|
OMIM |
Link |
Information gain |
01 |
|
MCOPS1
|
[NCBI]
|
0.00504731
|
|
|
MCOP1
|
[NCBI]
|
0.00330266
|
|
|
NNO1
|
[NCBI]
|
0.00290322
|
|
|
MCOPS7
|
[NCBI]
|
0.00247159
|
|
|
MCOPCB2
|
[NCBI]
|
0.00174232
|
|
|
kenny-caffey syndrome, type 2
|
[NCBI]
|
0.00161141
|
|
|
persistent hyperplastic primary vitreous, autosomal recessive
|
[NCBI]
|
0.0013076
|
|
|
MCOPS4
|
[NCBI]
|
0.0013076
|
|
|
RNANC
|
[NCBI]
|
0.00108688
|
|
|
MCOPCB1
|
[NCBI]
|
0.000868983
|
|
|
MCOPS10
|
[NCBI]
|
0.000868983
|
|
|
branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging
|
[NCBI]
|
0.000846808
|
|
|
lymphedema, microcephaly, chorioretinopathy syndrome
|
[NCBI]
|
0.000802936
|
|
|
MCOPCT1
|
[NCBI]
|
0.000651642
|
|
|
WS2B
|
[NCBI]
|
0.000569992
|
|
|
MCOPS9
|
[NCBI]
|
0.00053211
|
|
|
oculodentoosseous dysplasia, recessive
|
[NCBI]
|
0.000517186
|
|
|
MITF
|
[NCBI]
|
0.000483879
|
|
|
CCA1
|
[NCBI]
|
0.000447038
|
|
|
acromelic frontonasal dysostosis
|
[NCBI]
|
0.000447038
|
|
|
MCOPS6
|
[NCBI]
|
0.00042133
|
|
|
MCOPS2
|
[NCBI]
|
0.000397603
|
|
|
MCOP2
|
[NCBI]
|
0.000395432
|
|
|
ODDD
|
[NCBI]
|
0.000392502
|
|
|
HYPX
|
[NCBI]
|
0.000380325
|
|
|
NHS
|
[NCBI]
|
0.000363316
|
|
|
MCOPCB3
|
[NCBI]
|
0.000326751
|
|
|
MCOPS3
|
[NCBI]
|
0.000285866
|
|
|
CHX10
|
[NCBI]
|
0.000273192
|
|
|
WARBM
|
[NCBI]
|
0.000241053
|
|
|
NLS
|
[NCBI]
|
0.000218042
|
|
|
MCOPCB4
|
[NCBI]
|
0.000217683
|
|
|
GJA8
|
[NCBI]
|
0.000214002
|
|
|
HCCS
|
[NCBI]
|
0.000210747
|
|
|
coloboma, uveal, with cleft lip and palate and mental retardation
|
[NCBI]
|
0.000186748
|
|
|
moved to 310600
|
[NCBI]
|
0.000186748
|
|
|
gombo syndrome
|
[NCBI]
|
0.000172777
|
|
|
GJA3
|
[NCBI]
|
0.000166058
|
|
|
MLRD
|
[NCBI]
|
0.000163192
|
|
|
ARHGAP6
|
[NCBI]
|
0.000155232
|
|
|
coloboma, ocular
|
[NCBI]
|
0.000136721
|
|
|
HRD
|
[NCBI]
|
0.000133312
|
|
|
KCS
|
[NCBI]
|
0.000133312
|
|
|
BCOR
|
[NCBI]
|
0.000127678
|
|
|
WS2A
|
[NCBI]
|
0.000124842
|
|
|
MFRP
|
[NCBI]
|
0.000117283
|
|
|
NHS
|
[NCBI]
|
0.000113621
|
|
|
tachycardia, hypertension, microphthalmia, and hyperglycinuria
|
[NCBI]
|
0.000108767
|
|
|
retinal degeneration with nanophthalmos, cystic macular degeneration, and angle closure glaucoma
|
[NCBI]
|
0.000108767
|
|
|
retinal nonattachment and falciform detachment
|
[NCBI]
|
0.000108767
|
|
|
microphthalmia, posterior, with retinitis pigmentosa, foveoschisis, and optic disc drusen
|
[NCBI]
|
0.000108767
|
|
|
macrosomia with microphthalmia, lethal
|
[NCBI]
|
0.000108767
|
|
|
SOX2
|
[NCBI]
|
9.53617e-05
|
|
|
walker-warburg syndrome
