Symptom Information: Sort according to HPO 

1
 (HPO:0000006) Autosomal dominant inheritance 2518 / 7739
2
 (HPO:0000613) Photophobia rare [HPO:skoehler] 158 / 7739
3
 (HPO:0000662) Nyctalopia rare [HPO:skoehler] 92 / 7739
4
 (HPO:0007754) Macular dystrophy 26 / 7739
5
 (HPO:0007913) Reticular retinal dystrophy 2 / 7739
6
 (HPO:0012508) Metamorphopsia rare [HPO:skoehler] 3 / 7739