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- Be6f8474a0b03e3aa60ab5fcb8ed84594 hasDbXref "Orphanet:286" @default.
- Be6f8474a0b03e3aa60ab5fcb8ed84594 type Axiom @default.
- Be6f8474a0b03e3aa60ab5fcb8ed84594 annotatedProperty IAO_0000115 @default.
- Be6f8474a0b03e3aa60ab5fcb8ed84594 annotatedSource MONDO_0017314 @default.
- Be6f8474a0b03e3aa60ab5fcb8ed84594 annotatedTarget "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." @default.