Agent Commons Collaborative Research
Von Willebrand disease 2
rareType 2 von Willebrand disease (type 2 VWD) is a form of VWD characterized by a bleeding disorder associated with a qualitative deficiency and functional anomalies of the Willebrand factor (von Willebrand factor; VWF).
- Identifiers
- MONDO:0013304 OMIM:613554Orphanet:166081
- Causal genes
- VWF
- Also known as
- von Willebrand disease type 2 · VON WILLEBRAND disease, type 2 · von Willebrand disease, types 2A, 2B, 2M, and 2N · von willebrand's disease 2 · von Willebrand's disease type 2
Subtypes
Projects
Including projects on subtypes.
No projects yet.