|
1
|
(HPO:0000505)
|
Visual impairment |
Very frequent [Orphanet]
|
|
|
|
297 / 7739
|
|
2
|
(HPO:0000512)
|
Abnormal electroretinogram |
Very frequent [Orphanet]
|
|
|
|
61 / 7739
|
|
3
|
(HPO:0000613)
|
Photophobia |
Very frequent [Orphanet]
|
|
|
|
158 / 7739
|
|
4
|
(HPO:0000510)
|
Rod-cone dystrophy |
Very frequent [Orphanet]
|
|
|
|
266 / 7739
|
|
5
|
(HPO:0000642)
|
Red-green dyschromatopsia |
Very frequent [Orphanet]
|
|
|
|
25 / 7739
|
|
6
|
(HPO:0000006)
|
Autosomal dominant inheritance |
|
|
|
|
2518 / 7739
|
|
7
|
(HPO:0000529)
|
Progressive visual loss |
|
|
|
|
54 / 7739
|
|
8
|
(HPO:0000551)
|
Abnormality of color vision |
|
|
|
|
20 / 7739
|
|
9
|
(HPO:0007829)
|
Diffuse retinal cone degeneration |
|
|
|
|
2 / 7739
|
|
10
|
(HPO:0011504)
|
Bull's eye maculopathy |
|
|
|
|
8 / 7739
|