Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B3c724db4a2b150ff5d611de1dc14d74d> ?p ?o ?g. }
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- B3c724db4a2b150ff5d611de1dc14d74d hasDbXref "Orphanet:166096" @default.
- B3c724db4a2b150ff5d611de1dc14d74d type Axiom @default.
- B3c724db4a2b150ff5d611de1dc14d74d annotatedProperty IAO_0000115 @default.
- B3c724db4a2b150ff5d611de1dc14d74d annotatedSource MONDO_0010191 @default.
- B3c724db4a2b150ff5d611de1dc14d74d annotatedTarget "Type 3 von Willebrand disease (type 3 VWD) is the most severe form of VWD characterized by a bleeding disorder associated with a total or near-total absence of Willebrand factor (von Willebrand factor; VWF) in the plasma and cellular compartments, also leading to a profound deficiency of plasmatic factor VIII (FVIII)." @default.