|
1
|
(HPO:0000501)
|
Glaucoma |
|
|
|
|
180 / 7739
|
|
2
|
(HPO:0000518)
|
Cataract |
|
|
|
|
454 / 7739
|
|
3
|
(HPO:0000533)
|
Chorioretinal atrophy |
|
|
|
|
24 / 7739
|
|
4
|
(HPO:0000545)
|
Myopia |
|
|
|
|
286 / 7739
|
|
5
|
(HPO:0000572)
|
Visual loss |
|
|
|
|
272 / 7739
|
|
6
|
(HPO:0000648)
|
Optic atrophy |
|
|
|
|
238 / 7739
|
|
7
|
(HPO:0000655)
|
Vitreoretinal degeneration |
|
|
|
|
8 / 7739
|
|
8
|
(HPO:0001123)
|
Visual field defect |
|
|
|
|
30 / 7739
|
|
9
|
(HPO:0007643)
|
Peripheral traction retinal detachment |
|
|
|
|
1 / 7739
|
|
10
|
(HPO:0007722)
|
Retinal pigment epithelial atrophy |
|
|
|
|
10 / 7739
|
|
11
|
(HPO:0000575)
|
Scotoma |
|
|
|
|
11 / 7739
|
|
12
|
(OMIM)
|
Vision loss with age (middle age) |
|
|
|
|
1 / 7739
|
|
13
|
(OMIM)
|
Myopia, mild |
|
|
|
|
1 / 7739
|
|
14
|
(OMIM)
|
Exudative vitreoretinopathy |
|
|
|
|
2 / 7739
|
|
15
|
(OMIM)
|
'Empty' vitreous with fibrillary condensations (childhood) |
|
|
|
|
1 / 7739
|
|
16
|
(OMIM)
|
Impairment of dark adaptation with age |
|
|
|
|
1 / 7739
|
|
17
|
(HPO:0000006)
|
Autosomal dominant inheritance |
|
|
|
|
2518 / 7739
|
|
18
|
(HPO:0030490)
|
Exudative vitreoretinopathy |
rare [HPO:skoehler]
|
|
|
|
5 / 7739
|