1
|
(HPO:0000006)
|
Autosomal dominant inheritance |
|
|
|
|
2518 / 7739
|
2
|
(HPO:0000523)
|
Subcapsular cataract |
|
|
|
|
12 / 7739
|
3
|
(HPO:0000541)
|
Retinal detachment |
|
|
|
|
87 / 7739
|
4
|
(HPO:0000618)
|
Blindness |
|
|
|
|
124 / 7739
|
5
|
(HPO:0001146)
|
Pigmentary retinal degeneration |
|
|
|
|
15 / 7739
|
6
|
(HPO:0001147)
|
Retinal exudate |
|
|
|
|
8 / 7739
|
7
|
(HPO:0001489)
|
Posterior vitreous detachment |
|
|
|
|
3 / 7739
|
8
|
(HPO:0001493)
|
Falciform retinal fold |
|
|
|
|
6 / 7739
|
9
|
(HPO:0002757)
|
Recurrent fractures |
|
|
|
|
47 / 7739
|
10
|
(HPO:0003593)
|
Infantile onset |
|
|
|
|
249 / 7739
|
11
|
(HPO:0003677)
|
Slow progression |
|
|
|
|
134 / 7739
|
12
|
(HPO:0007663)
|
Reduced visual acuity |
|
|
|
|
100 / 7739
|
13
|
(HPO:0007685)
|
Peripheral retinal avascularization |
|
|
|
|
3 / 7739
|
14
|
(HPO:0007902)
|
Vitreous hemorrhage |
|
|
|
|
9 / 7739
|
15
|
(HPO:0030490)
|
Exudative vitreoretinopathy |
|
|
|
|
5 / 7739
|