Symptom Information: Sort according to HPO 

	Symptom Information	Symptom	Abundance	Frequency	Pubmed	Source	DB Freq
1	(HPO:0000243)	Trigonocephaly					40 / 7739
2	(HPO:0000252)	Microcephaly	rare [HPO:skoehler]				832 / 7739
3	(HPO:0000316)	Hypertelorism	rare [HPO:skoehler]				644 / 7739
4	(OMIM)	Metopic craniosynostosis					1 / 7739
5	(HPO:0000006)	Autosomal dominant inheritance					2518 / 7739
6	(HPO:0011330)	Metopic synostosis					3 / 7739