Symptom Information: Sort according to HPO 

1
(HPO:0100026) Arteriovenous malformation Very frequent [Orphanet] 38 / 7739
2
(HPO:0011276) Vascular skin abnormality Very frequent [Orphanet] 24 / 7739
3
(HPO:0000153) Abnormality of the mouth 60 / 7739
4
(HPO:0002584) Intestinal bleeding 16 / 7739
5
(OMIM) Mucosal bleeding 2 / 7739
6
(OMIM) Maxillary and mandibular deformity 1 / 7739
7
(OMIM) Variable gastrointestinal bleeding 1 / 7739
8
(OMIM) Cutaneous and mucosal venous malformations 1 / 7739
9
(HPO:0000006) Autosomal dominant inheritance 2518 / 7739
10
(HPO:0012721) Venous malformation 3 / 7739