Symptom Information: Sort according to HPO 

1
(HPO:0000572) Visual loss Occasional [Orphanet] 272 / 7739
2
(HPO:0000610) Abnormality of the choroid Frequent [Orphanet] 11 / 7739
3
(HPO:0000478) Abnormality of the eye Very frequent [Orphanet] 126 / 7739
4
(HPO:0000541) Retinal detachment Occasional [Orphanet] 87 / 7739
5
(HPO:0000510) Rod-cone dystrophy Frequent [Orphanet] 266 / 7739
6
(HPO:0000505) Visual impairment Very frequent [Orphanet] 297 / 7739
7
(HPO:0000642) Red-green dyschromatopsia Frequent [Orphanet] 25 / 7739
8
(HPO:0001123) Visual field defect Frequent [Orphanet] 30 / 7739
9
(HPO:0007677) Vitelliform-like macular lesions 4 / 7739
10
(HPO:0008059) Aplasia/Hypoplasia of the macula Very frequent [Orphanet] 21 / 7739
11
(HPO:0000006) Autosomal dominant inheritance 2518 / 7739
12
(HPO:0000613) Photophobia 158 / 7739
13
(HPO:0007401) Macular atrophy 14 / 7739
14
(HPO:0007663) Reduced visual acuity 100 / 7739
15
(HPO:0007754) Macular dystrophy 26 / 7739
16
(HPO:0012508) Metamorphopsia 3 / 7739