|
1
|
(HPO:0000545)
|
Myopia |
Very frequent [Orphanet]
|
|
|
|
286 / 7739
|
|
2
|
(HPO:0000572)
|
Visual loss |
Frequent [Orphanet]
|
|
|
|
272 / 7739
|
|
3
|
(HPO:0000662)
|
Nyctalopia |
|
|
|
|
92 / 7739
|
|
4
|
(HPO:0000478)
|
Abnormality of the eye |
Very frequent [Orphanet]
|
|
|
|
126 / 7739
|
|
5
|
(HPO:0000512)
|
Abnormal electroretinogram |
Very frequent [Orphanet]
|
|
|
|
61 / 7739
|
|
6
|
(HPO:0000510)
|
Rod-cone dystrophy |
Very frequent [Orphanet]
|
|
|
|
266 / 7739
|
|
7
|
(HPO:0000505)
|
Visual impairment |
Very frequent [Orphanet]
|
|
|
|
297 / 7739
|
|
8
|
(HPO:0000529)
|
Progressive visual loss |
|
|
|
|
54 / 7739
|
|
9
|
(HPO:0001133)
|
Constriction of peripheral visual field |
|
|
|
|
33 / 7739
|
|
10
|
(HPO:0001139)
|
Choroideremia |
|
|
|
|
7 / 7739
|
|
11
|
(HPO:0001150)
|
Choroidal sclerosis |
|
|
|
|
5 / 7739
|
|
12
|
(HPO:0200065)
|
Chorioretinal degeneration |
|
|
|
|
7 / 7739
|
|
13
|
(OMIM)
|
Reduced central vision (occurs last) |
|
|
|
|
2 / 7739
|
|
14
|
(OMIM)
|
Atrophy around the optic disc (in carrier females) |
|
|
|
|
2 / 7739
|
|
15
|
(OMIM)
|
Irregular pigmentation of fundus (in carrier females) |
|
|
|
|
2 / 7739
|
|
16
|
(HPO:0000504)
|
Abnormality of vision |
Very frequent [Orphanet]
|
|
|
|
22 / 7739
|
|
17
|
(HPO:0000533)
|
Chorioretinal atrophy |
|
|
|
|
24 / 7739
|
|
18
|
(HPO:0001423)
|
X-linked dominant inheritance |
|
|
|
|
69 / 7739
|