Symptom Information: Sort according to HPO 

	Symptom Information	Symptom	Abundance	Frequency	Pubmed	Source	DB Freq
1	(HPO:0000519)	Congenital cataract					73 / 7739
2	(OMIM)	Floriform cataract					1 / 7739
3	(HPO:0000006)	Autosomal dominant inheritance					2518 / 7739
4	(HPO:0000501)	Glaucoma	rare [HPO:skoehler]				180 / 7739
5	(HPO:0000545)	Myopia	rare [HPO:skoehler]				286 / 7739