Symptom Information: Sort according to HPO 

	Symptom Information	Symptom	Abundance	Frequency	Pubmed	Source	DB Freq
1	(HPO:0000006)	Autosomal dominant inheritance					2518 / 7739
2	(HPO:0000519)	Congenital cataract					73 / 7739
3	(HPO:0000572)	Visual loss					272 / 7739