Symptom Information: Sort according to HPO 

	Symptom Information	Symptom	Abundance	Frequency	Pubmed	Source	DB Freq
1	(HPO:0000316)	Hypertelorism	Occasional [Orphanet]				644 / 7739
2	(HPO:0000366)	Abnormality of the nose	Very frequent [Orphanet]				56 / 7739
3	(HPO:0000006)	Autosomal dominant inheritance					2518 / 7739
4	(HPO:0000028)	Cryptorchidism					347 / 7739
5	(HPO:0000508)	Ptosis					459 / 7739
6	(HPO:0000924)	Abnormality of the skeletal system					114 / 7739
7	(HPO:0011803)	Bifid nose					12 / 7739