Symptom Information: Sort according to HPO 

	Symptom Information	Symptom	Abundance	Frequency	Pubmed	Source	DB Freq
1	(HPO:0000478)	Abnormality of the eye					126 / 7739
2	(OMIM)	Upper eyelid epiblepharon					1 / 7739
3	(HPO:0000006)	Autosomal dominant inheritance					2518 / 7739
4	(HPO:0040150)	Epiblepharon of upper lid					1 / 7739