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- B9a48a7149a650bce7f966d7c90049fa8 hasDbXref "Orphanet:286" @default.
- B9a48a7149a650bce7f966d7c90049fa8 type Axiom @default.
- B9a48a7149a650bce7f966d7c90049fa8 annotatedProperty IAO_0000115 @default.
- B9a48a7149a650bce7f966d7c90049fa8 annotatedSource MONDO_0017314 @default.
- B9a48a7149a650bce7f966d7c90049fa8 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.