|
1
|
(HPO:0000505)
|
Visual impairment |
Occasional [Orphanet]
|
|
|
|
297 / 7739
|
|
2
|
(HPO:0000613)
|
Photophobia |
Very frequent [Orphanet]
|
|
|
|
158 / 7739
|
|
3
|
(HPO:0000510)
|
Rod-cone dystrophy |
Very frequent [Orphanet]
|
|
|
|
266 / 7739
|
|
4
|
(HPO:0000642)
|
Red-green dyschromatopsia |
Frequent [Orphanet]
|
|
|
|
25 / 7739
|
|
5
|
(HPO:0000504)
|
Abnormality of vision |
Very frequent [Orphanet]
|
|
|
|
22 / 7739
|
|
6
|
(HPO:0000006)
|
Autosomal dominant inheritance |
|
|
|
|
2518 / 7739
|
|
7
|
(HPO:0000533)
|
Chorioretinal atrophy |
|
|
|
|
24 / 7739
|
|
8
|
(HPO:0000548)
|
Cone/cone-rod dystrophy |
|
|
|
|
47 / 7739
|
|
9
|
(HPO:0000551)
|
Abnormality of color vision |
|
|
|
|
20 / 7739
|
|
10
|
(HPO:0000618)
|
Blindness |
|
|
|
|
124 / 7739
|
|
11
|
(HPO:0000662)
|
Nyctalopia |
|
|
|
|
92 / 7739
|
|
12
|
(HPO:0001133)
|
Constriction of peripheral visual field |
|
|
|
|
33 / 7739
|
|
13
|
(HPO:0007663)
|
Reduced visual acuity |
|
|
|
|
100 / 7739
|
|
14
|
(HPO:0007994)
|
Peripheral visual field loss |
|
|
|
|
13 / 7739
|