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Von Willebrand disease 3
rareType 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).
- Identifiers
- MONDO:0010191 OMIM:277480Orphanet:166096
- Causal genes
- VWF
- Also known as
- von Willebrand disease type 3 · VON WILLEBRAND disease, type 3 · von Willebrand's disease 3 · von Willebrand's disease type 3 · VWD3
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