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- Ba6f0f1121de2aecda90f2348b747be33 hasDbXref "Orphanet:903" @default.
- Ba6f0f1121de2aecda90f2348b747be33 type Axiom @default.
- Ba6f0f1121de2aecda90f2348b747be33 annotatedProperty IAO_0000115 @default.
- Ba6f0f1121de2aecda90f2348b747be33 annotatedSource MONDO_0019565 @default.
- Ba6f0f1121de2aecda90f2348b747be33 annotatedTarget "Hereditary von Willebrand disease (VWD) is a hereditary bleeding disorder caused by a genetic anomaly leading to quantitative, structural or functional abnormalities of the Willebrand factor (von Willebrand factor; VWF). Two major groups of VWF deficiency have been defined: quantitative and partial (type 1) or total (type 3), and qualitative (type 2) with several subtypes (2A, 2B, 2M, 2N)." @default.