
|
coats disease
|
[NCBI]
|
5.52808e-05
|
|
|
TST
|
[NCBI]
|
5.23214e-05
|
|
|
SLC4A7
|
[NCBI]
|
5.23214e-05
|
|
|
LCA5
|
[NCBI]
|
5.23214e-05
|
|
|
DNAJC5
|
[NCBI]
|
5.23214e-05
|
|
|
musical perfect pitch
|
[NCBI]
|
4.93909e-05
|
|
|
CSNB1B
|
[NCBI]
|
4.93909e-05
|
|
|
renal tubular acidosis, proximal, with ocular abnormalities and mental retardation
|
[NCBI]
|
4.93909e-05
|
|
|
USH1G
|
[NCBI]
|
4.89512e-05
|
|
|
SLC4A4
|
[NCBI]
|
4.89512e-05
|
|
|
CNGB1
|
[NCBI]
|
4.89512e-05
|
|
|
LRAT
|
[NCBI]
|
4.89512e-05
|
|
|
ARL6
|
[NCBI]
|
4.89512e-05
|
|
|
SEMA4A
|
[NCBI]
|
4.89512e-05
|
|
|
CLN5
|
[NCBI]
|
4.89512e-05
|
|
|
adenylosuccinase deficiency
|
[NCBI]
|
4.71115e-05
|
|
|
PDC
|
[NCBI]
|
4.64471e-05
|
|
|
RHO
|
[NCBI]
|
4.63381e-05
|
|
|
NPHP3
|
[NCBI]
|
4.51242e-05
|
|
|
RP12
|
[NCBI]
|
4.51242e-05
|
|
|
VLDLRCH
|
[NCBI]
|
4.51242e-05
|
|
|
NPHP2
|
[NCBI]
|
4.51242e-05
|
|
|
NPHP3
|
[NCBI]
|
4.4453e-05
|
|
|
IMPDH1
|
[NCBI]
|
4.4453e-05
|
|
|
sarcosinemia
|
[NCBI]
|
4.33636e-05
|
|
|
fundus albipunctatus
|
[NCBI]
|
4.33636e-05
|
|
|
USH3A
|
[NCBI]
|
4.27961e-05
|
|
|
sturge-weber syndrome
|
[NCBI]
|
4.17842e-05
|
|
|
CLN5
|
[NCBI]
|
4.03528e-05
|
|
|
ALMS1
|
[NCBI]
|
4.01405e-05
|
|
|
TTC10
|
[NCBI]
|
4.01405e-05
|
|
|
STGD3
|
[NCBI]
|
3.90446e-05
|
|
|
WZS
|
[NCBI]
|
3.90446e-05
|
|
|
USH1C
|
[NCBI]
|
3.90446e-05
|
|
|
CEP290
|
[NCBI]
|
3.80532e-05
|
|
|
TIMM8A
|
[NCBI]
|
3.80532e-05
|
|
|
OPTA2
|
[NCBI]
|
3.78408e-05
|
|
|
SFD
|
[NCBI]
|
3.67262e-05
|
|
|
CTSD
|
[NCBI]
|
3.55763e-05
|
|
|
COL11A1
|
[NCBI]
|
3.55763e-05
|
|
|
TIMP1
|
[NCBI]
|
3.48732e-05
|
|
|
synovitis, granulomatous, with uveitis and cranial neuropathies
|
[NCBI]
|
3.47195e-05
|
|
|
pseudoxanthoma elasticum, forme fruste
|
[NCBI]
|
3.47195e-05
|
|
|
RLBP1
|
[NCBI]
|
3.24811e-05
|
|
|
ESCS
|
[NCBI]
|
3.21438e-05
|
|
|
MAOB
|
[NCBI]
|
3.19653e-05
|
|
|
CLN2
|
[NCBI]
|
3.06494e-05
|
|
|
OMP
|
[NCBI]
|
3.01406e-05
|
|
|
BBS
|
[NCBI]
|
2.99548e-05
|
|
|
SOX10
|
[NCBI]
|
2.97339e-05
|
|
|
MTND1
|
[NCBI]
|
2.86083e-05
|
|
|
EVR1
|
[NCBI]
|
2.80603e-05
|
|
|
STGD1
|
[NCBI]
|
2.63901e-05
|
|
|
PPT1
|
[NCBI]
|
2.56009e-05
|
|
|
ornithine aminotransferase deficiency
|
[NCBI]
|
2.53469e-05
|
|
|
RS1
|
[NCBI]
|
2.53469e-05
|
|
|
OPA1
|
[NCBI]
|
2.49005e-05
|
|
|
myoclonic epilepsy of lafora
|
[NCBI]
|
2.44382e-05
|
|
|
MSD
|
[NCBI]
|
2.39913e-05
|
|
|
SHH
|
[NCBI]
|
2.38599e-05
|
|
|
CADASIL
|
[NCBI]
|
2.234e-05
|
|
|
MEB
|
[NCBI]
|
2.234e-05
|
|
|
MTND4
|
[NCBI]
|
2.20137e-05
|
|
|
BSG
|
[NCBI]
|
2.15038e-05
|
|
|
walker-warburg syndrome
|
[NCBI]
|
2.12254e-05
|
|
|
OCA1A
|
[NCBI]
|
2.05326e-05
|
|
|
VMD
|
[NCBI]
|
1.98759e-05
|
|
|
FDH
|
[NCBI]
|
1.98759e-05
|
|
|
WFS1
|
[NCBI]
|
1.95599e-05
|
|
|
COL2A1
|
[NCBI]
|
1.88102e-05
|
|
|
MYOC
|
[NCBI]
|
1.67496e-05
|
|
|
FCMD
|
[NCBI]
|
1.65376e-05
|
|
|
metachromatic leukodystrophy
|
[NCBI]
|
1.26809e-05
|
|
|
PEDF
|
[NCBI]
|
1.24165e-05
|
|
|
KLK3
|
[NCBI]
|
1.02479e-05
|
|
|
VRNI
|
[NCBI]
|
8.35077e-06
|
|
|
VHL
|
[NCBI]
|
6.41192e-06
|
|
|
GNRH1
|
[NCBI]
|
5.99991e-06
|
|
|
EV
|
[NCBI]
|
4.63995e-06
|
|
|
VEGF
|
[NCBI]
|
3.67652e-06
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
2.84154e-06
|
|
|
EPO
|
[NCBI]
|
1.89358e-06
|
|
|
PJS
|
[NCBI]
|
1.77364e-06
|
|
|
GFAP
|
[NCBI]
|
1.60878e-06
|
|
|
PXE
|
[NCBI]
|
1.49579e-06
|
|
|
TS
|
[NCBI]
|
1.31107e-06
|
|
|
AVP
|
[NCBI]
|
5.01171e-07
|
|
|
G6PD
|
[NCBI]
|
3.09291e-07
|
|
|
ALD
|
[NCBI]
|
2.07354e-07
|
|
|
NPY
|
[NCBI]
|
1.84224e-07
|
|
|
BDNF
|
[NCBI]
|
7.78476e-08
|
|