Inherited coagulation factor deficiency without bleeding tendency (Q39583): Difference between revisions

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CID11:3B15
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Revision as of 05:03, 13 August 2026

A disease caused by a genetically inherited mutation leading to decreased levels of coagulation factor. This disease is characterised by decreased levels of coagulation factor without leading to increased haemorrhaging. Confirmation is by identification of decreased levels of coagulation factor in a blood sample.
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3B15
    English
    Inherited coagulation factor deficiency without bleeding tendency
    A disease caused by a genetically inherited mutation leading to decreased levels of coagulation factor. This disease is characterised by decreased levels of coagulation factor without leading to increased haemorrhaging. Confirmation is by identification of decreased levels of coagulation factor in a blood sample.

      Statements

      CID11:3B15
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