Von Willebrand disease type 2A (Q100601): Difference between revisions
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A doença de von Willebrand tipo 2A (DVW tipo 2A) é um subtipo de DVW tipo 2 caracterizada por um transtorno hemorrágico associado a uma redução da afinidade do fator de von Willebrand (FVW) pelas plaquetas e pelo subendotélio, causada por uma deficiência de multímeros de FVW de alto peso molecular. A doença manifesta-se anomalias do sangramento mucocutâneo (menorragia, epistaxe, hemorragia gastrointestinal, etc.). | |||||||||||||||
| description / en | description / en | ||||||||||||||
Type 2A von Willebrand disease (type 2A VWD) is a subtype of type 2 VWD characterised by a bleeding disorder associated with a decrease in the affinity of the Willebrand factor (von Willebrand factor; VWF) for platelets and the subendothelium caused by a deficiency of high molecular weight VWF multimers. The disease manifests as mucocutaneous bleeding anomalies (menorrhagia, epistaxis, gastrointestinal haemorrhage, etc.). | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1009291548 / rank | |||||||||||||||
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CID11:ID_1009291548 | |||||||||||||||
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dki-india-ID_1009291548 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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15 August 2026
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| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
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Latest revision as of 17:19, 16 August 2026
Type 2A von Willebrand disease (type 2A VWD) is a subtype of type 2 VWD characterised by a bleeding disorder associated with a decrease in the affinity of the Willebrand factor (von Willebrand factor; VWF) for platelets and the subendothelium caused by a deficiency of high molecular weight VWF multimers. The disease manifests as mucocutaneous bleeding anomalies (menorrhagia, epistaxis, gastrointestinal haemorrhage, etc.).
| Language | Label | Description | Also known as |
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| default for all languages | ID_1009291548 |
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| English | Von Willebrand disease type 2A |
Type 2A von Willebrand disease (type 2A VWD) is a subtype of type 2 VWD characterised by a bleeding disorder associated with a decrease in the affinity of the Willebrand factor (von Willebrand factor; VWF) for platelets and the subendothelium caused by a deficiency of high molecular weight VWF multimers. The disease manifests as mucocutaneous bleeding anomalies (menorrhagia, epistaxis, gastrointestinal haemorrhage, etc.). |
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CID11:ID_1009291548
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dki-india-ID_1009291548
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Concluído
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15 August 2026
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