Von Willebrand Testing
|
0030284 |
von Willebrand Modified Panel |
Order in conjunction with Factor VIII Activity (0030095) for the workup of suspected von Willebrand disease. |
0030285 |
von Willebrand Factor Antigen |
Order in conjunction with von Willebrand Factor Activity (Ristocetin Cofactor) (0030250) and Factor VIII Activity (0030095) as part of initial workup of suspected von Willebrand disease. |
0030250 |
von Willebrand Factor Activity (Ristocetin Cofactor) |
Order in conjunction with von Willebrand Factor Antigen (0030285) and Factor VIII Activity (0030095) as part of initial orkup of suspected von Willebrand disease. |
0030125 |
von Willebrand Panel |
Recommended panel for the initial workup of suspected von Willebrand disease. |
0030002 |
von Willebrand Multimeric Panel |
Not recommended for initial screening except in suspected cases of acquired von Willebrand disease (vWD) or high suspicion of vWD. Preferred initial test is von Willebrand Panel with Reflex to von Willebrand Multimeric Analysis (2003387). |
0092281 |
von WIllebrand Factor Multimers |
Order to subclassify established von WIllebrand disease. |
2003387 |
von Willebrand Panel with Reflex to von Willebrand Multimeric Analysis |
Recommended reflex panel to diagnose and subclassify suspected von Willebrand disease. |
Molecular
|
2005476 |
von Willebrand Disease, Platelet Type (GP1BA) 4 Mutations |
Molecular testing to distinguish von Willebrand disease (vWD) type 2B from pseudo (platelet-type) vWD. |
2005486 |
von Willebrand Disease, Type 2B (VWF) Sequencing |
Molecular testing to confirm a phenotypic diagnosis of von Willebrand disease type 2B and to distinguish from pseudo (platelet-type) vWD. |
2005490 |
von Willebrand Disease, Type 2M (VWF) Sequencing |
Molecular testing to confirm a phenotypic diagnosis of von Willebrand disease type 2M. |
2005494 |
von Willebrand Disease, Type 2N (VWF) Sequencing |
Molecular testing to distinguish von Willebrand disease type 2N from hemophilia A. |
2005480 |
von Willebrand Disease, Type 2A (VWF) Sequencing Exon 28 with Reflex to 9 Exons |
Molecular testing to confirm a phenotypic diagnosis of von Willebrand disease type 2A. |