vascular disorder Ehlers-Danlos syndrome, vascular type https://github.com/monarch-initiative/mondo/issues/10692 Ehlers-Danlos syndrome type IV, also known as the vascular type of Ehlers-Danlos syndrome (EDS), is an inherited connective tissue disorder defined by characteristic facial features (acrogeria) in most patients, translucent skin with highly visible subcutaneous vessels on the trunk and lower back, easy bruising, and severe arterial, digestive and uterine complications, which are rarely, if at all, observed in the other forms of EDS. EDS type 4 GARD:0002082 Ehlers-Danlos syndrome, vascular type EDS IV Ehlers Danlos syndrome, ecchymotic type Ehlers-Danlos syndrome type IV MEDGEN:82790 EDS4 (formerly) icd11.foundation:1202686415 EDS type 4 (formerly) Ehlers-Danlos syndrome type IV (formerly) vascular EDS MONDO:0017314 sack-Barabas syndrome NCIT:C125699 NANDO:2201258 vascular Ehlers-Danlos syndrome Ehlers Danlos syndrome, arterial type EDS IV (formerly) Ehlers-Danlos syndrome type 4 Ehlers-Danlos syndrome type 4 (formerly) Ehlers-Danlos syndrome, type IV UMLS:C0268338 vEDS ICD10CM:Q79.63 NANDO:1200648 Orphanet:286 Ehlers Danlos syndrome, sack-Barabas type SCTID:17025000 Ehlers-Danlos syndrome