|
1
|
(HPO:0000545)
|
Myopia |
Very frequent [Orphanet]
|
|
|
|
286 / 7739
|
|
2
|
(HPO:0000639)
|
Nystagmus |
Very frequent [Orphanet]
|
|
|
|
555 / 7739
|
|
3
|
(HPO:0000505)
|
Visual impairment |
|
|
|
|
297 / 7739
|
|
4
|
(HPO:0000541)
|
Retinal detachment |
|
|
|
|
87 / 7739
|
|
5
|
(HPO:0007810)
|
Progressive bifocal chorioretinal atrophy |
|
|
|
|
1 / 7739
|
|
6
|
(HPO:0007920)
|
Congenital chorioretinal dystrophy |
|
|
|
|
1 / 7739
|
|
7
|
(HPO:0008046)
|
Abnormality of the retinal vasculature |
Very frequent [Orphanet]
|
|
|
|
41 / 7739
|
|
8
|
(OMIM)
|
Progressive macular and nasal retinal atrophic lesions |
|
|
|
|
1 / 7739
|
|
9
|
(OMIM)
|
Congenital temporal atrophy |
|
|
|
|
1 / 7739
|
|
10
|
(HPO:0000006)
|
Autosomal dominant inheritance |
|
|
|
|
2518 / 7739
|
|
11
|
(HPO:0000533)
|
Chorioretinal atrophy |
|
|
|
|
24 / 7739
|
|
12
|
(HPO:0001135)
|
Chorioretinal dystrophy |
|
|
|
|
18 / 7739
|