Symptom Information: Sort according to HPO 

1
(HPO:0000478) Abnormality of the eye Very frequent [Orphanet] 126 / 7739
2
(HPO:0000502) Abnormality of the conjunctiva 6 / 7739
3
(HPO:0001059) Pterygium 16 / 7739
4
(OMIM) Wing-shaped conjunctival thickening in interpalpebral fissure 1 / 7739
5
(HPO:0000481) Abnormality of the cornea Frequent [Orphanet] 124 / 7739
6
(HPO:0000006) Autosomal dominant inheritance 2518 / 7739