Symptom Information: Sort according to HPO 

	Symptom Information	Symptom	Abundance	Frequency	Pubmed	Source	DB Freq
1	(HPO:0200018)	Protanomaly					1 / 7739
2	(OMIM)	Red series defect					1 / 7739
3	(HPO:0001419)	X-linked recessive inheritance					189 / 7739