Symptom Information: Sort according to HPO 

1
(HPO:0100612) Odontogenic neoplasm Very frequent [Orphanet] 5 / 7739
2
(HPO:0001399) Hepatic failure Very frequent [Orphanet] 80 / 7739
3
(HPO:0002575) Tracheoesophageal fistula Very frequent [Orphanet] 54 / 7739
4
(HPO:0002621) Atherosclerosis Very frequent [Orphanet] 33 / 7739
5
(HPO:0030680) Abnormality of cardiovascular system morphology Very frequent [Orphanet] 355 / 7739
6
(HPO:0002015) Dysphagia 301 / 7739
7
(HPO:0011068) Odontoma 6 / 7739
8
(OMIM) Esophageal smooth muscle hypertrophy 1 / 7739
9
(HPO:0000006) Autosomal dominant inheritance 2518 / 7739