|
[NCBI]
|
8.89011e-05
|
|
|
microphthalmia, isolated, with cataract 4
|
[NCBI]
|
8.63138e-05
|
|
|
NNO2
|
[NCBI]
|
8.63138e-05
|
|
|
teebi-shaltout syndrome
|
[NCBI]
|
8.63138e-05
|
|
|
dextrocardia with unusual facies and microphthalmia
|
[NCBI]
|
8.63138e-05
|
|
|
cataract, lamellar 2
|
[NCBI]
|
8.63138e-05
|
|
|
AN2
|
[NCBI]
|
8.18604e-05
|
|
|
CES
|
[NCBI]
|
8.12378e-05
|
|
|
MCOP3
|
[NCBI]
|
7.78513e-05
|
|
|
arhinia, choanal atresia, and microphthalmia
|
[NCBI]
|
7.78513e-05
|
|
|
coloboma of optic nerve
|
[NCBI]
|
7.78513e-05
|
|
|
MCOPS5
|
[NCBI]
|
7.78513e-05
|
|
|
yemenite deaf-blind hypopigmentation syndrome
|
[NCBI]
|
7.78513e-05
|
|
|
CLCN4
|
[NCBI]
|
7.75317e-05
|
|
|
SOLH
|
[NCBI]
|
7.75317e-05
|
|
|
MCOPS8
|
[NCBI]
|
7.23626e-05
|
|
|
fryns microphthalmia syndrome
|
[NCBI]
|
7.23626e-05
|
|
|
PAX6
|
[NCBI]
|
6.86314e-05
|
|
|
jejunal atresia with microcephaly and ocular anomalies
|
[NCBI]
|
6.82864e-05
|
|
|
CTPP4
|
[NCBI]
|
6.3755e-05
|
|
|
CCA2
|
[NCBI]
|
6.23472e-05
|
|
|
SNX3
|
[NCBI]
|
5.85576e-05
|
|
|
UBE2I
|
[NCBI]
|
5.85576e-05
|
|
|
STRA6
|
[NCBI]
|
5.85576e-05
|
|
|
IRID1
|
[NCBI]
|
5.46419e-05
|
|
|
wagr syndrome
|
[NCBI]
|
5.31859e-05
|
|
|
oculocerebrocutaneous syndrome
|
[NCBI]
|
5.31859e-05
|
|
|
CCT
|
[NCBI]
|
5.26761e-05
|
|
|
RENS1
|
[NCBI]
|
5.18531e-05
|
|
|
CRYBA4
|
[NCBI]
|
5.06786e-05
|
|
|
TFAP2A
|
[NCBI]
|
4.90181e-05
|
|
|
COFS1
|
[NCBI]
|
4.84236e-05
|
|
|
GJA1
|
[NCBI]
|
4.80384e-05
|
|
|
SMMCI
|
[NCBI]
|
4.56137e-05
|
|
|
AIED
|
[NCBI]
|
4.47798e-05
|
|
|
MSX2
|
[NCBI]
|
4.42609e-05
|
|
|
PITX3
|
[NCBI]
|
4.42609e-05
|
|
|
AGS1
|
[NCBI]
|
4.39886e-05
|
|
|
RB1
|
[NCBI]
|
4.20909e-05
|
|
|
PQBP1
|
[NCBI]
|
3.97898e-05
|
|
|
OPTB1
|
[NCBI]
|
3.93636e-05
|
|
|
RIEG1
|
[NCBI]
|
3.93636e-05
|
|
|
BOR1
|
[NCBI]
|
3.72408e-05
|
|
|
SOX10
|
[NCBI]
|
3.58917e-05
|
|
|
FIH
|
[NCBI]
|
3.49508e-05
|
|
|
charge syndrome
|
[NCBI]
|
3.45323e-05
|
|
|
PIGA
|
[NCBI]
|
3.25292e-05
|
|
|
ACP5
|
[NCBI]
|
3.22526e-05
|
|
|
PHS
|
[NCBI]
|
3.22444e-05
|
|
|
FDH
|
[NCBI]
|
3.18956e-05
|
|
|
VMD
|
[NCBI]
|
3.18956e-05
|
|
|
KIT
|
[NCBI]
|
3.17124e-05
|
|
|
FANCA
|
[NCBI]
|
3.14548e-05
|
|
|
MKS1
|
[NCBI]
|
2.7482e-05
|
|
|
PAX3
|
[NCBI]
|
2.70505e-05
|
|
|
IP
|
[NCBI]
|
1.55387e-05
|
|
|
TP53
|
[NCBI]
|
1.46794e-05
|
|
|
DGS
|
[NCBI]
|
1.18071e-05
|
|
|
SHH
|
[NCBI]
|
1.13165e-05
|
|
|
VEGF
|
[NCBI]
|
1.05281e-05
|
|
|
AVP
|
[NCBI]
|
7.676e-06
|
|
|
G6PD
|
[NCBI]
|
2.98e-06
|
|
|
FA
|
[NCBI]
|
8.80678e-07
|
|
|
NPY
|
[NCBI]
|
8.41416e-07
|
|
|
RP
|
[NCBI]
|
2.53815e-07
|
|