Von Willebrand disease type 1 (Q84138)
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Type 1 von Willebrand disease (type 1 VWD) is a form of VWD (see this term) characterised by a bleeding disorder associated with a partial quantitative plasmatic deficiency of an otherwise structurally and functionally normal Willebrand factor (von Willebrand factor; VWF). The type 1 disease is considered to be the most common form of VWD, accounting for between 50 and 75% of cases but its prevalence is probably overestimated. Age of onset of bleeding anomalies varies, with earlier onset and more severe symptoms being associated with more severe VWF deficiency.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1861858008 |
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| English | Von Willebrand disease type 1 |
Type 1 von Willebrand disease (type 1 VWD) is a form of VWD (see this term) characterised by a bleeding disorder associated with a partial quantitative plasmatic deficiency of an otherwise structurally and functionally normal Willebrand factor (von Willebrand factor; VWF). The type 1 disease is considered to be the most common form of VWD, accounting for between 50 and 75% of cases but its prevalence is probably overestimated. Age of onset of bleeding anomalies varies, with earlier onset and more severe symptoms being associated with more severe VWF deficiency. |
