Symptom Information: Sort according to HPO 

1
 (HPO:0000613) Photophobia 158 / 7739
2
 (OMIM) Cone dystrophy 2 / 7739
3
 (OMIM) Color and central vision loss 1 / 7739
4
 (HPO:0000006) Autosomal dominant inheritance 2518 / 7739
5
 (HPO:0000548) Cone/cone-rod dystrophy 47 / 7739