Von Willebrand disease type 2N (Q100619): Difference between revisions
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Revision as of 17:21, 16 August 2026
Type 2N von Willebrand disease (type 2N VWD) is a subtype of type 2 VWD characterised by a bleeding disorder associated with a marked decrease in the affinity of the Willebrand factor (von Willebrand factor; VWF) for factor VIII (FVIII). Abnormal bleeding manifestations are much less frequent in this VWD subtype than in other forms of the disease.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1091176565 |
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| English | Von Willebrand disease type 2N |
Type 2N von Willebrand disease (type 2N VWD) is a subtype of type 2 VWD characterised by a bleeding disorder associated with a marked decrease in the affinity of the Willebrand factor (von Willebrand factor; VWF) for factor VIII (FVIII). Abnormal bleeding manifestations are much less frequent in this VWD subtype than in other forms of the disease. |
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CID11:ID_1091176565
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