Symptom Information: Sort according to HPO 

1
 (HPO:0000572) Visual loss Very frequent [Orphanet] 272 / 7739
2
 (HPO:0000615) Abnormality of the pupil Frequent [Orphanet] 39 / 7739
3
 (HPO:0000478) Abnormality of the eye 126 / 7739
4
 (OMIM) Corneal dermoid 1 / 7739
5
 (OMIM) Congenital opaque corneas 1 / 7739
6
 (HPO:0000481) Abnormality of the cornea Very frequent [Orphanet] 124 / 7739
7
 (HPO:0001417) X-linked inheritance 173 / 7739