(Q32146609)
English
platelet-type bleeding disorder 3
A inherited blood coagulation disease characterized by enhanced binding of von Willebrand factor by the platelet glycoprotein Ib receptor complex that has material basis in mutation in the GP1BA gene on chromosome 17p13.2.
- BDPLT3
- platelet type-von Willebrand disease
- von Willebrand disease platelet-type
- PT-VWD
- pseudo-von Willebrand disease
- Pseudo-von Willebrand disease type 2B
- PSEUDO-VON WILLEBRAND DISEASE; VWDP
- Platelet-Type von Willebrand Disease
- Von Willebrand Disease, Platelet-Type
- VWDP
- Bleeding Disorder, Platelet-Type, 3
Statements
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C131681
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Identifiers
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