Hereditary factor VIII deficiency (Q39575): Difference between revisions

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Latest revision as of 05:03, 13 August 2026

A disease caused by a genetically inherited mutation leading to a deficiency in clotting due to lack of factor VIII. This disease is characterised by increasing haemorrhaging and bruising. Confirmation is by identification of mutations by genetic testing.

Language	Label	Description	Also known as
default for all languages	3B10
English	Hereditary factor VIII deficiency	A disease caused by a genetically inherited mutation leading to a deficiency in clotting due to lack of factor VIII. This disease is characterised by increasing haemorrhaging and bruising. Confirmation is by identification of mutations by genetic testing.