Von Willebrand disease type 2N (Q100619): Difference between revisions
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A doença de von Willebrand tipo 2N (DVW tipo 2N) é um subtipo de DVW tipo 2 caracterizada por um transtorno hemorrágico associado a uma redução acentuada da afinidade do fator de von Willebrand (FVW) pelo fator VIII (FVIII). Manifestações hemorrágiacas anormais são muito menos frequentes neste subtipo de DVW do que nas outras formas da doença. | |||||||||||||||
| description / en | description / en | ||||||||||||||
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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| Property / Canonical URI: https://id.who.int/icd/entity/1091176565 / rank | |||||||||||||||
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CID11:ID_1091176565 | |||||||||||||||
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dki-india-ID_1091176565 | |||||||||||||||
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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 17:21, 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 |
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| 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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dki-india-ID_1091176565
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Concluído
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15 August 2026
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