Hereditary factor IX deficiency (Q39576): Difference between revisions

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+August 2026Timestamp +2026-08-13T00:00:00Z
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Latest revision as of 05:03, 13 August 2026

A disease caused by a genetically inherited X-linked recessive trait leading to a defective gene located on the X chromosome. This disease is characterised by low levels of the protein factor IX in the body leading to increased haemorrhaging and bruising due to clotting abnormalities. Confirmation is by identification of recessive trait by genetic testing.

Language	Label	Description	Also known as
default for all languages	3B11
English	Hereditary factor IX deficiency	A disease caused by a genetically inherited X-linked recessive trait leading to a defective gene located on the X chromosome. This disease is characterised by low levels of the protein factor IX in the body leading to increased haemorrhaging and bruising due to clotting abnormalities. Confirmation is by identification of recessive trait by genetic testing.