|
OMIM |
Link |
Information
gain |
01 |
|
|
ectopia lentis with ectopia of pupil
|
[NCBI]
|
0.0041473
|
|
|
|
ataxia, spastic, with congenital miosis
|
[NCBI]
|
0.00158502
|
|
|
|
microcoria, congenital
|
[NCBI]
|
0.00115699
|
|
|
|
aniridia, cerebellar ataxia, and mental deficiency
|
[NCBI]
|
0.000979436
|
|
|
|
melanoma, uveal
|
[NCBI]
|
0.000530815
|
|
|
|
mydriatic response to pharmacologic agents
|
[NCBI]
|
0.000367332
|
|
|
|
adie pupil
|
[NCBI]
|
0.000342895
|
|
|
|
NRCLP1
|
[NCBI]
|
0.00027977
|
|
|
|
congenital corneal opacities, cornea guttata, and corectopia
|
[NCBI]
|
0.000210237
|
|
|
|
ptosis, strabismus, and ectopic pupils
|
[NCBI]
|
0.000210237
|
|
|
|
MCOPCT2
|
[NCBI]
|
0.000210237
|
|
|
|
stormorken syndrome
|
[NCBI]
|
0.000210237
|
|
|
|
mydriasis, congenital
|
[NCBI]
|
0.000210237
|
|
|
|
RP
|
[NCBI]
|
0.000208538
|
|
|
|
telecanthus
|
[NCBI]
|
0.000170976
|
|
|
|
axenfeld-rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities
|
[NCBI]
|
0.000146557
|
|
|
|
weill-marchesani syndrome, autosomal recessive
|
[NCBI]
|
0.000121421
|
|
|
|
HSAN1
|
[NCBI]
|
0.000102749
|
|
|
|
ACHE
|
[NCBI]
|
9.51683e-05
|
|
|
|
CMT1B
|
[NCBI]
|
7.83973e-05
|
|
|
|
TTR
|
[NCBI]
|
6.83327e-05
|
|
|
|
OPRM1
|
[NCBI]
|
6.09163e-05
|
|
|
|
fabry disease
|
[NCBI]
|
5.92481e-05
|
|
|
|
OPN4
|
[NCBI]
|
3.95374e-05
|
|
|
|
CRY2
|
[NCBI]
|
3.5039e-05
|
|
|
|
PDE6B
|
[NCBI]
|
3.2768e-05
|
|
|
|
CRY1
|
[NCBI]
|
3.2768e-05
|
|
|
|
MDD
|
[NCBI]
|
2.89317e-05
|
|
|
|
MPZ
|
[NCBI]
|
2.71668e-05
|
|
|
|
CCK
|
[NCBI]
|
2.56719e-05
|
|
|
|
APOE
|
[NCBI]
|
2.34594e-05
|
|
|
|
NPY
|
[NCBI]
|
1.88899e-05
|
|
|
|
FTD
|
[NCBI]
|
1.72791e-05
|
|
|
|
AD
|
[NCBI]
|
1.56828e-05
|
|
|
|
CF
|
[NCBI]
|
1.14567e-05
|
|
|
|
AVP
|
[NCBI]
|
1.13895e-05
|
|
|
|
NPPA
|
[NCBI]
|
5.86292e-06
|
|
|
|
MG
|
[NCBI]
|
5.22237e-06
|
|
|
|
CHAT
|
[NCBI]
|
3.84148e-06
|
|
|
|
TH
|
[NCBI]
|
1.27988e-06
|
|
|
|
VEGF
|
[NCBI]
|
1.70262e-08
|
|
