A inherited blood coagulation disease characterized by enhanced binding of von Willebrand factor by the platelet glycoprotein Ib receptor complex that has material basis in mutation in the GP1BA gene on chromosome 17p13.2.
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description |
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exact match | |
exact match | |
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genetic association | |
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on focus list of Wikimedia project | |
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MeSH descriptor ID |
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on focus list of Wikimedia project | |
is about of | |
is genetic association of | |
is genetic association of |