|
1
|
(HPO:0000610)
|
Abnormality of the choroid |
Occasional [Orphanet]
|
|
|
|
11 / 7739
|
|
2
|
(HPO:0000505)
|
Visual impairment |
Very frequent [Orphanet]
|
|
|
|
297 / 7739
|
|
3
|
(HPO:0000642)
|
Red-green dyschromatopsia |
Frequent [Orphanet]
|
|
|
|
25 / 7739
|
|
4
|
(HPO:0000512)
|
Abnormal electroretinogram |
|
|
|
|
61 / 7739
|
|
5
|
(HPO:0001123)
|
Visual field defect |
Occasional [Orphanet]
|
|
|
|
30 / 7739
|
|
6
|
(HPO:0008028)
|
Cystoid macular degeneration |
|
|
|
|
3 / 7739
|
|
7
|
(OMIM)
|
Deeply and irregularly pigmented yellow macular mass |
|
|
|
|
1 / 7739
|
|
8
|
(MedDRA:10014456)
|
Electrooculogram abnormal |
|
|
|
|
3 / 7739
|
|
9
|
(HPO:0008059)
|
Aplasia/Hypoplasia of the macula |
Very frequent [Orphanet]
|
|
|
|
21 / 7739
|
|
10
|
(HPO:0000006)
|
Autosomal dominant inheritance |
|
|
|
|
2518 / 7739
|
|
11
|
(HPO:0007663)
|
Reduced visual acuity |
|
|
|
|
100 / 7739
|
|
12
|
(HPO:0007754)
|
Macular dystrophy |
|
|
|
|
26 / 7739
|