Symptom Information: Sort according to HPO 

	Symptom Information	Symptom	Abundance	Frequency	Pubmed	Source	DB Freq
1	(HPO:0000962)	Hyperkeratosis					216 / 7739
2	(HPO:0007479)	Congenital nonbullous ichthyosiform erythroderma					13 / 7739
3	(HPO:0000007)	Autosomal recessive inheritance					2538 / 7739
4	(HPO:0000656)	Ectropion	rare [HPO:skoehler]				25 / 7739
5	(HPO:0000966)	Hypohidrosis					41 / 7739
6	(HPO:0012472)	Eclabion	rare [HPO:skoehler]				7 / 7739